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F Hentati

Showing results (11-20 of 120) with videos related to

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Neuromuscular Disorders : NMD|April 18, 2006
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genesK Fendri, M Kefi, F Hentati, et al.
Journal of Inherited Metabolic Disease|September 10, 2008
L-2-hydroxyglutaric aciduria: clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variabilityA Larnaout, R Amouri, M Kefi, et al.
Neurology|February 1, 1990
Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindredM Ben Hamida, F Hentati, C Ben Hamida
Revue Neurologique|January 1, 1992
[Candida albicans meningitis and neurosarcoidosis]A Larnaout, M Haddad, F Hentati, et al.
Clinical Genetics|April 12, 2001
Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian familiesN Marzouki, S Belal, C Benhamida, et al.
Acta Neuropathologica|January 1, 1987
Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen casesM Ben Hamida, F Letaief, F Hentati, et al.
La Tunisie Medicale|May 20, 1999
[Treatment of cervical dystonia with botulinum toxin]N Gouider-Khouja, I Turki, M Ben Hamida, et al.
Advances in Neurology|January 1, 1993
Early onset ataxias in Tunisia. Intrafamilial heterogeneityM Ben Hamida, N Attia-Romdhane, F Hentati, et al.
La Tunisie Medicale|May 20, 1999
[Hemifacial spasm and its treatment with botulinum toxin]N Gouider-Khouja, I Turki, M Ben Hamida, et al.
Neurology|April 13, 2000
Clinical and genetic study of familial Parkinson's disease in TunisiaN Gouider-Khouja, S Belal, M B Hamida, et al.
Pageof 12

Showing results (11-20 of 120) with videos related to

Sort By:
Pageof 12
Neuromuscular Disorders : NMD|April 18, 2006
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genesK Fendri, M Kefi, F Hentati, et al.
Journal of Inherited Metabolic Disease|September 10, 2008
L-2-hydroxyglutaric aciduria: clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variabilityA Larnaout, R Amouri, M Kefi, et al.
Neurology|February 1, 1990
Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindredM Ben Hamida, F Hentati, C Ben Hamida
Revue Neurologique|January 1, 1992
[Candida albicans meningitis and neurosarcoidosis]A Larnaout, M Haddad, F Hentati, et al.
Clinical Genetics|April 12, 2001
Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian familiesN Marzouki, S Belal, C Benhamida, et al.
Acta Neuropathologica|January 1, 1987
Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen casesM Ben Hamida, F Letaief, F Hentati, et al.
La Tunisie Medicale|May 20, 1999
[Treatment of cervical dystonia with botulinum toxin]N Gouider-Khouja, I Turki, M Ben Hamida, et al.
Advances in Neurology|January 1, 1993
Early onset ataxias in Tunisia. Intrafamilial heterogeneityM Ben Hamida, N Attia-Romdhane, F Hentati, et al.
La Tunisie Medicale|May 20, 1999
[Hemifacial spasm and its treatment with botulinum toxin]N Gouider-Khouja, I Turki, M Ben Hamida, et al.
Neurology|April 13, 2000
Clinical and genetic study of familial Parkinson's disease in TunisiaN Gouider-Khouja, S Belal, M B Hamida, et al.
Pageof 12