|1.||Solomon, Benjamin D: 2 articles (12/2012 - 01/2011)|
|2.||Magid, S K: 2 articles (01/2001 - 09/2000)|
|3.||Yazici, Y: 2 articles (01/2001 - 09/2000)|
|4.||Erkan, D: 2 articles (01/2001 - 09/2000)|
|5.||Lam, L A: 2 articles (01/2001 - 09/2000)|
|6.||Hyodo, Yoji: 1 article (01/2015)|
|7.||Shishido, Seiichiro: 1 article (01/2015)|
|8.||Hamasaki, Yuko: 1 article (01/2015)|
|9.||Nihei, Hiroshi: 1 article (01/2015)|
|10.||Muramatsu, Masaki: 1 article (01/2015)|
12/01/1994 - "The authors report the case of a 1,500-g baby boy with microgastria, vascular ring, tracheoesophageal fistula (TEF), and the VATER association. "
01/01/2004 - "Tracheoesophageal fistula (H-type) in neonates with imperforate anus and the VATER association."
09/01/1999 - "We examined the potential role of sonography in the prenatal diagnosis of the VATER association, a spectrum of fetal anomalies that includes vertebral defects, imperforate anus, tracheoesophageal fistula, and radial and renal dysplasia. "
01/01/2014 - "We described a patient with a 1.4 Mb duplication at 17q12 detected by SNP-array study and validated using qRT-PCR, who presented with an oesophageal atresia accompanied with tracheoesophageal fistula and anal atresia as well as other symptoms resembling VATER association (thumb hypoplasia, sacral bone defect, cryptorchidism). "
02/01/2010 - "In this report we present a young woman with mild bilateral CTS, based on electrophysiological studies, in whom marked thenar atrophy was on a congenital basis related to the VATER association (vertebral anomalies, anal atresia, tracheoesophageal fistula, and radial or renal abnormalities)."
03/01/2005 - "Anal atresia is a relatively common congenital malformation that occurs in about 1 out of 5000 infants, caused by abnormal hindgut development of the embryo, often associated with other developmental anomalies (e.g., Currarino, Townes-Brock, Pallister-Hall syndromes, and VATER association). "
03/01/1977 - "The radial dysplasia/imperforate anus/vertebral anomalies syndrome (the VATER association): Developmental aspects and eye findings."
02/01/2013 - "VACTERL/VATER association is a group of congenital malformations characterized by at least 3 of the following findings: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. "
01/01/2011 - "The management of patients with VACTERL/VATER association typically centers around surgical correction of the specific congenital anomalies (typically anal atresia, certain types of cardiac malformations, and/or tracheo-esophageal fistula) in the immediate postnatal period, followed by long-term medical management of sequelae of the congenital malformations. "
01/01/2011 - "VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. "
03/01/1999 - "The aim of this study was to reproduce the animal model of esophageal atresia and the VATER association. "
01/01/2006 - "Here, we report on a girl presenting with pre- and postnatal growth retardation, esophageal atresia, vertebral and costal anomalies and a unilateral radial defect, consistent with the diagnosis of VATER association. "
01/01/1988 - "High proximal pouch esophageal atresia accompanied by vertebral, rib, and sternal anomalies constitutes a heretofore unrecognized high risk group with the VATER association."
01/01/1988 - "The base of the proximal esophageal pouch in babies born with esophageal atresia varies in location from the low cervical region to the upper third of the mediastinum, but the relevance of this finding to the VATER association is not known. "
01/01/1988 - "High proximal pouch esophageal atresia with vertebral, rib, and sternal anomalies: an additional component to the VATER association."
|4.||Congenital Abnormalities (Deformity)
05/01/2006 - "Patient registries of women who take TNF-a antagonists during pregnancy also need to be followed to see if there is an increase in the birth defects that are part of VATER association."
01/01/2000 - "The indications are that this model will continue to clarify the processes that lead to many of the structural congenital abnormalities that are seen in infants born with the VATER association."
07/11/1997 - "To assess the spectrum of congenital anomalies associated with VATER while minimizing the distortions due to small samples and referral patterns typical of clinical series, we studied infants with VATER association reported to the combined registry of infants with multiple congenital anomalies from 17 birth defects registries worldwide that are part of the International Clearinghouse for Birth Defects Monitoring Systems (ICB-DMS). "
02/01/1993 - "At postmortem tracheal atresia was diagnosed, in combination with other congenital abnormalities, which pointed to a VATER-association. "
06/01/2003 - "Vater association is an extremely rare and complex event and this report aimed at describing for the first time a renal transplantation with cadaver donor in a child with this congenital defect, the result of which has been fully satisfactory."
03/01/1998 - "This report supports the hypothesis that VATER association, VACTERL-H association, and sirenomelia may represent pathophysiologically related entities."
03/01/1998 - "It has been suggested that the VATER association may represent a less severe form of sirenomelia. "
11/01/1991 - "In addition, sirenomelia patients were found in 12%, the VATER association in 27%, and 27% could not be classified. "
01/01/1986 - "Review of the literature indicates that the basic defect in sirenomelia and the VATER association lies in the formation and differentiation of mesodermal tissue and that sirenomelia, the VATER association, and monozygotic twinning show a complex etiological interrelationship."
01/01/2003 - "Syndromes with associated preaxial reduction defects mainly Fanconi pancytopenia, VATER association, Rothmund-Thompson and Roberts phocomelia syndrome were excluded by proper clinical and cytogenetic studies. "
|5.||Hereditary renal agenesis
|10.||tranilast (N 5')
|2.||Urinary Diversion (Ileal Conduit)
|4.||Transplantation (Transplant Recipients)