Murad Alturkustani
Overview
Explore the profile of Murad Alturkustani including associated specialties, affiliations and a list of published articles.
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39
Citations
133
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Recent Articles
1.
Nmezi B, Bey G, Oranburg T, Dudnyk K, Lardo S, Herdman N, et al.
Nat Commun
. 2025 Feb;
16(1):1373.
PMID: 39910058
The role of non-coding regulatory elements and how they might contribute to tissue type specificity of disease phenotypes is poorly understood. Autosomal Dominant Leukodystrophy (ADLD) is a fatal, adult-onset, neurological...
2.
Alturkustani M, Ang L
Diagnostics (Basel)
. 2024 Oct;
14(19).
PMID: 39410644
Background: Multiple sclerosis (MS) is characterized by white matter demyelinating plaques, which can be classified as active, chronic active, or chronic inactive based on the extent of demyelination, cellularity, and...
3.
Alturkustani M, Alomran A, Al-Thomali H
Cureus
. 2024 Sep;
16(8):e66153.
PMID: 39233958
Background and objective Standardizing placental pathology diagnoses is crucial for improving diagnostic accuracy and clinical communication. The Amsterdam Consensus Criteria were developed to address inconsistencies in diagnosing significant placental pathologies....
4.
Alturkustani M, Walker A, Castaneda E, Cotter J
J Neuropathol Exp Neurol
. 2024 Jul;
83(12):1039-1046.
PMID: 39067019
This study evaluates the diagnostic utility of OLIG2 immunohistochemistry for distinguishing between pediatric high-grade gliomas (pHGG) and embryonal tumors (ETs) of the CNS. Utilizing a retrospective pediatric cohort (1990-2021) of...
5.
Alnajjar S, Ahyad R, Alhashmi G, Alturkustani M, Alharthi M, Bustangi N
Radiol Case Rep
. 2024 Jul;
19(8):3211-3215.
PMID: 39022112
Multiple theories have been proposed about the pathophysiology of Fetus-in-fetu (FIF). The most widely accepted theory is abnormal embryogenesis in diamniotic monochorionic pregnancies, in which a malformed parasitic fetus is...
6.
Alturkustani M
Neurosciences (Riyadh)
. 2024 Jul;
29(3):168-176.
PMID: 38981632
Objectives: To elucidate the relationship between DNA methylation profiling (DMP) and pathological diagnosis (PD) in pediatric glial and glioneuronal tumors with B-Raf proto-oncogene, serine/threonine kinase mutations, addressing their diagnostic challenges....
7.
Alturkustani M, Yang B, Bockoven C, Mahabir R, Shillingford N, Schmidt R, et al.
Transl Pediatr
. 2024 May;
13(4):624-633.
PMID: 38715664
Background: -associated tumors are heterogeneous and affect several organs. -associated primary intracranial sarcoma is associated with histone H3 trimethylation on lysine 27 (H3K27me3) loss in nucleus by immunohistochemistry. Methods: We...
8.
Albalawi S, Hafiz B, Turki A, Alturkustani M, Bakhsh S, Sabbagh A
Cureus
. 2024 Feb;
16(1):e52341.
PMID: 38361697
Infantile hemangioma is a common benign vascular tumor in children, but it is very unusual to be found intracranially. Our literature review identified 44 reported cases. Presentation can vary from...
9.
Alturkustani M
Diagnostics (Basel)
. 2023 Nov;
13(22).
PMID: 37998600
This study adopts an innovative approach to utilize the DNA methylation class (MC) by prioritizing the understanding of discrepancies over traditional direct comparisons with the pathological diagnosis (PD). The aim...
10.
Nmezi B, Bey G, Oranburg T, Dudnyk K, Lardo S, Herdman N, et al.
bioRxiv
. 2023 Aug;
PMID: 37609196
The role of non-coding regulatory elements and how they might contribute to tissue type specificity of disease phenotypes is poorly understood. Autosomal Dominant Leukodystrophy (ADLD) is a fatal, adult-onset, neurological...