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

Year Number of Results
1994 2
1995 5
1996 5
1997 1
1998 1
1999 3
2000 2
2002 2
2003 8
2004 5
2005 6
2006 6
2007 3
2008 14
2009 10
2010 13
2011 5
2012 6
2013 8
2014 9
2015 12
2016 9
2017 12
2018 13
2019 13
2020 13
2021 9
2022 12
2023 2
2024 2

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180 results

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Page 1
The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?
Weinreb NJ, Goker-Alpan O, Kishnani PS, Longo N, Burrow TA, Bernat JA, Gupta P, Henderson N, Pedro H, Prada CE, Vats D, Pathak RR, Wright E, Ficicioglu C. Weinreb NJ, et al. Among authors: ficicioglu c. Mol Genet Metab. 2022 May;136(1):4-21. doi: 10.1016/j.ymgme.2022.03.001. Epub 2022 Mar 9. Mol Genet Metab. 2022. PMID: 35367141 Free article. Review.
3-methylcrotonyl-CoA carboxylase deficiency: clinical, biochemical, enzymatic and molecular studies in 88 individuals.
Grünert SC, Stucki M, Morscher RJ, Suormala T, Bürer C, Burda P, Christensen E, Ficicioglu C, Herwig J, Kölker S, Möslinger D, Pasquini E, Santer R, Schwab KO, Wilcken B, Fowler B, Yue WW, Baumgartner MR. Grünert SC, et al. Among authors: ficicioglu c. Orphanet J Rare Dis. 2012 May 29;7:31. doi: 10.1186/1750-1172-7-31. Orphanet J Rare Dis. 2012. PMID: 22642865 Free PMC article.
Erratum.
Edmondson AC, Salant J, Ierardi-Curto LA, Ficicioglu C. Edmondson AC, et al. Among authors: ficicioglu c. JIMD Rep. 2017;33:109-110. doi: 10.1007/8904_2017_587. JIMD Rep. 2017. PMID: 28409479 Free PMC article. No abstract available.
Agnathia-holoprosencephaly-situs inversus.
Ozden S, Fiçicioğlu C, Kara M, Oral O, Bilgiç R. Ozden S, et al. Among authors: ficicioglu c. Am J Med Genet. 2000 Mar 20;91(3):235-6. doi: 10.1002/(sici)1096-8628(20000320)91:3<235::aid-ajmg16>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10756350 No abstract available.
Predicting the disease severity in male individuals with ornithine transcarbamylase deficiency.
Scharre S, Posset R, Garbade SF, Gleich F, Seidl MJ, Druck AC, Okun JG, Gropman AL, Nagamani SCS, Hoffmann GF, Kölker S, Zielonka M; Urea Cycle Disorders Consortium (UCDC) and the European registry and network for Intoxication type Metabolic Diseases (E-IMD) Consortia Study Group. Scharre S, et al. Ann Clin Transl Neurol. 2022 Nov;9(11):1715-1726. doi: 10.1002/acn3.51668. Epub 2022 Oct 10. Ann Clin Transl Neurol. 2022. PMID: 36217298 Free PMC article.
Adolescent presentations of inborn errors of metabolism.
Ahrens-Nicklas RC, Slap G, Ficicioglu C. Ahrens-Nicklas RC, et al. Among authors: ficicioglu c. J Adolesc Health. 2015 May;56(5):477-82. doi: 10.1016/j.jadohealth.2015.01.008. J Adolesc Health. 2015. PMID: 25907648 Review.
180 results