Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2002 1
2006 1
2009 1
2010 1
2011 1
2012 1
2014 1
2015 1
2016 1
2017 2
2018 6
2019 2
2020 1
2021 3
2022 2
2023 2
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

26 results

Results by year

Filters applied: . Clear all
Page 1
Succinate dehydrogenase (SDH)-deficient neoplasia.
Gill AJ. Gill AJ. Histopathology. 2018 Jan;72(1):106-116. doi: 10.1111/his.13277. Histopathology. 2018. PMID: 29239034 Review.
SDH-deficient gastrointestinal stromal tumours (GISTs) show distinctive features, including absent KIT proto-oncogene receptor tyrosine kinase/platelet-derived growth factor receptor A (KIT/PDGFRA) mutations [but positive staining for cKIT and DOG1], virtually exclusive gastric l …
SDH-deficient gastrointestinal stromal tumours (GISTs) show distinctive features, including absent KIT proto-oncogene receptor tyrosine kina …
Systemic diseases associated with retinal dystrophies.
Werdich XQ, Place EM, Pierce EA. Werdich XQ, et al. Semin Ophthalmol. 2014 Sep-Nov;29(5-6):319-28. doi: 10.3109/08820538.2014.959202. Semin Ophthalmol. 2014. PMID: 25325857 Review.
A genetic diagnosis may also be informative with regard to prognosis and potential therapies. Effective management and rehabilitation for patients with syndromic retinal dystrophy requires a comprehensive genetic-based team approach involving patients, family members, opht …
A genetic diagnosis may also be informative with regard to prognosis and potential therapies. Effective management and rehabilitation …
Genetics of hereditary forms of primary hyperparathyroidism.
English KA, Lines KE, Thakker RV. English KA, et al. Hormones (Athens). 2024 Mar;23(1):3-14. doi: 10.1007/s42000-023-00508-9. Epub 2023 Dec 1. Hormones (Athens). 2024. PMID: 38038882 Free PMC article. Review.
Some patients with non-syndromic PHPT may have mutations of the MEN1 gene or the calcium-sensing receptor (CASR), whose loss of function mutations usually cause FHH1, a disorder associated with mild hypercalcemia and may follow a benign clinical course. Measurement of the …
Some patients with non-syndromic PHPT may have mutations of the MEN1 gene or the calcium-sensing receptor (CASR), whose loss of function mut …
Old, New, and Emerging Immunohistochemical Markers in Pheochromocytoma and Paraganglioma.
Cheung VKY, Gill AJ, Chou A. Cheung VKY, et al. Endocr Pathol. 2018 Jun;29(2):169-175. doi: 10.1007/s12022-018-9534-7. Endocr Pathol. 2018. PMID: 29779206 Review.
It is now accepted that more than one third of pheochromocytoma and paragangliomas arise in the context of syndromic disease, usually hereditary. The genetic profile of these tumors also has important prognostic implications which may help guide treatment. Accompanying the …
It is now accepted that more than one third of pheochromocytoma and paragangliomas arise in the context of syndromic disease, usually heredi …
"Wild type" GIST: Clinicopathological features and clinical practice.
Wada R, Arai H, Kure S, Peng WX, Naito Z. Wada R, et al. Pathol Int. 2016 Aug;66(8):431-7. doi: 10.1111/pin.12431. Epub 2016 Jul 18. Pathol Int. 2016. PMID: 27427238 Review.
Attention to the age, gender, family history and other neoplasms may raise the prediction of syndromic disease. Location of the tumor, morphology, and pleomorphism of the tumor cells are further informative. ...
Attention to the age, gender, family history and other neoplasms may raise the prediction of syndromic disease. Location of the tumor …
The COVID-19 Pandemic in a Hispanic Population: A Primary Care Perspective.
Owens CD, Pertuz GM, Sanchez JC, Ayala J, Pimentel LH, Lamb C, Lopez Mayo YE, Yunez AL. Owens CD, et al. J Am Board Fam Med. 2022 Jul-Aug;35(4):686-694. doi: 10.3122/jabfm.2022.04.210163. J Am Board Fam Med. 2022. PMID: 35896459 Free article.
Essential workers and uninsured health status may lead to more prolonged disease course....
Essential workers and uninsured health status may lead to more prolonged disease course....
Outcomes following general anaesthesia in children with hypertrophic cardiomyopathy.
Norrish G, Forshaw N, Woo C, Avanis MC, Field E, Cervi E, Iguchi A, Kaski JP. Norrish G, et al. Arch Dis Child. 2019 May;104(5):471-475. doi: 10.1136/archdischild-2018-315366. Epub 2018 Nov 9. Arch Dis Child. 2019. PMID: 30413484 Free PMC article.
Future studies are required to systematically identify clinical features that may predict anaesthetic risk....
Future studies are required to systematically identify clinical features that may predict anaesthetic risk....
Stem cell modeling of mitochondrial parkinsonism reveals key functions of OPA1.
Jonikas M, Madill M, Mathy A, Zekoll T, Zois CE, Wigfield S, Kurzawa-Akanbi M, Browne C, Sims D, Chinnery PF, Cowley SA, Tofaris GK. Jonikas M, et al. Ann Neurol. 2018 May;83(5):915-925. doi: 10.1002/ana.25221. Epub 2018 Apr 25. Ann Neurol. 2018. PMID: 29604226 Free PMC article.
Severity of OPA1 disease associates primarily with the extent of OPA1-mediated fusion, suggesting that activation of this mechanism or identification of its genetic modifiers may have therapeutic or prognostic value. Ann Neurol 2018;83:915-925....
Severity of OPA1 disease associates primarily with the extent of OPA1-mediated fusion, suggesting that activation of this mechanism or ident …
26 results