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M F Ben Dridi

Showing results (11-20 of 26) with videos related to

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Annales De Pediatrie|December 1, 1990
[Nesidioblastosis. Apropos of 12 new cases]A Samoud, D Dey, R Brauner, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|January 30, 2009
Phenotypic continuum of type 2 Gaucher's disease: an intermediate phenotype between perinatal-lethal and classic type 2 Gaucher's diseaseH Ben Turkia, N Tebib, H Azzouz, et al.
Pediatric Radiology|January 1, 1987
Radiological abnormalities of the skeleton in patients with sickle-cell anemia. A study of 222 cases in TunisiaM F Ben Dridi, A Oumaya, H Gastli, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 26, 2008
[Congenital generalized lipodystrophy: a case report with neurological involvement]H Ben Turkia, N Tebib, H Azzouz, et al.
Pathologie-Biologie|May 11, 2012
A novel 22bp deletion in a Tunisian phenylketonuria familyS Khemir, H Siala, H Azzouz, et al.
Journal Des Maladies Vasculaires|November 22, 2008
[Atypical presentation of Wegener disease in childhood]H Ben Turkia, N Amdouni, H Azzouz, et al.
Archives Francaises De Pediatrie|August 1, 1992
[Recessive osteopetrosis. Identification of a form of medium severity]M Bejaoui, M Baraket, R Lakhoua, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 14, 2011
Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patientsS Ouesleti, V Brunel, H Ben Turkia, et al.
Pathologie-Biologie|November 10, 2009
Homogénéité mutationnelle de la glycogénose de type Ia en TunisieW Cherif, F Ben Rhouma, A Ben Chehida, et al.
Journal of Inherited Metabolic Disease|July 25, 2008
Phenotypic spectrum of fucosidosis in TunisiaH Ben Turkia, N Tebib, H Azzouz, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Annales De Pediatrie|December 1, 1990
[Nesidioblastosis. Apropos of 12 new cases]A Samoud, D Dey, R Brauner, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|January 30, 2009
Phenotypic continuum of type 2 Gaucher's disease: an intermediate phenotype between perinatal-lethal and classic type 2 Gaucher's diseaseH Ben Turkia, N Tebib, H Azzouz, et al.
Pediatric Radiology|January 1, 1987
Radiological abnormalities of the skeleton in patients with sickle-cell anemia. A study of 222 cases in TunisiaM F Ben Dridi, A Oumaya, H Gastli, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 26, 2008
[Congenital generalized lipodystrophy: a case report with neurological involvement]H Ben Turkia, N Tebib, H Azzouz, et al.
Pathologie-Biologie|May 11, 2012
A novel 22bp deletion in a Tunisian phenylketonuria familyS Khemir, H Siala, H Azzouz, et al.
Journal Des Maladies Vasculaires|November 22, 2008
[Atypical presentation of Wegener disease in childhood]H Ben Turkia, N Amdouni, H Azzouz, et al.
Archives Francaises De Pediatrie|August 1, 1992
[Recessive osteopetrosis. Identification of a form of medium severity]M Bejaoui, M Baraket, R Lakhoua, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 14, 2011
Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patientsS Ouesleti, V Brunel, H Ben Turkia, et al.
Pathologie-Biologie|November 10, 2009
Homogénéité mutationnelle de la glycogénose de type Ia en TunisieW Cherif, F Ben Rhouma, A Ben Chehida, et al.
Journal of Inherited Metabolic Disease|July 25, 2008
Phenotypic spectrum of fucosidosis in TunisiaH Ben Turkia, N Tebib, H Azzouz, et al.
Pageof 3