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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 disease
H 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 Tunisia
M 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 family
S 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 patients
S Ouesleti, V Brunel, H Ben Turkia, et al.
Pathologie-Biologie
|
November 10, 2009
Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie
W Cherif, F Ben Rhouma, A Ben Chehida, et al.
Journal of Inherited Metabolic Disease
|
July 25, 2008
Phenotypic spectrum of fucosidosis in Tunisia
H Ben Turkia, N Tebib, H Azzouz, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 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 disease
H 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 Tunisia
M 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 family
S 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 patients
S Ouesleti, V Brunel, H Ben Turkia, et al.
Pathologie-Biologie
|
November 10, 2009
Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie
W Cherif, F Ben Rhouma, A Ben Chehida, et al.
Journal of Inherited Metabolic Disease
|
July 25, 2008
Phenotypic spectrum of fucosidosis in Tunisia
H Ben Turkia, N Tebib, H Azzouz, et al.
Page
of 3