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Neuropediatrics
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August 2, 2008
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutations
M 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-up
A 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 sclerosis
M 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 loci
Y 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 children
A 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 locus
S 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 capillaries
F M Tomé, P Brunet, M Fardeau, et al.
Journal of Inherited Metabolic Disease
|
October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduria
A 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.
Page
of 12
Search research articles
Search
Showing results (21-30 of 120) with videos related to
Sort By:
Page
of 12
Neuropediatrics
|
August 2, 2008
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutations
M 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-up
A 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 sclerosis
M 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 loci
Y 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 children
A 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 locus
S 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 capillaries
F M Tomé, P Brunet, M Fardeau, et al.
Journal of Inherited Metabolic Disease
|
October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduria
A 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.
Page
of 12