-
1
-
-
0025943622
-
Bulbo-pontine paralysis with deafness: The Vialetto-Van Laere syndrome
-
ABARBANEL J.-M., ASHBY P., MARQUEZ-JULIO A., CHAPMAN K.R. (1991). Bulbo-pontine paralysis with deafness: the Vialetto-Van Laere syndrome. Can J Neurol Sei, 18:349-351.
-
(1991)
Can J Neurol Sei
, vol.18
, pp. 349-351
-
-
Abarbanel, J.-M.1
Ashby, P.2
Marquez-Julio, A.3
Chapman, K.R.4
-
2
-
-
84939120484
-
Infantile amyotrophic lateral sclerosis of the family type
-
BROWN C.H. (1894). Infantile amyotrophic lateral sclerosis of the family type. J Nerv Ment Dis, 21:707-716.
-
(1894)
J Nerv Ment Dis
, vol.21
, pp. 707-716
-
-
Brown, C.H.1
-
3
-
-
0019510555
-
Progressive pontobulbar palsy with deafness
-
BRUCHER J.-M., DOM R., LOMBAERT A., CARTON H. (1981). Progressive pontobulbar palsy with deafness. Clinical and pathological study of two cases. Arch Neural, 38 :186-190.
-
(1981)
Clinical and Pathological Study of Two Cases. Arch Neural
, vol.38
, pp. 186-190
-
-
Brucher, J.-M.1
Dom, R.2
Lombaert, A.3
Carton, H.4
-
4
-
-
85005372628
-
The Brown-Vialetto-Van Laere syndrome: A case report and literature review
-
DAVENPORT R.J., MUMFORD C.J. (1994). The Brown-Vialetto-Van Laere syndrome: a case report and literature review. Eur j Neural, 1:51-5.
-
(1994)
Eur J Neural
, vol.1
, pp. 51-55
-
-
Davenport, R.J.1
Mumford, C.J.2
-
5
-
-
0019431614
-
Ponto-bulbar palsy with deafness (Brown-Vialetto-Van Laere syndrome)
-
GALLAI V., HOCKADAY J.-M., HUGHES J.T., LANE D.J., OPPENHEIMER D.R., RUSHWORTH G. (1981). Ponto-bulbar palsy with deafness (Brown-Vialetto-Van Laere syndrome). A report on three cases. J Neural Sei, 50:259-275.
-
(1981)
A Report on Three Cases. J Neural Sei
, vol.50
, pp. 259-275
-
-
Gallai, V.1
Hockaday, J.-M.2
Hughes, J.T.3
Lane, D.J.4
Oppenheimer, D.R.5
Rushworth, G.6
-
6
-
-
0025193469
-
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible dominant heritance
-
HAWKINS S.A., NEVIN N.C., HARDING A.E. (1990). Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible dominant heritance. J Med Genet, 27 :176179.
-
(1990)
J Med Genet
, vol.27
, pp. 176179
-
-
Hawkins, S.A.1
Nevin, N.C.2
Harding, A.E.3
-
7
-
-
0025771612
-
Invited review: Motor neuropathies, motor neuron disorders, and antiglycolipid antibodies
-
PESTRONK A. (1991). Invited review: Motor neuropathies, motor neuron disorders, and antiglycolipid antibodies. Muscle Nerve, ! 14:927-936.
-
(1991)
Muscle Nerve, !
, vol.14
, pp. 927-936
-
-
Pestronk, A.1
-
8
-
-
0026629712
-
Recovery from respiratory failure in a sporadic . case of Brown-Vialetto-Van Laere syndrome with unusually late onset
-
PICCOLO G., MARCHIONI E., MAURELLI M., SIMONETTI F., BIZZETTI F., SAVOLDI F. (1992). Recovery from respiratory failure in a sporadic . case of Brown-Vialetto-Van Laere syndrome with unusually late onset. J Neural, 239:355-356.
-
(1992)
J Neural
, vol.239
, pp. 355-356
-
-
Piccolo, G.1
Marchioni, E.2
Maurelli, M.3
Simonetti, F.4
Bizzetti, F.5
Savoldi, F.6
-
10
-
-
0002915627
-
Contributo alla forma ereditaria délia paralisi bulbare progressiva
-
VIALETTO E. (1936). Contributo alla forma ereditaria délia paralisi bulbare progressiva. Riv Sper Frenatr Med Légale Mondiali, 40 : 1-24.
-
(1936)
Riv Sper Frenatr Med Légale Mondiali
, vol.40
, pp. 1-24
-
-
Vialetto, E.1
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