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Ben Chehida, Amel
164
results:
Search for persons
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Format
Online (164)
Mediatypes
E-Books (2)
Articles (Online) (141)
Bookchapter (Online) (12)
OpenAccess-fulltext (9)
Languages
english (135)
french (20)
Sorted by: Relevance
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?
1
Mutation delTTCT 1471 de l'intolérance aux protéines dibasi..:
Jbebli, Elhem
;
Jbeli, Yosra
;
Amdouni, Rym
...
La Tunisie Médicale. 102 (2024) 5 - p. , 2024
Link:
https://doi.org/10.62438..
?
2
High Frequency of Cardiovascular Complications in Tunisian ..:
Ben Chehida, Amel
;
Ben Messaoud, Sana
;
Ben Abdelaziz, Rim
...
Journal of Tropical Pediatrics. 65 (2018) 3 - p. 217-223 , 2018
Link:
https://doi.org/10.1093/..
?
3
Correction to: Full title: peripheral venous catheter compl..:
Ben Abdelaziz, Rim
;
Hafsi, Habiba
;
Hajji, Hela
...
BMC Pediatrics. 18 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
4
Full title: peripheral venous catheter complications in chi..:
Ben Abdelaziz, Rim
;
Hafsi, Habiba
;
Hajji, Hela
...
BMC Pediatrics. 17 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
5
Clinical and Genetic Characterization of 26 Tunisian Patien..:
Kallabi, Fakhri
;
Belghuith, Neila
;
Aloulou, Hajer
...
Archives of Medical Research. 47 (2016) 2 - p. 105-110 , 2016
Link:
https://doi.org/10.1016/..
?
6
A novel homozygous missense mutation in the insulin recepto..:
Ben Abdelaziz, Rim
;
Ben Chehida, Amel
;
Azzouz, Hatem
...
European Journal of Medical Genetics. 59 (2016) 1 - p. 16-19 , 2016
Link:
https://doi.org/10.1016/..
?
7
Splicing defects in ABCD1 gene leading to both exon skippin..:
Kallabi, Fakhri
;
Hadj Salem, Ikhlass
;
Ben Chehida, Amel
...
Neuroscience Research. 97 (2015) - p. 7-12 , 2015
Link:
https://doi.org/10.1016/..
?
8
Molecular and computational characterization of ABCB11 and ..:
Khabou, Boudour
;
Kallabi, Fakhri
;
Abdelaziz, Rim Ben
...
Annals of Human Genetics. 88 (2023) 3 - p. 194-211 , 2023
Link:
https://doi.org/10.1111/..
?
9
Identification of mutations that causes glucose-6-phosphate..:
Chkioua, Latifa
;
Amri, Yessine
;
Sahli, Chayma
...
Diabetology & Metabolic Syndrome. 15 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
10
Self-Reported Anxiety, Depression and Coping in Parents of ..:
Abdelaziz, Rim Ben
;
Chehida, Amel Ben
;
Chakchouk, Henda Kachouri
...
Journal of Developmental and Physical Disabilities. 31 (2019) 6 - p. 753-776 , 2019
Link:
https://doi.org/10.1007/..
?
11
A severe clinical phenotype of Noonan syndrome with neonata..:
Jaouadi, Hager
;
Chehida, Amel Ben
;
Kraoua, Lilia
...
Genetics Research. 101 (2019) - p. , 2019
Link:
https://doi.org/10.1017/..
?
12
Molecular and biochemical characterization of a novel intro..:
Ben Rhouma, Faten
;
Azzouz, Hatem
;
Petit, François M.
...
Molecular Biology Reports. 40 (2013) 7 - p. 4197-4202 , 2013
Link:
https://doi.org/10.1007/..
?
13
A severe clinical phenotype of Noonan syndrome with neonata..:
Jaouadi, Hager
;
Ben Chehida, Amel
;
Kraoua, Lilia
...
info:eu-repo/semantics/altIdentifier/doi/10.1017/S0016672319000041. , 2019
Link:
https://amu.hal.science/..
?
14
A severe clinical phenotype of Noonan syndrome with neonata..:
Jaouadi, Hager
;
Ben Chehida, Amel
;
Kraoua, Lilia
...
info:eu-repo/semantics/altIdentifier/doi/10.1017/S0016672319000041. , 2019
Link:
https://amu.hal.science/..
?
15
A severe clinical phenotype of Noonan syndrome with neonata..:
Jaouadi, Hager
;
Ben Chehida, Amel
;
Kraoua, Lilia
...
info:eu-repo/semantics/altIdentifier/doi/10.1017/S0016672319000041. , 2019
Link:
https://hal-amu.archives..
1-15