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Results by year

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

Year Number of Results
1993 2
1994 1
1999 1
2000 1
2001 1
2003 2
2004 2
2005 4
2006 4
2007 4
2008 6
2009 7
2010 11
2011 5
2012 7
2013 8
2014 13
2015 8
2016 5
2017 13
2018 19
2019 15
2020 16
2021 13
2022 12
2023 5
Text availability
Article attribute
Article type
Publication date

Search Results

151 results
Results by year
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Page 1
CLCN7-Related Osteopetrosis.
Sobacchi C, Villa A, Schulz A, Kornak U. Sobacchi C, et al. Among authors: kornak u. 2007 Feb 12 [updated 2022 Jan 20]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2007 Feb 12 [updated 2022 Jan 20]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301306 Free Books & Documents. Review.
Congenital disorders of glycosylation (CDG): Quo vadis?
Péanne R, de Lonlay P, Foulquier F, Kornak U, Lefeber DJ, Morava E, Pérez B, Seta N, Thiel C, Van Schaftingen E, Matthijs G, Jaeken J. Péanne R, et al. Among authors: kornak u. Eur J Med Genet. 2018 Nov;61(11):643-663. doi: 10.1016/j.ejmg.2017.10.012. Epub 2017 Oct 25. Eur J Med Genet. 2018. PMID: 29079546 Free article. Review.
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.
Fischer-Zirnsak B, Segebrecht L, Schubach M, Charles P, Alderman E, Brown K, Cadieux-Dion M, Cartwright T, Chen Y, Costin C, Fehr S, Fitzgerald KM, Fleming E, Foss K, Ha T, Hildebrand G, Horn D, Liu S, Marco EJ, McDonald M, McWalter K, Race S, Rush ET, Si Y, Saunders C, Slavotinek A, Stockler-Ipsiroglu S, Telegrafi A, Thiffault I, Torti E, Tsai AC, Wang X, Zafar M, Keren B, Kornak U, Boerkoel CF, Mirzaa G, Ehmke N. Fischer-Zirnsak B, et al. Among authors: kornak u. Am J Hum Genet. 2019 Sep 5;105(3):631-639. doi: 10.1016/j.ajhg.2019.07.002. Epub 2019 Jul 25. Am J Hum Genet. 2019. PMID: 31353024 Free PMC article.
ATP6V0A2-Related Cutis Laxa.
Van Maldergem L, Dobyns W, Kornak U. Van Maldergem L, et al. Among authors: kornak u. 2009 Mar 19 [updated 2023 Mar 16]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2009 Mar 19 [updated 2023 Mar 16]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301755 Free Books & Documents. Review.
Bone remodeling: facts and perspectives.
Marie P, Kornak U, Teti A. Marie P, et al. Among authors: kornak u. Arch Biochem Biophys. 2008 May 15;473(2):97. doi: 10.1016/j.abb.2008.04.002. Arch Biochem Biophys. 2008. PMID: 18455550 No abstract available.
Response to "Letter to the editor".
Kornak U. Kornak U. Bone. 2019 Nov;128:115065. doi: 10.1016/j.bone.2019.115065. Epub 2019 Sep 24. Bone. 2019. PMID: 31561010 No abstract available.
Metabolic cutis laxa syndromes.
Mohamed M, Kouwenberg D, Gardeitchik T, Kornak U, Wevers RA, Morava E. Mohamed M, et al. Among authors: kornak u. J Inherit Metab Dis. 2011 Aug;34(4):907-16. doi: 10.1007/s10545-011-9305-9. Epub 2011 Mar 23. J Inherit Metab Dis. 2011. PMID: 21431621 Free PMC article. Review.
[Osteoimmunology-IMMUNOBONE : Regulation of bone by inflammation].
Rauner M, Buttgereit F, Distler J, Garbe AI, Herrmann M, Hofbauer L, Hoffmann M, Jessberger R, Kornak U, Krönke G, Mundlos S, Spies C, Tuckermann J, Zwerina J. Rauner M, et al. Among authors: kornak u. Z Rheumatol. 2018 May;77(Suppl 1):12-15. doi: 10.1007/s00393-018-0455-0. Z Rheumatol. 2018. PMID: 29691689 Review. German. No abstract available.
151 results