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F Hentati

Showing results (21-30 of 120) with videos related to

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Neuropediatrics|August 2, 2008
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutationsM Kefi, R Amouri, S Chabrak, et al.
Neuropediatrics|November 11, 2008
Wilson's disease: appreciable improvement of sub-cortical white matter abnormalities after copper chelating treatment: five years follow-upA Larnaout, N Ammar, Z Mourad, et al.
Journal of the Neurological Sciences|May 1, 1987
Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosisM Ben Hamida, F Letaief, F Hentati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Distinct phenotypes within autosomal recessive ataxias not linked to already known lociY Bouhlal, G El-Euch-Fayeche, R Amouri, et al.
La Tunisie Medicale|March 24, 2000
Prognostic factors in congenital hemiplegia in full-term and preterm childrenA Larnaout, M T De Lattore, G Lyon, et al.
Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locusS Belal, F Hentati, C Ben Hamida, et al.
Revue Neurologique|April 1, 1995
[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty]M Ben Hamida, K Ben Othmane, S Belal, et al.
Acta Neuropathologica|January 1, 1985
Familial disorder of the central and peripheral nervous systems with particular cytoplasmic lamellated inclusions in peripheral nerves, muscle satellite cells, and blood capillariesF M Tomé, P Brunet, M Fardeau, et al.
Journal of Inherited Metabolic Disease|October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduriaA Larnaout, R Amouri, S Neji, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 1, 1994
[Congenital fibrolipoma of the mesencephalic protuberation area]A Larnaout, F Hentati, C Ben Hamida, et al.
Pageof 12

Showing results (21-30 of 120) with videos related to

Sort By:
Pageof 12
Neuropediatrics|August 2, 2008
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutationsM Kefi, R Amouri, S Chabrak, et al.
Neuropediatrics|November 11, 2008
Wilson's disease: appreciable improvement of sub-cortical white matter abnormalities after copper chelating treatment: five years follow-upA Larnaout, N Ammar, Z Mourad, et al.
Journal of the Neurological Sciences|May 1, 1987
Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosisM Ben Hamida, F Letaief, F Hentati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Distinct phenotypes within autosomal recessive ataxias not linked to already known lociY Bouhlal, G El-Euch-Fayeche, R Amouri, et al.
La Tunisie Medicale|March 24, 2000
Prognostic factors in congenital hemiplegia in full-term and preterm childrenA Larnaout, M T De Lattore, G Lyon, et al.
Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locusS Belal, F Hentati, C Ben Hamida, et al.
Revue Neurologique|April 1, 1995
[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty]M Ben Hamida, K Ben Othmane, S Belal, et al.
Acta Neuropathologica|January 1, 1985
Familial disorder of the central and peripheral nervous systems with particular cytoplasmic lamellated inclusions in peripheral nerves, muscle satellite cells, and blood capillariesF M Tomé, P Brunet, M Fardeau, et al.
Journal of Inherited Metabolic Disease|October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduriaA Larnaout, R Amouri, S Neji, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 1, 1994
[Congenital fibrolipoma of the mesencephalic protuberation area]A Larnaout, F Hentati, C Ben Hamida, et al.
Pageof 12