Detalhe da pesquisa
1.
Effects of 12 weeks of recreational football (soccer) with caloric control on glycemia and cardiovascular health of adolescent boys with type 1 diabetes.
Pediatr Diabetes
; 22(4): 625-637, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33745203
2.
A novel mutation in ATM gene in a Saudi female with ataxia telangiectasia.
Int J Neurosci
; 131(2): 206-211, 2021 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-32172615
3.
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
Inglês
| MEDLINE | ID: mdl-34154525
4.
Molecular and enzoinformatics perspectives of targeting Polo-like kinase 1 in cancer therapy.
Semin Cancer Biol
; 56: 47-55, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-29122685
5.
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
Inglês
| MEDLINE | ID: mdl-32414585
6.
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
Inglês
| MEDLINE | ID: mdl-32968423
7.
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
Inglês
| MEDLINE | ID: mdl-30392057
8.
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
Inglês
| MEDLINE | ID: mdl-31258591
9.
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
Inglês
| MEDLINE | ID: mdl-29541814
10.
Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family.
Neurosciences (Riyadh)
; 23(4): 347-350, 2018 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-30351297
11.
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
Inglês
| MEDLINE | ID: mdl-28181300
12.
Copy number variations in Saudi family with intellectual disability and epilepsy.
BMC Genomics
; 17(Suppl 9): 757, 2016 10 17.
Artigo
Inglês
| MEDLINE | ID: mdl-27766957
13.
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
Inglês
| MEDLINE | ID: mdl-27531570
14.
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
Inglês
| MEDLINE | ID: mdl-33065750
15.
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
Inglês
| MEDLINE | ID: mdl-34454412
16.
Sleep Patterns and Predictors of Poor Sleep Quality among Medical Students in King Khalid University, Saudi Arabia.
Malays J Med Sci
; 23(6): 94-102, 2016 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-28090183
17.
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
Inglês
| MEDLINE | ID: mdl-25923336
18.
Effect of BRAF mutational status on expression profiles in conventional papillary thyroid carcinomas.
BMC Genomics
; 16 Suppl 1: S6, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25922907
19.
Comparison of microarray expression profiles between follicular variant of papillary thyroid carcinomas and follicular adenomas of the thyroid.
BMC Genomics
; 16 Suppl 1: S7, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25923053
20.
c-MET immunostaining in colorectal carcinoma is associated with local disease recurrence.
BMC Cancer
; 15: 676, 2015 Oct 12.
Artigo
Inglês
| MEDLINE | ID: mdl-26459369