Literature DB >> 5781468

Cutis gyratum, acanthosis nigricans and other congenital anomalies. A new syndrome.

J M Beare, J A Dodge, N C Nevin.   

Abstract

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Year:  1969        PMID： 5781468

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  11 in total

Review 1.  Infantile hypertrophic pyloric stenosis--genetics and syndromes.

Authors:  Babette Peeters; Marc A Benninga; Raoul C M Hennekam
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2012-07-10       Impact factor: 46.802

2.  Acanthosis nigricans, congenital heart disease and other congenital defects.

Authors:  J F Costello
Journal:  Proc R Soc Med       Date:  1972-09

3.  Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndrome.

Authors:  N Flanagan; S A Boyadjiev; J Harper; L Kyne; M Earley; R Watson; E W Jabs; M T Geraghty
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

4.  Congenital craniofacial dysostosis and cutis gyratum: the Beare-Stevenson syndrome.

Authors:  B Bratanic; M Praprotnik; M Novosel-Sever
Journal:  Eur J Pediatr       Date:  1994-03       Impact factor: 3.183

5.  p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.

Authors:  Yingli Wang; Xueyan Zhou; Kurun Oberoi; Robert Phelps; Ross Couwenhoven; Miao Sun; Amélie Rezza; Greg Holmes; Christopher J Percival; Jenna Friedenthal; Pavel Krejci; Joan T Richtsmeier; David L Huso; Michael Rendl; Ethylin Wang Jabs
Journal:  J Clin Invest       Date:  2012-05-15       Impact factor: 14.808

Review 6.  Genetic insights into the mechanisms of Fgf signaling.

Authors:  J Richard Brewer; Pierre Mazot; Philippe Soriano
Journal:  Genes Dev       Date:  2016-04-01       Impact factor: 11.361

Review 7.  Fibroblast Growth Factor Receptor 2 (FGFR2) Mutation Related Syndromic Craniosynostosis.

Authors:  Saïd C Azoury; Sashank Reddy; Vivek Shukla; Chu-Xia Deng
Journal:  Int J Biol Sci       Date:  2017-11-02       Impact factor: 6.580

8.  The first Korean case of Beare-Stevenson syndrome with a Tyr375Cys mutation in the fibroblast growth factor receptor 2 gene.

Authors:  So-Hee Eun; Ki Ssu Ha; Bo-Kyung Je; Eung Seok Lee; Byung Min Choi; Jung Hwa Lee; Baik-Lin Eun; Kee Hwan Yoo
Journal:  J Korean Med Sci       Date:  2007-04       Impact factor: 2.153

9.  A Case of Beare-Stevenson Syndrome with Unusual Manifestations.

Authors:  Nitin Ron; Samuel Leung; Erin Carney; Alexis Gerber; Karen Laurie David
Journal:  Am J Case Rep       Date:  2016-04-15

10.  Report of a Father With Congenital Bilateral Absence of the Vas Deferens Fathering a Child With Beare-Stevenson Syndrome.

Authors:  Leonardo C Ferreira; José H Dantas Junior
Journal:  Front Genet       Date:  2020-02-25       Impact factor: 4.599
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