Detalhe da pesquisa
1.
Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan Patients.
J Clin Immunol;
43(2): 485-494, 2023 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36367635
2.
Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds.
J Clin Immunol;
43(4): 728-740, 2023 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36630059
3.
Implementing the WHO Global Initiative for Childhood Cancer in Morocco: Survival study for the six indexed childhood cancers.
Pediatr Blood Cancer;
69(10): e29788, 2022 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35796382
4.
Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades' Experience.
J Clin Immunol;
41(3): 631-638, 2021 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33411152
5.
Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.
J Clin Immunol;
34(4): 452-8, 2014 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24596025
6.
A rare case of steroid 11 beta-hydroxylase deficiency in a child revealed by acute pulmonary edema.
Oxf Med Case Reports;
2024(5): omae042, 2024 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38784773
7.
Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis.
Mol Syndromol;
15(2): 96-103, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38585542
8.
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array.
Arch Pediatr;
31(2): 112-116, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38262863
9.
Chronic renal failure revealing a spinal arachnoid cyst, a case report with literature review.
Int J Surg Case Rep;
107: 108310, 2023 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37172393
10.
Corrigendum to Acute pancreatitis following L-asparaginase in acute lymphoblastic leukemia.
Leuk Res Rep;
20: 100375, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38098958
11.
A very rare case of bacteraemia in a 4-year-old girl with osteopetrosis with probable Leuconostoc lactis infection.
Access Microbiol;
5(10): 000439, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37970073
12.
Malignant Rhabdoid Tumor of the Kidney in a Child With Xeroderma Pigmentosum: Incidence or Coincidence?
Cureus;
14(7): e27049, 2022 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36000096
13.
What Lies Behind the Cannonball Pulmonary Metastases: Hodgkin's Lymphoma?
Cureus;
14(4): e24351, 2022 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35607589
14.
Bean Syndrome in a Child Treated with Sirolimus: About a Case.
Case Rep Pediatr;
2022: 8245139, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35656331
15.
Acute pancreatitis following L-asparaginase in acute lymphoblastic leukemia.
Leuk Res Rep;
18: 100357, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36405565
16.
Hemiparesis Revealing a Unique Neurological Hemophagocytic Lymphohistiocytosis in a Patient With Griscelli Syndrome Type 2.
Cureus;
14(9): e29159, 2022 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36259028
17.
Molecular heterogeneity of ß-thalassemia variants in the Eastern region of Morocco.
Mol Genet Genomic Med;
10(8): e1970, 2022 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35615994
18.
Complicated primary intestinal lymphangiectasia (Waldmann's disease) in a child successfully treated with octreotide: A case report from a low-resource setting.
Ann Med Surg (Lond);
68: 102588, 2021 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34401115
19.
Atypical Kawasaki Disease in an Adolescent with Multivisceral Involvement.
Case Rep Pediatr;
2021: 8941847, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34367708
20.
Visceral leishmaniasis associated with macrophage activation syndrome: Case report and literature review.
IDCases;
26: e01247, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34430207