-
1
-
-
0019402976
-
Benign (nonparoxysmal) familial chorea. Paediatric perspectives
-
Sleigh G, Lindenbaum R. Benign (nonparoxysmal) familial chorea. Paediatric perspectives. Arch Dis Child 1981;56: 616-621.
-
(1981)
Arch Dis Child
, vol.56
, pp. 616-621
-
-
Sleigh, G.1
Lindenbaum, R.2
-
2
-
-
0014084736
-
Familial benign chorea with intention tremor: A clinical entity
-
Pincus JH, Chutorian A. Familial benign chorea with intention tremor: a clinical entity. J Pediatr 1967;70:724-729.
-
(1967)
J Pediatr
, vol.70
, pp. 724-729
-
-
Pincus, J.H.1
Chutorian, A.2
-
3
-
-
0014093159
-
Hereditary nonprogressive chorea of early onset
-
Haerer AF, Currier RD, Jackson JF. Hereditary nonprogressive chorea of early onset. N Engl J Med 1967;276:1220-1224.
-
(1967)
N Engl J Med
, vol.276
, pp. 1220-1224
-
-
Haerer, A.F.1
Currier, R.D.2
Jackson, J.F.3
-
4
-
-
0001174173
-
Chronic juvenile hereditary chorea (benign hereditary chorea of early onset)
-
Vinken PJ, Bruyn GW, Klawans HL, eds. Amsterdam: Elsevier Science
-
Bruyn GW, Myrianthopoulos NC. Chronic juvenile hereditary chorea (benign hereditary chorea of early onset). In: Vinken PJ, Bruyn GW, Klawans HL, eds. Handbook of clinical neurology. Extrapyramidal disorders: vol. 5. Amsterdam: Elsevier Science, 1986:335-348.
-
(1986)
Handbook of Clinical Neurology. Extrapyramidal Disorders
, vol.5
, pp. 335-348
-
-
Bruyn, G.W.1
Myrianthopoulos, N.C.2
-
6
-
-
0014622938
-
Benign, recessively inherited choreo-athetosis of early onset
-
Nutting PA, Cole BR, Schimke RN. Benign, recessively inherited choreo-athetosis of early onset. J Med Genet 1969; 6:408-410.
-
(1969)
J Med Genet
, vol.6
, pp. 408-410
-
-
Nutting, P.A.1
Cole, B.R.2
Schimke, R.N.3
-
7
-
-
0017499042
-
Familial nonprogressive involuntary movements of childhood
-
Damasio H, Antunes L, Damasio AR. Familial nonprogressive involuntary movements of childhood. Ann Neurol 1977; 1:602-603.
-
(1977)
Ann Neurol
, vol.1
, pp. 602-603
-
-
Damasio, H.1
Antunes, L.2
Damasio, A.R.3
-
8
-
-
0021243344
-
Chorée familiale non progressive, liée au sexe
-
Landrieu P, Benchet ML, Tardieu M, Lapresle J. Chorée familiale non progressive, liée au sexe. Rev Neurol (Paris) 1984;140:432-433.
-
(1984)
Rev Neurol (Paris)
, vol.140
, pp. 432-433
-
-
Landrieu, P.1
Benchet, M.L.2
Tardieu, M.3
Lapresle, J.4
-
9
-
-
9044241396
-
Benign hereditary chorea. A neuroradiologic, physiologic and psychometric investigation
-
London: Academic Press
-
Lange HW, Aulich A, Hefter H, et al. Benign hereditary chorea. A neuroradiologic, physiologic and psychometric investigation. In: Motor disturbances I. London: Academic Press, 1987:253-264.
-
(1987)
Motor Disturbances I
, pp. 253-264
-
-
Lange, H.W.1
Aulich, A.2
Hefter, H.3
-
10
-
-
0023835859
-
Benign hereditary chorea. A case report
-
Loosmore SJ, Wood K. Benign hereditary chorea. A case report. Br J Psychiatry 1988;152:131-134.
-
(1988)
Br J Psychiatry
, vol.152
, pp. 131-134
-
-
Loosmore, S.J.1
Wood, K.2
-
11
-
-
0001490037
-
Contribution à l'indépendance de l'athétose double idiopathique el congénitale
-
Syllaba L, Henner K. Contribution à l'indépendance de l'athétose double idiopathique el congénitale. Rev Neurol 1926;1:541-562.
-
(1926)
Rev Neurol
, vol.1
, pp. 541-562
-
-
Syllaba, L.1
Henner, K.2
-
12
-
-
9044237429
-
Progressive familial choreoathetosis with cutaneous telangiectasia
-
Wells CE, Shy GM. Progressive familial choreoathetosis with cutaneous telangiectasia. J Neurol Neurosurg Psychiatry 1957;20:98-104.
-
(1957)
J Neurol Neurosurg Psychiatry
, vol.20
, pp. 98-104
-
-
Wells, C.E.1
Shy, G.M.2
-
13
-
-
0022292043
-
Ataxia-telangiectasia: An overview
-
Gatti RA, Swift M, eds. New York: Liss
-
Boder E. Ataxia-telangiectasia: an overview. In: Gatti RA, Swift M, eds. Ataxia-telangiectasia. Genetics, neuropathology, and immunology of a degenerative disease of childhood. New York: Liss, 1985:1-63.
-
(1985)
Ataxia-telangiectasia. Genetics, Neuropathology, and Immunology of a Degenerative Disease of Childhood
, pp. 1-63
-
-
Boder, E.1
-
14
-
-
0023763764
-
Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: An area of confusion
-
Quinn NP, Rothwell JC, Thompson PD, Marsden CD. Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion. Adv Neurol 1988;50:391-401.
-
(1988)
Adv Neurol
, vol.50
, pp. 391-401
-
-
Quinn, N.P.1
Rothwell, J.C.2
Thompson, P.D.3
Marsden, C.D.4
-
15
-
-
0002535394
-
Sur un syndrome progressif comprenant des télangiectasies capillaires cutanées et conjonctivales symétriques, à disposition nævoïde et de troubles cérébelleux
-
Louis-Bar D. Sur un syndrome progressif comprenant des télangiectasies capillaires cutanées et conjonctivales symétriques, à disposition nævoïde et de troubles cérébelleux. Conf Neurol 1941;4:32-42.
-
(1941)
Conf Neurol
, vol.4
, pp. 32-42
-
-
Louis-Bar, D.1
-
16
-
-
9044221106
-
Palaeocerebellar atrophy with extrapyramidal manifestations in association with bronchiectasis and telangiectasis of the conjunctiva bulbi as a familial syndrome
-
van Bogaert L, Radermecker J, eds. London: Pergamon Press
-
Biemond A. Palaeocerebellar atrophy with extrapyramidal manifestations in association with bronchiectasis and telangiectasis of the conjunctiva bulbi as a familial syndrome. In: van Bogaert L, Radermecker J, eds. Proceedings 1st International Congress of Neurological Sciences, Brussels, July 1957. London: Pergamon Press, 1957:206.
-
(1957)
Proceedings 1st International Congress of Neurological Sciences, Brussels, July 1957
, pp. 206
-
-
Biemond, A.1
-
17
-
-
0002590341
-
Ataxia-telangiectasia. a familial syndrome of progressive cerebellar ataxia, oculocutaneous telangiectasia and frequent pulmonary infection. a preliminary report on 7 children, an autopsy, and a case history
-
Boder E, Sedgwick RP. Ataxia-telangiectasia. A familial syndrome of progressive cerebellar ataxia, oculocutaneous telangiectasia and frequent pulmonary infection. A preliminary report on 7 children, an autopsy, and a case history. USC Med Bull 1957;9:15-28.
-
(1957)
USC Med Bull
, vol.9
, pp. 15-28
-
-
Boder, E.1
Sedgwick, R.P.2
-
18
-
-
0001174049
-
Ataxia-telangiectasia. a review of 101 cases
-
Walsh G, ed. London: Heinemann Medical Books
-
Boder E, Sedgwick RP. Ataxia-telangiectasia. A review of 101 cases. In: Walsh G, ed. Little club clinics in developmental medicine, No. 8. London: Heinemann Medical Books, 1967:110-118.
-
(1967)
Little Club Clinics in Developmental Medicine, No. 8
, pp. 110-118
-
-
Boder, E.1
Sedgwick, R.P.2
-
20
-
-
0026575779
-
Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia
-
Lanzi G, Balottin U, Franciotta D, et al. Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia. Eur Neurol 1992;32:121-125.
-
(1992)
Eur Neurol
, vol.32
, pp. 121-125
-
-
Lanzi, G.1
Balottin, U.2
Franciotta, D.3
-
21
-
-
0021741547
-
Ataxia-without-telangiectasia. Progressive multisystem degeneration with IgE deficiency and chromosomal instability
-
Byrne E, Hallpike JF, Manson JI, Sutherland GR, Thory YH. Ataxia-without-telangiectasia. Progressive multisystem degeneration with IgE deficiency and chromosomal instability. J Neurol Sci 1984;66:307-317.
-
(1984)
J Neurol Sci
, vol.66
, pp. 307-317
-
-
Byrne, E.1
Hallpike, J.F.2
Manson, J.I.3
Sutherland, G.R.4
Thory, Y.H.5
-
22
-
-
0027357002
-
Genetic aspects of ataxia telangiectasia
-
Swift M, Hein RA, Lench NJ. Genetic aspects of ataxia telangiectasia. Adv Neurol 1993;61:115-125.
-
(1993)
Adv Neurol
, vol.61
, pp. 115-125
-
-
Swift, M.1
Hein, R.A.2
Lench, N.J.3
-
23
-
-
0027208059
-
Ataxia without telangiectasia
-
Friedman JH, Weitberg A. Ataxia without telangiectasia. Mov Disord 1993;8:223-226.
-
(1993)
Mov Disord
, vol.8
, pp. 223-226
-
-
Friedman, J.H.1
Weitberg, A.2
-
24
-
-
9044228178
-
Ataxic disorders associated with defective DNA repair. Ataxia telangiectasia
-
Harding AE. New York: Churchill Livingstone
-
Harding AE. Ataxic disorders associated with defective DNA repair. Ataxia telangiectasia. In: Harding AE. The hereditary ataxias. New York: Churchill Livingstone, 1984: 45-52.
-
(1984)
The Hereditary Ataxias
, pp. 45-52
-
-
Harding, A.E.1
-
25
-
-
0027350413
-
Candidates for the molecular defect in ataxia telangiectasia
-
Gatti RA. Candidates for the molecular defect in ataxia telangiectasia. Adv Neurol 1993;61:127-132.
-
(1993)
Adv Neurol
, vol.61
, pp. 127-132
-
-
Gatti, R.A.1
-
26
-
-
0018163187
-
Eye movements in ataxia-telangiectasia
-
Baloh RW, Yce RD, Boder E. Eye movements in ataxia-telangiectasia. Neurology 1978;28:1099-1104.
-
(1978)
Neurology
, vol.28
, pp. 1099-1104
-
-
Baloh, R.W.1
Yce, R.D.2
Boder, E.3
-
28
-
-
0027443824
-
Identification of an expanded CAG repeat in the Huntington's disease gene (IT 15) in a family reported to have benign hereditary chorea
-
MacMillan JC, Morrison PJ, Nevin NC, et al. Identification of an expanded CAG repeat in the Huntington's disease gene (IT 15) in a family reported to have benign hereditary chorea. J Med Genet 1993;30:1012-1013.
-
(1993)
J Med Genet
, vol.30
, pp. 1012-1013
-
-
MacMillan, J.C.1
Morrison, P.J.2
Nevin, N.C.3
-
29
-
-
0015448074
-
Hereditary nonprogressive involuntary movements with early onset and intention tremor, without dementia
-
Refsum S, Sjaastad O. Hereditary nonprogressive involuntary movements with early onset and intention tremor, without dementia. Acta Neurol Scand Suppl 1972;51:489-491.
-
(1972)
Acta Neurol Scand Suppl
, vol.51
, pp. 489-491
-
-
Refsum, S.1
Sjaastad, O.2
-
30
-
-
0021000171
-
Benign familial myoclonus-like movements, partly of early onset
-
Sjaastad O, Sulg I, Refsum S. Benign familial myoclonus-like movements, partly of early onset. J Neural Transm 1983;19:291-303.
-
(1983)
J Neural Transm
, vol.19
, pp. 291-303
-
-
Sjaastad, O.1
Sulg, I.2
Refsum, S.3
-
31
-
-
0027638258
-
Benign hereditary chorea or hereditary idiopathic dystonia?
-
Quinn NP. Benign hereditary chorea or hereditary idiopathic dystonia? Mov Disord 1993;8:401-402.
-
(1993)
Mov Disord
, vol.8
, pp. 401-402
-
-
Quinn, N.P.1
|