E-LIB Suche - Ergebnisse für: Ben Charfeddine, Ilhem

1

Macrozoospermia: screening for the homozygous c.144delC mut..:

Ghédir, Houda ; Gribaa, Moez ; Mamaî, Ons...
Journal of Assisted Reproduction and Genetics. 32 (2015) 11 - p. 1651-1658 , 2015

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

2

Multiple Self-Healing Palmoplantar Carcinoma: A Familial Pr..:

Mamaï, Ons ; Boussofara, Lobna ; Denguezli, Mohamed...
Journal of Investigative Dermatology. 135 (2015) 1 - p. 304-308 , 2015

Link: https://doi.org/10.1038/..

3

Circadian heart rate and blood pressure variability in inte..:

Ben Lazreg, Taheni ; Ben Charfeddine, Ilhem ; Mammai, Ons...
Biological Rhythm Research. 45 (2013) 2 - p. 285-292 , 2013

Link: https://doi.org/10.1080/..

4

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunis..:

Ben Charfeddine, Ilhem ; Riepe, Felix G. ; Clauser, Eric...
Gene. 507 (2012) 1 - p. 20-26 , 2012

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

5

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes cop..:

Amara, Abdelbasset ; Adala, Labiba ; Ben Charfeddine, Ilhem...
European Journal of Paediatric Neurology. 16 (2012) 2 - p. 167-174 , 2012

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

6

Two novel CYP11B1 mutations in congenital adrenal hyperplas..:

Ben Charfeddine, Ilhem ; Riepe, Felix G. ; Kahloul, Najoua...
General and Comparative Endocrinology. 175 (2012) 3 - p. 514-518 , 2012

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

7

Molecular and biochemical characterization of Tunisian pati..:

Mili, Amira ; Ben Charfeddine, Ilhem ; Mamaï, Ons...
Journal of Human Genetics. 57 (2011) 3 - p. 170-175 , 2011

Link: https://doi.org/10.1038/..

8

An autosomal dominant hypophosphatemic rickets phenotype in..:

Gribaa, Moez ; Younes, Mohamed ; Bouyacoub, Yosra...
Journal of Bone and Mineral Metabolism. 28 (2009) 1 - p. 111-115 , 2009

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

9

Clinical, genetic, and structural basis of congenital adren..:

Khattab, Ahmed ; Haider, Shozeb ; Kumar, Ameet...
Proceedings of the National Academy of Sciences. 114 (2017) 10 - p. , 2017

Link: https://doi.org/10.1073/..

10

The predominance of codon 39 (c>t) mutation of HBB gene in ..:

Kamilia, Belhadi ; Mouloud, Yahia ; Moez, Gribaa...
Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale. 90 (2017) 1 - p. , 2017

Link: https://doi.org/10.4081/..

11

Clinical, genetic, and structural basis of congenital adren..:

Khattab, Ahmed ; Haider, Shozeb ; Kumar, Ameet...
Proceedings of the National Academy of Sciences of the United States of America. 114 (2017) 10 - p. E1933-E1940 , 2017

Link: https://www.jstor.org/st..

12

Erratum: Molecular and biochemical characterization of Tuni..:

Mili, Amira ; Charfeddine, Ilhem Ben ; Mama, Ons...
Journal of Human Genetics. 57 (2012) 3 - p. 221-221 , 2012

Link: https://doi.org/10.1038/..

13

The predominance of codon 39 (c>t) mutation of HBB gene in ..:

Belhadi Kamilia ; Yahia Mouloud ; Gribaa Moez...
http://www.pagepressjournals.org/index.php/jbr/article/view/6407. , 2017

Link: https://doi.org/10.4081/..

14

Genetic Analysis of Mu and Kappa Opioid Receptor and COMT E..:

Imen CHATTI ; Jean-Baptiste WOILLARD ; Amira MILI...
https://ijph.tums.ac.ir/index.php/ijph/article/view/11769. , 2017

Link: https://doaj.org/article..

15

Frequency of HNF4A-P.I463V Variant in the Tunisian North-Af..:

Abdelbasset Amara ; Ilhem Ben Charfeddine ; Houda Ghédir...
https://ijph.tums.ac.ir/index.php/ijph/article/view/3633. , 2015

Link: https://doaj.org/article..