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Revue Neurologique
|
January 1, 1991
[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias]
M Ben Hamida, N Attia-Romdhane, C H Triki, et al.
Pathologie-Biologie
|
August 18, 2015
Association of TGFB1 -509C/T polymorphism gene with clinical variability in cystic fibrosis patients: A case-control study
S Oueslati, S Hadj Fredj, B Dakhlaoui, et al.
Acta Physiologica Hungarica
|
December 8, 2014
Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation
S Oueslati, S Hadj Fredj, R Belhaj, et al.
Journal De Radiologie
|
August 12, 2003
[MRI in the diagnosis of Rathke's cleft cyst]
N Mnif, A Hamrouni, C Iffenecker, et al.
Revue Neurologique
|
January 1, 1990
[Subacute brainstem hematoma. A surgically treated case]
H Cambon, J Shen, P Cornu, et al.
European Journal of Gynaecological Oncology
|
May 23, 2012
Impact of sampling origin on molecular detection of high-risk human papillomavirus and oncogene expression
S Kahla, M Achour, S Oueslati, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
March 8, 2003
[MRI of cerebral cortical dysgenesis]
N Mnif, S Oueslati, M Fredj, et al.
Journal De Radiologie
|
June 9, 2009
[Imaging features of Takayasu's arteritis]
L Charrada-Ben Farhat, A Miaoui, A Askri, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
November 8, 2006
[Ectopic thyroid]
S Oueslati, W Douira, L Charada, et al.
The Journal of Antimicrobial Chemotherapy
|
January 30, 2015
OXY-2-15, a novel variant showing increased ceftazidime hydrolytic activity
R H T Nijhuis, S Oueslati, K Zhou, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Revue Neurologique
|
January 1, 1991
[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias]
M Ben Hamida, N Attia-Romdhane, C H Triki, et al.
Pathologie-Biologie
|
August 18, 2015
Association of TGFB1 -509C/T polymorphism gene with clinical variability in cystic fibrosis patients: A case-control study
S Oueslati, S Hadj Fredj, B Dakhlaoui, et al.
Acta Physiologica Hungarica
|
December 8, 2014
Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation
S Oueslati, S Hadj Fredj, R Belhaj, et al.
Journal De Radiologie
|
August 12, 2003
[MRI in the diagnosis of Rathke's cleft cyst]
N Mnif, A Hamrouni, C Iffenecker, et al.
Revue Neurologique
|
January 1, 1990
[Subacute brainstem hematoma. A surgically treated case]
H Cambon, J Shen, P Cornu, et al.
European Journal of Gynaecological Oncology
|
May 23, 2012
Impact of sampling origin on molecular detection of high-risk human papillomavirus and oncogene expression
S Kahla, M Achour, S Oueslati, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
March 8, 2003
[MRI of cerebral cortical dysgenesis]
N Mnif, S Oueslati, M Fredj, et al.
Journal De Radiologie
|
June 9, 2009
[Imaging features of Takayasu's arteritis]
L Charrada-Ben Farhat, A Miaoui, A Askri, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
November 8, 2006
[Ectopic thyroid]
S Oueslati, W Douira, L Charada, et al.
The Journal of Antimicrobial Chemotherapy
|
January 30, 2015
OXY-2-15, a novel variant showing increased ceftazidime hydrolytic activity
R H T Nijhuis, S Oueslati, K Zhou, et al.
Page
of 3