الرئيسية › دليل الباحثين › Aomar Agadr

Aomar Agadr

الانتماء : Mohammed V University

• 33منشورات (انتماء مغربي)
• 124مجموع المنشورات
• 225الاستشهادات
• 8مؤشر h

OpenAlex

مجالات البحث

• Metabolism and Genetic Disorders
• Lysosomal Storage Disorders Research
• Genomics and Rare Diseases
• Glycogen Storage Diseases and Myoclonus
• Immunodeficiency and Autoimmune Disorders

المنشورات (33)

• Sly Disease: First Case Report in Morocco
  2025 · Asian Journal of Pediatric Research
• Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay with Early-Onset Epilepsy and Novel Clinical Features: A rare entity from Morocco in the Middle East and North Africa region
  2025 · Sultan Qaboos University medical journal
• Severe congenital hyperinsulinism with progressive neurological deterioration due to novel HADH-GHSR digenic mutations: the first case report
  2025 · Pediatric Endocrinology Diabetes and Metabolism
• Complicated meconium ileus in a male neonate with cystic fibrosis: Case report
  2024 · Radiology Case Reports · استُشهد به 1 مرة
• A Novel NRAS Variant Near the Splice Junction in Moroccan Childhood Acute Lymphoblastic Leukemia: A Molecular Dynamics Study
  2024 · Biochemical Genetics · استُشهد به 1 مرة
• Late Infantile Metachromatic Leukodystrophy: Arylsulfatase A and Saposin B Deficiency
  2024 · SAS Journal of Medicine
• Cri Du Chat Syndrome: A Case Study
  2024 · SAS Journal of Medicine
• Cytogenetic abnormalities and TP53 and RAS gene profiles of childhood acute lymphoblastic leukemia in Morocco
  2024 · Archives de Pédiatrie
• Adams-Oliver Syndrome (OSA)
  2023 · Asian Journal of Pediatric Research
• Coeliac disease hidden by cryptogenic hypertransaminasaemia in children: a case report
  2022 · Pan African Medical Journal · استُشهد به 2 مرة
• Pycnodysostose Associated with Stridor: Case Report
  2022 · Asian Journal of Pediatric Research · استُشهد به 1 مرة
• Macrophagic Activation Syndrome Revealing Hodgkin Lymphoma: Case Report
  2022 · Asian Journal of Pediatric Research
• COVID-19 Infection in Premature Twins: A Case Report
  2022 · Scholars Journal of Medical Case Reports
• Infantile-Onset Pompe Disease: About 5 Cases
  2022 · Scholars Journal of Medical Case Reports
• Vitamin B12 deficiency: case report and review of literature.
  2021 · PubMed Central · استُشهد به 29 مرة
• Congenital hepatic fibrosis: case report and review of literature
  2021 · Pan African Medical Journal · استُشهد به 23 مرة
• Clinical and Molecular Findings in a Moroccan Family with Primary Distal Renal Tubular Acidosis and Deafness by Mutation of ATP60A4 Gene: Case Report
  2021 · Asian Journal of Pediatric Research
• Nijmegen breakage syndrome: case report and review of literature
  2020 · Pan African Medical Journal · استُشهد به 26 مرة
• Congenital hyperinsulinsim: case report and review of literature
  2020 · Pan African Medical Journal · استُشهد به 10 مرة
• COVID-19 et greffe de cellules souches hématopoïétiques : recommandations et situation au Maroc
  2020 · Bulletin du Cancer · استُشهد به 1 مرة
• Congenital Isolated Folic Acid Malabsorption: Case Report
  2020 · Asian Journal of Pediatric Research · استُشهد به 1 مرة
• Congenital Deficiency in Factor VII Revealed by Menorrhagia: Case Report
  2020 · Asian Journal of Pediatric Research
• [Diagnosis and management of severe neonatal thrombocytopenia due to maternal alloimmunization against fetal platelet antigens: case study and literature review].
  2020 · PubMed Central
• Macrophage activation syndrome associated with griscelli syndrome type 2: case report and review of literature.
  2018 · Europe PMC (PubMed Central) · استُشهد به 10 مرة
• A three-year-old boy with hypodipsic hypernatremia syndrome
  2018 · Pan African Medical Journal · استُشهد به 4 مرة
• Pycnodysostose: à propos d’un cas
  2018 · Pan African Medical Journal · استُشهد به 1 مرة
• Vomissements associés à une stagnation pondérale et convulsions: penser à une anomalie du cycle d’urée
  2018 · Pan African Medical Journal
• Von Willebrand's disease: case report and review of literature
  2017 · Pan African Medical Journal · استُشهد به 31 مرة
• Déficit congénital en facteur V: à propos d’un cas
  2017 · Pan African Medical Journal · استُشهد به 4 مرة
• Report on paediatric care in the Moroccan military mission in the Gaza Strip
  2017 · Eastern Mediterranean Health Journal · استُشهد به 2 مرة
• Utility of the QuantiFERON®-TB Gold In-Tube assay for the diagnosis of tuberculosis in Moroccan children
  2016 · The International Journal of Tuberculosis and Lung Disease · استُشهد به 12 مرة
• Grisel’s syndrome: a rare complication following traditional uvulectomy
  2015 · Pan African Medical Journal · استُشهد به 19 مرة
• [Aplasia cutis congenita of the vertex in the newborn].
  2013 · Europe PMC (PubMed Central)

مجلات النشر

• Pan African Medical Journal × 10
• Asian Journal of Pediatric Research × 7
• SAS Journal of Medicine × 2
• Scholars Journal of Medical Case Reports × 2
• PubMed Central × 2
• Europe PMC (PubMed Central) × 2

المنشورات حسب السنة

• 20253
• 20245
• 20231
• 20225
• 20213
• 20206
• 20184
• 20173
• 20161
• 20151

التعاون العلمي

المؤسسات الشريكة : Centre Hospitalier Ibn Sina · Université Mohammed VI des Sciences et de la Santé · Université Ibn-Tofail · Centre Hospitalier Universitaire Ibn Rochd · Hôpital Universitaire International Cheikh Khalifa

المؤلفون المشاركون

• Rachid Abilkassem
• Brahim El Hasbaoui
• Abdelhakim Ourrai
• Abdelilah Radi
• Rachid Abilkacem
• Amal Hassani
• Mohamed Kmari
• Abdelhakim Elyajouri
• Abdelhkim Elyajouri
• Mohamed Sellouti
• A. Hassani
• Mohammed Khattab

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).