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

Year Number of Results
1953 1
1962 1
1963 1
1964 3
1967 2
1970 1
1971 3
1972 3
1973 7
1974 7
1975 2
1976 3
1977 5
1978 9
1979 2
1980 3
1981 5
1982 4
1983 3
1984 3
1985 3
1986 5
1987 6
1988 10
1989 6
1990 7
1991 2
1992 5
1993 8
1994 9
1995 10
1996 11
1997 7
1998 12
1999 13
2000 18
2001 25
2002 21
2003 16
2004 14
2005 21
2006 20
2007 17
2008 36
2009 28
2010 45
2011 38
2012 43
2013 50
2014 34
2015 41
2016 38
2017 41
2018 36
2019 32
2020 42
2021 59
2022 41
2023 33
2024 17

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894 results

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Page 1
Silver-Russell Syndrome.
Saal HM, Harbison MD, Netchine I. Saal HM, et al. 2002 Nov 2 [updated 2019 Oct 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2002 Nov 2 [updated 2019 Oct 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301499 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Silver-Russell Syndrome (SRS) is typically characterized by asymmetric gestational growth restriction resulting in affected individuals being born small for gestational age, with relative macrocephaly at birth (head circumference 1.5 …
CLINICAL CHARACTERISTICS: Silver-Russell Syndrome (SRS) is typically characterized by asymmetric gestational growth res …
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
This Consensus Statement summarizes recommendations for clinical diagnosis, investigation and management of patients with Silver-Russell syndrome (SRS), an imprinting disorder that causes prenatal and postnatal growth retardation. ...
This Consensus Statement summarizes recommendations for clinical diagnosis, investigation and management of patients with Silver-R …
Silver-Russell syndrome.
Wakeling EL. Wakeling EL. Arch Dis Child. 2011 Dec;96(12):1156-61. doi: 10.1136/adc.2010.190165. Epub 2011 Feb 24. Arch Dis Child. 2011. PMID: 21349887 Review.
Silver-Russell syndrome (SRS) is characterised by intrauterine growth restriction, poor postnatal growth, relative macrocephaly, triangular face, asymmetry and feeding difficulties. ...
Silver-Russell syndrome (SRS) is characterised by intrauterine growth restriction, poor postnatal growth, relative macr …
Silver-Russell Syndrome: A Review.
Spiteri BS, Stafrace Y, Calleja-Agius J. Spiteri BS, et al. Neonatal Netw. 2017 Jul 1;36(4):206-212. doi: 10.1891/0730-0832.36.4.206. Neonatal Netw. 2017. PMID: 28764823 Review.
Silver-Russell syndrome (SRS) is a rare congenital imprinting disorder. ...
Silver-Russell syndrome (SRS) is a rare congenital imprinting disorder. ...
Russell-Silver syndrome.
Eggermann T. Eggermann T. Am J Med Genet C Semin Med Genet. 2010 Aug 15;154C(3):355-64. doi: 10.1002/ajmg.c.30274. Am J Med Genet C Semin Med Genet. 2010. PMID: 20803658 Review.
In comparison to Prader-Willi or Angelman syndrome, Russell-Silver syndrome (RSS) is a relatively "young" imprinting disorder. ...
In comparison to Prader-Willi or Angelman syndrome, Russell-Silver syndrome (RSS) is a relatively "young" imprin …
Silver-Russell syndrome.
Binder G, Begemann M, Eggermann T, Kannenberg K. Binder G, et al. Best Pract Res Clin Endocrinol Metab. 2011 Feb;25(1):153-60. doi: 10.1016/j.beem.2010.06.005. Best Pract Res Clin Endocrinol Metab. 2011. PMID: 21396582
The Silver-Russell syndrome (SRS) is a sporadic clinically and genetically heterogeneous disorder. ...
The Silver-Russell syndrome (SRS) is a sporadic clinically and genetically heterogeneous disorder. ...
Silver-Russell Syndrome: Orthodontic Perspective.
Khalid Z, Iqbal K, Jan A, Khurshid A. Khalid Z, et al. J Coll Physicians Surg Pak. 2020 Dec;30(12):1352-1354. doi: 10.29271/jcpsp.2020.12.1352. J Coll Physicians Surg Pak. 2020. PMID: 33397069
Silver-Russell syndrome (SRS) is a rare disorder characterised by prenatal and postnatal growth deficiency, a relatively large head size with triangular face, a prominent forehead, body asymmetry, feeding difficulties, clinodactyly and other features. ...The …
Silver-Russell syndrome (SRS) is a rare disorder characterised by prenatal and postnatal growth deficiency, a relativel …
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology.
Õunap K. Õunap K. Mol Syndromol. 2016 Jul;7(3):110-21. doi: 10.1159/000447413. Epub 2016 Jul 6. Mol Syndromol. 2016. PMID: 27587987 Free PMC article. Review.
Silver-Russell syndrome (SRS) and Beckwith-Wiedemann syndrome (BWS) are 2 clinically opposite growth-affecting disorders belonging to the group of congenital imprinting disorders. ...Six diagnostic scoring systems for SRS and 4 for BWS have been previo …
Silver-Russell syndrome (SRS) and Beckwith-Wiedemann syndrome (BWS) are 2 clinically opposite growth-affecting d …
Silver-Russell Syndrome - Part I: Clinical Characteristics and Genetic Background.
Marczak-Hałupka A, Kalina MA, Tańska A, Chrzanowska KH. Marczak-Hałupka A, et al. Pediatr Endocrinol Diabetes Metab. 2015;20(3):101-6. doi: 10.18544/PEDM-20.03.0009. Pediatr Endocrinol Diabetes Metab. 2015. PMID: 26615046 Free article. Review.
Silver-Russell syndrome (SRS) is a rare, clinically and genetically heterogeneous entity, caused by (epi)genetic alternations. ...
Silver-Russell syndrome (SRS) is a rare, clinically and genetically heterogeneous entity, caused by (epi)genetic altern …
Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
Chang S, Bartolomei MS. Chang S, et al. Dis Model Mech. 2020 May 26;13(5):dmm044123. doi: 10.1242/dmm.044123. Dis Model Mech. 2020. PMID: 32424032 Free PMC article. Review.
Dysregulation of genomic imprinting can cause developmental disorders such as Beckwith-Wiedemann syndrome (BWS) and Silver-Russell syndrome (SRS). In this Review, we discuss (1) how various (epi)genetic lesions lead to the dysregulation of clinically r …
Dysregulation of genomic imprinting can cause developmental disorders such as Beckwith-Wiedemann syndrome (BWS) and Silver- …
894 results