-
2
-
-
84655161342
-
Novel mutation in GLRB in a large family with hereditary hyperekplexia
-
Al-Owain M., Colak D., Al-Bakheet A., Al-Hashmi N., Shuaib T., Al-Hemidan A., et al. Novel mutation in GLRB in a large family with hereditary hyperekplexia. Clin Genet 2011.
-
(2011)
Clin Genet
-
-
Al-Owain, M.1
Colak, D.2
Al-Bakheet, A.3
Al-Hashmi, N.4
Shuaib, T.5
Al-Hemidan, A.6
-
4
-
-
0019225609
-
Startle disease or hyperekplexia: further delineation of the syndrome
-
Andermann F., Keene D.L., Andermann E., Quesney L.F. Startle disease or hyperekplexia: further delineation of the syndrome. Brain 1980, 103:985-997.
-
(1980)
Brain
, vol.103
, pp. 985-997
-
-
Andermann, F.1
Keene, D.L.2
Andermann, E.3
Quesney, L.F.4
-
5
-
-
0020526971
-
Evidence for sensory-selective set in young infants
-
Anthony B.J., Graham F.K. Evidence for sensory-selective set in young infants. Science 1983, 220:742-744.
-
(1983)
Science
, vol.220
, pp. 742-744
-
-
Anthony, B.J.1
Graham, F.K.2
-
6
-
-
0028915733
-
Sympathetic skin response: a decade later
-
Arunodaya G.R., Taly A.B. Sympathetic skin response: a decade later. J Neurol Sci 1995, 129:81-89.
-
(1995)
J Neurol Sci
, vol.129
, pp. 81-89
-
-
Arunodaya, G.R.1
Taly, A.B.2
-
7
-
-
59149098653
-
Quantification of the auditory startle reflex in children
-
Bakker M.J., Boer F., van der Meer J.N., Koelman J.H., Boeree T., Bour L., et al. Quantification of the auditory startle reflex in children. Clin Neurophysiol 2009, 120:424-430.
-
(2009)
Clin Neurophysiol
, vol.120
, pp. 424-430
-
-
Bakker, M.J.1
Boer, F.2
van der Meer, J.N.3
Koelman, J.H.4
Boeree, T.5
Bour, L.6
-
8
-
-
70449990554
-
Clonazepam is an effective treatment for hyperekplexia due to a SLC6A5 (GlyT2) mutation
-
Bakker M.J., Peeters E.A., Tijssen M.A. Clonazepam is an effective treatment for hyperekplexia due to a SLC6A5 (GlyT2) mutation. Mov Disord 2009, 24:1852-1854.
-
(2009)
Mov Disord
, vol.24
, pp. 1852-1854
-
-
Bakker, M.J.1
Peeters, E.A.2
Tijssen, M.A.3
-
9
-
-
84655164853
-
Normalization of the auditory startle reflex after symptom reduction in children with anxiety disorders
-
Bakker M.J., Tijssen M.A., Koelman J.H., Boer F. Normalization of the auditory startle reflex after symptom reduction in children with anxiety disorders. J Psychiatr Res 2010.
-
(2010)
J Psychiatr Res
-
-
Bakker, M.J.1
Tijssen, M.A.2
Koelman, J.H.3
Boer, F.4
-
10
-
-
70149123005
-
Increased whole-body auditory startle reflex and autonomic reactivity in children with anxiety disorders
-
Bakker M.J., Tijssen M.A., van der Meer J.N., Koelman J.H., Boer F. Increased whole-body auditory startle reflex and autonomic reactivity in children with anxiety disorders. J Psychiatry Neurosci 2009, 34:314-322.
-
(2009)
J Psychiatry Neurosci
, vol.34
, pp. 314-322
-
-
Bakker, M.J.1
Tijssen, M.A.2
van der Meer, J.N.3
Koelman, J.H.4
Boer, F.5
-
11
-
-
33646502644
-
Startle syndromes
-
Bakker M.J., van Dijk J.G., van den Maagdenberg A.M., Tijssen M.A. Startle syndromes. Lancet Neurol 2006, 5:513-524.
-
(2006)
Lancet Neurol
, vol.5
, pp. 513-524
-
-
Bakker, M.J.1
van Dijk, J.G.2
van den Maagdenberg, A.M.3
Tijssen, M.A.4
-
12
-
-
0029240989
-
Affective influences on startle in five-month-old infants: reactions to facial expressions of emotions
-
Balaban M.T. Affective influences on startle in five-month-old infants: reactions to facial expressions of emotions. Child Dev 1995, 66:28-36.
-
(1995)
Child Dev
, vol.66
, pp. 28-36
-
-
Balaban, M.T.1
-
13
-
-
0028363338
-
Disease, disorder, or deception? Latah as habit in a Malay extended family
-
Bartholomew R.E. Disease, disorder, or deception? Latah as habit in a Malay extended family. J Nerv Ment Dis 1994, 182:331-338.
-
(1994)
J Nerv Ment Dis
, vol.182
, pp. 331-338
-
-
Bartholomew, R.E.1
-
14
-
-
0031828117
-
Spectroscopic imaging of frontal neuronal dysfunction in hyperekplexia
-
Bernasconi A., Cendes F., Shoubridge E.A., Andermann E., Li L.M., Arnold D.L., et al. Spectroscopic imaging of frontal neuronal dysfunction in hyperekplexia. Brain 1998, 121:1507-1512.
-
(1998)
Brain
, vol.121
, pp. 1507-1512
-
-
Bernasconi, A.1
Cendes, F.2
Shoubridge, E.A.3
Andermann, E.4
Li, L.M.5
Arnold, D.L.6
-
15
-
-
0030157847
-
Familial hyperekplexia: startle disease clinical, electrophysiological and genetic study of a family
-
Bernasconi A., Regli F., Schorderet D.F., Pescia G. Familial hyperekplexia: startle disease clinical, electrophysiological and genetic study of a family. Rev Neurol (Paris) 1996, 152:447-450.
-
(1996)
Rev Neurol (Paris)
, vol.152
, pp. 447-450
-
-
Bernasconi, A.1
Regli, F.2
Schorderet, D.F.3
Pescia, G.4
-
16
-
-
0032941645
-
The paroxysmal dyskinesias
-
Bhatia K.P. The paroxysmal dyskinesias. J Neurol 1999, 246:149-155.
-
(1999)
J Neurol
, vol.246
, pp. 149-155
-
-
Bhatia, K.P.1
-
17
-
-
0036359905
-
Neurophysiology of the startle syndrome and hyperekplexia
-
Brown P. Neurophysiology of the startle syndrome and hyperekplexia. Adv Neurol 2002, 89:153-159.
-
(2002)
Adv Neurol
, vol.89
, pp. 153-159
-
-
Brown, P.1
-
18
-
-
0025955618
-
The effect of posture on the normal and pathological auditory startle reflex
-
Brown P., Day B.L., Rothwell J.C., Thompson P.D., Marsden C.D. The effect of posture on the normal and pathological auditory startle reflex. J Neurol Neurosurg Psychiatry 1991, 54:892-897.
-
(1991)
J Neurol Neurosurg Psychiatry
, vol.54
, pp. 892-897
-
-
Brown, P.1
Day, B.L.2
Rothwell, J.C.3
Thompson, P.D.4
Marsden, C.D.5
-
19
-
-
0032843971
-
The stiff man and stiff man plus syndromes
-
Brown P., Marsden C.D. The stiff man and stiff man plus syndromes. J Neurol 1999, 246:648-652.
-
(1999)
J Neurol
, vol.246
, pp. 648-652
-
-
Brown, P.1
Marsden, C.D.2
-
20
-
-
0025788588
-
New observations on the normal auditory startle reflex in man
-
Brown P., Rothwell J.C., Thompson P.D., Britton T.C., Day B.L., Marsden C.D. New observations on the normal auditory startle reflex in man. Brain 1991, 114:1891-1902.
-
(1991)
Brain
, vol.114
, pp. 1891-1902
-
-
Brown, P.1
Rothwell, J.C.2
Thompson, P.D.3
Britton, T.C.4
Day, B.L.5
Marsden, C.D.6
-
21
-
-
0025900901
-
The hyperekplexias and their relationship to the normal startle reflex
-
Brown P., Rothwell J.C., Thompson P.D., Britton T.C., Day B.L., Marsden C.D. The hyperekplexias and their relationship to the normal startle reflex. Brain 1991, 114:1903-1928.
-
(1991)
Brain
, vol.114
, pp. 1903-1928
-
-
Brown, P.1
Rothwell, J.C.2
Thompson, P.D.3
Britton, T.C.4
Day, B.L.5
Marsden, C.D.6
-
22
-
-
0035412909
-
Electrophysiological aids to the diagnosis of psychogenic jerks, spasms, and tremor
-
Brown P., Thompson P.D. Electrophysiological aids to the diagnosis of psychogenic jerks, spasms, and tremor. Mov Disord 2001, 16:595-599.
-
(2001)
Mov Disord
, vol.16
, pp. 595-599
-
-
Brown, P.1
Thompson, P.D.2
-
23
-
-
0025897365
-
A case of postanoxic encephalopathy with cortical action and brainstem reticular reflex myoclonus
-
Brown P., Thompson P.D., Rothwell J.C., Day B.L., Marsden C.D. A case of postanoxic encephalopathy with cortical action and brainstem reticular reflex myoclonus. Mov Disord 1991, 6:139-144.
-
(1991)
Mov Disord
, vol.6
, pp. 139-144
-
-
Brown, P.1
Thompson, P.D.2
Rothwell, J.C.3
Day, B.L.4
Marsden, C.D.5
-
24
-
-
0029962877
-
A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors
-
Brune W., Weber R.G., Saul B., von Knebel D.M., Grond-Ginsbach C., Kellerman K., et al. A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors. Am J Hum Genet 1996, 58:989-997.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 989-997
-
-
Brune, W.1
Weber, R.G.2
Saul, B.3
von Knebel, D.M.4
Grond-Ginsbach, C.5
Kellerman, K.6
-
26
-
-
0033867246
-
Early fatal pontocerebellar hypoplasia in premature twin sisters
-
Chaves-Vischer V., Pizzolato G.P., Hanquinet S., Maret A., Bottani A., Haenggeli C.A. Early fatal pontocerebellar hypoplasia in premature twin sisters. Eur J Paediatr Neurol 2000, 4:171-176.
-
(2000)
Eur J Paediatr Neurol
, vol.4
, pp. 171-176
-
-
Chaves-Vischer, V.1
Pizzolato, G.P.2
Hanquinet, S.3
Maret, A.4
Bottani, A.5
Haenggeli, C.A.6
-
28
-
-
0032621044
-
Sympathetic skin response. The International Federation of Clinical Neurophysiology
-
Claus D., Schondorf R. Sympathetic skin response. The International Federation of Clinical Neurophysiology. Electroencephalogr Clin Neurophysiol Suppl 1999, 52:277-282.
-
(1999)
Electroencephalogr Clin Neurophysiol Suppl
, vol.52
, pp. 277-282
-
-
Claus, D.1
Schondorf, R.2
-
29
-
-
0026733490
-
Sensory phenomena associated with Gilles de la Tourette's syndrome
-
Cohen A.J., Leckman J.F. Sensory phenomena associated with Gilles de la Tourette's syndrome. J Clin Psychiatry 1992, 53:319-323.
-
(1992)
J Clin Psychiatry
, vol.53
, pp. 319-323
-
-
Cohen, A.J.1
Leckman, J.F.2
-
30
-
-
33644941595
-
Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 gene
-
Coto E., Armenta D., Espinosa R., Argente J., Castro M.G., Alvarez V. Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 gene. Mov Disord 2005, 20:1626-1629.
-
(2005)
Mov Disord
, vol.20
, pp. 1626-1629
-
-
Coto, E.1
Armenta, D.2
Espinosa, R.3
Argente, J.4
Castro, M.G.5
Alvarez, V.6
-
31
-
-
0035728365
-
Patients with the major and minor form of hyperekplexia differ with regards to disynaptic reciprocal inhibition between ankle flexor and extensor muscles
-
Crone C., Nielsen J., Petersen N., Tijssen M.A., van Dijk J.G. Patients with the major and minor form of hyperekplexia differ with regards to disynaptic reciprocal inhibition between ankle flexor and extensor muscles. Exp Brain Res 2001, 140:190-197.
-
(2001)
Exp Brain Res
, vol.140
, pp. 190-197
-
-
Crone, C.1
Nielsen, J.2
Petersen, N.3
Tijssen, M.A.4
van Dijk, J.G.5
-
32
-
-
84873454709
-
The glycinergic system in human startle disease: a genetic screening approach
-
Davies J.S., Chung S.K., Thomas R.H., Robinson A., Hammond C.L., Mullins J.G., et al. The glycinergic system in human startle disease: a genetic screening approach. Front Mol Neurosci 2010, 3:8.
-
(2010)
Front Mol Neurosci
, vol.3
, pp. 8
-
-
Davies, J.S.1
Chung, S.K.2
Thomas, R.H.3
Robinson, A.4
Hammond, C.L.5
Mullins, J.G.6
-
34
-
-
0019957992
-
A primary acoustic startle circuit: lesion and stimulation studies
-
Davis M., Gendelman D.S., Tischler M.D., Gendelman P.M. A primary acoustic startle circuit: lesion and stimulation studies. J Neurosci 1982, 2:791-805.
-
(1982)
J Neurosci
, vol.2
, pp. 791-805
-
-
Davis, M.1
Gendelman, D.S.2
Tischler, M.D.3
Gendelman, P.M.4
-
35
-
-
84655167045
-
The muscular tension reflex and two of its modifying conditions
-
Davis R. The muscular tension reflex and two of its modifying conditions. Science series 1935, 3:21.
-
(1935)
Science series
, vol.3
, pp. 21
-
-
Davis, R.1
-
36
-
-
0007514950
-
Motor effects of strong auditory stimuli
-
Davis R. Motor effects of strong auditory stimuli. J Exp Psychol 1948, 38:257-275.
-
(1948)
J Exp Psychol
, vol.38
, pp. 257-275
-
-
Davis, R.1
-
37
-
-
0035666557
-
A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia
-
del Giudice E.M., Coppola G., Bellini G., Cirillo G., Scuccimarra G., Pascotto A. A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia. Eur J Hum Genet 2001, 9:873-876.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 873-876
-
-
del Giudice, E.M.1
Coppola, G.2
Bellini, G.3
Cirillo, G.4
Scuccimarra, G.5
Pascotto, A.6
-
38
-
-
0024583109
-
Startle disease or hyperekplexia: adolescent onset and response to valproate
-
Dooley J.M., Andermann F. Startle disease or hyperekplexia: adolescent onset and response to valproate. Pediatr Neurol 1989, 5:126-127.
-
(1989)
Pediatr Neurol
, vol.5
, pp. 126-127
-
-
Dooley, J.M.1
Andermann, F.2
-
39
-
-
34447116860
-
A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam
-
Doria L.L., Giribaldi G., De N.E., Follo R., De G.E., Pintaudi M., et al. A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam. J Child Neurol 2007, 22:769-772.
-
(2007)
J Child Neurol
, vol.22
, pp. 769-772
-
-
Doria, L.L.1
Giribaldi, G.2
De, N.E.3
Follo, R.4
De, G.E.5
Pintaudi, M.6
-
40
-
-
0008330701
-
Schreckreflex und schreckreaktion als hirnorganische zeichen
-
Duensing F. Schreckreflex und schreckreaktion als hirnorganische zeichen. Arch Psychiatr Nervenkr 1952, 188:162-192.
-
(1952)
Arch Psychiatr Nervenkr
, vol.188
, pp. 162-192
-
-
Duensing, F.1
-
41
-
-
0005079207
-
Ein Mensch ohne Grosshirn
-
Edinger, Fischer Ein Mensch ohne Grosshirn. Arch f d ges Physiol 1913, 152:535-562.
-
(1913)
Arch f d ges Physiol
, vol.152
, pp. 535-562
-
-
Edinger, F.1
-
42
-
-
0020692623
-
Hyperekplexia exacerbated by occlusion of posterior thalamic arteries
-
Fariello R.G., Schwartzman R.J., Beall S.S. Hyperekplexia exacerbated by occlusion of posterior thalamic arteries. Arch Neurol 1983, 40:244-246.
-
(1983)
Arch Neurol
, vol.40
, pp. 244-246
-
-
Fariello, R.G.1
Schwartzman, R.J.2
Beall, S.S.3
-
43
-
-
34748907434
-
A novel GLRA1 mutation in a recessive hyperekplexia pedigree
-
Forsyth R.J., Gika A.D., Ginjaar I., Tijssen M.A. A novel GLRA1 mutation in a recessive hyperekplexia pedigree. Mov Disord 2007, 22:1643-1645.
-
(2007)
Mov Disord
, vol.22
, pp. 1643-1645
-
-
Forsyth, R.J.1
Gika, A.D.2
Ginjaar, I.3
Tijssen, M.A.4
-
44
-
-
0019564238
-
Committee report. Publication recommendations for electrodermal measurements
-
Fowles D.C., Christie M.J., Edelberg R., Grings W.W., Lykken D.T., Venables P.H. Committee report. Publication recommendations for electrodermal measurements. Psychophysiology 1981, 18:232-239.
-
(1981)
Psychophysiology
, vol.18
, pp. 232-239
-
-
Fowles, D.C.1
Christie, M.J.2
Edelberg, R.3
Grings, W.W.4
Lykken, D.T.5
Venables, P.H.6
-
45
-
-
0017813348
-
Excitatory and inhibitory components of the eyeblink responses to startle evoking stimuli, studied in the human subject
-
Fox J.E. Excitatory and inhibitory components of the eyeblink responses to startle evoking stimuli, studied in the human subject. Electroencephalogr Clin Neurophysiol 1977, 44:490-501.
-
(1977)
Electroencephalogr Clin Neurophysiol
, vol.44
, pp. 490-501
-
-
Fox, J.E.1
-
46
-
-
1142285239
-
Frontal lobe dysfunction in sporadic hyperekplexia-case study and literature review
-
Gaitazis A., Karsounis L.D., Gacinovic S., Costa D.C., Harvey K., Harvey R.J., et al. Frontal lobe dysfunction in sporadic hyperekplexia-case study and literature review. J Neurol 2004, 251:91-98.
-
(2004)
J Neurol
, vol.251
, pp. 91-98
-
-
Gaitazis, A.1
Karsounis, L.D.2
Gacinovic, S.3
Costa, D.C.4
Harvey, K.5
Harvey, R.J.6
-
47
-
-
0014151623
-
The startle disease or hyperekplexia. Pathological surprise reaction
-
Gastaut H., Villeneuve A. The startle disease or hyperekplexia. Pathological surprise reaction. J Neurol Sci 1967, 5:523-542.
-
(1967)
J Neurol Sci
, vol.5
, pp. 523-542
-
-
Gastaut, H.1
Villeneuve, A.2
-
48
-
-
0342656586
-
Abnormalities of the acoustic startle reflex and reaction time in gilles de la tourette syndrome
-
Gironell A., Rodriguez-Fornells A., Kulisevsky J., Pascual B., Riba J., Barbanoj M., et al. Abnormalities of the acoustic startle reflex and reaction time in gilles de la tourette syndrome. Clin Neurophysiol 2000, 111:1366-1371.
-
(2000)
Clin Neurophysiol
, vol.111
, pp. 1366-1371
-
-
Gironell, A.1
Rodriguez-Fornells, A.2
Kulisevsky, J.3
Pascual, B.4
Riba, J.5
Barbanoj, M.6
-
49
-
-
0014952522
-
The startle and orienting reactions in man. A study of their characteristics and habituation
-
Gogan P. The startle and orienting reactions in man. A study of their characteristics and habituation. Brain Res 1970, 18:117-135.
-
(1970)
Brain Res
, vol.18
, pp. 117-135
-
-
Gogan, P.1
-
50
-
-
0036257442
-
Hyperekplexia in a girl with posterior fossa malformations
-
Goraya J.S., Shah D., Poddar B. Hyperekplexia in a girl with posterior fossa malformations. J Child Neurol 2002, 17:147-149.
-
(2002)
J Child Neurol
, vol.17
, pp. 147-149
-
-
Goraya, J.S.1
Shah, D.2
Poddar, B.3
-
52
-
-
0021962790
-
Atypical presentations of pyridoxine-dependent seizures: a treatable cause of intractable epilepsy in infants
-
Goutieres F., Aicardi J. Atypical presentations of pyridoxine-dependent seizures: a treatable cause of intractable epilepsy in infants. Ann Neurol 1985, 17:117-120.
-
(1985)
Ann Neurol
, vol.17
, pp. 117-120
-
-
Goutieres, F.1
Aicardi, J.2
-
53
-
-
57749200449
-
A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype
-
Gregory M.L., Guzauskas G.F., Edgar T.S., Clarkson K.B., Srivastava A.K., Holden K.R. A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. J Child Neurol 2008, 23:1433-1438.
-
(2008)
J Child Neurol
, vol.23
, pp. 1433-1438
-
-
Gregory, M.L.1
Guzauskas, G.F.2
Edgar, T.S.3
Clarkson, K.B.4
Srivastava, A.K.5
Holden, K.R.6
-
54
-
-
0028196695
-
Baseline and fear-potentiated startle in panic disorder patients
-
Grillon C., Ameli R., Goddard A., Woods S.W., Davis M. Baseline and fear-potentiated startle in panic disorder patients. Biol Psychiatry 1994, 35:431-439.
-
(1994)
Biol Psychiatry
, vol.35
, pp. 431-439
-
-
Grillon, C.1
Ameli, R.2
Goddard, A.3
Woods, S.W.4
Davis, M.5
-
55
-
-
0042426146
-
A review of the modulation of the startle reflex by affective states and its application in psychiatry
-
Grillon C., Baas J. A review of the modulation of the startle reflex by affective states and its application in psychiatry. Clin Neurophysiol 2003, 114:1557-1579.
-
(2003)
Clin Neurophysiol
, vol.114
, pp. 1557-1579
-
-
Grillon, C.1
Baas, J.2
-
57
-
-
0017413125
-
Reticular reflex myoclonus: a physiological type of human post-hypoxic myoclonus
-
Hallett M., Chadwick D., Adam J., Marsden C.D. Reticular reflex myoclonus: a physiological type of human post-hypoxic myoclonus. J Neurol Neurosurg Psychiatry 1977, 40:253-264.
-
(1977)
J Neurol Neurosurg Psychiatry
, vol.40
, pp. 253-264
-
-
Hallett, M.1
Chadwick, D.2
Adam, J.3
Marsden, C.D.4
-
59
-
-
7944236819
-
Late onset hyperekplexia
-
Hamelin S., Rohr P., Kahane P., Minotti L., Vercueil L. Late onset hyperekplexia. Epileptic Disord 2004, 6:169-172.
-
(2004)
Epileptic Disord
, vol.6
, pp. 169-172
-
-
Hamelin, S.1
Rohr, P.2
Kahane, P.3
Minotti, L.4
Vercueil, L.5
-
60
-
-
49849098981
-
-
Harvey R.J., Topf M., Harvey K., Rees M.I. The genetics of hyperekplexia: more than startle! Trends Genet 2008, 24:439-447.
-
(2008)
The genetics of hyperekplexia: more than startle! Trends Genet
, vol.24
, pp. 439-447
-
-
Harvey, R.J.1
Topf, M.2
Harvey, K.3
Rees, M.I.4
-
61
-
-
0025781128
-
Hyperekplexia: pedigree studies in two families
-
Hayashi T., Tachibana H., Kajii T. Hyperekplexia: pedigree studies in two families. Am J Med Genet 1991, 40:138-143.
-
(1991)
Am J Med Genet
, vol.40
, pp. 138-143
-
-
Hayashi, T.1
Tachibana, H.2
Kajii, T.3
-
62
-
-
0026043048
-
Efferent pathway of the amygdala involved in conditioned fear as measured with the fear-potentiated startle paradigm
-
Hitchcock J.M., Davis M. Efferent pathway of the amygdala involved in conditioned fear as measured with the fear-potentiated startle paradigm. Behav Neurosci 1991, 105:826-842.
-
(1991)
Behav Neurosci
, vol.105
, pp. 826-842
-
-
Hitchcock, J.M.1
Davis, M.2
-
63
-
-
0023273724
-
Neurologic, audiologic, and electrophysiologic sequelae of bilateral temporal lobe lesions
-
Ho K.J., Kileny P., Paccioretti D., McLean D.R. Neurologic, audiologic, and electrophysiologic sequelae of bilateral temporal lobe lesions. Arch Neurol 1987, 44:982-987.
-
(1987)
Arch Neurol
, vol.44
, pp. 982-987
-
-
Ho, K.J.1
Kileny, P.2
Paccioretti, D.3
McLean, D.R.4
-
64
-
-
0022508188
-
Blink reflex elicited by auditory stimulation in the rabbit
-
Hori A., Yasuhara A., Naito H., Yasuhara M. Blink reflex elicited by auditory stimulation in the rabbit. J Neurol Sci 1986, 76:49-59.
-
(1986)
J Neurol Sci
, vol.76
, pp. 49-59
-
-
Hori, A.1
Yasuhara, A.2
Naito, H.3
Yasuhara, M.4
-
65
-
-
0026660291
-
From the jumping Frenchmen of Maine to post-traumatic stress disorder: the startle response in neuropsychiatry
-
Howard R., Ford R. From the jumping Frenchmen of Maine to post-traumatic stress disorder: the startle response in neuropsychiatry. Psychol Med 1992, 22:695-707.
-
(1992)
Psychol Med
, vol.22
, pp. 695-707
-
-
Howard, R.1
Ford, R.2
-
66
-
-
85047700016
-
A novel recessive hyperekplexia allele GLRA1 (S231R): genotyping by MALDI-TOF mass spectrometry and functional characterisation as a determinant of cellular glycine receptor trafficking
-
Humeny A., Bonk T., Becker K., Jafari-Boroujerdi M., Stephani U., Reuter K., et al. A novel recessive hyperekplexia allele GLRA1 (S231R): genotyping by MALDI-TOF mass spectrometry and functional characterisation as a determinant of cellular glycine receptor trafficking. Eur J Hum Genet 2002, 10:188-196.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 188-196
-
-
Humeny, A.1
Bonk, T.2
Becker, K.3
Jafari-Boroujerdi, M.4
Stephani, U.5
Reuter, K.6
-
67
-
-
0343448192
-
Response to a sudden unexpected stimulus
-
Jacobsen E. Response to a sudden unexpected stimulus. J Exp Psychol 1926, 9:19-25.
-
(1926)
J Exp Psychol
, vol.9
, pp. 19-25
-
-
Jacobsen, E.1
-
68
-
-
0347092038
-
The acoustic startle reflex in ischemic stroke
-
Jankelowitz S.K., Colebatch J.G. The acoustic startle reflex in ischemic stroke. Neurology 2004, 62:114-116.
-
(2004)
Neurology
, vol.62
, pp. 114-116
-
-
Jankelowitz, S.K.1
Colebatch, J.G.2
-
69
-
-
4344605185
-
An electromyographic technique for recording the startle pattern
-
Jones F.P., Kennedy J.L. An electromyographic technique for recording the startle pattern. J Psychol 1951, 32:63-68.
-
(1951)
J Psychol
, vol.32
, pp. 63-68
-
-
Jones, F.P.1
Kennedy, J.L.2
-
70
-
-
0031840419
-
Hyperekplexia and trismus due to brainstem encephalopathy
-
Kellett M.W., Humphrey P.R., Tedman B.M., Steiger M.J. Hyperekplexia and trismus due to brainstem encephalopathy. J Neurol Neurosurg Psychiatry 1998, 65:122-125.
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.65
, pp. 122-125
-
-
Kellett, M.W.1
Humphrey, P.R.2
Tedman, B.M.3
Steiger, M.J.4
-
71
-
-
4344563108
-
Hyperekplexia and stiff-man syndrome: abnormal brainstem reflexes suggest a physiological relationship
-
Khasani S., Becker K., Meinck H.M. Hyperekplexia and stiff-man syndrome: abnormal brainstem reflexes suggest a physiological relationship. J Neurol Neurosurg Psychiatry 2004, 75:1265-1269.
-
(2004)
J Neurol Neurosurg Psychiatry
, vol.75
, pp. 1265-1269
-
-
Khasani, S.1
Becker, K.2
Meinck, H.M.3
-
73
-
-
0032880711
-
The neurobiology of startle
-
Koch M. The neurobiology of startle. Prog Neurobiol 1999, 59:107-128.
-
(1999)
Prog Neurobiol
, vol.59
, pp. 107-128
-
-
Koch, M.1
-
74
-
-
0035854614
-
Influence of age on auditory startle responses in humans
-
Kofler M., Muller J., Reggiani L., Valls-Sole J. Influence of age on auditory startle responses in humans. Neurosci Lett 2001, 307:65-68.
-
(2001)
Neurosci Lett
, vol.307
, pp. 65-68
-
-
Kofler, M.1
Muller, J.2
Reggiani, L.3
Valls-Sole, J.4
-
75
-
-
0035824290
-
Influence of gender on auditory startle responses
-
Kofler M., Muller J., Reggiani L., Valls-Sole J. Influence of gender on auditory startle responses. Brain Res 2001, 921:206-210.
-
(2001)
Brain Res
, vol.921
, pp. 206-210
-
-
Kofler, M.1
Muller, J.2
Reggiani, L.3
Valls-Sole, J.4
-
76
-
-
0037687971
-
Exaggerated auditory startle responses in multiple system atrophy: a comparative study of parkinson and cerebellar subtypes
-
Kofler M., Muller J., Seppi K., Wenning G.K. Exaggerated auditory startle responses in multiple system atrophy: a comparative study of parkinson and cerebellar subtypes. Clin Neurophysiol 2003, 114:541-547.
-
(2003)
Clin Neurophysiol
, vol.114
, pp. 541-547
-
-
Kofler, M.1
Muller, J.2
Seppi, K.3
Wenning, G.K.4
-
77
-
-
0033709567
-
Hyperekplexia in the first year of life
-
Koning-Tijssen M.A., Brouwer O.F. Hyperekplexia in the first year of life. Mov Disord 2000, 15:1293-1296.
-
(2000)
Mov Disord
, vol.15
, pp. 1293-1296
-
-
Koning-Tijssen, M.A.1
Brouwer, O.F.2
-
78
-
-
0029838455
-
Non-obscene complex socially inappropriate behavior in Tourette's syndrome
-
Kurlan R., Daragjati C., Como P.G., McDermott M.P., Trinidad K.S., Roddy S., et al. Non-obscene complex socially inappropriate behavior in Tourette's syndrome. J Neuropsychiatry Clin Neurosci 1996, 8:311-317.
-
(1996)
J Neuropsychiatry Clin Neurosci
, vol.8
, pp. 311-317
-
-
Kurlan, R.1
Daragjati, C.2
Como, P.G.3
McDermott, M.P.4
Trinidad, K.S.5
Roddy, S.6
-
79
-
-
0035378693
-
Mutations in the glycine receptor alpha1 subunit (GLRA1) gene in hereditary hyperekplexia pedigrees: evidence for non-penetrance of mutation Y279C
-
Kwok J.B., Raskin S., Morgan G., Antoniuk S.A., Bruk I., Schofield P.R. Mutations in the glycine receptor alpha1 subunit (GLRA1) gene in hereditary hyperekplexia pedigrees: evidence for non-penetrance of mutation Y279C. J Med Genet 2001, 38:E17.
-
(2001)
J Med Genet
, vol.38
-
-
Kwok, J.B.1
Raskin, S.2
Morgan, G.3
Antoniuk, S.A.4
Bruk, I.5
Schofield, P.R.6
-
80
-
-
0034237481
-
Effects of startle and laughter in cataplectic subjects: a neurophysiological study between attacks
-
Lammers G.J., Overeem S., Tijssen M.A., van Dijk J.G. Effects of startle and laughter in cataplectic subjects: a neurophysiological study between attacks. Clin Neurophysiol 2000, 111:1276-1281.
-
(2000)
Clin Neurophysiol
, vol.111
, pp. 1276-1281
-
-
Lammers, G.J.1
Overeem, S.2
Tijssen, M.A.3
van Dijk, J.G.4
-
82
-
-
0025455754
-
Emotion, attention, and the startle reflex
-
Lang P.J., Bradley M.M., Cuthbert B.N. Emotion, attention, and the startle reflex. Psychol Rev 1990, 97:377-395.
-
(1990)
Psychol Rev
, vol.97
, pp. 377-395
-
-
Lang, P.J.1
Bradley, M.M.2
Cuthbert, B.N.3
-
83
-
-
0029983622
-
A primary acoustic startle pathway: obligatory role of cochlear root neurons and the nucleus reticularis pontis caudalis
-
Lee Y., Lopez D.E., Meloni E.G., Davis M. A primary acoustic startle pathway: obligatory role of cochlear root neurons and the nucleus reticularis pontis caudalis. J Neurosci 1996, 16:3775-3789.
-
(1996)
J Neurosci
, vol.16
, pp. 3775-3789
-
-
Lee, Y.1
Lopez, D.E.2
Meloni, E.G.3
Davis, M.4
-
84
-
-
0019201234
-
A patient with reflex myoclonus and muscle rigidity: " jerking stiff-man syndrome"
-
Leigh P.N., Rothwell J.C., Traub M., Marsden C.D. A patient with reflex myoclonus and muscle rigidity: " jerking stiff-man syndrome" J Neurol Neurosurg Psychiatry 1980, 43:1125-1131.
-
(1980)
J Neurol Neurosurg Psychiatry
, vol.43
, pp. 1125-1131
-
-
Leigh, P.N.1
Rothwell, J.C.2
Traub, M.3
Marsden, C.D.4
-
86
-
-
0024510219
-
Evidence for a contribution of the auditory cortex to audiospinal facilitation in man
-
Liegeois-Chauvel C., Morin C., Musolino A., Bancaud J., Chauvel P. Evidence for a contribution of the auditory cortex to audiospinal facilitation in man. Brain 1989, 112:375-391.
-
(1989)
Brain
, vol.112
, pp. 375-391
-
-
Liegeois-Chauvel, C.1
Morin, C.2
Musolino, A.3
Bancaud, J.4
Chauvel, P.5
-
87
-
-
0028324413
-
Giant neurons in the rat reticular formation: a sensorimotor interface in the elementary acoustic startle circuit?
-
Lingenhohl K., Friauf E. Giant neurons in the rat reticular formation: a sensorimotor interface in the elementary acoustic startle circuit?. J Neurosci 1994, 14:1176-1194.
-
(1994)
J Neurosci
, vol.14
, pp. 1176-1194
-
-
Lingenhohl, K.1
Friauf, E.2
-
88
-
-
22644438619
-
Baseline and modulated acoustic startle responses in adolescent girls with posttraumatic stress disorder
-
Lipschitz D.S., Mayes L.M., Rasmusson A.M., Anyan W., Billingslea E., Gueorguieva R., et al. Baseline and modulated acoustic startle responses in adolescent girls with posttraumatic stress disorder. J Am Acad Child Adolesc Psychiatry 2005, 44:807-814.
-
(2005)
J Am Acad Child Adolesc Psychiatry
, vol.44
, pp. 807-814
-
-
Lipschitz, D.S.1
Mayes, L.M.2
Rasmusson, A.M.3
Anyan, W.4
Billingslea, E.5
Gueorguieva, R.6
-
90
-
-
0015342462
-
Range correction applied to heart rate and to GSR data
-
Lykken D.T. Range correction applied to heart rate and to GSR data. Psychophysiology 1972, 9:373-379.
-
(1972)
Psychophysiology
, vol.9
, pp. 373-379
-
-
Lykken, D.T.1
-
91
-
-
0013985598
-
Correcting psychophysiological measures for individual differences in range
-
Lykken D.T., Rose R., Luther B., Maley M. Correcting psychophysiological measures for individual differences in range. Psychol Bull 1966, 66:481-484.
-
(1966)
Psychol Bull
, vol.66
, pp. 481-484
-
-
Lykken, D.T.1
Rose, R.2
Luther, B.3
Maley, M.4
-
93
-
-
0021357407
-
Familial startle disease (hyperexplexia). Electrophysiologic studies
-
Markand O.N., Garg B.P., Weaver D.D. Familial startle disease (hyperexplexia). Electrophysiologic studies. Arch Neurol 1984, 41:71-74.
-
(1984)
Arch Neurol
, vol.41
, pp. 71-74
-
-
Markand, O.N.1
Garg, B.P.2
Weaver, D.D.3
-
94
-
-
34547855884
-
Clinical and inheritance profiles of hyperekplexia in Jordan
-
Masri A.T., Hamamy H.A. Clinical and inheritance profiles of hyperekplexia in Jordan. J Child Neurol 2007, 22:895-900.
-
(2007)
J Child Neurol
, vol.22
, pp. 895-900
-
-
Masri, A.T.1
Hamamy, H.A.2
-
95
-
-
0026758875
-
Physiological abnormalities in hereditary hyperekplexia
-
Matsumoto J., Fuhr P., Nigro M., Hallett M. Physiological abnormalities in hereditary hyperekplexia. Ann Neurol 1992, 32:41-50.
-
(1992)
Ann Neurol
, vol.32
, pp. 41-50
-
-
Matsumoto, J.1
Fuhr, P.2
Nigro, M.3
Hallett, M.4
-
96
-
-
0027943248
-
The acoustic startle reflex in stiff-man syndrome
-
Matsumoto J.Y., Caviness J.N., McEvoy K.M. The acoustic startle reflex in stiff-man syndrome. Neurology 1994, 44:1952-1955.
-
(1994)
Neurology
, vol.44
, pp. 1952-1955
-
-
Matsumoto, J.Y.1
Caviness, J.N.2
McEvoy, K.M.3
-
98
-
-
77649092419
-
An FMRI study of frontostriatal circuits during the inhibition of eye blinking in persons with Tourette syndrome
-
Mazzone L., Yu S., Blair C., Gunter B.C., Wang Z., Marsh R., et al. An FMRI study of frontostriatal circuits during the inhibition of eye blinking in persons with Tourette syndrome. Am J Psychiatry 2010, 167:341-349.
-
(2010)
Am J Psychiatry
, vol.167
, pp. 341-349
-
-
Mazzone, L.1
Yu, S.2
Blair, C.3
Gunter, B.C.4
Wang, Z.5
Marsh, R.6
-
99
-
-
0030023318
-
A novel mutation (Gln266-His) in the alpha 1 subunit of the inhibitory glycine-receptor gene (GLRA1) in hereditary hyperekplexia
-
Milani N., Dalpra L., del P.A., Zanini R., Larizza L. A novel mutation (Gln266-His) in the alpha 1 subunit of the inhibitory glycine-receptor gene (GLRA1) in hereditary hyperekplexia. Am J Hum Genet 1996, 58:420-422.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 420-422
-
-
Milani, N.1
Dalpra, L.2
del, P.A.3
Zanini, R.4
Larizza, L.5
-
100
-
-
16344378367
-
A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia
-
Miraglia del G.E., Coppola G., Bellini G., Ledaal P., Hertz J.M., Pascotto A. A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia. J Med Genet 2003, 40:e71.
-
(2003)
J Med Genet
, vol.40
-
-
Miraglia del, G.E.1
Coppola, G.2
Bellini, G.3
Ledaal, P.4
Hertz, J.M.5
Pascotto, A.6
-
101
-
-
0019980517
-
Hyperexplexia: an inherited disorder of the startle response
-
Morley D.J., Weaver D.D., Garg B.P., Markand O. Hyperexplexia: an inherited disorder of the startle response. Clin Genet 1982, 21:388-396.
-
(1982)
Clin Genet
, vol.21
, pp. 388-396
-
-
Morley, D.J.1
Weaver, D.D.2
Garg, B.P.3
Markand, O.4
-
102
-
-
0034978708
-
Different responses to auditory and somaesthetic stimulation in patients with an excessive startle: a report of pediatric experience
-
Oguro K., Aiba H., Hojo H. Different responses to auditory and somaesthetic stimulation in patients with an excessive startle: a report of pediatric experience. Clin Neurophysiol 2001, 112:1266-1272.
-
(2001)
Clin Neurophysiol
, vol.112
, pp. 1266-1272
-
-
Oguro, K.1
Aiba, H.2
Hojo, H.3
-
103
-
-
20344399664
-
Trigeminally induced startle in children with hyperekplexia
-
Oguro K., Hirano K., Aiba H. Trigeminally induced startle in children with hyperekplexia. Mov Disord 2005, 20:484-489.
-
(2005)
Mov Disord
, vol.20
, pp. 484-489
-
-
Oguro, K.1
Hirano, K.2
Aiba, H.3
-
104
-
-
0022907537
-
Maturation of startle modulation
-
Ornitz E.M., Guthrie D., Kaplan A.R., Lane S.J., Norman R.J. Maturation of startle modulation. Psychophysiology 1986, 23:624-634.
-
(1986)
Psychophysiology
, vol.23
, pp. 624-634
-
-
Ornitz, E.M.1
Guthrie, D.2
Kaplan, A.R.3
Lane, S.J.4
Norman, R.J.5
-
106
-
-
0026795017
-
Neonatal hyperekplexia: a case report
-
Pascotto A., Coppola G. Neonatal hyperekplexia: a case report. Epilepsia 1992, 33:817-820.
-
(1992)
Epilepsia
, vol.33
, pp. 817-820
-
-
Pascotto, A.1
Coppola, G.2
-
108
-
-
0028580443
-
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor
-
Rees M.I., Andrew M., Jawad S., Owen M.J. Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor. Hum Mol Genet 1994, 3:2175-2179.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2175-2179
-
-
Rees, M.I.1
Andrew, M.2
Jawad, S.3
Owen, M.J.4
-
109
-
-
33745552512
-
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease
-
Rees M.I., Harvey K., Pearce B.R., Chung S.K., Duguid I.C., Thomas P., et al. Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nat Genet 2006, 38:801-806.
-
(2006)
Nat Genet
, vol.38
, pp. 801-806
-
-
Rees, M.I.1
Harvey, K.2
Pearce, B.R.3
Chung, S.K.4
Duguid, I.C.5
Thomas, P.6
-
110
-
-
0036538280
-
Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)
-
Rees M.I., Lewis T.M., Kwok J.B., Mortier G.R., Govaert P., Snell R.G., et al. Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB). Hum Mol Genet 2002, 11:853-860.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 853-860
-
-
Rees, M.I.1
Lewis, T.M.2
Kwok, J.B.3
Mortier, G.R.4
Govaert, P.5
Snell, R.G.6
-
111
-
-
0034804087
-
Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia
-
Rees M.I., Lewis T.M., Vafa B., Ferrie C., Corry P., Muntoni F., et al. Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia. Hum Genet 2001, 109:267-270.
-
(2001)
Hum Genet
, vol.109
, pp. 267-270
-
-
Rees, M.I.1
Lewis, T.M.2
Vafa, B.3
Ferrie, C.4
Corry, P.5
Muntoni, F.6
-
112
-
-
29744448760
-
Congenital hyperekplexia: five sporadic cases
-
Rivera S., Villega F., de Saint-Martin A., Matis J., Escande B., Chaigne D., et al. Congenital hyperekplexia: five sporadic cases. Eur J Pediatr 2006, 165:104-107.
-
(2006)
Eur J Pediatr
, vol.165
, pp. 104-107
-
-
Rivera, S.1
Villega, F.2
de Saint-Martin, A.3
Matis, J.4
Escande, B.5
Chaigne, D.6
-
113
-
-
0028316166
-
Annotation: Gilles de la Tourette syndrome-an update
-
Robertson M.M. Annotation: Gilles de la Tourette syndrome-an update. J Child Psychol Psychiatry 1994, 35:597-611.
-
(1994)
J Child Psychol Psychiatry
, vol.35
, pp. 597-611
-
-
Robertson, M.M.1
-
114
-
-
0033983916
-
Tourette syndrome, associated conditions and the complexities of treatment
-
Robertson M.M. Tourette syndrome, associated conditions and the complexities of treatment. Brain 2000, 123:425-462.
-
(2000)
Brain
, vol.123
, pp. 425-462
-
-
Robertson, M.M.1
-
116
-
-
0025142537
-
Differences in heart rate and blood pressure in children with conduct disorder, major depression, and separation anxiety
-
Rogeness G.A., Cepeda C., Macedo C.A., Fischer C., Harris W.R. Differences in heart rate and blood pressure in children with conduct disorder, major depression, and separation anxiety. Psychiatry Res 1990, 33:199-206.
-
(1990)
Psychiatry Res
, vol.33
, pp. 199-206
-
-
Rogeness, G.A.1
Cepeda, C.2
Macedo, C.A.3
Fischer, C.4
Harris, W.R.5
-
117
-
-
0016695404
-
Startle responses recorded in the leg of man
-
Rossignol S. Startle responses recorded in the leg of man. Electroencephalogr Clin Neurophysiol 1975, 39:389-397.
-
(1975)
Electroencephalogr Clin Neurophysiol
, vol.39
, pp. 389-397
-
-
Rossignol, S.1
-
118
-
-
0037065768
-
Symptomatic hyperekplexia in a patient with multiple sclerosis
-
Ruprecht K., Warmuth-Metz M., Waespe W., Gold R. Symptomatic hyperekplexia in a patient with multiple sclerosis. Neurology 2002, 58:503-504.
-
(2002)
Neurology
, vol.58
, pp. 503-504
-
-
Ruprecht, K.1
Warmuth-Metz, M.2
Waespe, W.3
Gold, R.4
-
119
-
-
0026651547
-
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis
-
Ryan S.G., Sherman S.L., Terry J.C., Sparkes R.S., Torres M.C., Mackey R.W. Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis. Ann Neurol 1992, 31:663-668.
-
(1992)
Ann Neurol
, vol.31
, pp. 663-668
-
-
Ryan, S.G.1
Sherman, S.L.2
Terry, J.C.3
Sparkes, R.S.4
Torres, M.C.5
Mackey, R.W.6
-
120
-
-
0030964891
-
The audiogenic startle reflex in Tourette's syndrome
-
Sachdev P.S., Chee K.Y., Aniss A.M. The audiogenic startle reflex in Tourette's syndrome. Biol Psychiatry 1997, 41:796-803.
-
(1997)
Biol Psychiatry
, vol.41
, pp. 796-803
-
-
Sachdev, P.S.1
Chee, K.Y.2
Aniss, A.M.3
-
122
-
-
0021350671
-
Hyperekplexia: a syndrome of pathological startle responses
-
Saenz-Lope E., Herranz-Tanarro F.J., Masdeu J.C., Chacon Pena J.R. Hyperekplexia: a syndrome of pathological startle responses. Ann Neurol 1984, 15:36-41.
-
(1984)
Ann Neurol
, vol.15
, pp. 36-41
-
-
Saenz-Lope, E.1
Herranz-Tanarro, F.J.2
Masdeu, J.C.3
Chacon Pena, J.R.4
-
125
-
-
0034649380
-
Hypertension, hyperekplexia, and pyramidal paresis due to vascular compression of the medulla
-
Salvi F., Mascalchi M., Bortolotti C., Meletti S., Plasmati R., Rubboli G., et al. Hypertension, hyperekplexia, and pyramidal paresis due to vascular compression of the medulla. Neurology 2000, 55:1381-1384.
-
(2000)
Neurology
, vol.55
, pp. 1381-1384
-
-
Salvi, F.1
Mascalchi, M.2
Bortolotti, C.3
Meletti, S.4
Plasmati, R.5
Rubboli, G.6
-
126
-
-
0033080914
-
Novel GLRA1 missense mutation (P250T) in dominant hyperekplexia defines an intracellular determinant of glycine receptor channel gating
-
Saul B., Kuner T., Sobetzko D., Brune W., Hanefeld F., Meinck H.M., et al. Novel GLRA1 missense mutation (P250T) in dominant hyperekplexia defines an intracellular determinant of glycine receptor channel gating. J Neurosci 1999, 19:869-877.
-
(1999)
J Neurosci
, vol.19
, pp. 869-877
-
-
Saul, B.1
Kuner, T.2
Sobetzko, D.3
Brune, W.4
Hanefeld, F.5
Meinck, H.M.6
-
127
-
-
0032869017
-
Behavioral and psychophysiological correlates of self-presentation in temperamentally shy children
-
Schmidt L.A., Fox N.A., Schulkin J., Gold P.W. Behavioral and psychophysiological correlates of self-presentation in temperamentally shy children. Dev Psychobiol 1999, 35:119-135.
-
(1999)
Dev Psychobiol
, vol.35
, pp. 119-135
-
-
Schmidt, L.A.1
Fox, N.A.2
Schulkin, J.3
Gold, P.W.4
-
128
-
-
0034130236
-
Beneficial effect of fluoxetine in a case of sporadic hyperekplexia
-
Sechi G., Sotgiu S., Valenti M.P., Pitzolu M.G., Peterlongo P., Larizza L., et al. Beneficial effect of fluoxetine in a case of sporadic hyperekplexia. Clin Neuropharmacol 2000, 23:161-163.
-
(2000)
Clin Neuropharmacol
, vol.23
, pp. 161-163
-
-
Sechi, G.1
Sotgiu, S.2
Valenti, M.P.3
Pitzolu, M.G.4
Peterlongo, P.5
Larizza, L.6
-
129
-
-
0026006850
-
Nose tapping test inducing a generalized flexor spasm: a hallmark of hyperexplexia
-
Shahar E., Brand N., Uziel Y., Barak Y. Nose tapping test inducing a generalized flexor spasm: a hallmark of hyperexplexia. Acta Paediatr Scand 1991, 80:1073-1077.
-
(1991)
Acta Paediatr Scand
, vol.80
, pp. 1073-1077
-
-
Shahar, E.1
Brand, N.2
Uziel, Y.3
Barak, Y.4
-
130
-
-
3142645008
-
Sporadic major hyperekplexia in neonates and infants: clinical manifestations and outcome
-
Shahar E., Raviv R. Sporadic major hyperekplexia in neonates and infants: clinical manifestations and outcome. Pediatr Neurol 2004, 31:30-34.
-
(2004)
Pediatr Neurol
, vol.31
, pp. 30-34
-
-
Shahar, E.1
Raviv, R.2
-
131
-
-
0029038869
-
Mutational analysis of familial and sporadic hyperekplexia
-
Shiang R., Ryan S.G., Zhu Y.Z., Fielder T.J., Allen R.J., Fryer A., et al. Mutational analysis of familial and sporadic hyperekplexia. Ann Neurol 1995, 38:85-91.
-
(1995)
Ann Neurol
, vol.38
, pp. 85-91
-
-
Shiang, R.1
Ryan, S.G.2
Zhu, Y.Z.3
Fielder, T.J.4
Allen, R.J.5
Fryer, A.6
-
132
-
-
0023924673
-
Somatosensory and acoustic brain stem reflex myoclonus
-
Shibasaki H., Kakigi R., Oda K., Masukawa S. Somatosensory and acoustic brain stem reflex myoclonus. J Neurol Neurosurg Psychiatry 1988, 51:572-575.
-
(1988)
J Neurol Neurosurg Psychiatry
, vol.51
, pp. 572-575
-
-
Shibasaki, H.1
Kakigi, R.2
Oda, K.3
Masukawa, S.4
-
134
-
-
33748375151
-
The auditory startle response in post-traumatic stress disorder
-
Siegelaar S.E., Olff M., Bour L.J., Veelo D., Zwinderman A.H., van B.G., et al. The auditory startle response in post-traumatic stress disorder. Exp Brain Res 2006, 174:1-6.
-
(2006)
Exp Brain Res
, vol.174
, pp. 1-6
-
-
Siegelaar, S.E.1
Olff, M.2
Bour, L.J.3
Veelo, D.4
Zwinderman, A.H.5
van, B.G.6
-
136
-
-
33746811061
-
Hyperekplexia in Kurdish families: a possible GLRA1 founder mutation
-
Siren A., Legros B., Chahine L., Misson J.P., Pandolfo M. Hyperekplexia in Kurdish families: a possible GLRA1 founder mutation. Neurology 2006, 67:137-139.
-
(2006)
Neurology
, vol.67
, pp. 137-139
-
-
Siren, A.1
Legros, B.2
Chahine, L.3
Misson, J.P.4
Pandolfo, M.5
-
138
-
-
0029622348
-
The audiogenic startle response in Tourette's syndrome
-
Stell R., Thickbroom G.W., Mastaglia F.L. The audiogenic startle response in Tourette's syndrome. Mov Disord 1995, 10:723-730.
-
(1995)
Mov Disord
, vol.10
, pp. 723-730
-
-
Stell, R.1
Thickbroom, G.W.2
Mastaglia, F.L.3
-
139
-
-
0242480735
-
Das Zusammenschrecken: experimental Kinomatographische Studie zur Physiologie und Pathofysiologie der Reaktivbewegungen
-
Strauss H. Das Zusammenschrecken: experimental Kinomatographische Studie zur Physiologie und Pathofysiologie der Reaktivbewegungen. Journal für Psychologie und Neurologie 1929, 39:111-232.
-
(1929)
Journal für Psychologie und Neurologie
, vol.39
, pp. 111-232
-
-
Strauss, H.1
-
140
-
-
0000069083
-
Hyperexplexia, a hereditary startle syndrome
-
Suhren O., Bruyn G.W., Tuynman A. Hyperexplexia, a hereditary startle syndrome. J Neurol Science 1966, 3:577-605.
-
(1966)
J Neurol Science
, vol.3
, pp. 577-605
-
-
Suhren, O.1
Bruyn, G.W.2
Tuynman, A.3
-
141
-
-
0035353729
-
Latah in Jakarta, Indonesia
-
Tanner C.M., Chamberland J. Latah in Jakarta, Indonesia. Mov Disord 2001, 16:526-529.
-
(2001)
Mov Disord
, vol.16
, pp. 526-529
-
-
Tanner, C.M.1
Chamberland, J.2
-
142
-
-
84886019254
-
-
Lippincott, Philadelphia
-
Thompson P.D. The phenomenology of startle, latah, and related conditions. Psychogenic movement disorders 2006, Lippincott, Philadelphia, p. 48-52.
-
(2006)
The phenomenology of startle, latah, and related conditions. Psychogenic movement disorders
, pp. 48-52
-
-
Thompson, P.D.1
-
143
-
-
0026681011
-
Voluntary stimulus-sensitive jerks and jumps mimicking myoclonus or pathological startle syndromes
-
Thompson P.D., Colebatch J.G., Brown P., Rothwell J.C., Day B.L., Obeso J.A., et al. Voluntary stimulus-sensitive jerks and jumps mimicking myoclonus or pathological startle syndromes. Mov Disord 1992, 7:257-262.
-
(1992)
Mov Disord
, vol.7
, pp. 257-262
-
-
Thompson, P.D.1
Colebatch, J.G.2
Brown, P.3
Rothwell, J.C.4
Day, B.L.5
Obeso, J.A.6
-
144
-
-
33744487403
-
Proven startle-provoked epileptic seizures in childhood: semiologic and electrophysiologic variability
-
Tibussek D., Wohlrab G., Boltshauser E., Schmitt B. Proven startle-provoked epileptic seizures in childhood: semiologic and electrophysiologic variability. Epilepsia 2006, 47:1050-1058.
-
(2006)
Epilepsia
, vol.47
, pp. 1050-1058
-
-
Tibussek, D.1
Wohlrab, G.2
Boltshauser, E.3
Schmitt, B.4
-
145
-
-
0029620382
-
Saccadic eye movements in hyperekplexia
-
Tijssen M.A., Bollen E., van E.E., van Dijk J.G. Saccadic eye movements in hyperekplexia. Mov Disord 1995, 10:749-753.
-
(1995)
Mov Disord
, vol.10
, pp. 749-753
-
-
Tijssen, M.A.1
Bollen, E.2
van, E.E.3
van Dijk, J.G.4
-
146
-
-
0347031390
-
Magnetic resonance spectroscopy of cerebral cortex is normal in hereditary hyperekplexia due to mutations in the GLRA1 gene
-
Tijssen M.A., Brown P., MacManus D., McLean M.A., Davie C. Magnetic resonance spectroscopy of cerebral cortex is normal in hereditary hyperekplexia due to mutations in the GLRA1 gene. Mov Disord 2003, 18:1538-1541.
-
(2003)
Mov Disord
, vol.18
, pp. 1538-1541
-
-
Tijssen, M.A.1
Brown, P.2
MacManus, D.3
McLean, M.A.4
Davie, C.5
-
147
-
-
0032702397
-
Late onset startle induced tics
-
Tijssen M.A., Brown P., Morris H.R., Lees A. Late onset startle induced tics. J Neurol Neurosurg Psychiatry 1999, 67:782-784.
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.67
, pp. 782-784
-
-
Tijssen, M.A.1
Brown, P.2
Morris, H.R.3
Lees, A.4
-
148
-
-
0029900087
-
The startle pattern in the minor form of hyperekplexia
-
Tijssen M.A., Padberg G.W., van Dijk J.G. The startle pattern in the minor form of hyperekplexia. Arch Neurol 1996, 53:608-613.
-
(1996)
Arch Neurol
, vol.53
, pp. 608-613
-
-
Tijssen, M.A.1
Padberg, G.W.2
van Dijk, J.G.3
-
149
-
-
0030987119
-
The effects of clonazepam and vigabatrin in hyperekplexia
-
Tijssen M.A., Schoemaker H.C., Edelbroek P.J., Roos R.A., Cohen A.F., van Dijk J.G. The effects of clonazepam and vigabatrin in hyperekplexia. J Neurol Sci 1997, 149:63-67.
-
(1997)
J Neurol Sci
, vol.149
, pp. 63-67
-
-
Tijssen, M.A.1
Schoemaker, H.C.2
Edelbroek, P.J.3
Roos, R.A.4
Cohen, A.F.5
van Dijk, J.G.6
-
150
-
-
0029016226
-
Molecular genetic reevaluation of the Dutch hyperekplexia family
-
Tijssen M.A., Shiang R., van D.J., Boerman R.H., Wasmuth J.J., Sandkuijl L.A., et al. Molecular genetic reevaluation of the Dutch hyperekplexia family. Arch Neurol 1995, 52:578-582.
-
(1995)
Arch Neurol
, vol.52
, pp. 578-582
-
-
Tijssen, M.A.1
Shiang, R.2
van, D.J.3
Boerman, R.H.4
Wasmuth, J.J.5
Sandkuijl, L.A.6
-
151
-
-
0036652637
-
Major and minor form of hereditary hyperekplexia
-
Tijssen M.A., Vergouwe M.N., van Dijk J.G., Rees M., Frants R.R., Brown P. Major and minor form of hereditary hyperekplexia. Mov Disord 2002, 17:826-830.
-
(2002)
Mov Disord
, vol.17
, pp. 826-830
-
-
Tijssen, M.A.1
Vergouwe, M.N.2
van Dijk, J.G.3
Rees, M.4
Frants, R.R.5
Brown, P.6
-
152
-
-
0030896290
-
Startle responses in hereditary hyperekplexia
-
Tijssen M.A., Voorkamp L.M., Padberg G.W., van Dijk J.G. Startle responses in hereditary hyperekplexia. Arch Neurol 1997, 54:388-393.
-
(1997)
Arch Neurol
, vol.54
, pp. 388-393
-
-
Tijssen, M.A.1
Voorkamp, L.M.2
Padberg, G.W.3
van Dijk, J.G.4
-
153
-
-
0025876599
-
Hyperexplexia or stiff baby syndrome
-
Tohier C., Roze J.C., David A., Veccierini M.F., Renaud P., Mouzard A. Hyperexplexia or stiff baby syndrome. Arch Dis Child 1991, 66:460-461.
-
(1991)
Arch Dis Child
, vol.66
, pp. 460-461
-
-
Tohier, C.1
Roze, J.C.2
David, A.3
Veccierini, M.F.4
Renaud, P.5
Mouzard, A.6
-
154
-
-
4644369714
-
Two novel mutations of the glycine receptor gene in a Taiwanese hyperekplexia family
-
Tsai C.H., Chang F.C., Su Y.C., Tsai F.J., Lu M.K., Lee C.C., et al. Two novel mutations of the glycine receptor gene in a Taiwanese hyperekplexia family. Neurology 2004, 63:893-896.
-
(2004)
Neurology
, vol.63
, pp. 893-896
-
-
Tsai, C.H.1
Chang, F.C.2
Su, Y.C.3
Tsai, F.J.4
Lu, M.K.5
Lee, C.C.6
-
155
-
-
44349152308
-
Interaction between startle and voluntary reactions in humans
-
Valls-Sole J., Kumru H., Kofler M. Interaction between startle and voluntary reactions in humans. Exp Brain Res 2008, 187:497-507.
-
(2008)
Exp Brain Res
, vol.187
, pp. 497-507
-
-
Valls-Sole, J.1
Kumru, H.2
Kofler, M.3
-
156
-
-
0033135541
-
Patterned ballistic movements triggered by a startle in healthy humans
-
Valls-Sole J., Rothwell J.C., Goulart F., Cossu G., Munoz E. Patterned ballistic movements triggered by a startle in healthy humans. J Physiol 1999, 516:931-938.
-
(1999)
J Physiol
, vol.516
, pp. 931-938
-
-
Valls-Sole, J.1
Rothwell, J.C.2
Goulart, F.3
Cossu, G.4
Munoz, E.5
-
157
-
-
34347207264
-
Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy
-
van de Warrenburg B.P., Cordivari C., Brown P., Bhatia K.P. Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy. Mov Disord 2007, 22:1017-1020.
-
(2007)
Mov Disord
, vol.22
, pp. 1017-1020
-
-
van de Warrenburg, B.P.1
Cordivari, C.2
Brown, P.3
Bhatia, K.P.4
-
158
-
-
0032829753
-
Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations
-
Vergouwe M.N., Tijssen M.A., Peters A.C., Wielaard R., Frants R.R. Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations. Ann Neurol 1999, 46:634-638.
-
(1999)
Ann Neurol
, vol.46
, pp. 634-638
-
-
Vergouwe, M.N.1
Tijssen, M.A.2
Peters, A.C.3
Wielaard, R.4
Frants, R.R.5
-
159
-
-
0030864920
-
Hyperekplexia-like syndromes without mutations in the GLRA1 gene
-
Vergouwe M.N., Tijssen M.A., Shiang R., van Dijk J.G., al S.S., Ophoff R.A., et al. Hyperekplexia-like syndromes without mutations in the GLRA1 gene. Clin Neurol Neurosurg 1997, 99:172-178.
-
(1997)
Clin Neurol Neurosurg
, vol.99
, pp. 172-178
-
-
Vergouwe, M.N.1
Tijssen, M.A.2
Shiang, R.3
van Dijk, J.G.4
al, S.S.5
Ophoff, R.A.6
-
160
-
-
34548181827
-
Pontine hyperperfusion in sporadic hyperekplexia
-
Vetrugno R., Mascalchi M., Vella A., Della N.R., Guerrini L., Vattimo A., et al. Pontine hyperperfusion in sporadic hyperekplexia. J Neurol Neurosurg Psychiatry 2007, 78:1001-1004.
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, pp. 1001-1004
-
-
Vetrugno, R.1
Mascalchi, M.2
Vella, A.3
Della, N.R.4
Guerrini, L.5
Vattimo, A.6
-
161
-
-
0024492904
-
Startle disease: an avoidable cause of sudden infant death
-
Vigevano F., Di C.M., Dalla B.B. Startle disease: an avoidable cause of sudden infant death. Lancet 1989, 1:216.
-
(1989)
Lancet
, vol.1
, pp. 216
-
-
Vigevano, F.1
Di, C.M.2
Dalla, B.B.3
-
162
-
-
0024118211
-
The startle probe response: a new measure of emotion?
-
Vrana S.R., Spence E.L., Lang P.J. The startle probe response: a new measure of emotion?. J Abnorm Psychol 1988, 97:487-491.
-
(1988)
J Abnorm Psychol
, vol.97
, pp. 487-491
-
-
Vrana, S.R.1
Spence, E.L.2
Lang, P.J.3
-
163
-
-
55749108347
-
Developmental changes in startle reactivity in school-age children at risk for and with actual anxiety disorder
-
Waters A.M., Craske M.G., Bergman R.L., Naliboff B.D., Negoro H., Ornitz E.M. Developmental changes in startle reactivity in school-age children at risk for and with actual anxiety disorder. Int J Psychophysiol 2008, 70:158-164.
-
(2008)
Int J Psychophysiol
, vol.70
, pp. 158-164
-
-
Waters, A.M.1
Craske, M.G.2
Bergman, R.L.3
Naliboff, B.D.4
Negoro, H.5
Ornitz, E.M.6
-
164
-
-
0036460919
-
Focal pathological startle following pontine infarction
-
Watson S.R., Colebatch J.G. Focal pathological startle following pontine infarction. Mov Disord 2002, 17:212-218.
-
(2002)
Mov Disord
, vol.17
, pp. 212-218
-
-
Watson, S.R.1
Colebatch, J.G.2
-
165
-
-
0022587642
-
Audiogenic startle reflex of man and its relationship to startle syndromes. A review
-
Wilkins D.E., Hallett M., Wess M.M. Audiogenic startle reflex of man and its relationship to startle syndromes. A review. Brain 1986, 109:561-573.
-
(1986)
Brain
, vol.109
, pp. 561-573
-
-
Wilkins, D.E.1
Hallett, M.2
Wess, M.M.3
-
166
-
-
77950299743
-
Clinical and electrophysiological characteristics of startle epilepsy in childhood
-
Yang Z., Liu X., Qin J., Zhang Y., Bao X., Wang S., et al. Clinical and electrophysiological characteristics of startle epilepsy in childhood. Clin Neurophysiol 2010, 121:658-664.
-
(2010)
Clin Neurophysiol
, vol.121
, pp. 658-664
-
-
Yang, Z.1
Liu, X.2
Qin, J.3
Zhang, Y.4
Bao, X.5
Wang, S.6
-
167
-
-
0029555859
-
The acoustic startle reflex: neurons and connections
-
Yeomans J.S., Frankland P.W. The acoustic startle reflex: neurons and connections. Brain Res Brain Res Rev 1995, 21:301-314.
-
(1995)
Brain Res Brain Res Rev
, vol.21
, pp. 301-314
-
-
Yeomans, J.S.1
Frankland, P.W.2
-
168
-
-
0037461315
-
Primary lateral sclerosis: a heterogeneous disorder composed of different subtypes?
-
Zhai P., Pagan F., Statland J., Butman J.A., Floeter M.K. Primary lateral sclerosis: a heterogeneous disorder composed of different subtypes?. Neurology 2003, 60:1258-1265.
-
(2003)
Neurology
, vol.60
, pp. 1258-1265
-
-
Zhai, P.1
Pagan, F.2
Statland, J.3
Butman, J.A.4
Floeter, M.K.5
-
169
-
-
0036806404
-
Hyperekplexia: a treatable neurogenetic disease
-
Zhou L., Chillag K.L., Nigro M.A. Hyperekplexia: a treatable neurogenetic disease. Brain Dev 2002, 24:669-674.
-
(2002)
Brain Dev
, vol.24
, pp. 669-674
-
-
Zhou, L.1
Chillag, K.L.2
Nigro, M.A.3
|