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Informations du chercheur

Nom complet

bourrahouat aicha

Grade

PES

Spécialité

Pediatrie

Thématique de recherche

Peditrie enfant

Laboratoire

Laboratoire DE RECHERCHE L'ENFANCE, LA SANTE ET LE DEVELOPPEMENT DURABLE

Établissement

Faculté de Médecine et de Pharmacie de Marrakech

Ouvrages (0 au total)

Aucun ouvrage disponible.

Projets (0 au total)

Aucun projet disponible.

Publications (93 au total)

Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients

Auteur: Karima Lafhal, Es-said Sabir, Abdelmalek Hakmaoui, Miloud Hammoud, Abdelmohcine Aimrane, Samira Najeh, Imane Assiri, Abdelaati Berrachid, Najwa Imad, Chaima Ait Boujemaa, Faissal Aziz, Fatima Zahra El Hanafi, Abdessamad Lalaoui, Hasna Aamri, Iryna Boyko, Ana Sánchez-Monteagudo, Carmen Espinós, Imane Ait Sab, Nisrine Aboussair, Aicha Bourrahouat, Naima Fdil

Revue: Molecular Genetics and Metabolism Reports

Année: 2023

DOI: 10.1016/j.ymgmr.2023.100984

Sphingolipidoses in Morocco: Chemical profiling for an affordable and rapid diagnosis strategy

Auteur: M. Hammoud, A.M.S. Rodrigues, I. Assiri, Es Sabir, K. Lafhal, S. Najeh, M. Jakani, N. Imad, A. Bourrahouat, I. Ait Sab, R. Elqadiry, H. Nassih, A. Outzourit, M. Elamiri, F. Maoulainine, N. Slitine Elidrissi, F. Bennaoui, M. Bourous, S. Mrhar, L. Essaadouni, D. Stien, N. Rada, M. Bouskraoui, E. Houël, N. Fdil

Revue: Prostaglandins & Other Lipid Mediators

Année: 2023

DOI: 10.1016/j.prostaglandins.2023.106751

ACUTE RENAL FAILURE DURING POISONINGATTETRAHYDROCANNABIOL: ABOUT A CASE

Auteur: J. Fahri, undefined undefined, H. Nassih, R. Elqadiry, A. Bourrahouat, I. Ait Sab, undefined undefined, undefined undefined, undefined undefined, undefined undefined

Revue: International Journal of Advanced Research

Année: 2023

DOI: 10.21474/ijar01/16876

Glomerulonephritis in Children: Epidemiological, Clinical, Paraclinical and Therapeutic Profile

Auteur: Hasna Aamri, D. Kaouani, R. Elqadiry, H. Nassih, A. Bourrahouat, I. Ait Sab

Revue: SAS Journal of Medicine

Année: 2023

DOI: 10.36347/sasjm.2023.v09i04.006

Case Reports of Children with Vogt_Koyanagi_Harada Syndrome

Auteur: Hasna Aamri, FZ Azzouzi, R. Elqadiry, H. Nassih, A. Bourrahouat, I. Ait Sab

Revue: Scholars Journal of Medical Case Reports

Année: 2023

DOI: 10.36347/sjmcr.2023.v11i03.017

Secondary cutaneous aspergillosis in a child with Behçet’s disease: a case-based update

Auteur: Soumia Nachate, Mouad El Mouhtadi, Yousra Zouine, Mohamed Amine Haouane, Mohamed Amine Azami, Mohamed Oulad Saiad, Dounia Basraoui, Hicham Jalal, Houda Nassih, Rabiy Elqadiry, Aicha Bourrahouat, Imane Ait Sab, Awatif El Hakkouni

Revue: Annals of Pediatric Surgery

Année: 2023

DOI: 10.1186/s43159-023-00242-2

The role of combination between TLC and UHPL/MS-MS in the diagnosis and prognosis of metachromatic leukodystrophy

Auteur: Miloud Hammoud, Es-said Sabir, Imane Assiri, Karima Lafhal, Samira Najeh, Imane ait Saab, Aicha Bourrahouat, Rabiy Elqadiry, Houda Nassih, My Ahmed Elamiri, Fadl Mrabih Rabou Maoulainine, Nadia Elidriss Slitine, Fatiha Bennaoui, Mounir Bourrous, Alice M.S. Rodrigues, Didier Stien, Soumia Mrhar, Nourddine Rada, Mohammed Bouskraoui, Fdil Naima

Revue: Molecular Genetics and Metabolism

Année: 2023

DOI: 10.1016/j.ymgme.2022.107138

The case of glycosylation defects mimicking Wilson disease: A case report

Auteur: Karima Lafhal, Es-Said Sabir, Miloud Hammoud, Abdelmohcine Aimrane, Samira Najeh, Imane Assiri, Fadl Mrabih Rabou Maoulainine, Aicha Bourrahouat, Elouafi Elaouni Kamili, Naima Fdil

Revue: Molecular Genetics and Metabolism

Année: 2023

DOI: 10.1016/j.ymgme.2022.107191

Timely diagnosis of Niemann Pick disease using thin layer chromatography with identification of SMPD1 mutations causing NPD type A/B among Moroccan population

Auteur: Imane Assiri, Miloud Hammoud, Samira Najeh, Es-said Sabir, Karima Lafhal, Aicha Bourrahouat, Mounir Bourrous, My Ahmed Elamiri, Naima Fdil

Revue: Molecular Genetics and Metabolism

Année: 2023

DOI: 10.1016/j.ymgme.2022.107013