Detalhe da pesquisa
1.
RAS Mutations Predict Recurrence-Free Survival and Recurrence Patterns in Colon Cancer: A Unicenter Study in Morocco.
Cancer Control
; 31: 10732748241229290, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38270484
2.
Identification of novel and de novo variant in the SCN1A gene confirms Dravet syndrome in Moroccan child: a case report.
Mol Biol Rep
; 51(1): 233, 2024 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38282049
3.
Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population.
Audiol Neurootol
; : 1-8, 2024 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38253033
4.
A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2.
Am J Med Genet A
; 191(11): 2673-2678, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37596802
5.
Novel APOE Mutation in a Moroccan Subject Suffering from Alzheimer Disease: A Case Study and Exploration of Pathogenic Implication.
Alzheimer Dis Assoc Disord
; 37(4): 370-372, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38015425
6.
Genetic characterization of Schuurs-Hoeijmakers syndrome in a moroccan individual with heterozygote PACS1 mutation.
Mol Biol Rep
; 50(11): 9121-9128, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37747683
7.
Correlation of Epidermal Growth Factor Receptor Mutation With Major Histologic Subtype of Lung Adenocarcinoma According to IASLC/ATS/ERS Classification.
Cancer Control
; 29: 10732748221084930, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35348028
8.
Associations between nutritional factors and KRAS mutations in colorectal cancer: a systematic review.
BMC Cancer
; 20(1): 696, 2020 Jul 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32723394
9.
Williams-Beuren syndrome in diverse populations.
Am J Med Genet A
; 176(5): 1128-1136, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29681090
10.
Impact of Deletion on Angelman Syndrome Phenotype Variability: Phenotype-Genotype Correlation in 97 Patients with Motor Developmental Delay.
J Pediatr Genet
; 13(1): 15-21, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38567176
11.
Genotypic and Allelic Distribution of the CD36 rs1761667 Polymorphism in High-Level Moroccan Athletes: A Pilot Study.
Genes (Basel)
; 15(4)2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38674354
12.
An epidermal growth factor receptor compound mutation of L858R with S768I in advanced non-small-cell lung cancer: a case report.
J Med Case Rep
; 18(1): 118, 2024 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38494473
13.
A Mosaic PIK3CA Mutation in a Moroccan Female: Exploring the Diagnostic Challenges of PIK3CA-Related Overgrowth Spectrum.
Cureus
; 15(4): e36996, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37139028
14.
The burden of cystic fibrosis in North Africa.
Front Genet
; 14: 1295008, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38269366
15.
Clinical Evidence of Circulating Tumor DNA Application in Aggressive Breast Cancer.
Diagnostics (Basel)
; 13(3)2023 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36766575
16.
Rare and Atypical Case of Turner Syndrome With Three Cell Lines.
Cureus
; 15(6): e41128, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37519544
17.
The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study.
Cureus
; 15(4): e37866, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37223137
18.
New Biomarkers and Treatment Advances in Triple-Negative Breast Cancer.
Diagnostics (Basel)
; 13(11)2023 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37296801
19.
Influence of CYP450 Enzymes and ABCB1 Polymorphisms on Clopidogrel Response in Moroccan Patients with Acute Coronary Syndromes.
Pharmgenomics Pers Med
; 16: 901-909, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37810546
20.
Heterogeneous distribution of EGFR mutation in NSCLC: Case report.
Respir Med Case Rep
; 44: 101871, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37251359