-
1
-
-
42549117636
-
Brown-Vialetto-Van Laere syndrome
-
Sathasivam S. Brown-Vialetto-Van Laere syndrome. Orphanet J Rare Dis 2008;3:9.
-
(2008)
Orphanet J Rare Dis
, vol.3
, pp. 9
-
-
Sathasivam, S.1
-
2
-
-
77949273807
-
Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54
-
Green P, Wiseman M, Crow YJ, Houlden H, Riphagen S, Lin JP, et al. Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54. Am J Hum Genet 2010;86:485-9.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 485-489
-
-
Green, P.1
Wiseman, M.2
Crow, Y.J.3
Houlden, H.4
Riphagen, S.5
Lin, J.P.6
-
3
-
-
0342314442
-
Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance?
-
Mégarbané A, Desguerres I, Rizkallah E, Delague V, Nabbout R, Barois A, et al. Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? Am J Med Genet 2000;92:117-21.
-
(2000)
Am J Med Genet
, vol.92
, pp. 117-121
-
-
Mégarbané, A.1
Desguerres, I.2
Rizkallah, E.3
Delague, V.4
Nabbout, R.5
Barois, A.6
-
4
-
-
84891935835
-
Four cases of Brown-Vialetto-van Laere syndrome from Iran: Clinical and electrophysiologic findings
-
Yadegari S, Dezfouli MA, Nafissi S, Ghorbani A. Four cases of Brown-Vialetto-van Laere syndrome from Iran: Clinical and electrophysiologic findings. Iran J Neurol 2011;10: 54-7.
-
(2011)
Iran J Neurol
, vol.10
, pp. 54-57
-
-
Yadegari, S.1
Dezfouli, M.A.2
Nafissi, S.3
Ghorbani, A.4
-
5
-
-
0034278928
-
Brown-Vialetto-Van Laere syndrome: Case report and literature review
-
Sathasivam S, O'Sullivan S, Nicolson A, Tilley PJ, Shaw PJ. Brown-Vialetto-Van Laere syndrome: Case report and literature review. Amyotroph Lateral Scler Other Motor Neuron Disord 2000;1:277-81.
-
(2000)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.1
, pp. 277-281
-
-
Sathasivam, S.1
O'sullivan, S.2
Nicolson, A.3
Tilley, P.J.4
Shaw, P.J.5
-
6
-
-
0023390542
-
Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-van Laere syndrome or Madras-type motor neuron disease?
-
Summers BA, Swash M, Schwartz MS, Ingram DA. Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-van Laere syndrome or Madras-type motor neuron disease? J Neurol 1987;234:440-2.
-
(1987)
J Neurol
, vol.234
, pp. 440-442
-
-
Summers, B.A.1
Swash, M.2
Schwartz, M.S.3
Ingram, D.A.4
-
7
-
-
0027064530
-
Progressive bulbar paralysis of childhood
-
McShane MA, Boyd S, Harding B, Brett EM, Wilson J. Progressive bulbar paralysis of childhood. A reappraisal of Fazio-Londe disease. Brain 1992;115 (Pt 6):1889-900.
-
(1992)
A Reappraisal of Fazio-Londe Disease. Brain
, vol.115
, Issue.PART 6
, pp. 1889-1900
-
-
McShane, M.A.1
Boyd, S.2
Harding, B.3
Brett, E.M.4
Wilson, J.5
-
9
-
-
0024509068
-
Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: A dominant form of spinal muscular atrophy?
-
Boltshauser E, Lang W, Spillmann T, Hof E. Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: A dominant form of spinal muscular atrophy? J Med Genet 1989;26:105-8.
-
(1989)
J Med Genet
, vol.26
, pp. 105-108
-
-
Boltshauser, E.1
Lang, W.2
Spillmann, T.3
Hof, E.4
-
10
-
-
0014913987
-
Clinical pattern of motor neuron disease seen in younger age groups in Madras
-
Meenakshisundaram E, Jagannathan K, Ramamurthi B. Clinical pattern of motor neuron disease seen in younger age groups in Madras. Neurol India 1970;18 Suppl 1:109-12.
-
(1970)
Neurol India
, vol.18
, Issue.SUPPL. 1
, pp. 109-112
-
-
Meenakshisundaram, E.1
Jagannathan, K.2
Ramamurthi, B.3
|