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Page 1
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
Brioude F, Kalish JM, Mussa A, Foster AC, Bliek J, Ferrero GB, Boonen SE, Cole T, Baker R, Bertoletti M, Cocchi G, Coze C, De Pellegrin M, Hussain K, Ibrahim A, Kilby MD, Krajewska-Walasek M, Kratz CP, Ladusans EJ, Lapunzina P, Le Bouc Y, Maas SM, Macdonald F, Õunap K, Peruzzi L, Rossignol S, Russo S, Shipster C, Skórka A, Tatton-Brown K, Tenorio J, Tortora C, Grønskov K, Netchine I, Hennekam RC, Prawitt D, Tümer Z, Eggermann T, Mackay DJG, Riccio A, Maher ER. Brioude F, et al. Nat Rev Endocrinol. 2018 Apr;14(4):229-249. doi: 10.1038/nrendo.2017.166. Epub 2018 Jan 29. Nat Rev Endocrinol. 2018. PMID: 29377879 Free PMC article. Review.
Beckwith-Wiedemann syndrome (BWS), a human genomic imprinting disorder, is characterized by phenotypic variability that might include overgrowth, macroglossia, abdominal wall defects, neonatal hypoglycaemia, lateralized overgrowth and predisposition to embryo
Beckwith-Wiedemann syndrome (BWS), a human genomic imprinting disorder, is characterized by phenotypic variability that
Beckwith-Wiedemann syndrome.
Mishra D, Chakole V. Mishra D, et al. Pan Afr Med J. 2023 May 5;45:17. doi: 10.11604/pamj.2023.45.17.38741. eCollection 2023. Pan Afr Med J. 2023. PMID: 37426460 Free PMC article. No abstract available.
Beckwith-Wiedemann syndrome.
Weksberg R, Shuman C, Beckwith JB. Weksberg R, et al. Eur J Hum Genet. 2010 Jan;18(1):8-14. doi: 10.1038/ejhg.2009.106. Eur J Hum Genet. 2010. PMID: 19550435 Free PMC article. Review.
Beckwith-Wiedemann syndrome (BWS) is a model disorder for the study of imprinting, growth dysregulation, and tumorigenesis. ...
Beckwith-Wiedemann syndrome (BWS) is a model disorder for the study of imprinting, growth dysregulation, and tumorigene
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature.
Elefante P, Spedicati B, Faletra F, Pignata L, Cerrato F, Riccio A, Barbi E, Memo L, Travan L. Elefante P, et al. Ital J Pediatr. 2023 Sep 25;49(1):127. doi: 10.1186/s13052-023-01530-8. Ital J Pediatr. 2023. PMID: 37749604 Free PMC article. Review.
BACKGROUND: Beckwith-Wiedemann syndrome (BWS, OMIM #130,650) is a pediatric overgrowth disorder involving a predisposition to tumor development. ...
BACKGROUND: Beckwith-Wiedemann syndrome (BWS, OMIM #130,650) is a pediatric overgrowth disorder involving a predisposit …
Wiedemann-Beckwith syndrome.
Engström W, Lindham S, Schofield P. Engström W, et al. Eur J Pediatr. 1988 Jun;147(5):450-7. doi: 10.1007/BF00441965. Eur J Pediatr. 1988. PMID: 3044795 Review.
The Wiedemann-Beckwith syndrome (WBS) comprises an accumulation of multiple congenital anomalies. Exomphalos, macroglossia and gigantism are considered the most common manifestations, hence the alternative designation EMG-syndrome. The syndrome
The Wiedemann-Beckwith syndrome (WBS) comprises an accumulation of multiple congenital anomalies. Exomphalos, macroglos …
Beckwith-Wiedemann Syndrome Review: A Guide for the Neonatal Nurse.
Zammit M, Caruana E, Cassar D, Calleja-Agius J. Zammit M, et al. Neonatal Netw. 2017 May 1;36(3):129-133. doi: 10.1891/0730-0832.36.3.129. Neonatal Netw. 2017. PMID: 28494824 Review.
Beckwith-Wiedemann syndrome (BWS) is the most common pediatric overgrowth syndrome. Features characteristic of the BWS phenotype include both physical attributes, such as macroglossia, abdominal wall defects, gigantism, nevus flammeus, visceromegaly, a
Beckwith-Wiedemann syndrome (BWS) is the most common pediatric overgrowth syndrome. Features characteristic of t
Beckwith-Wiedemann syndrome.
Weksberg R, Shuman C, Smith AC. Weksberg R, et al. Am J Med Genet C Semin Med Genet. 2005 Aug 15;137C(1):12-23. doi: 10.1002/ajmg.c.30058. Am J Med Genet C Semin Med Genet. 2005. PMID: 16010676 Review.
Beckwith-Wiedemann syndrome (BWS) is a clinically heterogeneous overgrowth syndrome associated with an increased risk for embryonal tumor development. ...
Beckwith-Wiedemann syndrome (BWS) is a clinically heterogeneous overgrowth syndrome associated with an increased
Beckwith-Wiedemann syndrome: clinical and etiopathogenic aspects of a model genomic imprinting entity.
Cammarata-Scalisi F, Avendaño A, Stock F, Callea M, Sparago A, Riccio A. Cammarata-Scalisi F, et al. Arch Argent Pediatr. 2018 Oct 1;116(5):368-373. doi: 10.5546/aap.2018.eng.368. Arch Argent Pediatr. 2018. PMID: 30204990 Free article. Review. English, Spanish.
The Beckwith-Wiedemann syndrome is the most common genetic entity in overgrowth, with an approximate incidence of 1 in 10 00013 700births. ...The objective of this article is to describe the current status of the Beckwith-Wiedemann syndrome
The Beckwith-Wiedemann syndrome is the most common genetic entity in overgrowth, with an approximate incidence of 1 in …
Ocular manifestations of Beckwith-Wiedemann syndrome.
Rohowetz LJ, Kalavar M, Al-Khersan H, Kiryakoza L, Patel NA, Yannuzzi NA, Capo H, Berrocal AM. Rohowetz LJ, et al. J AAPOS. 2021 Oct;25(5):303-305.e1. doi: 10.1016/j.jaapos.2021.04.012. Epub 2021 Sep 25. J AAPOS. 2021. PMID: 34582951
Beckwith-Wiedemann syndrome (BWS; OMIM #130650) is a pediatric overgrowth disorder with few known ocular manifestations. ...
Beckwith-Wiedemann syndrome (BWS; OMIM #130650) is a pediatric overgrowth disorder with few known ocular manifestations
Beckwith-Wiedemann syndrome.
Elliott M, Maher ER. Elliott M, et al. J Med Genet. 1994 Jul;31(7):560-4. doi: 10.1136/jmg.31.7.560. J Med Genet. 1994. PMID: 7966193 Free PMC article. Review. No abstract available.
1,959 results