Detalhe da pesquisa
1.
A novel mutation in ATM gene in a Saudi female with ataxia telangiectasia.
Int J Neurosci
; 131(2): 206-211, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32172615
2.
Characteristics of visits and predictors of admission from a paediatric emergency room in Saudi Arabia.
BMC Emerg Med
; 21(1): 72, 2021 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34154525
3.
Molecular and enzoinformatics perspectives of targeting Polo-like kinase 1 in cancer therapy.
Semin Cancer Biol
; 56: 47-55, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29122685
4.
A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
J Stroke Cerebrovasc Dis
; 29(7): 104832, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32414585
5.
Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family.
Pak J Med Sci
; 36(6): 1425-1428, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32968423
6.
A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family.
Neurol Sci
; 40(2): 299-303, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30392057
7.
Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family.
Pak J Med Sci
; 35(3): 764-770, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31258591
8.
Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Pediatr Cardiol
; 39(5): 924-940, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29541814
9.
Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family.
Neurosciences (Riyadh)
; 23(4): 347-350, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30351297
10.
Synthesis and Characterization of Cefotaxime Conjugated Gold Nanoparticles and Their Use to Target Drug-Resistant CTX-M-Producing Bacterial Pathogens.
J Cell Biochem
; 118(9): 2802-2808, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28181300
11.
Copy number variations in Saudi family with intellectual disability and epilepsy.
BMC Genomics
; 17(Suppl 9): 757, 2016 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27766957
12.
Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing.
Am J Med Genet A
; 170(11): 3018-3022, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27531570
13.
A Novel Mutation in HERC2 Gene in a Patient with Global Developmental Delay, Intellectual Disability, and Refractory Seizures.
Neuropediatrics
; 52(2): 150-152, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33065750
14.
Correction to: Characteristics of visits and predictors of admission from a paediatric emergency room in Saudi Arabia.
BMC Emerg Med
; 21(1): 99, 2021 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34454412
15.
Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia.
BMC Genomics
; 16 Suppl 1: S10, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25923336
16.
Thyroid Disorders Spectrum in Pediatric Endocrine Clinic; Seven-Year Experience of a Teaching Hospital in Saudi Arabia.
Children (Basel)
; 10(2)2023 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36832519
17.
A Clinical and Biochemical Comparative Study Of Diabetic Ketoacidosis (DKA) in Newly Diagnosed Vs Known Cases of Type 1 Diabetic Children.
Rev Diabet Stud
; 19(1): 28-33, 2023 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37185051
18.
Diabetic Ketoacidosis and its Severity Predictors in Type 1 Diabetic Children; A 10-year Experience of A Teaching Hospital in Saudi Arabia.
Rev Diabet Stud
; 18(3): 146-151, 2022 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36309773
19.
Myocarditis in Children: Impact of Early Presentation on Disease Outcomes at a Single Tertiary Center in Saudi Arabia.
Int J Gen Med
; 15: 5627-5633, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35726274
20.
Innovative Method to Digitize a Web-Based OSCE Evaluation System for Medical Students: A Cross-Sectional Study in University Hospital in Saudi Arabia.
Int J Gen Med
; 15: 1085-1095, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35140510