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K Monastiri

Showing results (21-30 of 29) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 2, 2015
Sanjad-Sakati syndrome in a Tunisian childE Kerkeni, R Sakka, S Sfar, 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.
La Revue De Medecine Interne|January 28, 2004
[Gaucher's disease in Tunisia (multicenter study)]M Chaabouni, H Aoulou, N Tebib, et al.
Annales De Biologie Clinique|November 28, 2007
[Biochemical and molecular diagnosis of Gaucher disease in Tunisia]A Dandana, S Ferchichi, S Khedhiri, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 10, 2013
[Cervical teratoma in a child]A Ksia, S Mosbahi, A Zrig, et al.
Clinical Genetics|May 27, 2015
Comorbidity in the Tunisian populationL Romdhane, O Messaoud, Y Bouyacoub, et al.
Journal of Inherited Metabolic Disease|November 17, 2007
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosisE 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 mutationsC Charfeddine, K Monastiri, M Mokni, et al.
La Tunisie Medicale|June 1, 2026
Abstracts Association Tunisienne de Médecine Néonatale (ATMN)M Abid, A Abdennadher, F Abdelhaedi, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 2, 2015
Sanjad-Sakati syndrome in a Tunisian childE Kerkeni, R Sakka, S Sfar, 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.
La Revue De Medecine Interne|January 28, 2004
[Gaucher's disease in Tunisia (multicenter study)]M Chaabouni, H Aoulou, N Tebib, et al.
Annales De Biologie Clinique|November 28, 2007
[Biochemical and molecular diagnosis of Gaucher disease in Tunisia]A Dandana, S Ferchichi, S Khedhiri, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 10, 2013
[Cervical teratoma in a child]A Ksia, S Mosbahi, A Zrig, et al.
Clinical Genetics|May 27, 2015
Comorbidity in the Tunisian populationL Romdhane, O Messaoud, Y Bouyacoub, et al.
Journal of Inherited Metabolic Disease|November 17, 2007
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosisE 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 mutationsC Charfeddine, K Monastiri, M Mokni, et al.
La Tunisie Medicale|June 1, 2026
Abstracts Association Tunisienne de Médecine Néonatale (ATMN)M Abid, A Abdennadher, F Abdelhaedi, et al.
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