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Tebib, N.
57
results:
Search for persons
X
Format
Online (57)
Mediatypes
Articles (Online) (51)
OpenAccess-fulltext (6)
Languages
english (32)
french (25)
Sorted by: Relevance
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?
1
The mutational spectrum of hunter syndrome reveals correlat..:
Chkioua, L
;
Grissa, O
;
Leban, N
...
BMC Medical Genetics. 21 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
2
Une cause insolite d'insuffisance surrénalienne : le syndro..:
Boudiche, I.
;
Ben Massaoud, S.
;
Ben Hassine, S.
...
Annales d'Endocrinologie. 81 (2020) 4 - p. 364 , 2020
Link:
https://doi.org/10.1016/..
?
3
Factors predictive of prognosis of infantile spasms. A retr..:
Ben Abdelaziz, R.
;
Ben Chehida, A.
;
Lamouchi, M.
...
Archives de Pédiatrie. 26 (2019) 1 - p. 1-5 , 2019
Link:
https://doi.org/10.1016/..
?
4
An uncommon complication of Listeria monocytogenes infectio..:
Tebib, N.
;
Bill, O.
;
Niederhauser, J.
.
IDCases. 12 (2018) - p. 101-103 , 2018
Link:
https://doi.org/10.1016/..
?
5
Contribution of M470V variant to cystic fibrosis: First stu..:
Nefzi, M.
;
Hadj Fredj, S.
;
Tebib, N.
...
Pathologie Biologie. 63 (2015) 4-5 - p. 169-174 , 2015
Link:
https://doi.org/10.1016/..
?
6
P-236 – Déficit immunitaire primitif de l'enfant en Tunisie:
Halioui-Louhaichi, S.
;
Abdelkefi, S.
;
Mattoussi, N.
...
Archives de Pédiatrie. 22 (2015) 5 - p. 293 , 2015
Link:
https://doi.org/10.1016/..
?
7
P-405 – Étude de 10 cas pédiatriques de Maladie de Wilson: ..:
Ben Chehida, A.
;
Besbes, T.
;
Bouslah, M.
...
Archives de Pédiatrie. 22 (2015) 5 - p. 335-336 , 2015
Link:
https://doi.org/10.1016/..
?
8
P-332 – La maladie de Gaucher type 2: hétérogénéité et cont..:
Boudabous, H.
;
Jlassi, M.
;
Ben Chehida, A.
...
Archives de Pédiatrie. 22 (2015) 5 - p. 318 , 2015
Link:
https://doi.org/10.1016/..
?
9
Les maladies héréditaires du métabolisme en Tunisie: défis,..:
Ben Dridi, M.-F.
;
Ben Turkia, H.
;
Azzouz, H.
...
Archives de Pédiatrie. 22 (2015) 5 - p. 3-4 , 2015
Link:
https://doi.org/10.1016/..
?
10
P-330 – Maladie de Gaucher de type 1 et atteinte neurologiq..:
Boudabous, H.
;
Jlassi, M.
;
Ben Chehida, A.
...
Archives de Pédiatrie. 22 (2015) 5 - p. 317 , 2015
Link:
https://doi.org/10.1016/..
?
11
La myasthénie à révélation tardive : analyse rétrospective ..:
Tebib, N.
;
Mzahem, A.
;
Bouchenak, M.
..
Revue Neurologique. 170 (2014) - p. A44 , 2014
Link:
https://doi.org/10.1016/..
?
12
SFP PC-45 - Validité de la version en Arabe dialectal Tunis..:
Ben Chehida Chaari, A.
;
Ben Salah, F.Z.
;
Ben Abdelaziz, R.
...
Archives de Pédiatrie. 21 (2014) 5 - p. 935 , 2014
Link:
https://doi.org/10.1016/..
?
13
SFP P-047 – Validité d'un check-list (CCL) évaluant la comp..:
Ben Chehida Chaari, A.
;
Ben Ameur, Z.
;
Ben Abdelaziz, R.
...
Archives de Pédiatrie. 21 (2014) 5 - p. 757 , 2014
Link:
https://doi.org/10.1016/..
?
14
SFP PC-33 - L'atteinte cardiaque de la glycogénose type III..:
Ben Chehida Chaari, A.
;
Mansouri, H.
;
Azzouz, H.
...
Archives de Pédiatrie. 21 (2014) 5 - p. 923 , 2014
Link:
https://doi.org/10.1016/..
?
15
SFP P-135 – La mucoviscidose chez l'enfant Tunisien:
Halioui-Louhaichi, S.
;
Abdelkefi, S.
;
Ben Chehida, A.
...
Archives de Pédiatrie. 21 (2014) 5 - p. 845 , 2014
Link:
https://doi.org/10.1016/..
1-15