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Makrelouf, Mohamed
41
results:
Search for persons
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Format
Online (41)
Mediatypes
Articles (Online) (16)
OpenAccess-fulltext (25)
Languages
english (38)
french (2)
Sorted by: Relevance
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?
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
Link:
https://doi.org/10.1016/..
?
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
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/..
?
5
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/..
?
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
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/..
?
9
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/..
?
10
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/..
?
11
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..
?
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
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/..
?
15
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/..
1-15