-
1
-
-
0014952522
-
The startle and orientation reaction in man: A study of their characteristics and habituation
-
Gogan P. The startle and orientation reaction in man A study of their characteristics and habituation. Brain Res. 18:1970;117-135
-
(1970)
Brain Res
, vol.18
, pp. 117-135
-
-
Gogan, P.1
-
3
-
-
0013865890
-
Habituation: A model phenomenon for the study of neuronal substrates of behavior
-
Thompson R.F., Spencer W.A. Habituation A model phenomenon for the study of neuronal substrates of behavior. Psychol Rev. 73:1966;16-43
-
(1966)
Psychol Rev
, vol.73
, pp. 16-43
-
-
Thompson, R.F.1
Spencer, W.A.2
-
4
-
-
0019964425
-
Motor functions: Associated primitive reflex profile
-
Capute A.J., Shapiro B.K., Accardo P.J., Wachtel R.C., Ross A., Palmar F.B. Motor functions Associated primitive reflex profile. Dev Med Child Neurol. 24:1982;662-669
-
(1982)
Dev Med Child Neurol
, vol.24
, pp. 662-669
-
-
Capute, A.J.1
Shapiro, B.K.2
Accardo, P.J.3
Wachtel, R.C.4
Ross, A.5
Palmar, F.B.6
-
5
-
-
0000069083
-
Hyperexplexia, a hereditary startle syndrome
-
Shuren O., Bruin G.W., Tuyman A. Hyperexplexia, a hereditary startle syndrome. J Neurol Sci. 3:1966;577-605
-
(1966)
J Neurol Sci
, vol.3
, pp. 577-605
-
-
Shuren, O.1
Bruin, G.W.2
Tuyman, A.3
-
6
-
-
0017842343
-
Periodic nocturnal myoclonus in a patient with hyperexplexia
-
de Groen J.H., Kamphuisen H.A. Periodic nocturnal myoclonus in a patient with hyperexplexia. J Neurol Sci. 38:1978;207-213
-
(1978)
J Neurol Sci
, vol.38
, pp. 207-213
-
-
De Groen, J.H.1
Kamphuisen, H.A.2
-
7
-
-
0019980517
-
Hyperexplexia: An inherited disorder of the startle response
-
Morely D.J., Weaver D.D., Garg B.P., Markand O. Hyperexplexia An inherited disorder of the startle response. Clin Genet. 21:1982;388-396
-
(1982)
Clin Genet
, vol.21
, pp. 388-396
-
-
Morely, D.J.1
Weaver, D.D.2
Garg, B.P.3
Markand, O.4
-
8
-
-
0021357407
-
Familial startle disease (hyperexplexia) Electrophysiologic studies
-
Markand O.N., Garg B.P., Weaver D.D. Familial startle disease (hyperexplexia) Electrophysiologic studies. Ann Neurol. 41:1984;71-74
-
(1984)
Ann Neurol
, vol.41
, pp. 71-74
-
-
Markand, O.N.1
Garg, B.P.2
Weaver, D.D.3
-
9
-
-
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. 80:1991;1073-1077
-
(1991)
Acta Paediatr Scand
, vol.80
, pp. 1073-1077
-
-
Shahar, E.1
Brand, N.2
Uziel, Y.3
Barak, Y.4
-
10
-
-
0014151623
-
The startle disease or hyperekplexia, pathological surprise reaction
-
Gastaut H., Villeneuve A. The startle disease or hyperekplexia, pathological surprise reaction. J Neurol Sci. 5:1967;523-542
-
(1967)
J Neurol Sci
, vol.5
, pp. 523-542
-
-
Gastaut, H.1
Villeneuve, A.2
-
11
-
-
0019225609
-
Startle disease or hyperekplexia: Further delineation of the syndrome
-
Andermann F, Keen DL, Andermann E, Quesnwy LF. Startle disease or hyperekplexia: Further delineation of the syndrome. Brain 1980;985-97
-
(1980)
Brain
, pp. 985-997
-
-
Andermann, F.1
Keen, D.L.2
Andermann, E.3
Quesnwy, L.F.4
-
12
-
-
0020693750
-
Hyperekplexia
-
Kurczynski T.W. Hyperekplexia. Arch Neurol. 40:1983;246-248
-
(1983)
Arch Neurol
, vol.40
, pp. 246-248
-
-
Kurczynski, T.W.1
-
14
-
-
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. 114:1991;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
-
15
-
-
0025781128
-
Hyperekplexia: Pedigree studies in two families
-
Hayashi T., Tachubana H., Kajii T. Hyperekplexia Pedigree studies in two families. Am J Med Genet. 40:1991;138-143
-
(1991)
Am J Med Genet
, vol.40
, pp. 138-143
-
-
Hayashi, T.1
Tachubana, H.2
Kajii, T.3
-
16
-
-
3142639557
-
Hyperekplexia and sudden neonatal death
-
Nigro M.A., Lim H.C. Hyperekplexia and sudden neonatal death. Pediatr Neurol. 31:1992;63-68
-
(1992)
Pediatr Neurol
, vol.31
, pp. 63-68
-
-
Nigro, M.A.1
Lim, H.C.2
-
17
-
-
0026795017
-
Neonatal hyperekplexia: A case report
-
Pascoto A., Coppola G. Neonatal hyperekplexia A case report. Epilepsia. 33:1992;817-820
-
(1992)
Epilepsia
, vol.33
, pp. 817-820
-
-
Pascoto, A.1
Coppola, G.2
-
18
-
-
0026758875
-
Physiological abnormalities in hereditary hyperekplexia
-
Matsumoto J., Fuhr P., Nigro M., Hallet M. Physiological abnormalities in hereditary hyperekplexia. Ann Neurol. 32:1992;41-50
-
(1992)
Ann Neurol
, vol.32
, pp. 41-50
-
-
Matsumoto, J.1
Fuhr, P.2
Nigro, M.3
Hallet, M.4
-
19
-
-
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. 31:1992;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
-
20
-
-
0027437603
-
Startle disease or hyperekplexia
-
Gordon N. Startle disease or hyperekplexia. Dev Med Child Neurol. 35:1993;1015-1024
-
(1993)
Dev Med Child Neurol
, vol.35
, pp. 1015-1024
-
-
Gordon, N.1
-
21
-
-
0028287870
-
Hyperekplexia associated with apnea and sudden death syndrome
-
Giacoia G.P., Ryan S.G. Hyperekplexia associated with apnea and sudden death syndrome. Arch Pediatr Adolesc Med. 148:1994;540-543
-
(1994)
Arch Pediatr Adolesc Med
, vol.148
, pp. 540-543
-
-
Giacoia, G.P.1
Ryan, S.G.2
-
22
-
-
0028933543
-
Hyperekplexia, a cause of neonatal apnea: A case report
-
Gherpeli J.L.D., Nogueira A.R., Troster E.J., et al. Hyperekplexia, a cause of neonatal apnea A case report. Brain Dev. 17:1995;114-116
-
(1995)
Brain Dev
, vol.17
, pp. 114-116
-
-
Gherpeli, J.L.D.1
Nogueira, A.R.2
Troster, E.J.3
-
23
-
-
0028967379
-
Hyperekplexia as cause of abnormal intrauterine movements
-
[Letter]
-
Leventer R.J., Hopkins I.J., Shield L.K. Hyperekplexia as cause of abnormal intrauterine movements. [Letter] Lancet. 345:1995;461
-
(1995)
Lancet
, vol.345
, pp. 461
-
-
Leventer, R.J.1
Hopkins, I.J.2
Shield, L.K.3
-
24
-
-
0028927041
-
Complete heart block in nonfamilial hyperekplexia
-
McAbee G.N., Kadakia S.K., Sisley K.C., Eegt R., Delfiner J.S. Complete heart block in nonfamilial hyperekplexia. Pediatr Neurol. 12:1995;149-151
-
(1995)
Pediatr Neurol
, vol.12
, pp. 149-151
-
-
McAbee, G.N.1
Kadakia, S.K.2
Sisley, K.C.3
Eegt, R.4
Delfiner, J.S.5
-
25
-
-
0029805655
-
Startle disease-Hyperekplexia (two sibling cases)
-
Altunbasak S., Baytok V. Startle disease-Hyperekplexia (two sibling cases). Epilepsia. 5:1996;313-315
-
(1996)
Epilepsia
, vol.5
, pp. 313-315
-
-
Altunbasak, S.1
Baytok, V.2
-
26
-
-
0030905427
-
Neonatal sporadic hyperekplexia: A rare and often unrecognized entity
-
Scarcella A., Coppola G. Neonatal sporadic hyperekplexia A rare and often unrecognized entity. Brain Dev. 19:1997;226-228
-
(1997)
Brain Dev
, vol.19
, pp. 226-228
-
-
Scarcella, A.1
Coppola, G.2
-
27
-
-
0033709567
-
Hyperekplexia in the first year of life
-
Koning-Tijssen M.A.J., Brower O.F. Hyperekplexia in the first year of life. Mov Disord. 15:2000;1293-1296
-
(2000)
Mov Disord
, vol.15
, pp. 1293-1296
-
-
Koning-Tijssen, M.A.J.1
Brower, O.F.2
-
28
-
-
0036247190
-
Successful treatment of severe infantile hyperekplexia with low-dose clobazam
-
Stewart W.A., Wood E.P., Gordon K.E., Camfield P.R. Successful treatment of severe infantile hyperekplexia with low-dose clobazam. J Child Neurol. 17:2002;154-156
-
(2002)
J Child Neurol
, vol.17
, pp. 154-156
-
-
Stewart, W.A.1
Wood, E.P.2
Gordon, K.E.3
Camfield, P.R.4
-
29
-
-
0036652637
-
Major and minor form of hereditary hyperekplexia
-
Tijssen M.A.J., Vergouwe M.N., Gert van Dijk J., Rees M., Frants R.R., Brown P. Major and minor form of hereditary hyperekplexia. Mov Disord. 17:2002;826-830
-
(2002)
Mov Disord
, vol.17
, pp. 826-830
-
-
Tijssen, M.A.J.1
Vergouwe, M.N.2
Gert Van Dijk, J.3
Rees, M.4
Frants, R.R.5
Brown, P.6
-
30
-
-
0024492904
-
Startle disease: An avoidable cause of sudden infant death
-
Vigevano F., Capua M.D., Bernadina B.D. Startle disease An avoidable cause of sudden infant death. Lancet. 1:1989;216
-
(1989)
Lancet
, vol.1
, pp. 216
-
-
Vigevano, F.1
Capua, M.D.2
Bernadina, B.D.3
-
31
-
-
3142529288
-
An abnormal proprioceptive startle in children implies grave irreversible neurologic damage
-
[Abstract]
-
Shahar E., Seifert M. An abnormal proprioceptive startle in children implies grave irreversible neurologic damage. [Abstract] Ann Neurol. 44:1998;559
-
(1998)
Ann Neurol
, vol.44
, pp. 559
-
-
Shahar, E.1
Seifert, M.2
-
32
-
-
0026683048
-
Low cerebrospinal fluid concentrations of free gamma-amino butyric acid in startle disease
-
Dubowitz L.M.S., Buoza H., Hird M.F., Janken J. Low cerebrospinal fluid concentrations of free gamma-amino butyric acid in startle disease. Lancet. 340:1992;80-81
-
(1992)
Lancet
, vol.340
, pp. 80-81
-
-
Dubowitz, L.M.S.1
Buoza, H.2
Hird, M.F.3
Janken, J.4
-
33
-
-
0025375519
-
Anesthetic complications in an infant with hyperekplexia
-
Doolitle G.M., Greiner A.S. Anesthetic complications in an infant with hyperekplexia. Anesthesiology. 73:1990;181-183
-
(1990)
Anesthesiology
, vol.73
, pp. 181-183
-
-
Doolitle, G.M.1
Greiner, A.S.2
-
34
-
-
0018677961
-
Stiff-man syndrome in a black girl
-
Isaacs H. Stiff-man syndrome in a black girl. J Neuro Neurosurg Psych. 42:1979;988-994
-
(1979)
J Neuro Neurosurg Psych
, vol.42
, pp. 988-994
-
-
Isaacs, H.1
-
35
-
-
0036265916
-
Isaacs' syndrome as a potassium channelopathy of the nerve
-
Arimura K, Sonoda Y, Watanabe O, et al. Isaacs' syndrome as a potassium channelopathy of the nerve. Muscle Nerve 2002;11(Suppl. 1):S55-8
-
(2002)
Muscle Nerve
, vol.11
, Issue.1 SUPPL.
-
-
Arimura, K.1
Sonoda, Y.2
Watanabe, O.3
-
36
-
-
0028346293
-
Continuous muscle fibre activity (Isaacs syndrome) in infancy: A report of two cases
-
Thomas N.H., Heckmatt J.Z., Rodillo E., Ransley Y.F., Dubowitz V. Continuous muscle fibre activity (Isaacs syndrome) in infancy A report of two cases. Neuromusc Disord. 4:1994;147-151
-
(1994)
Neuromusc Disord
, vol.4
, pp. 147-151
-
-
Thomas, N.H.1
Heckmatt, J.Z.2
Rodillo, E.3
Ransley, Y.F.4
Dubowitz, V.5
-
37
-
-
13344257514
-
Congenital blepharophimosis associated with a unique generalized myopathy
-
Schwartz O., Jampel R.S. Congenital blepharophimosis associated with a unique generalized myopathy. Arch Ophthalmol. 68:1962;52-57
-
(1962)
Arch Ophthalmol
, vol.68
, pp. 52-57
-
-
Schwartz, O.1
Jampel, R.S.2
-
38
-
-
0030249048
-
Neonatal diagnosis of Schwartz-Jampel syndrome with dramatic response to carbamazepine
-
Squires L.A., Prangley J. Neonatal diagnosis of Schwartz-Jampel syndrome with dramatic response to carbamazepine. Pediatr Neurol. 15:1996;172-174
-
(1996)
Pediatr Neurol
, vol.15
, pp. 172-174
-
-
Squires, L.A.1
Prangley, J.2
-
39
-
-
0036359905
-
Neurophysiology of the startle syndrome and hyperekplexia
-
Brown P. Neurophysiology of the startle syndrome and hyperekplexia. Adv Neurol. 89:2002;153-159
-
(2002)
Adv Neurol
, vol.89
, pp. 153-159
-
-
Brown, P.1
-
40
-
-
0022487715
-
Central- and peripheral-type benzodiazepines receptors
-
G. Biggio, & E. Costa. New York: Raven Press
-
Martini C., Lucacchini A., Hrelia S., Rossi C.A. Central- and peripheral-type benzodiazepines receptors. Biggio G., Costa E. GABAergic transmission and anxiety. 1986;1-10 Raven Press, New York
-
(1986)
GABAergic Transmission and Anxiety
, pp. 1-10
-
-
Martini, C.1
Lucacchini, A.2
Hrelia, S.3
Rossi, C.A.4
|