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1 . Academic Journal
Chronic progressive external ophthalmoplegia in a Saudi patient with a mutation in the POLG gene successfully managed with bilateral frontalis sling
저자
by
Hussein Algahtani
;
Bader Shirah
;
Khalid Alsaggaf
;
Mohammad H. Al-Qahtani
;
Angham Abdulrahman Abdulkareem
, et al.
소스
대한의학유전학회지 18. 2 (2021): 121-126.
Full Text(스콜라)
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7 . Academic Journal
A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy
저자
by
Muhammad Imran Naseer
;
Mohammad Khalid Alwasiyah
;
Angham Abdulrahman Abdulkareem
;
Rayan Abdullah Bajammal
;
Carlos Trujillo
, et al.
소스
Genes & Genomics, 40(11), pp.1149-1155 Nov, 2018
Web of Science
Scopus
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7 . Academic Journal
A novel homozygous frameshift variant in the MCPH1 gene causes primary microcephaly in a consanguineous Saudi family
저자
by
Muhammad Imran Naseer
;
Mahmood Rasool
;
Osama Yousef Muthaffar
;
Abdulrahman J. Sabbagh
;
Adeel G. Chaudhary
, et al.
소스
Genes & Genomics, 39(12), pp.1317-1323 Dec, 2017
Web of Science
Scopus
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7 . Academic Journal
Effect of quercetin on steroidogenesis and folliculogenesis in ovary of mice with experimentally-induced polycystic ovarian syndrome
저자
by
Mohd Zahoor ul haq Shah
;
Vinoy kumar Shrivastva
;
Manzoor Ahmad Mir
;
Wajid Mohammad Sheikh
;
Mohd Ashraf Ganie
, et al.
소스
Frontiers in Endocrinology, Vol 14 (2023)
Open Access (DOAJ)
Web of Science
Scopus
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7 . Academic Journal
Characteristics of visits and predictors of admission from a paediatric emergency room in Saudi Arabia
저자
by
Mohammad H. Al-Qahtani
;
Abdullah A. Yousef
;
Bassam H. Awary
;
Waleed H. Albuali
;
Mohammed A. Al Ghamdi
, et al.
소스
BMC Emergency Medicine, Vol 21, Iss 1, Pp 1-8 (2021)
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7 . Academic Journal
Thyroid Disorders Spectrum in Pediatric Endocrine Clinic; Seven-Year Experience of a Teaching Hospital in Saudi Arabia
저자
by
Mohammad H. Al-Qahtani
;
Sufian A. ElYahia
;
Abdulaziz S. AlQahtani
;
Abdulrahman J. AlQahtani
;
Abdulaziz A. Alamer
, et al.
소스
Children, Vol 10, Iss 2, p 390 (2023)
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7 . Academic Journal
Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in GBA2 gene in a large consanguineous Saudi family
저자
by
Hussein Algahtani
;
Bader Shirah
;
Ikram Ullah
;
Mohammad H. Al-Qahtani
;
Angham Abdulrahman Abdulkareem
, et al.
소스
Genes and Diseases, Vol 8, Iss 1, Pp 110-114 (2021)
Full Text (ScienceDirect)
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Full Text (ScienceDirect O/A)
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7 . Academic Journal
Child Abuse and Neglect Awareness among Medical Students
저자
by
Mohammad H. Al-Qahtani
;
Haitham H. Almanamin
;
Ahmed M. Alasiri
;
Mohammed H. Alqudaihi
;
Mohammed H. AlSaffar
, et al.
소스
Children, Vol 9, Iss 6, p 885 (2022)
Open Access (DOAJ)
Web of Science
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7 . Academic Journal
Predictors of Recurrent Acute Chest Syndrome in Pediatric Sickle Cell Disease: A Retrospective Case-Control Study
저자
by
Abdullah A. Yousef
;
Hwazen A. Shash
;
Ali N. Almajid
;
Ammar A. Binammar
;
Hamza Ali Almusabeh
, et al.
소스
Children, Vol 9, Iss 6, p 894 (2022)
Open Access (DOAJ)
Web of Science
Scopus
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7 . Academic Journal
A novel variant c.3706C>T p.(Avg 1236Cys) in the ABCA7 gene in a Saudi patient with susceptibility to Alzheimer's disease 9
저자
by
Alhusain Alshareef
;
Angham Abdulrahman Abdulkareem
;
Bader Shirah
;
Hussein Algahtani
;
Mohammad H. Al-Qahtani
, et al.
소스
Intractable & Rare Diseases Research. 2020, 9(3):151
Open Access (JSTAGE)
Scopus
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