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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 25, 2012
[Neonatal renal vein thrombosis in a heterozygous carrier of both factor V Leiden and the MTHFR gene mutation]
S Wannes, H Soua, S Ghanmi, et al.
Diagnostic and Interventional Imaging
|
August 28, 2012
Pfeiffer syndrome type II discovered perinatally: Report of an observation and review of the literature
H Ben Hamouda, Y Tlili, S Ghanmi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 30, 2017
[Prenatal diagnosis and management of two cases of bilateral ureteroceles on simplex ureters]
H Ben Hamouda, H Bouchahda, S Ghanmi, et al.
Acta Orthopaedica Belgica
|
February 2, 2002
Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum
H Ben Hamouda, M N Sfar, R Braham, et al.
Annales D'Endocrinologie
|
June 18, 2010
[Long-term follow-up of permanent neonatal diabetes in Tunisian infant]
H Ben Hamouda, F Chioukh, B Boussetta, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
September 19, 2009
Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX
H Ben Hamouda, N Mkacher, H Elghezal, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie
|
June 23, 2011
[Management and follow-up of antenatally diagnosed primary megaureters]
S Ghanmi, H Ben Hamouda, I Krichene, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 5, 2014
[Prenatal diagnosis of a giant cystic lymphangioma in the axillothoracic wall]
H Ben Hamouda, O Gasmi, S Wannes, 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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Search research articles
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Showing results (21-30 of 29) with videos related to
Sort By:
Page
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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
|
February 25, 2012
[Neonatal renal vein thrombosis in a heterozygous carrier of both factor V Leiden and the MTHFR gene mutation]
S Wannes, H Soua, S Ghanmi, et al.
Diagnostic and Interventional Imaging
|
August 28, 2012
Pfeiffer syndrome type II discovered perinatally: Report of an observation and review of the literature
H Ben Hamouda, Y Tlili, S Ghanmi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 30, 2017
[Prenatal diagnosis and management of two cases of bilateral ureteroceles on simplex ureters]
H Ben Hamouda, H Bouchahda, S Ghanmi, et al.
Acta Orthopaedica Belgica
|
February 2, 2002
Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum
H Ben Hamouda, M N Sfar, R Braham, et al.
Annales D'Endocrinologie
|
June 18, 2010
[Long-term follow-up of permanent neonatal diabetes in Tunisian infant]
H Ben Hamouda, F Chioukh, B Boussetta, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
September 19, 2009
Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX
H Ben Hamouda, N Mkacher, H Elghezal, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie
|
June 23, 2011
[Management and follow-up of antenatally diagnosed primary megaureters]
S Ghanmi, H Ben Hamouda, I Krichene, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 5, 2014
[Prenatal diagnosis of a giant cystic lymphangioma in the axillothoracic wall]
H Ben Hamouda, O Gasmi, S Wannes, 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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of 3