Works matching DE "VATER syndrome"
Results: 81
EP10.37: Prenatal diagnosis of cloacal malformation with VATER syndrome: a case report.
- Published in:
- 2016
- By:
- Publication type:
- journal article
P12.11: Discordant VACTERL association in a dichorionic twin pregnancy after insemination.
- Published in:
- Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 251, doi. 10.1002/uog.14222
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- Publication type:
- Article
GROSS HEMATURIA IN THE VATER ASSOCIATION: COINCIDENCE OR ASSOCIATION.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Ventricular Septal Defect Closure in a Patient with VACTERL Syndrome.
- Published in:
- 2008
- By:
- Publication type:
- Case Study
HEMIVERTEBRAE, ARE THEY ALWAYS SYMPTOMATIC?
- Published in:
- 2010
- By:
- Publication type:
- Case Study
PCSK5 mutation in a patient with the VACTERL association.
- Published in:
- BMC Research Notes, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13104-015-1166-0
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- Publication type:
- Article
VACTEL association at autopsy of a foetus.
- Published in:
- Acta Paediatrica, 2003, v. 92, n. 11, p. 1351, doi. 10.1111/j.1651-2227.2003.tb00509.x
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- Publication type:
- Article
A Female Infant Who Had both Complete VACTERL Association and MURCS Association: Report of a Case.
- Published in:
- Surgery Today, 2007, v. 37, n. 10, p. 878, doi. 10.1007/s00595-007-3478-8
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- Publication type:
- Article
Neuroendocrine tumours of the ampulla of Vater: clinico-pathological features, surgical approach and assessment of prognosis.
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- Langenbeck's Archives of Surgery, 2012, v. 397, n. 6, p. 933, doi. 10.1007/s00423-012-0951-7
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- Publication type:
- Article
Evidence for inheritance in patients with VACTERL association.
- Published in:
- 2010
- By:
- Publication type:
- Report
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 561, doi. 10.1007/s00439-002-0733-3
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- Publication type:
- Article
Somatic mosaicism of an intragenic <italic>FANCB</italic> duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 1, p. 77, doi. 10.1002/mgg3.350
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- Publication type:
- Article
Association of difficult airway to VACTERL anomaly: An anesthetic challenge.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Eyelid Coloboma in a Newborn with VACTERL Association.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A case of VACTERL and non-VACTERL association without the "V and L".
- Published in:
- Indian Journal of Nuclear Medicine, 2014, v. 29, n. 1, p. 46, doi. 10.4103/0972-3919.125776
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- Publication type:
- Article
Prenatal Diagnosis of Persistent Cloaca Associated with VATER (Vertebral Defects, Anal Atresia, Tracheo-Esophageal Fistula, and Renal Dysplasia).
- Published in:
- Tohoku Journal of Experimental Medicine, 2007, v. 213, n. 4, p. 291, doi. 10.1620/tjem.213.291
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- Publication type:
- Article
Asociación VACTER: reporte de un caso.
- Published in:
- Revista Mexicana de Pediatria, 2013, v. 80, n. 3, p. 109
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- Publication type:
- Article
Surgical correction of tracheo-oesophageal fistula and oesophageal atresia in infants with VACTERL association: a retrospective case-control study.
- Published in:
- Pediatric Surgery International, 2012, v. 28, n. 10, p. 967, doi. 10.1007/s00383-012-3165-8
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- Publication type:
- Article
Inheritance of the VATER/VACTERL association.
- Published in:
- Pediatric Surgery International, 2012, v. 28, n. 7, p. 681, doi. 10.1007/s00383-012-3100-z
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- Publication type:
- Article
Familial occurrence of the VATER/VACTERL association.
- Published in:
- 2012
- By:
- Publication type:
- Report
PP-18 Prenatal sonographic diagnosis of VACTERL syndrome.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Coexistence of VATER association and recurrent urolithiasis: a case report.
- Published in:
- Pediatric Nephrology, 1998, v. 12, n. 2, p. 141
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- Publication type:
- Article
Anesthetic management in VACTERL syndrome.
- Published in:
- Journal of Clinical & Experimental Investigations, 2014, v. 5, n. 1, p. 103, doi. 10.5799/ahinjs.01.2014.01.0369
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- Publication type:
- Article
ASOCIACIÓN VACTERL: REPORTE DE UN CASO.
- Published in:
- CIMEL, 2012, v. 17, n. 1, p. 46
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- Publication type:
- Article
VATER/VACTERL Association and Caudal Regression with Xq25-q27.3 Microdeletion: A Case Report.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
A Fetus with Hemifacial Microsomia and Sirenomelia. The Same Mesodermal Defect Spectrum?
- Published in:
- Fetal & Pediatric Pathology, 2013, v. 32, n. 2, p. 152, doi. 10.3109/15513815.2012.684846
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- Publication type:
- Article
‘Double trouble’: incidental diagnosis of colonic duplication on spinal MRI.
- Published in:
- Pediatric Radiology, 2008, v. 38, n. 10, p. 1143, doi. 10.1007/s00247-008-0927-5
- By:
- Publication type:
- Article
Tracheoesophageal fistula (H-type) in neonates with imperforate anus and the VATER association.
- Published in:
- 2004
- By:
- Publication type:
- journal article
MURCS and VACTERL association in a 27 year old female.
- Published in:
- Journal of Obstetrics & Gynaecology, 2009, v. 29, n. 8, p. 762, doi. 10.3109/01443610903191293
- By:
- Publication type:
- Article
Sporadic neonatal Fanconi's anemia with VACTERL association.
- Published in:
- Pediatrics International, 2010, v. 52, n. 1, p. 141, doi. 10.1111/j.1442-200X.2009.02945.x
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- Publication type:
- Article
A case of esophageal atresia with tracheoesophageal fistula, imperforate anus, persistent cloaca, incomplete fusion of the labium and chronic renal failure due to urethral obstruction.
- Published in:
- Pediatrics International, 2000, v. 42, n. 5, p. 585, doi. 10.1046/j.1442-200x.2000.01283.x
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- Publication type:
- Article
Prune-Belly syndrome with VACTERL association: A rare case.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
First trimester diagnosis of VACTERL association.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Adriamycin mouse model: a variable but reproducible model of tracheo-oesophageal malformations.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Expression of homeotic genes Hoxa3, Hoxb3, Hoxd3 and Hoxc4 is decreased in the lungs but not in the hearts of adriamycin-exposed mice.
- Published in:
- 2007
- By:
- Publication type:
- journal article
VACTERL anomalies in patients with esophageal atresia: an updated delineation of the spectrum and review of the literature.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Neuroendocrine carcinoma of the ampulla of Vater causing ectopic adrenocorticotropic hormone-dependent Cushing's syndrome.
- Published in:
- Molecular & Clinical Oncology, 2016, v. 5, n. 1, p. 113, doi. 10.3892/mco.2016.869
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- Publication type:
- Article
Mixed adenoneuroendocrine carcinoma of the ampulla of Vater: A case report.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Medical genetics and genomic medicine in Turkey: a bright future at a new era in life sciences.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 5, p. 466, doi. 10.1002/mgg3.326
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- Publication type:
- Article
Female pseudohermaphroditism caused by caudal dysgenesis.
- Published in:
- Cytogenetics & Cell Genetics, 2000, v. 91, n. 1-4, p. 296, doi. 10.1159/000056860
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- Publication type:
- Article
A pulmonary artery sling with a vascular ring in a toddler: an uncommon combination.
- Published in:
- Cardiology in the Young, 2018, v. 28, n. 5, p. 783, doi. 10.1017/S1047951118000148
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- Publication type:
- Article
An overview of isolated and syndromic oesophageal atresia.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 5, p. 392, doi. 10.1111/j.1399-0004.2007.00798.x
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- Publication type:
- Article
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 12, p. 1377, doi. 10.1038/ejhg.2013.58
- By:
- Publication type:
- Article
A case of carcinoma of the papilla of Vater in a young man after subtotal colectomy for familial adenomatous polyposis.
- Published in:
- World Journal of Surgical Oncology, 2016, v. 14, p. 1, doi. 10.1186/s12957-016-0806-8
- By:
- Publication type:
- Article
Psychomotor Retardation and Agenesis of Vena Cava Inferior and Sacrum Associated with Unusual Features of Vacterl Anomalies.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Vestibular Derangement and Motion Intolerance in VATER Association.
- Published in:
- Case Reports in Otolaryngology, 2017, p. 1, doi. 10.1155/2017/4507323
- By:
- Publication type:
- Article
Genetic and physical mapping of the McKusick-Kaufman syndrome.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 3, p. 475, doi. 10.1093/hmg/7.3.475
- By:
- Publication type:
- Article
Tracheal bronchus associated with VACTERL.
- Published in:
- European Journal of Pediatrics, 2003, v. 162, n. 3, p. 165, doi. 10.1007/s00431-002-1109-3
- By:
- Publication type:
- Article
Dermoid Cyst and Ipsilateral Defects in VATER Association.
- Published in:
- Clinical Pediatrics, 1992, v. 31, n. 3, p. 184, doi. 10.1177/000992289203100312
- By:
- Publication type:
- Article