Angham Abdulrhman Abdulkareem
Overview
Explore the profile of Angham Abdulrhman Abdulkareem including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
22
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0
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Recent Articles
1.
Bagabir H, Abdulkareem A, Muthaffar O, Shirah B, Naseer M
Pak J Med Sci
. 2024 Nov;
40(10):2243-2250.
PMID: 39554679
Background & Objective: Autosomal recessive cerebellar ataxias (ARCA) are rare heterogenous neurodegenerative disorders characterized by degeneration of the cerebellum and spinal cord with an early onset before the age of...
2.
Abdulkareem A, Shirah B, Bagabir H, Haque A, Naseer M
Biomed Rep
. 2024 Mar;
20(4):67.
PMID: 38476606
Partner and localiser of BRCA2 (), also known as , is a key tumour suppressor gene in maintaining genome integrity. Monoallelic mutations of are associated with breast and overian cancers,...
3.
Muthaffar O, Abdulkareem A, Ashi A, Naseer M
Front Pediatr
. 2023 Dec;
11:1288542.
PMID: 38046674
Background: The mitochondria are a cellular power house. Tissues are involved in frequent energy consumption, and any failure or irregularity in the continuous energy production could lead to abnormalities. The...
4.
Zaman Q, Khan J, Ahmad M, Khan H, Chaudhary H, Rehman G, et al.
Gene
. 2023 Nov;
894:147986.
PMID: 37956964
Background: Oculocutaneous albinism (OCA) is a group of skin depigmentation disorders. Clinical presentation of OCA includes defects in melanocyte differentiation, melanin biosynthesis, and melanosome maturation and transport. Objectives: A molecular...
5.
Algahtani H, Shirah B, Abdulkareem A, Bibi F, Pushparaj P, Naseer M
Bioinformation
. 2023 Oct;
19(3):226-229.
PMID: 37808372
Leber hereditary optic neuropathy (LHON) is a rare maternally inherited mitochondrial disorder that typically affects young male adults in their second and third decades of life. It usually manifests as...
6.
Abdulkareem A, Zaman Q, Khan H, Khan S, Rehman G, Tariq N, et al.
Front Genet
. 2023 Jun;
14:1185065.
PMID: 37359369
Epilepsy is a group of neurological disorders characterized by recurring seizures and fits. The Epilepsy genes can be classified into four distinct groups, based on involvement of these genes in...
7.
Iqbal M, Shams S, Rafiq H, Khan M, Khan S, Khattak U, et al.
Pharmaceuticals (Basel)
. 2023 Jun;
16(2).
PMID: 37259449
Liver fibrosis is currently one of the top ten causes of death worldwide. Stem cells transplantation using mesenchymal stem cells (MSCs) is an alternative therapy which is used in the...
8.
Rahat M, Akbar F, Rasool A, Ilyas M, Rakha A, Shams S, et al.
Biomedicines
. 2023 May;
11(4).
PMID: 37189847
Methods: Eye colour digital photographs and buccal swab samples of 893 individuals of different age groups were collected. Multiplexed SNaPshot single base extension chemistry was used, and the genotypic results...
9.
Zaman Q, Iftikhar A, Rehman G, Khan Q, Najumuddin , Jan A, et al.
J Gene Med
. 2023 Apr;
25(10):e3522.
PMID: 37119015
Background: Autosomal recessive cutis laxa type 2A (ARCL2A; OMIM: 219200) is characterized by neurovegetative, developmental and progeroid elastic skin anomalies. It is caused by biallelic variation in ATPase, H transporting...
10.
Bakar A, Shams S, Bibi N, Ullah A, Ahmad W, Jelani M, et al.
Genes (Basel)
. 2023 Feb;
14(2).
PMID: 36833437
(1) Background: Dyggve-Melchior-Clausen Syndrome is a skeletal dysplasia caused by a defect in the gene (OMIM number 607461). Pathogenic variants in the gene have been reported to cause Dyggve-Melchior-Clausen (DMC;...