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

द्वारा Sefiani, Arthur, Geoffroy, Cédric G.
में प्रकाशित Front Neurosci (2021)

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

द्वारा Lamzouri, Afaf, Ratbi, Ilham, Sefiani, Abdelaziz
प्रकाशित 2013

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

द्वारा Aziza Sbiti, Fatiha El Kerch, Abdelaziz Sefiani
प्रकाशित 2002-01-01

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

द्वारा Sbiti, Aziza, El Kerch, Fatiha, Sefiani, Abdelaziz
प्रकाशित 2002

The Moroccan human mutation database

द्वारा Ratbi, Ilham, Gati, Alae-eddine, Sefiani, Abdelaziz
प्रकाशित 2008

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

द्वारा Belhassan, Khadija, Ouldim, Karim, Sefiani, Abdel Aziz
में प्रकाशित Mol Genet Genomic Med (2016)

Autosomal recessive anhidrotic ectodermal dysplasia in a large Moroccan family.

द्वारा Kabbaj, K, Baala, L, Chhoul, H, Sefiani, A
प्रकाशित 1998

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

द्वारा Ouldim, Karim, Natiq, Abdelhafid, Jonveaux, Philippe, Sefiani, Abdelaziz
प्रकाशित 2007

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

द्वारा Lahlouh, Ilyas, Rerhrhaye, Fathallah, Elakkary, Ahmed, Sefiani, Nacer
में प्रकाशित 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]

द्वारा Lahlouh, Ilyas, Rerhrhaye, Fathallah, Elakkary, Ahmed, Sefiani, Nacer
में प्रकाशित Heliyon (2021)

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

द्वारा Yassamine Doubaj, Wiam Smaili, Fatima-Zahra Laarabi, Abdelaziz Sefiani
प्रकाशित 2017-06-01

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

द्वारा Cherkaoui Jaouad, Imane, Guaoua, Soukaina, Hajjioui, Aicha, Sefiani, Abdelaziz
प्रकाशित 2014

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

द्वारा Doubaj, Yassamine, Smaili, Wiam, Laarabi, Fatima-Zahra, Sefiani, Abdelaziz
में प्रकाशित 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

द्वारा Lamzouri, Afaf, Natiq, Abdelhafid, Tajir, Mariam, Sendid, Mohamed, Sefiani, Abdelaziz
प्रकाशित 2012

P321: Current status of pharmacovigilance in Africa

द्वारा Skalli, S, Sefiani, H, Soulaymani, R, Errkhis, R Ouled, Benkirane, R
प्रकाशित 2013

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

द्वारा Tajir, M, Lyahyai, J, Guaoua, S, El Alloussi, M, Sefiani, A
में प्रकाशित Balkan J Med Genet (2020)

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

द्वारा Bounssir, Ayoub, Bakkali, Tarik, Taghi, Houda, Sefiani, Yasser, Lekehal, Brahim
में प्रकाशित Int J Surg Case Rep (2020)

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

द्वारा Maria Zerkaoui, Fatima Zahra Laarabi, Yousra Ajhoun, Bouchra Chkirate, Abdelaziz Sefiani
प्रकाशित 2018-03-01

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

द्वारा Elalaoui, Siham Chafai, Mariam, Tajir, Ilham, Ratbi, Yassamine, Doubaj, Abdelaziz, Sefiani
प्रकाशित 2011

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

द्वारा Elalaoui, S.C., Garin, I., Sefiani, A., Perez de Nanclares, G.
प्रकाशित 2014