Hindi Al-Hindi
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Explore the profile of Hindi Al-Hindi including associated specialties, affiliations and a list of published articles.
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45
Citations
472
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Recent Articles
1.
Alzahrani A, Alswailem M, Buffet A, Alghamdi B, Alobaid L, Alsagheir O, et al.
Endocr Relat Cancer
. 2024 May;
31(8).
PMID: 38767322
In 2012, somatic EPAS1 pathogenic variants were found to cause a triad of pheochromocytoma/paragangliomas (PPGLs), polycythemia, and somatostatinoma. Since then, a limited number of studies on this subject have been...
2.
Murugan A, Al-Hindi H, Alzahrani A
Endocrine
. 2024 Apr;
85(3):1278-1288.
PMID: 38580894
Purpose: Long noncoding RNAs (lncRNAs) play an essential role in the epigenetic regulation of various key genes involved in vital cellular functions. A somatic dinucleotide mutation in the lncRNA GAS8-AS1...
3.
Alzahrani A, Bin Nafisah A, Alswailem M, Moria Y, Poprawski D, Al-Hindi H, et al.
Front Endocrinol (Lausanne)
. 2023 Dec;
14:1273093.
PMID: 38152133
Context: Germline succinate dehydrogenase subunit B () pathogenic variants are characteristic of familial paraganglioma (PGL) syndrome type 4. This syndrome frequently presents with abdominal PGL and has high tendency for...
4.
Altassan R, AlQudairy H, AlJebreen S, Almuhaizea M, Al-Hindi H, Pena-Guerra K, et al.
Am J Med Genet A
. 2023 Dec;
194(4):e63498.
PMID: 38129970
Congenital muscular dystrophies are a group of progressive disorders with wide range of symptoms associated with diverse cellular mechanisms. Recently, biallelic variants in GGPS1 were linked to a distinct autosomal...
5.
Alghamdi B, Al-Hindi H, Murugan A, Alzahrani A
J Endocr Soc
. 2023 May;
7(5):bvad035.
PMID: 37143695
Context: Multiple tumors in the same patient suggest a genetic predisposition. Here, we report a patient who presented with several unusual types of malignant and benign tumors, presumably due to...
6.
Alswailem M, Alghamdi B, AlOtaibi A, Aljomiah A, Al-Hindi H, Murugan A, et al.
J Clin Endocrinol Metab
. 2023 Mar;
108(9):e704-e711.
PMID: 36995892
Context: Diffuse sclerosing papillary thyroid cancer (DSPTC) is rare, with limited data on its molecular genetics. Objective: We studied the molecular genetics of a cohort of DSPTC. Methods: DNA was...
7.
AlShail E, Alahmari A, Dababo A, Alsagob M, Al-Hindi H, Khalil H, et al.
Front Oncol
. 2023 Mar;
13:1034292.
PMID: 36860324
Background: Pilocytic Astrocytoma (PA) is the most common pediatric brain tumors. PAs are slow-growing tumors with high survival rates. However, a distinct subgroup of tumors defined as pilomyxoid astrocytoma (PMA)...
8.
Barakeh D, Alsolme E, Alqubaishi F, Almutairi A, Alhabeeb L, Al Abdulmohsen S, et al.
Front Med (Lausanne)
. 2022 Dec;
9:947456.
PMID: 36507516
Central nervous system (CNS) metastasis is the most common brain tumor type in adults. Compared to their primary tumors, these metastases undergo a variety of genetic changes to be able...
9.
Alhamoudi K, Alghamdi B, Alswailem M, Nasir A, Aljomaiah A, Al-Hindi H, et al.
J Clin Endocrinol Metab
. 2022 Jul;
107(10):2883-2891.
PMID: 35896147
Context: Synonymous mutations are usually nonpathogenic. Objective: We report here a family with X-linked hypophosphatemia (XLH) due to a novel synonymous PHEX variant with a unique mechanism. Methods: We studied...
10.
Alhamoudi K, Alghamdi B, Aljomaiah A, Alswailem M, Al-Hindi H, Alzahrani A
Front Genet
. 2022 Jul;
13:885589.
PMID: 35865014
Mutations in the nuclear receptor subfamily 5 group A member 1 () are the underlying cause of 10-20% of 46,XY disorders of sex development (DSDs). We describe a young girl...