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Journal of the Neurological Sciences
|
May 1, 1994
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy
C B Hamida, N Soussi-Yanicostas, K Bejaoui, et al.
Neuromuscular Disorders : NMD
|
June 6, 2000
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
A Driss, R Amouri, C Ben Hamida, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
M Kefi, R Amouri, A Driss, et al.
Journal of the Neurological Sciences
|
July 1, 1991
Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome
N Soussi-Yanicostas, C Ben Hamida, G S Butler-Browne, et al.
La Tunisie Medicale
|
October 18, 2006
[Cardiac involvement in Emery-Dreifuss muscular dystrophy: a case report]
S Chabrak, S Ammar, N Ammar, et al.
Neurology
|
April 6, 2000
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
N Mrissa, S Belal, C B Hamida, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study
A Larnaout, M A Mongalgi, N Kaabachi, et al.
Acta Neuropathologica
|
June 1, 1997
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient
A Larnaout, S Belal, M Zouari, et al.
Journal De Genetique Humaine
|
August 1, 1986
[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence]
M Ben Hamida, H Chaabouni, S Madani, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
March 21, 2007
Reversible metronidazole-induced encephalopathy
N Hammami, C Drissi, R Sebai, et al.
Page
of 12
Search research articles
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Showing results (61-70 of 120) with videos related to
Sort By:
Page
of 12
Journal of the Neurological Sciences
|
May 1, 1994
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy
C B Hamida, N Soussi-Yanicostas, K Bejaoui, et al.
Neuromuscular Disorders : NMD
|
June 6, 2000
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
A Driss, R Amouri, C Ben Hamida, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
M Kefi, R Amouri, A Driss, et al.
Journal of the Neurological Sciences
|
July 1, 1991
Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome
N Soussi-Yanicostas, C Ben Hamida, G S Butler-Browne, et al.
La Tunisie Medicale
|
October 18, 2006
[Cardiac involvement in Emery-Dreifuss muscular dystrophy: a case report]
S Chabrak, S Ammar, N Ammar, et al.
Neurology
|
April 6, 2000
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
N Mrissa, S Belal, C B Hamida, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study
A Larnaout, M A Mongalgi, N Kaabachi, et al.
Acta Neuropathologica
|
June 1, 1997
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient
A Larnaout, S Belal, M Zouari, et al.
Journal De Genetique Humaine
|
August 1, 1986
[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence]
M Ben Hamida, H Chaabouni, S Madani, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
March 21, 2007
Reversible metronidazole-induced encephalopathy
N Hammami, C Drissi, R Sebai, et al.
Page
of 12