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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2008 1
2010 5
2011 3
2012 3
2013 4
2014 2
2015 6
2016 6
2017 2
2018 2
2019 5
2020 4
2021 5
2022 8
2023 6
2024 2

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56 results

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Page 1
Molecular Genetics of Diffuse Sclerosing Papillary Thyroid Cancer.
Alswailem M, Alghamdi B, Alotaibi A, Aljomiah A, Al-Hindi H, Murugan AK, Abouelhoda M, Shi Y, Alzahrani AS. Alswailem M, et al. Among authors: al hindi h. J Clin Endocrinol Metab. 2023 Aug 18;108(9):e704-e711. doi: 10.1210/clinem/dgad185. J Clin Endocrinol Metab. 2023. PMID: 36995892
Angiocentric glioma of brainstem.
Almubarak AO, Alahmari A, Al Hindi H, AlShail E. Almubarak AO, et al. Among authors: al hindi h. Neurosciences (Riyadh). 2020 Oct;25(5):416-420. doi: 10.17712/nsj.2020.5.20200026. Neurosciences (Riyadh). 2020. PMID: 33459294 Free PMC article.
Infantile atypical subependymal giant cell astrocytoma.
Almubarak AO, Abdullah J, Al Hindi H, AlShail E. Almubarak AO, et al. Among authors: al hindi h. Neurosciences (Riyadh). 2020 Jan;25(1):61-64. doi: 10.17712/nsj.2020.1.20190044. Neurosciences (Riyadh). 2020. PMID: 31982898 Free PMC article.
MYH1 is a candidate gene for recurrent rhabdomyolysis in humans.
Alsaif HS, Alshehri A, Sulaiman RA, Al-Hindi H, Guzmán-Vega FJ, Arold ST, Alkuraya FS. Alsaif HS, et al. Among authors: al hindi h. Am J Med Genet A. 2021 Jul;185(7):2131-2135. doi: 10.1002/ajmg.a.62188. Epub 2021 Mar 23. Am J Med Genet A. 2021. PMID: 33755318
An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline SDHB pathogenic variant in the absence of paraganglioma or pheochromocytoma.
Alzahrani AS, Bin Nafisah A, Alswailem M, Moria Y, Poprawski D, Al-Hindi H, Pacak K. Alzahrani AS, et al. Among authors: al hindi h. Front Endocrinol (Lausanne). 2023 Dec 13;14:1273093. doi: 10.3389/fendo.2023.1273093. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38152133 Free PMC article.
Clinicopathologic and genomic characterizations of brain metastases using a comprehensive genomic panel.
Barakeh DH, Alsolme E, Alqubaishi F, Almutairi A, Alhabeeb L, Al Abdulmohsen S, Almohsen SS, Alayed D, AlAnazi SR, AlZahrani M, Binowayn AM, AlOtaibi SS, Alkhureeb FA, Al Shakweer W, Al-Hindi H, Alassiri A, Robinson HA, Abedalthagafi M. Barakeh DH, et al. Among authors: al hindi h. Front Med (Lausanne). 2022 Nov 24;9:947456. doi: 10.3389/fmed.2022.947456. eCollection 2022. Front Med (Lausanne). 2022. PMID: 36507516 Free PMC article.
ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder.
Al-Hassnan ZN, Al-Dosary M, Alfadhel M, Faqeih EA, Alsagob M, Kenana R, Almass R, Al-Harazi OS, Al-Hindi H, Malibari OI, Almutari FB, Tulbah S, Alhadeq F, Al-Sheddi T, Alamro R, AlAsmari A, Almuntashri M, Alshaalan H, Al-Mohanna FA, Colak D, Kaya N. Al-Hassnan ZN, et al. Among authors: al hindi h. J Med Genet. 2015 Mar;52(3):186-94. doi: 10.1136/jmedgenet-2014-102592. Epub 2014 Dec 24. J Med Genet. 2015. PMID: 25539947
56 results