The Potential Role of Inflammation in Modulating Endogenous Hippocampal Neurogenesis After Spinal Cord Injury

Yazar: Sefiani, Arthur, Geoffroy, Cédric G.
Yayımlandı Front Neurosci (2021)

Syndrome de Silver Russell: à propos de 3 cas et revue de la litterature

Yazar: Lamzouri, Afaf, Ratbi, Ilham, Sefiani, Abdelaziz
Baskı/Yayın Bilgisi 2013

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

Yazar: Aziza Sbiti, Fatiha El Kerch, Abdelaziz Sefiani
Baskı/Yayın Bilgisi 2002-01-01

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

Yazar: Sbiti, Aziza, El Kerch, Fatiha, Sefiani, Abdelaziz
Baskı/Yayın Bilgisi 2002

The Moroccan human mutation database

Yazar: Ratbi, Ilham, Gati, Alae-eddine, Sefiani, Abdelaziz
Baskı/Yayın Bilgisi 2008

Genetics and genomic medicine in Morocco: the present hope can make the future bright

Yazar: Belhassan, Khadija, Ouldim, Karim, Sefiani, Abdel Aziz
Yayımlandı Mol Genet Genomic Med (2016)

Autosomal recessive anhidrotic ectodermal dysplasia in a large Moroccan family.

Yazar: Kabbaj, K, Baala, L, Chhoul, H, Sefiani, A
Baskı/Yayın Bilgisi 1998

Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Autistic Disorder

Yazar: Ouldim, Karim, Natiq, Abdelhafid, Jonveaux, Philippe, Sefiani, Abdelaziz
Baskı/Yayın Bilgisi 2007

Experimental implementation of a new multi input multi output fuzzy-PID controller in a poultry house system

Yazar: Lahlouh, Ilyas, Rerhrhaye, Fathallah, Elakkary, Ahmed, Sefiani, Nacer
Yayımlandı Heliyon (2020)

Corrigendum to “Experimental implementation of a new multi input multi output fuzzy-PID controller in a poultry house system” [Heliyon 6 (8) (2020) e04645]

Yazar: Lahlouh, Ilyas, Rerhrhaye, Fathallah, Elakkary, Ahmed, Sefiani, Nacer
Yayımlandı Heliyon (2021)

A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report

Yazar: Yassamine Doubaj, Wiam Smaili, Fatima-Zahra Laarabi, Abdelaziz Sefiani
Baskı/Yayın Bilgisi 2017-06-01

Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report

Yazar: Cherkaoui Jaouad, Imane, Guaoua, Soukaina, Hajjioui, Aicha, Sefiani, Abdelaziz
Baskı/Yayın Bilgisi 2014

A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report

Yazar: Doubaj, Yassamine, Smaili, Wiam, Laarabi, Fatima-Zahra, Sefiani, Abdelaziz
Yayımlandı J Med Case Rep (2017)

Le diagnostic anténatal de la trisomie 21 par l'hybridation in situ en fluorescence (FISH): à propos des premiers tests réalisés au Maroc

Yazar: Lamzouri, Afaf, Natiq, Abdelhafid, Tajir, Mariam, Sendid, Mohamed, Sefiani, Abdelaziz
Baskı/Yayın Bilgisi 2012

P321: Current status of pharmacovigilance in Africa

Yazar: Skalli, S, Sefiani, H, Soulaymani, R, Errkhis, R Ouled, Benkirane, R
Baskı/Yayın Bilgisi 2013

Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene

Yazar: Tajir, M, Lyahyai, J, Guaoua, S, El Alloussi, M, Sefiani, A
Yayımlandı Balkan J Med Genet (2020)

Best strategy in managing the association of Horse-shoe-Kidney and Abdominal Aortic Aneurysm: Case report

Yazar: Bounssir, Ayoub, Bakkali, Tarik, Taghi, Houda, Sefiani, Yasser, Lekehal, Brahim
Yayımlandı Int J Surg Case Rep (2020)

A novel single variant in the MEFV gene causing Mediterranean fever and Behçet’s disease: a case report

Yazar: Maria Zerkaoui, Fatima Zahra Laarabi, Yousra Ajhoun, Bouchra Chkirate, Abdelaziz Sefiani
Baskı/Yayın Bilgisi 2018-03-01

A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review

Yazar: Elalaoui, Siham Chafai, Mariam, Tajir, Ilham, Ratbi, Yassamine, Doubaj, Abdelaziz, Sefiani
Baskı/Yayın Bilgisi 2011

Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome

Yazar: Elalaoui, S.C., Garin, I., Sefiani, A., Perez de Nanclares, G.
Baskı/Yayın Bilgisi 2014