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

Year Number of Results
1995 1
1998 1
1999 2
2000 1
2001 2
2003 1
2005 2
2006 1
2009 2
2010 5
2011 2
2012 1
2013 4
2015 3
2016 4
2017 1
2018 2
2019 1
2020 0
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31 results
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Page 1
Hyperestrogenism Affects Adult Height Outcome in Growth Hormone Treated Boys With Silver-Russell Syndrome.
Kvernebo-Sunnergren K, Ankarberg-Lindgren C, Åkesson K, Andersson MX, Samuelsson L, Lovmar L, Dahlgren J. Kvernebo-Sunnergren K, et al. Front Endocrinol (Lausanne). 2018 Dec 21;9:780. doi: 10.3389/fendo.2018.00780. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 30622515 Free PMC article.
Genetic Analysis and Clinical Presentation in Silver Russell Syndrome.
Lohiya N, Lote-Oke R, Agarwal M, Phadke N, Khadilkar V, Khadilkar A. Lohiya N, et al. Indian J Pediatr. 2018 Dec;85(12):1141-1142. doi: 10.1007/s12098-018-2738-5. Epub 2018 Jul 23. Indian J Pediatr. 2018. PMID: 30039337 No abstract available.
Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
Wakeling EL, Brioude F, Lokulo-Sodipe O, O'Connell SM, Salem J, Bliek J, Canton AP, Chrzanowska KH, Davies JH, Dias RP, Dubern B, Elbracht M, Giabicani E, Grimberg A, Grønskov K, Hokken-Koelega AC, Jorge AA, Kagami M, Linglart A, Maghnie M, Mohnike K, Monk D, Moore GE, Murray PG, Ogata T, Petit IO, Russo S, Said E, Toumba M, Tümer Z, Binder G, Eggermann T, Harbison MD, Temple IK, Mackay DJ, Netchine I. Wakeling EL, et al. Nat Rev Endocrinol. 2017 Feb;13(2):105-124. doi: 10.1038/nrendo.2016.138. Epub 2016 Sep 2. Nat Rev Endocrinol. 2017. PMID: 27585961
Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci.
Eggermann T, Perez de Nanclares G, Maher ER, Temple IK, Tümer Z, Monk D, Mackay DJ, Grønskov K, Riccio A, Linglart A, Netchine I. Eggermann T, et al. Clin Epigenetics. 2015 Nov 14;7:123. doi: 10.1186/s13148-015-0143-8. eCollection 2015. Clin Epigenetics. 2015. PMID: 26583054 Free PMC article. Review.
Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling.
Eggermann T, Brioude F, Russo S, Lombardi MP, Bliek J, Maher ER, Larizza L, Prawitt D, Netchine I, Gonzales M, Grønskov K, Tümer Z, Monk D, Mannens M, Chrzanowska K, Walasek MK, Begemann M, Soellner L, Eggermann K, Tenorio J, Nevado J, Moore GE, Mackay DJ, Temple K, Gillessen-Kaesbach G, Ogata T, Weksberg R, Algar E, Lapunzina P. Eggermann T, et al. Eur J Hum Genet. 2016 Jun;24(6):784-93. doi: 10.1038/ejhg.2015.224. Epub 2015 Oct 28. Eur J Hum Genet. 2016. PMID: 26508573 Free PMC article. Review.
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