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F Hentati

Showing results (41-50 of 120) with videos related to

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Acta Neuropathologica|January 1, 1994
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduriaA Larnaout, F Hentati, S Belal, et al.
Molecular Genetics and Metabolism|April 7, 1999
Progress in neuropathology of the neuronal ceroid lipofuscinosesH H Goebel, S S Schochet, M Jaynes, et al.
Journal of Neurology|March 27, 2001
Wernicke's encephalopathy in a patient with Crohn's disease: a pathological studyA Larnaout, G El-Euch, N Kchir, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosumF Hentati, C Ben Hamida, M Zeghal, et al.
Annales De Medecine Interne|January 1, 1991
[Fatal acute pancreatitis in systemic lupus erythematosus]M Moalla, K Boussen, S Meddeb, et al.
Brain Research|March 20, 1999
Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disordersR P Copp, T Wisniewski, F Hentati, et al.
Archives Francaises De Pediatrie|December 1, 1992
[Antenatal bilateral sylvian infarction and congenital syphilis]A Larnaout, M A Mongalgi, H Ben Ameur, et al.
Clinical and Experimental Rheumatology|September 1, 1994
CD11/CD18 bearing lymphocytes in cerebrospinal fluid from patients with active Behçet's diseaseK Hamzaoui, F Hentati, A Hamzaoui, et al.
Neuropediatrics|February 24, 1999
Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patientsA Larnaout, S Belal, N Miladi, et al.
Human Genetics|September 10, 1999
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate geneS Nicole, P S White, H Topaloglu, et al.
Pageof 12

Showing results (41-50 of 120) with videos related to

Sort By:
Pageof 12
Acta Neuropathologica|January 1, 1994
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduriaA Larnaout, F Hentati, S Belal, et al.
Molecular Genetics and Metabolism|April 7, 1999
Progress in neuropathology of the neuronal ceroid lipofuscinosesH H Goebel, S S Schochet, M Jaynes, et al.
Journal of Neurology|March 27, 2001
Wernicke's encephalopathy in a patient with Crohn's disease: a pathological studyA Larnaout, G El-Euch, N Kchir, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosumF Hentati, C Ben Hamida, M Zeghal, et al.
Annales De Medecine Interne|January 1, 1991
[Fatal acute pancreatitis in systemic lupus erythematosus]M Moalla, K Boussen, S Meddeb, et al.
Brain Research|March 20, 1999
Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disordersR P Copp, T Wisniewski, F Hentati, et al.
Archives Francaises De Pediatrie|December 1, 1992
[Antenatal bilateral sylvian infarction and congenital syphilis]A Larnaout, M A Mongalgi, H Ben Ameur, et al.
Clinical and Experimental Rheumatology|September 1, 1994
CD11/CD18 bearing lymphocytes in cerebrospinal fluid from patients with active Behçet's diseaseK Hamzaoui, F Hentati, A Hamzaoui, et al.
Neuropediatrics|February 24, 1999
Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patientsA Larnaout, S Belal, N Miladi, et al.
Human Genetics|September 10, 1999
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate geneS Nicole, P S White, H Topaloglu, et al.
Pageof 12