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

Year Number of Results
1999 1
2000 1
2005 1
2006 1
2010 1
2011 2
2012 1
2013 1
2014 1
2017 1
2019 1
2020 0
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9 results
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Page 1
Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome.
Dror Y, Donadieu J, Koglmeier J, Dodge J, Toiviainen-Salo S, Makitie O, Kerr E, Zeidler C, Shimamura A, Shah N, Cipolli M, Kuijpers T, Durie P, Rommens J, Siderius L, Liu JM. Dror Y, et al. Among authors: Siderius L. Ann N Y Acad Sci. 2011 Dec;1242:40-55. doi: 10.1111/j.1749-6632.2011.06349.x. Ann N Y Acad Sci. 2011. PMID: 22191555
The importance of rare diseases: from the gene to society.
Dodge JA, Chigladze T, Donadieu J, Grossman Z, Ramos F, Serlicorni A, Siderius L, Stefanidis CJ, Tasic V, Valiulis A, Wierzba J. Dodge JA, et al. Among authors: Siderius L. Arch Dis Child. 2011 Sep;96(9):791-2. doi: 10.1136/adc.2010.193664. Epub 2010 Aug 12. Arch Dis Child. 2011. PMID: 20705719 No abstract available.
Introducing standards of the best medical practice for patients with inherited alpha-1-antitrypsin deficiency in Central Eastern Europe.
Valiulis A, Utkus A, Stukas R, Valiulis A, Siderius L; Leonardo da Vinci Alfa-1-Qual No. LLP-LdV-PRT-2011-LT-0300 project group. Valiulis A, et al. Among authors: Siderius L. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2014;35(1):107-14. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2014. PMID: 24798601 Review.
Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen.
Schwarze U, Cundy T, Pyott SM, Christiansen HE, Hegde MR, Bank RA, Pals G, Ankala A, Conneely K, Seaver L, Yandow SM, Raney E, Babovic-Vuksanovic D, Stoler J, Ben-Neriah Z, Segel R, Lieberman S, Siderius L, Al-Aqeel A, Hannibal M, Hudgins L, McPherson E, Clemens M, Sussman MD, Steiner RD, Mahan J, Smith R, Anyane-Yeboa K, Wynn J, Chong K, Uster T, Aftimos S, Sutton VR, Davis EC, Kim LS, Weis MA, Eyre D, Byers PH. Schwarze U, et al. Among authors: Siderius L. Hum Mol Genet. 2013 Jan 1;22(1):1-17. doi: 10.1093/hmg/dds371. Epub 2012 Sep 4. Hum Mol Genet. 2013. PMID: 22949511 Free PMC article.
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene.
Hoornaert KP, Dewinter C, Vereecke I, Beemer FA, Courtens W, Fryer A, Fryssira H, Lees M, Müllner-Eidenböck A, Rimoin DL, Siderius L, Superti-Furga A, Temple K, Willems PJ, Zankl A, Zweier C, De Paepe A, Coucke P, Mortier GR. Hoornaert KP, et al. Among authors: Siderius L. J Med Genet. 2006 May;43(5):406-13. doi: 10.1136/jmg.2005.035717. Epub 2005 Sep 9. J Med Genet. 2006. PMID: 16155195 Free PMC article.
RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems.
Hofstra RM, Wu Y, Stulp RP, Elfferich P, Osinga J, Maas SM, Siderius L, Brooks AS, vd Ende JJ, Heydendael VM, Severijnen RS, Bax KM, Meijers C, Buys CH. Hofstra RM, et al. Among authors: Siderius L. Hum Mutat. 2000;15(5):418-29. doi: 10.1002/(SICI)1098-1004(200005)15:5<418::AID-HUMU3>3.0.CO;2-2. Hum Mutat. 2000. PMID: 10790203
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