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Mohamed El Khorassani

Observed names: EL KHORASSANI, M., KHORASSANI Mohamed EL, M El Khorassani, M El khorassani, M Elkhorassani, M el Khorassani, M. El Khorassani, M. El khorassani, M. ElKhorassani, M. Elkhorassani, M. Khorassani, Mohamed El khorassani, Mohamed Elkhorassani, Mohamed Khorassani
Observed institutions: Mohammed V University, University of Freiburg, University Medical Center Freiburg, Radboud University Medical Center, Centre Hospitalier Ibn Sina, Centre Hospitalier Universitaire de Rabat-Salé, Hospital Fatuma Bourguiba Monastir
OpenAlex ID: A5113492910
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment
2019 · Vincenzo Salpietro, Nancy T. Malintan, et al. · The American Journal of Human Genetics · 134
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
2019 · Stephanie Efthymiou, Vincenzo Salpietro, et al. · Brain · 71
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The World Federation of Hemophilia World Bleeding Disorders Registry: insights from the first 10,000 patients
2023 · Donna Coffin, Emma Gouider, et al. · Research and Practice in Thrombosis and Haemostasis · 46
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Clinical pharmacology, efficacy and safety study of a triple‐secured fibrinogen concentrate in adults and adolescent patients with congenital fibrinogen deficiency
2019 · Claudia Djambas Khayat, Mohamed El Khorassani, et al. · Journal of Thrombosis and Haemostasis · 31
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Von Willebrand's disease: case report and review of literature
2017 · Hanae Echahdi, Brahim El Hasbaoui, et al. · Pan African Medical Journal · 31
Time to diagnosis of pediatric brain tumors: a report from the Pediatric Hematology and Oncology Center in Rabat, Morocco
2018 · Fatima Zahra Boutahar, Sarra Benmiloud, et al. · Child s Nervous System · 29
Pediatric rhabdomyosarcoma in Morocco
2009 · Laila Hessissen, Lamya Kanouni, et al. · Pediatric Blood & Cancer · 28
Sarcome rénal à cellules claires. À propos d'une série de 13 cas
2004 · M El Kababri, M Khattab, et al. · Archives de Pédiatrie · 19
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
2022 · Elisa Calì, Sheng-Jia Lin, et al. · Genetics in Medicine · 17
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Pharmacology, Efficacy and Safety of a Triple-Secured Fibrinogen Concentrate in Children Less than or Equal to 12 Years with Afibrinogenaemia
2020 · Claudia Djambas Khayat, Mohamed El Khorassani, et al. · Thrombosis and Haemostasis · 12
Leucémie aiguë lymphoblastique T/Lymphome lymphoblastique orbitaire chez l’enfant
2005 · K. Abdelouahed, M. Laghmari, et al. · Journal Français d Ophtalmologie · 12
Utilisation de la médecine alternative en oncologie pédiatrique au Maroc
2011 · L. Hessissen, M. Bhour, et al. · Journal africain du cancer / African Journal of Cancer · 10
Cytogenetic Profile of Moroccan Pediatric Acute Lymphoblastic Leukemia: Analysis of 155 Cases With a Review of the Literature
2018 · Zahra Takki Chebihi, Aziza Belkhayat, et al. · Clinical Lymphoma Myeloma & Leukemia · 8
A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream
2009 · H Robert-Ebadi, P de Moerloose, et al. · Blood Coagulation & Fibrinolysis · 7
Sarcome rénal à cellules claires. À propos d'une série de 13 cas Clear cell sarcoma of the kidney. A study of 13 cases
2004 · Maria El Kababri, Mohamed A. Khattab, et al. · 6
Hypertrophie thymique après une chimiothérapie pour un néphroblastome
2006 · L. Hessissen, M.N. Nachef, et al. · Archives de Pédiatrie · 5
Pediatric Hodgkins disease in Morocco
2004 · Laila Hessissen, N. Oulhiane, et al. · Pediatric Blood & Cancer · 5
A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration
2019 · Stephanie Efthymiou, Yamna Kriouile, et al. · Journal of the Neurological Sciences · 4
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Inhibitor Development in Previously Untreated Patients with Severe Hemophilia a Treated with Nuwiq®, a New Generation Recombinant FVIII of Human Origin
2016 · Raina Liesner, Marina Abashidze, et al. · Blood · 4
Histiocytose langerhansienne à localisation orbitaire
2005 · M. Charif Chefchaouni, L. Lahlou, et al. · Journal Français d Ophtalmologie · 4
[Pleuro-pulmonary blastoma. Report of 4 cases].
1999 · T Benouachane, M el Khorassani, et al. · PubMed · 4
The prevalence of anti-factor VIII and anti-factor IX antibodies among patients with hemophilia in Rabat, Morocco: a single center experience
2022 · Meryem Bouyadmar, Mohamed El khorassani, et al. · Pan African Medical Journal · 3
A hemophagocytic syndrome revealing a Griscelli syndrome type 2
2013 · Selim Jennane, Maria El Kababri, et al. · Annales de biologie clinique · 3
Use of alternative medicine in a Moroccan pediatric oncology unit
2011 · Laila Hessissen, M. Bhour, et al. · 3
Lymphome non hodgkinien associé à un déficit en protéine S
2003 · M El Kababri, M El Khorassani, et al. · Archives de Pédiatrie · 3
Works count: 69
Citation count: 516
H-index: 11
I10-index: 12
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