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A Larnaout

Showing results (1-10 of 31) with videos related to

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La Tunisie Medicale|June 1, 1992
[How to treat epilepsy in children?]N Miladi, A Larnaout, I Turki
La Tunisie Medicale|November 1, 1992
[Pregnancy and epilepsy. Management]A Larnaout, N Miladi, S Meddeb
Acta Neurologica Scandinavica|January 6, 1999
A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entitiesA Larnaout, M Ben Hamida, F Hentati
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1990
Guillain-Barré syndrome and idiopathic thrombocytopenic purpuraF Khaldi, A Larnaout, N Miladi, 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.
Revue Neurologique|January 1, 1992
[Candida albicans meningitis and neurosarcoidosis]A Larnaout, M Haddad, F Hentati, 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.
Annales De Pediatrie|April 1, 1988
[Meningoencephalomyelitis and exophthalmos disclosing acute myeloid leukemia, M1 type]M Trabelsi, A Larnaout, F Guerfallah, 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.
Journal of Child Neurology|January 1, 1992
Phenylketonuria: an underlying etiology of autistic syndrome. A case reportN Miladi, A Larnaout, N Kaabachi, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
La Tunisie Medicale|June 1, 1992
[How to treat epilepsy in children?]N Miladi, A Larnaout, I Turki
La Tunisie Medicale|November 1, 1992
[Pregnancy and epilepsy. Management]A Larnaout, N Miladi, S Meddeb
Acta Neurologica Scandinavica|January 6, 1999
A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entitiesA Larnaout, M Ben Hamida, F Hentati
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1990
Guillain-Barré syndrome and idiopathic thrombocytopenic purpuraF Khaldi, A Larnaout, N Miladi, 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.
Revue Neurologique|January 1, 1992
[Candida albicans meningitis and neurosarcoidosis]A Larnaout, M Haddad, F Hentati, 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.
Annales De Pediatrie|April 1, 1988
[Meningoencephalomyelitis and exophthalmos disclosing acute myeloid leukemia, M1 type]M Trabelsi, A Larnaout, F Guerfallah, 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.
Journal of Child Neurology|January 1, 1992
Phenylketonuria: an underlying etiology of autistic syndrome. A case reportN Miladi, A Larnaout, N Kaabachi, et al.
Pageof 4