M. Hamida

发表

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome

M. Hallett, K. Wessel, S. Subramony, 1997, Journal of the Neurological Sciences.

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.

Novel mutations in spastin gene and absence of correlation with age at onset of symptoms

W. Hung, T. Siddique, N. Laing, 2000, Neurology.

The gene encoding ganglioside- induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease

J. Gilbert, M. Pericak-Vance, J. Vance, 2001 .

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

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

Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein Po

M. Hamida, A. Steck, K. Dellagi, 1992, Annals of neurology.

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

J. Gilbert, M. Pericak-Vance, J. Vance, 2002, Nature Genetics.

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.

The dentato-olivary pathway. Somatotopic relationship between the dentate nucleus and the contralateral inferior olive.

M. Hamida, J. Lapresle, 1970, Archives of neurology.

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Pieter J. de Jong, Saeed Bohlega, Jing Liu, 1998, Nature Genetics.

Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

L. Kunkel, J. Vance, L. Middleton, 1995, Science.

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.

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.

Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred

M. Hamida, F. Hentati, Christiane Ben Hamida, PhD, 1990, Neurology.

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.

Clinical and genetic study of familial Parkinson’s disease in Tunisia

M. Hamida, N. Gouider-Khouja, F. Hentati, 2000, Neurology.

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.

M. Pericak-Vance, J. Vance, M. Hamida, 1999, Genomics.

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33

J. Haines, H. Horvitz, M. Hamida, 1998, Neurogenetics.

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.

Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency

M. Hamida, N. Gouider-Khouja, I. Turki, 2001, European journal of neurology.

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.

Localization of α-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders

T. Wisniewski, M. Hamida, F. Hentati, 1999, Brain Research.

Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

M. Koenig, J. Mandel, M. Hamida, 1995, Nature Genetics.

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.

Multiple cranial nerve deficits associated with the Arnold‐Chiari malformation

K. Shulman, M. Hamida, R. Sieben, 1971, Neurology.

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

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

Duchenne muscular dystrophy in Tunisia: A clinical and morphological study of 77 cases

M. Hamida, I. Turki, N. Miladi, 1992, Journal of the Neurological Sciences.

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.

Giant axonal neuropathy locus refinement to a < 590 kb critical interval

M. Hamida, D. Callen, H. Topaloglu, 2000, European Journal of Human Genetics.

Hypertrophic neuropathy in spinocerebellar degeneration

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

Prevalence of Epilepsy in Kelibia, Tunisia

M. Hamida, A. Mrabet, N. Attia-Romdhane, 1993, Epilepsia.

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.

Serum Vitamin E and Lipid-adjusted Vitamin E Assess- ment in Friedreich Ataxia Phenotype Patients and Un-

M. Hamida, M. Feki, M. Souissi, 2002 .

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.

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

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

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.

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.

M. Pericak-Vance, W. Hung, M. Angrist, 1994, Human molecular genetics.

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.

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

M. Pericak-Vance, W. Hung, T. Siddique, 1998, Neurogenetics.

A clinicopathological observation of Nyssen–van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities

M. Hamida, F. Hentati, A. Larnaout, 1998, Acta neurologica Scandinavica.

Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.

M. Pericak-Vance, J. Vance, M. Hamida, 1995, Genomics.

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

M. Pericak-Vance, J. Vance, M. Hamida, 1993, Human molecular genetics.

Methylmalonic acidaemia with bilateral globus pallidus involvement: A neuropathological study

M. Hamida, D. Khiari, M. Ben Hamida, 1998, Journal of Inherited Metabolic Disease.