Network Profiles
LinkedIn: Sellama Nadifi - Maroc | LinkedIn
Sellama Nadifi. Directeur de laboratoire chez Faculté de medecine Lieu Maroc Secteur Professions médicales
Private Homepages
Sellama Nadifi - YouTube
www.youtube.com
Teile deine Videos mit Freunden, Verwandten oder der ganzen Welt
Books & Literature
Duchenne and Becker Muscular Dystrophy: Contribution of a Molecular...
doaj.org
Information about the open-access article 'Duchenne and Becker Muscular Dystrophy: Contribution of a Molecular and Immunohistochemical Analysis in Diagnosis...
authors:"Sellama Nadifi" - Search | Paperity
paperity.org
Paperity: the 1st multidisciplinary aggregator of Open Access journals & papers. Free fulltext PDF articles from hundreds of disciplines, all in one place
FLT3-ITD Incidence and FLT-D835 Mutations in Acute Myeloid Leukemia...
doaj.org
Background: According to numerous studies, FMS-like tyrosine kinase 3, internal tandem duplication, and the D835 mutation are associated with a poor
Sellama Nadifi | XanEdu Customization Platform
www.academicpub.com
Author: Sellama Nadifi. Results. c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum Springer ...
Related Documents
CiteSeerX — ANGELMAN SYNDROME: ETIOLOGIES AND GENETIC COUNSELING
citeseerx.ist.psu.edu
@MISC{Hamzi_angelmansyndrome:, author = {Khalil Hamzi and Afaf Ben Itto and Sellama Nadifi and Paul Egwuonwu Dim}, title = {ANGELMAN SYNDROME: ...
Interaction and association between genetic mutations and clinical...
www.ijias.issr-journals.org
... Mariame El Messal, Mustapha El Alaoui Faris, Mohamed Yahyaoui, Saadia Aidi, Ahmed Adlouni, Rachida Habbal, and Sellama Nadifi, ...
Modeling of Genetic Risk Factors in Ischemic Stroke
www.ijisr.issr-journals.org
Khalid Balar 1, Sellama Nadifi 2, Khalil HAMZI 3, and Bréhima DIAKITE 4 1 Laboratory of Human Genetics and Molecular Pathology, University Hassan II, Faculty of ...
HCV genotypes in Morocco, Journal of Medical Virology | DeepDyve
www.deepdyve.com
... Genotypes in Morocco. Abdelouahab Benani, Joumana El-Turk, Soumaya Benjelloun, Souad Sekkat, Sellama Nadifi,. Nezha Hda, and Abdellah Benslimane*.
Scientific Publications
Hearing Research | Vol 210, Issues 1–2, Pages (December 2005) |...
www.sciencedirect.com
The online version of Hearing Research at ScienceDirect.com, the world's leading platform for high quality peer-reviewed full-text journals.
Association of methylenetetrahydrofolate reductase gene (C677T) with...
www.ncbi.nlm.nih.gov
... Email: rf.liamtoh@araf-ihcrok. Rachida Habbal, Email: moc.liamtoh@adihcarlabbah. Sellama Nadifi, Email: moc.demnegbal@ifidan. Go to: ...
Prader-Willi syndrome: Methylation study or fluorescence in situ...
www.ncbi.nlm.nih.gov
· Khalil Hamzi, Afaf Ben Itto, 1 Sanaa Nassereddine, and Sellama Nadifi Author information ... Prader–Willi syndrome (PWS; OMIM ) ...
Screening of exon 11 of BRCA1 gene using the high resolution melting...
www.ncbi.nlm.nih.gov
... Email: am.ruetsap@takarabdimah. Abdellatif Benider, Email: rf.oohay@ledbaredineb. Sellama Nadifi, Email: rf.oohay@lesifidan. Go to: ...
Publications
ANGELMAN SYNDROME: ETIOLOGIES AND GENETIC COUNSELING - CORE
core.ac.uk
By Pharm Res, Sellama Nadifi Et Al, Khalil Hamzi, ... Angelman syndrome (AS) is a neurogenetic disease involving mental retardation, dysmorphism and epilepsy.
Publications Authored by Nadifi Sellama | PubFacts
www.pubfacts.com
Publications Authored by Nadifi Sellama
Duchenne and Becker Muscular Dystrophy: Contribution of a Molecular...
www.hindawi.com
View at Publisher · View at Google Scholar; Afaf Ben Itto, Khalil Hamzi, Hanane Bellayou, Mohammed Itri, Ilham Slassi, and Sellama Nadifi, ...
A Proteomic Approach for the Involvement of the GAPDH in Alzheimer...
link.springer.com
A Proteomic Approach for the Involvement of the GAPDH in Alzheimer Disease in the Blood of Moroccan FAD Cases Journal ... Sellama Nadifi (1) Ahmed Hachem (5)
Miscellaneous
Sellama Nadifi Nadifisel | LinkedIn
www.linkedin.com
View Sellama Nadifi Nadifisel’s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Sellama Nadifi ...
Sellama Nadifi | LinkedIn
www.linkedin.com
View Sellama Nadifi’s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Sellama Nadifi discover inside ...
Sellama Nadifi
www.infona.pl
Search results for: Sellama Nadifi Thierry Paluku They-They, Omar Battas, Sellama Nadifi · Neuroscience Bulletin > > 29 > 6 >
SID.ir | Paper Search - SELLAMA NADIFI
www.sid.ir
SID has provided outstanding services both in Persian and English sections such as indexing the latest research-scientific journals of Iran, Journal Citation Reports ...
A rapid polymerase chain reaction …
www.neurologyindia.com
Neurol India is an peer-reviewed biomedical periodical of Neurological Society of India.
Altmetric – A novel mutation in the ABCD1 gene of a Moroccan patient...
www.altmetric.com
Adnane Karkar, Abdelhamid Barakat, Amina Bakhchane, Houda Fettah, Ilham Slassi, Imen Dorboz, Odile Boespflug-Tanguy, Sellama Nadifi.
Association of C677T MTHFR and G20210A FII prothrombin polymorphisms...
www.spandidos-publications.com
Wiam Hmimech; Hind Hassani Idrissi; Brehima Diakite; Dalila Baghdadi; Farah Korchi; Rachida Habbal; Sellama Nadifi. View Affiliations.
Association of gastric cancer incidence with MDR1 gene polymorphism...
www.indianjcancer.com
The Indian Journal of Cancer is an official publication of the Indian Cancer Society and Indian Society of Oncology.
Back - Medknow Publications: Publisher of peer reviewed ...
www.medknow.com
273. Khalil Hamzi, Bréhima Diakité, Amal Tazzite, Sellama Nadifi Amal Tazzite, Hassan Jouhadi, Khalil Hamzi, Abdellatif Benider, Sellama Nadifi.
Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations ...
mr.crossref.org
Sellama Nadifi Genetics and Molecular Pathology Laboratory, Medical School of Casablanca Morocco Login to access the Email id. Source of Support: None, ...
G2691A and C2491T mutations of factor V gene and pre-disposition to...
www.spandidospublications.net
Authors: Wiam Hmimech; Brehima Diakite; Hind Hassani Idrissi; Khalil Hamzi; Farah Korchi; Dalila Baghdadi; Rachida Habbal; Sellama Nadifi.
The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men...
www.hal.inserm.fr
INSERM - Institut national de la santé et de la recherche médicale
Polymorphisms in oxidative pathway related genes and susceptibility...
publons.com
Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease
The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men...
hal.univ-grenoble-alpes.fr
HAL Grenoble Alpes
Prothrombin G20210A and factor V Leiden polymorphisms in stroke...
ohsu.pure.elsevier.com
... V Leiden polymorphisms in stroke. Thierry Paluku They-They ; Omar Battas ; Ilham Slassi ; Mohamed Abdou Rafai ; Desire Tshala Katumbay ; Sellama Nadifi.
Saudi Journal of Gastroenterology (SJG): Table of Contents
www.saudijgastro.com
... among Moroccan Patients. Nezha Senhaji,Yaya Kassogue,Mina Fahimi,Nadia Serbati,Wafaa Badre,Sellama Nadifi. Mediators of Inflammation.2015;2015(6)1.
NCSTL
www.ncstl.org
DNA. Resource: Scientific Journals. Record Upload Date: September 2, Author: Faiza Chbel, Sellama Nadifi, Cristina Martinez-Bouzas, Said Louahlia, ...
The CHEK delC allelic variant is not present in familial and...
springerplus.springeropen.com
Chaymaa MaroufEmail author,; Omar Hajji,; Brehima Diakité,; Amal Tazzite,; Hassan Jouhadi,; Abdellatif Benider and; Sellama Nadifi. SpringerPlus20154:38.
Medknow Publications: Publisher of peer reviewed scholarly ...
www.medknow.com
... Sellama Nadifi [HTML Full text] Recovery of oculomotor nerve palsy following surgical clipping of posterior communicating artery aneurysms : p. 103: Vamsi K
Related search requests for Sellama Nadifi
| Omar Battas Khalil Hamzi Nicolas Roullet |
People Forename "Sellama" (2) Name "Nadifi" (32) |
sorted by relevance / date