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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 18, 2018
Factors predictive of prognosis of infantile spasms. A retrospective study in a low-income country
R Ben Abdelaziz, A Ben Chehida, M Lamouchi, 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.
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.
La Revue De Medecine Interne
|
January 28, 2004
[Gaucher's disease in Tunisia (multicenter study)]
M Chaabouni, H Aoulou, N Tebib, et al.
Archives De L'Institut Pasteur De Tunis
|
April 25, 2009
[Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous]
W Cherif, H Ben Turkia, N Tebib, et al.
Pathologie-Biologie
|
May 1, 2012
[Molecular diagnosis of Gaucher disease in Tunisia]
W Cherif, H Ben Turkia, F Ben Rhouma, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 14, 2011
[Rosai-Dorfman disease: therapeutic issues in 2 cases]
H Ben Turkia, M Ben Romdhane, H Azzouz, et al.
Journal of Human Genetics
|
August 29, 2006
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia
R El Kares, M R Barbouche, H Elloumi-Zghal, et al.
Journal of Inherited Metabolic Disease
|
November 17, 2007
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis
E Barkaoui, W Cherif, N Tebib, et al.
Molecular Genetics and Metabolism
|
April 1, 2006
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations
C Charfeddine, K Monastiri, M Mokni, et al.
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of 2
Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 18, 2018
Factors predictive of prognosis of infantile spasms. A retrospective study in a low-income country
R Ben Abdelaziz, A Ben Chehida, M Lamouchi, 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.
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.
La Revue De Medecine Interne
|
January 28, 2004
[Gaucher's disease in Tunisia (multicenter study)]
M Chaabouni, H Aoulou, N Tebib, et al.
Archives De L'Institut Pasteur De Tunis
|
April 25, 2009
[Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous]
W Cherif, H Ben Turkia, N Tebib, et al.
Pathologie-Biologie
|
May 1, 2012
[Molecular diagnosis of Gaucher disease in Tunisia]
W Cherif, H Ben Turkia, F Ben Rhouma, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 14, 2011
[Rosai-Dorfman disease: therapeutic issues in 2 cases]
H Ben Turkia, M Ben Romdhane, H Azzouz, et al.
Journal of Human Genetics
|
August 29, 2006
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia
R El Kares, M R Barbouche, H Elloumi-Zghal, et al.
Journal of Inherited Metabolic Disease
|
November 17, 2007
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis
E Barkaoui, W Cherif, N Tebib, et al.
Molecular Genetics and Metabolism
|
April 1, 2006
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations
C Charfeddine, K Monastiri, M Mokni, et al.
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of 2