-
1
-
-
0020621190
-
Not 'indifference to pain' but varieties of hereditary sensory and autonomic neuropathy
-
Dick PJ, Mellinger JF, Reagan TJ, et al. Not 'indifference to pain' but varieties of hereditary sensory and autonomic neuropathy. Brain 1983 106 : 373 390.
-
(1983)
Brain
, vol.106
, pp. 373-390
-
-
Dick, P.J.1
Mellinger, J.F.2
Reagan, T.J.3
-
2
-
-
0037316882
-
Congenital insensibility to pain: An update
-
Nagasako EOA, Dworkin RH. Congenital insensibility to pain: an update. Pain 2003 101 : 213 219.
-
(2003)
Pain
, vol.101
, pp. 213-219
-
-
Nagasako, E.O.A.1
Dworkin, R.H.2
-
3
-
-
0035072984
-
A novel TRK a (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V
-
Houlden H, King RH, Hashemi-Nejad A, et al. A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. Annals of Neurology 2001 49 : 521 525.
-
(2001)
Annals of Neurology
, vol.49
, pp. 521-525
-
-
Houlden, H.1
King, R.H.2
Hashemi-Nejad, A.3
-
4
-
-
0035093827
-
SPTLC1 is muteded in hereditary sensory neuropathy type 1
-
Bejaoui K, Wu C, Scheffler MD. SPTLC1 is muteded in hereditary sensory neuropathy type 1. Nature Genetics 2001 27 : 261 262.
-
(2001)
Nature Genetics
, vol.27
, pp. 261-262
-
-
Bejaoui, K.1
Wu, C.2
Scheffler, M.D.3
-
5
-
-
0036173752
-
A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci
-
Bellone E, Rodolico C, Toscano A, et al. A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci. Neuromuscular Disorders 2002 12 : 286 291.
-
(2002)
Neuromuscular Disorders
, vol.12
, pp. 286-291
-
-
Bellone, E.1
Rodolico, C.2
Toscano, A.3
-
6
-
-
0041385594
-
A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-24
-
Kok C, Kennerson ML, Spring PJ, Ing AJ, Pollard JD, Nicholson GA. A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-24. American Journal of Human Genetics 2003 73 : 632 637.
-
(2003)
American Journal of Human Genetics
, vol.73
, pp. 632-637
-
-
Kok, C.1
Kennerson, M.L.2
Spring, P.J.3
Ing, A.J.4
Pollard, J.D.5
Nicholson, G.A.6
-
7
-
-
0033982968
-
Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci
-
Auer-Grumbach M, Wagner K, Timmerman V, De Jonghe P, Hartung HP. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci. Neurology 2000 54 : 45 52.
-
(2000)
Neurology
, vol.54
, pp. 45-52
-
-
Auer-Grumbach, M.1
Wagner, K.2
Timmerman, V.3
De Jonghe, P.4
Hartung, H.P.5
-
8
-
-
30744457042
-
Disease mechanisms in hereditary sensory and autonomic neuropathies
-
Verpoorten N, De Jonghe P, Timmerman V. Disease mechanisms in hereditary sensory and autonomic neuropathies. Neurobiology of Disease 2006 21 : 247 255.
-
(2006)
Neurobiology of Disease
, vol.21
, pp. 247-255
-
-
Verpoorten, N.1
De Jonghe, P.2
Timmerman, V.3
-
9
-
-
2342557998
-
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates
-
Lafranière RG, MacDonald ML, Dube MP, et al. Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates. American Journal of Human Genetics 2004 74 : 1064 1073.
-
(2004)
American Journal of Human Genetics
, vol.74
, pp. 1064-1073
-
-
Lafranière, R.G.1
MacDonald, M.L.2
Dube, M.P.3
-
10
-
-
31544461547
-
Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I)
-
Houlden H, King R, Blake J, et al. Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). Brain 2006 129 (Pt 2 411 425.
-
(2006)
Brain
, vol.129
, Issue.2
, pp. 411-425
-
-
Houlden, H.1
King, R.2
Blake, J.3
-
11
-
-
3042628488
-
Congenital insensibility to pain with anhidrosis in Taiwan: A morphometric and genetic study
-
Guo YC, Liao KK, Soong BW, et al. Congenital insensibility to pain with anhidrosis in Taiwan: a morphometric and genetic study. European Neurology 2004 51 : 206 214.
-
(2004)
European Neurology
, vol.51
, pp. 206-214
-
-
Guo, Y.C.1
Liao, K.K.2
Soong, B.W.3
-
12
-
-
0025317398
-
Dominantly transmitted congenital indifference to pain
-
Landrieu P, Said G, Allaire C. Dominantly transmitted congenital indifference to pain. Annals of Neurology 1990 27 : 574 578.
-
(1990)
Annals of Neurology
, vol.27
, pp. 574-578
-
-
Landrieu, P.1
Said, G.2
Allaire, C.3
-
13
-
-
1942517847
-
A mutation in nerve growth factor beta gene (NGFB) causes loss of pain perception
-
Einarsdottir E, Carlsson A, Minde J, et al. A mutation in nerve growth factor beta gene (NGFB) causes loss of pain perception. Human Molecular genetics 2004 13 : 799 805.
-
(2004)
Human Molecular Genetics
, vol.13
, pp. 799-805
-
-
Einarsdottir, E.1
Carlsson, A.2
Minde, J.3
-
14
-
-
0015901434
-
Congetital insensibility to pain: A clinical and neurophysiological study of four children from the same family
-
Thrush DC. Congetital insensibility to pain: a clinical and neurophysiological study of four children from the same family. Brain 1973 96 : 369 386.
-
(1973)
Brain
, vol.96
, pp. 369-386
-
-
Thrush, D.C.1
-
15
-
-
0034917953
-
Viktor Hamburger and Rita Levi-Montalcini: The path to the discovery of nerve growth factor
-
Cowan W. Viktor Hamburger and Rita Levi-Montalcini: the path to the discovery of nerve growth factor. Annual Review of Neuroscience 2001 24 : 551 600.
-
(2001)
Annual Review of Neuroscience
, vol.24
, pp. 551-600
-
-
Cowan, W.1
-
16
-
-
33845901486
-
An SC9A channelopathy causes congenital inability to experience pain
-
Cox JJ, Reimann F, Nicholas AK, et al. An SC9A channelopathy causes congenital inability to experience pain. Nature 2006 444 : 894 898.
-
(2006)
Nature
, vol.444
, pp. 894-898
-
-
Cox, J.J.1
Reimann, F.2
Nicholas, A.K.3
-
17
-
-
34247874778
-
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations
-
Goldberg Y, MacFarlane J, MacDonald ML, et al. Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. Clinical Genetics 2007 71 : 311 319.
-
(2007)
Clinical Genetics
, vol.71
, pp. 311-319
-
-
Goldberg, Y.1
MacFarlane, J.2
MacDonald, M.L.3
-
18
-
-
0021347942
-
Sympatheric skin response - A method of assessing unmyelinated axon dysfunction in peripheral neuropathies
-
Shahani BT, Halperin JJ, Boulu P, Cohen J. Sympatheric skin response - a method of assessing unmyelinated axon dysfunction in peripheral neuropathies. Journal of Neurology, Neurosurgery and Psychiatry 1984 47 : 536 542.
-
(1984)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.47
, pp. 536-542
-
-
Shahani, B.T.1
Halperin, J.J.2
Boulu, P.3
Cohen, J.4
-
19
-
-
0037167524
-
Assessment of the neurogenic flare reaction in small-fiber neuropathies
-
Bickel A, Krämmer HH, Hilz MJ, Birklein F, Neundörfer B, Schmelz M. Assessment of the neurogenic flare reaction in small-fiber neuropathies. Neurology 2002 59 : 917 919.
-
(2002)
Neurology
, vol.59
, pp. 917-919
-
-
Bickel, A.1
Krämmer, H.H.2
Hilz, M.J.3
Birklein, F.4
Neundörfer, B.5
Schmelz, M.6
-
21
-
-
0028395290
-
The Mini-Mental State Examination in a general population: Impact of educational status
-
Bertolucci PH, Brucki BS, Campacci SR, et al. The Mini-Mental State Examination in a general population: impact of educational status. Arquivos de Neuro-Psiquiatria 1994 52 : 325 331.
-
(1994)
Arquivos de Neuro-Psiquiatria
, vol.52
, pp. 325-331
-
-
Bertolucci, P.H.1
Brucki, B.S.2
Campacci, S.R.3
-
22
-
-
0016823810
-
'Mini-mental state'. a practical method for grading the cognitive state of patients for the clinician
-
Folstein MF. 'Mini-mental state'. A practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research 1975 12 : 189 198.
-
(1975)
Journal of Psychiatric Research
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
-
23
-
-
0004235298
-
-
American Psychiatric Association. Washington DC: American Psychiatric Association
-
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders IV. Washington DC : American Psychiatric Association, 1994.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders IV.
-
-
-
25
-
-
0027154845
-
Development of the alcohol use disorders identification test (AUDIT): WHO collaborative project on early detection of persons with harmful alcohol consumption. II
-
Saunders JB, Aasland OG, Babor TF, de la Fuente JR, Grant M. Development of the alcohol use disorders identification test (AUDIT): WHO collaborative project on early detection of persons with harmful alcohol consumption. II. Addiction 1993 88 : 791 804.
-
(1993)
Addiction
, vol.88
, pp. 791-804
-
-
Saunders, J.B.1
Aasland, O.G.2
Babor, T.F.3
De La Fuente, J.R.4
Grant, M.5
-
26
-
-
0020075038
-
Measurement of functional activities in older adults in the community
-
Pfeffer RI, Kurosaki TT, Harrah CH Jr, Chance JM, Filos S. Measurement of functional activities in older adults in the community. Journal of Gerontology 1982 37 : 323 329.
-
(1982)
Journal of Gerontology
, vol.37
, pp. 323-329
-
-
Pfeffer, R.I.1
Kurosaki, T.T.2
Harrah Jr., C.H.3
Chance, J.M.4
Filos, S.5
-
27
-
-
0014579432
-
Assessment of older people: Self-maintaining and instrumental activities of daily living
-
Lawton M. Assessment of older people: self-maintaining and instrumental activities of daily living. Gerontologist 1969 9 : 179 186.
-
(1969)
Gerontologist
, vol.9
, pp. 179-186
-
-
Lawton, M.1
-
28
-
-
0024453856
-
The consortium to establish a registry for Alzheimer's disease (CERAD). Part 1. Clinical and neuropsychological assessment of Alzheimer's disease
-
Morris JC. The consortium to establish a registry for Alzheimer's disease (CERAD). Part 1. Clinical and neuropsychological assessment of Alzheimer's disease. Neurology 1989 39 : 1159 1165.
-
(1989)
Neurology
, vol.39
, pp. 1159-1165
-
-
Morris, J.C.1
-
30
-
-
57049145197
-
Studies of interference in serial verbal reactions
-
Stroop R. Studies of interference in serial verbal reactions. Journal of Experimentam Psychology 1935 18 : 643 662.
-
(1935)
Journal of Experimentam Psychology
, vol.18
, pp. 643-662
-
-
Stroop, R.1
-
32
-
-
33646063523
-
Congenital idiopathic inability to perceive pain: A new syndrome of insensitivity to pain and itch with preserved small fibers
-
Sandroni P, Martin DP, Bruce BK, Rome JD. Congenital idiopathic inability to perceive pain: a new syndrome of insensitivity to pain and itch with preserved small fibers. Pain 2006 122 : 210 215.
-
(2006)
Pain
, vol.122
, pp. 210-215
-
-
Sandroni, P.1
Martin, D.P.2
Bruce, B.K.3
Rome, J.D.4
-
33
-
-
33749268350
-
Is pain the price of empathy? the perception of others' pain in patients with congenital insensitivity to pain
-
Danziger N, Prkachin KM, Willer J-C. Is pain the price of empathy? The perception of others' pain in patients with congenital insensitivity to pain. Brain 2006 129 (Pt 9 2494 2507.
-
(2006)
Brain
, vol.129
, Issue.9
, pp. 2494-2507
-
-
Danziger, N.1
Prkachin, K.M.2
Willer, J.-C.3
-
34
-
-
25644432659
-
Tension-type headache as the unique pain experience of a patient with congenital insensitivity to pain
-
Danzinger N, Willer J-C. Tension-type headache as the unique pain experience of a patient with congenital insensitivity to pain. Pain 2005 117 : 478 483.
-
(2005)
Pain
, vol.117
, pp. 478-483
-
-
Danzinger, N.1
Willer, J.-C.2
-
35
-
-
0036327040
-
No mutation in the TRK a (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a apatient with hereditary sensory and autonomic neuropathy type V
-
Toscano E, Simonati A, Indo Y, Andria G. No mutation in the TRK A (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a apatient with hereditary sensory and autonomic neuropathy type V. Annals of Neurology 2002 52 : 224 227.
-
(2002)
Annals of Neurology
, vol.52
, pp. 224-227
-
-
Toscano, E.1
Simonati, A.2
Indo, Y.3
Andria, G.4
-
36
-
-
2342495016
-
The functional neuroanatomy of the human orbitofrontal cortex: Evidence from neuroimaging and neuropsychology
-
Kringelbach ML, Rolls ET. The functional neuroanatomy of the human orbitofrontal cortex: evidence from neuroimaging and neuropsychology. Progress in Neurobiology 2004 72 : 341 372.
-
(2004)
Progress in Neurobiology
, vol.72
, pp. 341-372
-
-
Kringelbach, M.L.1
Rolls, E.T.2
|