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

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1979 1
1993 1
1996 2
1997 1
1998 7
1999 3
2000 8
2001 8
2002 7
2003 3
2004 3
2005 4
2006 4
2007 7
2008 7
2009 5
2010 6
2011 9
2012 2
2013 6
2014 8
2015 3
2016 7
2017 9
2018 9
2019 8
2020 15
2021 6
2022 8
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Similar articles for PMID: 10190331

149 results

Results by year

Filters applied: . Clear all
Page 1
Histopathological Features of Pendred Syndrome Thyroids Align with Differences in the Expression of Thyroid-Specific Markers, Apical Iodide Transporters, and Ciliogenesis Process.
Vázquez-Román V, Cameselle-Teijeiro JM, Fernández-Santos JM, Ríos-Moreno MJ, Loidi L, Ortiz T, Martín-Lacave I. Vázquez-Román V, et al. Endocr Pathol. 2022 Dec;33(4):484-493. doi: 10.1007/s12022-022-09732-2. Epub 2022 Oct 15. Endocr Pathol. 2022. PMID: 36242759 Free PMC article.
H syndrome caused by a novel P324S mutation in SLC29A3 gene.
Bhandari M, Khullar G, Batra S, Garg A, Khunger N, Verma P, Singh A, Misra R, Yadav AK. Bhandari M, et al. Int J Dermatol. 2023 Mar;62(3):e138-e140. doi: 10.1111/ijd.16264. Epub 2022 May 12. Int J Dermatol. 2023. PMID: 35556244 No abstract available.
Dominant and recessive SLC12A2-syndrome.
McNeill A, Aurora P, Rajput K, Nash R, Stals K, Robinson H, Wakeling E. McNeill A, et al. Am J Med Genet A. 2022 Mar;188(3):996-999. doi: 10.1002/ajmg.a.62573. Epub 2021 Nov 19. Am J Med Genet A. 2022. PMID: 34797034 No abstract available.
149 results