C. Hamida

发表

Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis

M. Hamida, F. Hentati, F. Letaief, 1987, Journal of the Neurological Sciences.

Limb-girdle muscular dystrophy 2C: Clinical aspects

M. Hamida, F. Hentati, S. Belal, 1996, Neuromuscular Disorders.

Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1

M. Koenig, J. Mandel, M. Hamida, 1997, Neurogenetics.

Replicative potential and telomere length in human skeletal muscle: implications for satellite cell-mediated gene therapy.

G. Butler-Browne, V. Mouly, J. Barbet, 1997, Human gene therapy.

Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum

M. Hamida, F. Hentati, M. Kamoun, 1992, Neuromuscular Disorders.

Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children

G. Butler-Browne, V. Mouly, J. Barbet, 2000, Neuromuscular Disorders.

Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation

L. Kunkel, M. Hamida, F. Hentati, 2003, Neuromuscular Disorders.

Friedreich’s ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient

H. Goebel, M. Hamida, F. Hentati, 1997, Acta Neuropathologica.

Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency

M. Hamida, M. Feki, I. Turki, 1998, Neuromuscular Disorders.

HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS) CONDITIONS COMBINING A BILATERAL PYRAMIDAL SYNDROME WITH LIMB AND BULBAR AMYOTROPHY by MONGI BEN HAMIDA, FAY£AL HENTATI and CHRISTIANE BEN HAMIDA

C. Hamida, 2022 .

Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy

M. Hamida, G. Butler-Browne, F. Hentati, 1994, Muscle & nerve.

Evolution of muscle specific proteins in Werdnig-Hoffman's disease

M. Hamida, G. Butler-Browne, F. Hentati, 1992, Journal of the Neurological Sciences.

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

M. Koenig, B. Tüysüz, H. Topaloglu, 2000, Nature Genetics.

Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)

J. Weissenbach, P. Beighton, D. Samson, 2000, Nature Genetics.

Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval

J. Weissenbach, P. Beighton, M. Hamida, 1996, Human Genetics.

Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q

M. Pericak-Vance, A. Roses, A. Bowcock, 1992, Nature Genetics.

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35

J. Haines, M. Pericak-Vance, Robert H. Brown, 1994, Nature Genetics.

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

J. Haines, J. Weissenbach, R. Griggs, 1995, Neurology.

Autosomal Recessive Ataxia Caused by Three Distinct Gene Defects in a Single Consanguineous Family

F. Hentati, Y. Bouhlal, R. Amouri, 2008, Journal of neurogenetics.

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3

M. Hamida, N. Gouider-Khouja, F. Hentati, 2000, Neuromuscular Disorders.

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families

J. Beckmann, G. Sirugo, M. Koenig, 1993, Neurology.

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family

M. Hamida, I. Turki, F. Hentati, 2000, Neurology.

Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy

M. Hamida, G. Butler-Browne, F. Hentati, 1994, Journal of the Neurological Sciences.

Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy

M. Hamida, J. Kaplan, K. Dellagi, 1990, Neurology.

LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3

C. Bönnemann, L. Kunkel, M. Hamida, 1998, Neuromuscular Disorders.

Hypertrophic neuropathy in spinocerebellar degeneration

M. Hamida, F. Hentati, F. Letaief, 2004, Acta Neuropathologica.

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus

Y. Agid, G. Stevanin, M. Hamida, 1994, Neurology.

Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3

M. Hamida, F. Hentati, R. Amouri, 2001, Neuromuscular Disorders.

Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome

M. Hamida, G. Butler-Browne, F. Hentati, 1991, Journal of the Neurological Sciences.

Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping.

J. Weissenbach, P. Beighton, D. Viljoen, 1995, Human molecular genetics.

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy.

M. Hamida, M. Ben Hamida, F. Hentati, 1990, Brain : a journal of neurology.

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

G. Gyapay, J. Weissenbach, D. Le Paslier, 1995, American journal of human genetics.

Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria

M. Ben Hamida, F. Hentati, N. Kaabachi, 2004, Acta Neuropathologica.