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Annales De Dermatologie Et De Venereologie
|
January 29, 1999
[Childhood plaque milia of the inner canthus]
S Bouassida, T J Meziou, H Mlik, et al.
Journal Francais D'Ophtalmologie
|
May 5, 2000
[Effect of scleral indentation on the corneal topography and the axial length after retinal detachment surgery. A prospective study in 30 cases]
J Feki, M Mlik, M Ould El Hassan, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
September 18, 2003
[Diastematomyelia: antenatal diagnosis with successful outcome, two cases]
A Cherif, B Oueslati, Z Marrakchi, et al.
Annales De Biologie Clinique
|
August 7, 2004
[Determination of anti-transglutaminase antibodies in the diagnosis of coeliac disease in children: results of a five year prospective study]
L Laadhar, N Bouaziz, M Ben Ayed, et al.
Molecular Genetics & Genomic Medicine
|
November 2, 2020
SQSTM1 mutation: Description of the first Tunisian case and literature review
M Akkari, I Kraoua, H Klaa, et al.
Journal Francais D'Ophtalmologie
|
July 27, 1999
[Blepharitis due to Demodex: myth or reality?]
B Kamoun, M Fourati, J Feki, et al.
European Journal of Human Genetics : EJHG
|
May 11, 1999
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2
M Hmani, A Ghorbel, A Boulila-Elgaied, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 19, 2007
[Devic's neuromyelitis optica in children: a case report and review of the literature]
N Djemal, M Ben Salah, N Ben Hlima, et al.
La Tunisie Medicale
|
May 20, 1999
[Epidemiological and evolutionary profile of childhood celiac disease (report of 118 cases)]
M Hachicha, M Chaabouni, S Marrekchi, et al.
European Journal of Medical Genetics
|
June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region
M Chaabouni, M Le Merrer, O Raoul, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 66) with videos related to
Sort By:
Page
of 7
Annales De Dermatologie Et De Venereologie
|
January 29, 1999
[Childhood plaque milia of the inner canthus]
S Bouassida, T J Meziou, H Mlik, et al.
Journal Francais D'Ophtalmologie
|
May 5, 2000
[Effect of scleral indentation on the corneal topography and the axial length after retinal detachment surgery. A prospective study in 30 cases]
J Feki, M Mlik, M Ould El Hassan, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
September 18, 2003
[Diastematomyelia: antenatal diagnosis with successful outcome, two cases]
A Cherif, B Oueslati, Z Marrakchi, et al.
Annales De Biologie Clinique
|
August 7, 2004
[Determination of anti-transglutaminase antibodies in the diagnosis of coeliac disease in children: results of a five year prospective study]
L Laadhar, N Bouaziz, M Ben Ayed, et al.
Molecular Genetics & Genomic Medicine
|
November 2, 2020
SQSTM1 mutation: Description of the first Tunisian case and literature review
M Akkari, I Kraoua, H Klaa, et al.
Journal Francais D'Ophtalmologie
|
July 27, 1999
[Blepharitis due to Demodex: myth or reality?]
B Kamoun, M Fourati, J Feki, et al.
European Journal of Human Genetics : EJHG
|
May 11, 1999
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2
M Hmani, A Ghorbel, A Boulila-Elgaied, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 19, 2007
[Devic's neuromyelitis optica in children: a case report and review of the literature]
N Djemal, M Ben Salah, N Ben Hlima, et al.
La Tunisie Medicale
|
May 20, 1999
[Epidemiological and evolutionary profile of childhood celiac disease (report of 118 cases)]
M Hachicha, M Chaabouni, S Marrekchi, et al.
European Journal of Medical Genetics
|
June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region
M Chaabouni, M Le Merrer, O Raoul, et al.
Page
of 7