Literature DB >> 4812361

Caudal mesoderm pattern of anomalies: from renal agenesis to sirenomelia.

B Källén, J Winberg.   

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Year:  1974        PMID： 4812361     DOI： 10.1002/tera.1420090113

Source DB:  PubMed          Journal:  Teratology        ISSN： 0040-3709


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  17 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.  Renal anomalies in family members of infants with bilateral renal agenesis/adysplasia.

Authors:  Andrew L Schwaderer; Carlton M Bates; Kirk M McHugh; Kim L McBride
Journal:  Pediatr Nephrol       Date:  2006-09-15       Impact factor: 3.714

Review 3.  Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review.

Authors:  Iêda M Orioli; Emmanuelle Amar; Jazmin Arteaga-Vazquez; Marian K Bakker; Sebastiano Bianca; Lorenzo D Botto; Maurizio Clementi; Adolfo Correa; Melinda Csaky-Szunyogh; Emanuele Leoncini; Zhu Li; Jorge S López-Camelo; R Brian Lowry; Lisa Marengo; María-Luisa Martínez-Frías; Pierpaolo Mastroiacovo; Margery Morgan; Anna Pierini; Annukka Ritvanen; Gioacchino Scarano; Elena Szabova; Eduardo E Castilla
Journal:  Am J Med Genet C Semin Med Genet       Date:  2011-10-14       Impact factor: 3.908

4.  Posterior axial corneal malformation and uveoretinal angiodysgenesis--a neurocristopathy?

Authors:  C M Mooy; B J Clark; W R Lee
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1990       Impact factor: 3.117

5.  Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report.

Authors:  Pedro Acién; Francisco Galán; Irene Manchón; Eva Ruiz; Maribel Acién; Luis A Alcaraz
Journal:  Orphanet J Rare Dis       Date:  2010-04-14       Impact factor: 4.123

6.  Chiari I malformation, caudal regression syndrome, and Pierre Robin Syndrome: a previously unreported combination.

Authors:  R Shane Tubbs; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2006-10-05       Impact factor: 1.475

7.  Unusual association of two unilateral anomalies present in adulthood: pulmonary hypoplasia and renal agenesis. Embryology and clinical expression.

Authors:  R M Mirapeix; C Domingo; J R Sañudo; J M Mata
Journal:  Surg Radiol Anat       Date:  1995       Impact factor: 1.246

8.  Sirenomelia: mermaid syndrome.

Authors:  O G Goodlow; R I Sibley; B G Allen; W S Kamanda; A C Gullattee; W C Rayfield
Journal:  J Natl Med Assoc       Date:  1988-03       Impact factor: 1.798

9.  The cyclops and the mermaid: an epidemiological study of two types of rare malformation.

Authors:  B Källén; E E Castilla; P A Lancaster; O Mutchinick; L B Knudsen; M L Martínez-Frías; P Mastroiacovo; E Robert
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

10.  Cloacal dysgenesis sequence with bilateral renal agenesis and normal pulmonary development in twin pregnancy.

Authors:  Sundram Jegadeesh; Jai Kumar Mahajan
Journal:  BMJ Case Rep       Date:  2016-01-20
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