Detalhe da pesquisa
1.
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination.
Brain
; 142(10): 2948-2964, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31501903
2.
Time to diagnosis of pediatric brain tumors: a report from the Pediatric Hematology and Oncology Center in Rabat, Morocco.
Childs Nerv Syst
; 34(12): 2431-2440, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30054805
3.
REACH: A programme for improving care in haemophilia.
Haemophilia
; 25(3): e211-e215, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30888109
4.
Pediatric rhabdomyosarcoma in Morocco.
Pediatr Blood Cancer
; 54(1): 25-8, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19746454
5.
Pharmacology, Efficacy and Safety of a Triple-Secured Fibrinogen Concentrate in Children Less than or Equal to 12 Years with Afibrinogenaemia.
Thromb Haemost
; 120(6): 957-967, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32392604
6.
Clinical pharmacology, efficacy and safety study of a triple-secured fibrinogen concentrate in adults and adolescent patients with congenital fibrinogen deficiency.
J Thromb Haemost
; 17(4): 635-644, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30661302
7.
Cytogenetic Profile of Moroccan Pediatric Acute Lymphoblastic Leukemia: Analysis of 155 Cases With a Review of the Literature.
Clin Lymphoma Myeloma Leuk
; 18(6): e241-e248, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29748040
8.
Von Willebrand's disease: case report and review of literature.
Pan Afr Med J
; 27: 147, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28904675
9.
A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration.
J Neurol Sci
; 410: 116639, 2020 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31884352
10.
[A hemophagocytic syndrome revealing a Griscelli syndrome type 2]. / Un syndrome d'activation macrophagique révélant un syndrome de Griscelli de type 2.
Ann Biol Clin (Paris)
; 71(4): 461-4, 2013.
Artigo
em Francês
| MEDLINE | ID: mdl-23906575