E-LIB Suche - Ergebnisse für: Makrelouf, Mohamed

1

Biallelic variants in TMIE and PDE6B genes mimic Usher synd..:

Abdi, Samia ; Makrelouf, Mohamed ; Rous, Issa Nazim...
Gene Reports. 36 (2024) - p. 101954 , 2024

2

Proposal of a new diagnostic algorithm for adult-onset Stil..:

Daghor-Abbaci, Karima ; Ait Hamadouche, Nadia ; Makhloufi, Chafia Dahou...
Clinical Rheumatology. 42 (2023) 4 - p. 1125-1135 , 2023

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

3

Association Between Insulin Resistance and Uric Acid in Hyp..:

Otmane, Amel ; Makrelouf, Mohamed ; Zenati, Akila
Metabolism. 142 (2023) - p. 155479 , 2023

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

4

Comparison of three indexes HOMA, QUICKI and TyG to evaluat..:

OTMANE, Amel ; ACID, Sadjia ; ALLANE, Fahima..
Metabolism. 128 (2022) - p. 155110 , 2022

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

5

Validation of the neutrophil-to-lymphocyte ratio as a new s..:

Daghor Abbaci, Karima ; Ait Hamadouche, Nadia ; Otmani, Fifi...
Medicine. 101 (2022) 32 - p. e29970 , 2022

Link: https://doi.org/10.1097/..

6

Reconsidering vitamin D optimal values based on parathyroid..:

Bennouar, Salam ; Bachir Cherif, Abdelghani ; Makrelouf, Mohamed...
Archives of Osteoporosis. 17 (2022) 1 - p. , 2022

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

7

Variations of oxidized ldl and adipocytokine during metabol..:

Otmane, Amel ; Makrelouf, Mohamed ; Zenati, Akila
Archives of Cardiovascular Diseases Supplements. 11 (2019) 3 - p. e353 , 2019

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

8

A novel biallelic splice site mutation of TECTA causes mode..:

Behlouli, Asma ; Bonnet, Crystel ; Abdi, Samia...
International Journal of Pediatric Otorhinolaryngology. 87 (2016) - p. 28-33 , 2016

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

9

Diversity of the Genes Implicated in Algerian Patients Affe..:

Abdi, Samia ; Bahloul, Amel ; Behlouli, Asma...
PLOS ONE. 11 (2016) 9 - p. e0161893 , 2016

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

10

The CD2 isoform of protocadherin‐15 is an essential compone..:

Pepermans, Elise ; Michel, Vincent ; Goodyear, Richard...
EMBO Molecular Medicine. 6 (2014) 7 - p. 984-992 , 2014

Link: https://doi.org/10.15252..

11

EPS8, encoding an actin-binding protein of cochlear hair ce..:

Behlouli, Asma ; Bonnet, Crystel ; Abdi, Samia...
Orphanet Journal of Rare Diseases. 9 (2014) 1 - p. , 2014

Link: https://doi.org/10.1186/..

12

Polymorphisms in NAT2 Gene and Atherosclerosis in an Algeri..:

Khelil, Malika ; Zenati, Akila ; Makrelouf, Mohamed..
Archives of Medical Research. 41 (2010) 3 - p. 215-220 , 2010

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

13

Molecular screening of deafness in Algeria: High genetic he..:

Ammar-Khodja, Fatima ; Faugère, Valérie ; Baux, David...
European Journal of Medical Genetics. 52 (2009) 4 - p. 174-179 , 2009

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

14

Homocystéine et génotypage de l'apolipoprotéine E:

Makrelouf, Mohamed ; Otmane, Amel ; Bendib, Myriam...
Revue Francophone des Laboratoires. 2007 (2007) 396 - p. 25-29 , 2007

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

15

Dosage de l'homocystéine totale chez une cohorte de diabéti..:

Otmane, Amel ; Makrelouf, Mohamed ; Bouchama, Rym...
Revue Francophone des Laboratoires. 2007 (2007) 396 - p. 21-24 , 2007

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