Accueil › Annuaire des chercheurs › Aïcha Bourrahouat
Aïcha Bourrahouat
Affiliation : Cadi Ayyad University · Centre Hospitalier Universitaire Mohammed VI
- 55Publications (affiliation marocaine)
- 65Publications au total
- 194Citations
- 7Indice h
Profil de recherche
Aïcha Bourrahouat compte 55 publications référencées (2010–2026). Ses travaux paraissent principalement dans « Molecular Genetics and Metabolism », « Open Journal of Pediatrics » et « Cureus ». Son article le plus cité, « Third Cranial Nerve Palsy Presenting with Unilateral Diplopia and Strabismus in a 24-Year-Old Woman with COVID-19 » (2020), a été cité 65 fois. 16 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de France.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Metabolism and Genetic Disorders
- Lysosomal Storage Disorders Research
- Celiac Disease Research and Management
- Trace Elements in Health
- COVID-19 Clinical Research Studies
Publications (55)
- Urinary sphingomyelin measurement: A simple tool for diagnosis and monitoring in Niemann-Pick disease type A
- Macrophage Activation Syndrome Revealing Tuberculous Lymphadenitis in an Adolescent: A Case Report and Review of Literature
- Eosinophilic Esophagitis Revealed by Hematemesis in an Asthmatic Adolescent: A Case Report
- From guidelines to real-world practice: clinical, biochemical, and genetic insights in a series of Moroccan patients with acid sphingomyelinase deficiency
- The prevalence of non-celiac gluten sensitivity in the general population: Systematic review and meta-analysis
- Identification of a novel nonsense mutation in the AGL gene in glycogen storage disease type IIIa: first genetically confirmed case report from Morocco
- First comprehensive identification of urinary sphingomyelin species in Niemann-Pick disease patients using UHPLC-MS/MS
- Unmasking Visceral Leishmaniasis: Nephrotic Syndrome as a Rare Pediatric Complication in Morocco
- Acute Abdomen Revealing Abdominal Tuberculosis in a 9 Years Old Child
- Isolated anal tuberculosis presenting as an anal fistula in an immunocompetent child
- Phenotype and molecular characterization of Wilson's disease in Morocco
- Immunoglobulin E-Mediated Food Sensitization in a Moroccan Pediatric Population with Celiac Disease
- Assessment of the impact of adherence to gluten-free diet and other determinants on quality of life in children, adolescents and adults with celiac disease using specific instruments: A systematic review with meta-analysis
- Clinical features of Wilson disease in Moroccan cohort
- Juvenile Systemic Sclerosis: About 9 Cases
- Microbiological quality of gluten-free meals, naturally gluten free foods, and gluten free-labelled products
- Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients
- Sphingolipidoses in Morocco: Chemical profiling for an affordable and rapid diagnosis strategy
- HAV Infection Associated with Hemophagocytic Syndrome
- Digestive manifestations of Covid-19 in children: a retrospective study
- Timely diagnosis of Niemann Pick disease using thin layer chromatography with identification of SMPD1 mutations causing NPD type A/B among Moroccan population
- The role of combination between TLC and UHPL/MS-MS in the diagnosis and prognosis of metachromatic leukodystrophy
- The case of glycosylation defects mimicking Wilson disease: A case report
- Secondary cutaneous aspergillosis in a child with Behçet’s disease: a case-based update
- Nutritional Status of Moroccan Pediatric Patients With Celiac Disease
- Detection of gluten content in both naturally and labelled gluten-free products available in Morocco
- Quality of life of Moroccan patients with celiac disease: Arabic translation, cross-cultural adaptation, and validation of the celiac disease questionnaire
- Challenges in the Diagnosis and Management of Nephrotic Syndrome in a Child With Multisystemic Tuberculosis
- Acute Vision Loss and Conjunctival Hemorrhage as Telltale Symptoms of PIMS-TS
- Moyamoya Syndrome Associated with Polycystic Kidney Disease in a Moroccan Child: A Rare Case
- Rare Association between Two Genetic Conditions: Turner Syndrome and Neurofibromatosis Type 1
- Neonatal Cholestasis: A Rare and Unusual Presentation of Pituitary Stalk Interruption Syndrome
- The Congenital Absence of the Portal Vein
- Atypical Presentation of Celiac Disease: Recurrent Acute Small Bowel Obstruction
- Rosa damascena Mill attenuated the liver and kidneys injuries in copper-overloaded mice
- Acute pancreatitis complicating a case of pediatric Wilson's disease*
- Wilson disease in children: A series of 43 cases
- An Isolated Thrombocytopenia in a Newborn
- Third Cranial Nerve Palsy Presenting with Unilateral Diplopia and Strabismus in a 24-Year-Old Woman with COVID-19
- Laboratory abnormalities in children with novel Coronavirus Disease 2019
- Implementation of an Affordable Method for MPS Diagnosis from Urine Screening to Enzymatic Confirmation: Results of a Pilot Study in Morocco
- Hepatitis A Virus Infection Associated with Cryoglobulinemic Vasculitis
- A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
- Update of a colorimetric method for quantitative determination of galactose in blood samples: A simple and rapid method for the early detection of inherited metabolic diseases
- Distal Arthrogryposis Type Six and Systemic Lupus Erythematosus, in a Girl: First Pediatric Case
- NGS-based, 107-gene resequencing panel as first-line screening test for lysosomal diseases
- Recurrent Hemolytic Anemia as an Inaugural Manifestation of Wilson Disease in Children: A Case Report
- Autism and celiac disease: a case in Marrakesh and review of the literature
- Systemic Lupus Erythematosus‐Related Pancreatitis in Children: Severe and Lethal Form
- Chronic Granulomatous Disease Revealed by Multiple Cystic and Pseudo-tumoral Liver Lesions: One Case Report
- Le cyclophosphamide dans le syndrome néphrotique idiopathique : résultats et perspectives
- GYNECOMASTIE UNILATERALE PERSISTANTE CHEZ LE PETIT ENFANT : A PROPOS D UN CAS PERSISTENT UNILATERAL GYNECOMASTIA IN A SMALL CHILD: ONE CASE REPORT.
- Évolution spectaculaire sous évérolimus d’un syndrome de Kasabach-Merrit associé à un angiome en touffe
- Fistule œsotrachéale congénitale isolée sans atrésie de l’œsophage. À propos de deux observations
- Cardiomyopathie dilatée révélant une arthrite juvénile idiopathique
Revues de publication
- Molecular Genetics and Metabolism × 10
- Open Journal of Pediatrics × 2
- Cureus × 2
- Nutrition Clinique et Métabolisme × 2
- Global Pediatric Health × 2
- Case Reports in Endocrinology × 2
Publications par année
- 20264
- 20256
- 20246
- 20239
- 20226
- 20217
- 20207
- 20193
- 20184
- 20171
Collaborations
Établissements partenaires : Université Hassan 1er · Chouaib Doukkali University · Instituts Supérieurs des Professions Infirmières et Techniques de Santé · Centre Hospitalier Universitaire Hassan II · Université Ibn Zohr
Pays des co-auteurs : France
Co-auteurs
- Imane Ait Sab
- Houda Nassih
- Rabiy El Qadiry
- Es‐Said Sabir
- Naı̈ma Fdil
- Karima Lafhal
- Imane Assiri
- Samira Najeh
- Miloud Hammoud
- Mohamed Sbihi
- Noureddine Rada
- Brahim Admou
Données bibliographiques issues d’OpenAlex (base ouverte).
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