Home › Researcher directory › Aïcha Bourrahouat
Aïcha Bourrahouat
Affiliation : Cadi Ayyad University · Centre Hospitalier Universitaire Mohammed VI
- 55Publications (affiliation in Morocco)
- 65Total publications
- 194Citations
- 7h-index
Research profile
Aïcha Bourrahouat has 55 indexed publications (2010–2026). Their work appears mainly in “Molecular Genetics and Metabolism”, “Open Journal of Pediatrics” and “Cureus”. Their most cited article, “Third Cranial Nerve Palsy Presenting with Unilateral Diplopia and Strabismus in a 24-Year-Old Woman with COVID-19” (2020), has been cited 65 times. 16 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France.
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Create my free profile Add my publicationsResearch areas
- 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
Publication venues
- 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 per year
- 20264
- 20256
- 20246
- 20239
- 20226
- 20217
- 20207
- 20193
- 20184
- 20171
Collaborations
Partner institutions : Université Hassan 1er · Chouaib Doukkali University · Instituts Supérieurs des Professions Infirmières et Techniques de Santé · Centre Hospitalier Universitaire Hassan II · Université Ibn Zohr
Co-authors’ countries : France
Co-authors
- 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
Bibliographic data from OpenAlex (open database).
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