E-LIB Suche - Ergebnisse für: Trabelsi, Mediha

1

Pathologic complete response to neoadjuvant imatinib of a g..:

Rekaya, Mariem Ben ; Ksontini, Feryel ; Kacem, Linda Bel Haj...
Clinical Case Reports. 11 (2023) 6 - p. , 2023

Link: https://doi.org/10.1002/..

2

Clinical and genetic characteristics of Tunisian children w..:

El Younsi, Mariem ; Trabelsi, Médiha ; Ben Youssef, Sandra...
Pediatric Nephrology. 38 (2022) 1 - p. 119-129 , 2022

Link: https://doi.org/10.1007/..

3

Disease burden and management of Crigler‐Najjar syndrome: R..:

Aronson, Sem J. ; Junge, Norman ; Trabelsi, Mediha...
Liver International. 42 (2022) 7 - p. 1593-1604 , 2022

Link: https://doi.org/10.1111/..

4

Novel RAB3GAP1 Mutation in the First Tunisian Family With W..:

Kerkeni, Nesrine ; Kharrat, Maher ; Maazoul, Faouzi...
Journal of Clinical Neurology. 18 (2022) 2 - p. 214 , 2022

Link: https://doi.org/10.3988/..

5

Le syndrome Wolf–Hirschhorn : à propos de 9 cas:

Fredj, Hana ; Kraoua, Lilia ; Adhoum, Cyrine...
Morphologie. 105 (2021) 350 - p. S28 , 2021

Link: https://doi.org/10.1016/..

6

Alpha-mannosidosis in Tunisian consanguineous families: Pot..:

Mkaouar, Rahma ; Riahi, Zied ; Charfeddine, Cherine...
PLOS ONE. 16 (2021) 10 - p. e0258202 , 2021

Link: https://doi.org/10.1371/..

7

Le syndrome de Kabuki : étude clinique d'une série de 23 pa..:

Fredj, Hana ; Ouertani, Ines ; Trabelsi, Mediha...
Morphologie. 105 (2021) 350 - p. S33 , 2021

Link: https://doi.org/10.1016/..

8

In vitro functional characterization of androgen receptor g..:

Tajouri, Asma ; Kharrat, Maher ; Trabelsi, Mediha...
The Journal of Steroid Biochemistry and Molecular Biology. 208 (2021) - p. 105834 , 2021

Link: https://doi.org/10.1016/..

9

WDR73-related galloway mowat syndrome with collapsing glome..:

El Younsi, Mariem ; Kraoua, Lilia ; Meddeb, Rym...
European Journal of Medical Genetics. 62 (2019) 9 - p. 103550 , 2019

Link: https://doi.org/10.1016/..

10

Novel MED12 variant in a multiplex Fragile X syndrome famil..:

Lahbib, Saida ; Trabelsi, Mediha ; Dallali, Hamza...
Molecular Biology Reports. 46 (2019) 4 - p. 4185-4193 , 2019

Link: https://doi.org/10.1007/..

11

Identification of two additional novel mutations in the AR ..:

Kharrat, Maher ; Tajouri, Asma ; Nacef, Imen Ben...
Steroids. 152 (2019) - p. 108489 , 2019

Link: https://doi.org/10.1016/..

12

Novel PAX3 mutations causing Waardenburg syndrome type 1 in..:

Trabelsi, Mediha ; Nouira, Malek ; Maazoul, Faouzi...
International Journal of Pediatric Otorhinolaryngology. 103 (2017) - p. 14-19 , 2017

Link: https://doi.org/10.1016/..

13

Clinical and Molecular Cytogenetic Study of 38 Williams-Beu..:

Ouertani, Ines ; Chaabouni, Myriam ; Chelly, Imen...
Open Journal of Genetics. 4 (2014) 5 - p. 385-391 , 2014

Link: https://doi.org/10.4236/..

14

Epidemiologic and clinical characteristics of 458 Tunisian ..:

Trabelsi, Mediha ; Chelly, Imen ; Maazoul, Faouzi...
European Journal of Medical Genetics. 56 (2013) 1 - p. 13-19 , 2013

Link: https://doi.org/10.1016/..

15

GJB2 and GJB6 screening in Tunisian patients with autosomal..:

Trabelsi, Mediha ; Bahri, Wafa ; Habibi, Marwene...
International Journal of Pediatric Otorhinolaryngology. 77 (2013) 5 - p. 714-716 , 2013

Link: https://doi.org/10.1016/..