Literature DB >> 6789651

Triad of anorectal, sacral, and presacral anomalies.

G Currarino, D Coln, T Votteler.   

Abstract

Mesh：

Year:  1981        PMID： 6789651     DOI： 10.2214/ajr.137.2.395

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN： 0361-803X            Impact factor:   3.959


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  82 in total

1.  Involvement of the HLXB9 homeobox gene in Currarino syndrome.

Authors:  E Belloni; G Martucciello; D Verderio; E Ponti; M Seri; V Jasonni; M Torre; M Ferrari; L C Tsui; S W Scherer
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Complete Currarino syndrome in an adult, presenting as a fecalith obstruction: report of a case.

Authors:  Michael N Colapinto; Erika A M Vowinckel; Nicholas D Colapinto
Journal:  Can J Surg       Date:  2003-08       Impact factor: 2.089

3.  Caudal regression syndrome with bilateral popliteal webbing without maternal diabetes: a rare entity.

Authors:  Mukul Aggarwal; Vikrant Sood; Shivani Deswal; K C Aggarwal
Journal:  Childs Nerv Syst       Date:  2012-04-20       Impact factor: 1.475

4.  Sacrococcygeal masses other than meningomyelocele.

Authors:  Akhilesh Agarwal; Sukanta Das; Dipak Ghosh; Anshu Agarwal
Journal:  Indian J Surg       Date:  2011-04-27       Impact factor: 0.656

5.  Currarino syndrome.

Authors:  Ramesh S Iyer; Paritosh C Khanna
Journal:  Pediatr Radiol       Date:  2010-08-10

Review 6.  Congenital spine anomalies: the closed spinal dysraphisms.

Authors:  Erin Simon Schwartz; Andrea Rossi
Journal:  Pediatr Radiol       Date:  2015-09-07

Review 7.  Severe bacterial meningitis due to an enterothecal fistula in a 6-year-old child with Currarino syndrome: evaluation of surgical strategy with review of the literature.

Authors:  Hanne-Rinck Jeltema; Paul M A Broens; Oebele F Brouwer; Rob J M Groen
Journal:  Childs Nerv Syst       Date:  2019-04-09       Impact factor: 1.475

8.  Currarino triad with a terminal deletion 7q35-->qter.

Authors:  M Masuno; K Imaizumi; N Aida; Y Tanaka; K Sekido; Y Ohhama; T Nishi; Y Kuroki
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

9.  Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene.

Authors:  C Coutton; B Poreau; F Devillard; C Durand; S Odent; C Rozel; G Vieville; F Amblard; P-S Jouk; V Satre
Journal:  Mol Syndromol       Date:  2013-10-02

10.  An autosomal dominant syndrome of renal and anogenital malformations with syndactyly.

Authors:  A J Green; R N Sandford; B C Davison
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318
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