Congenital anomalies of the kidney and urinary tract in a cohort of 280 consecutive patients with Hirschsprung disease

Reference ranges for ultrasonographic renal dimensions as functions of age and body indices: A retrospective observational study in Taiwan

(2019) Hsuan-An Su et al.   PLoS One

Urinary Tract Anomalies and Urinary Tract Dysfunction in Children with Hirschsprung Disease – Is Follow-Up Indicated?

(2018) C Granéli et al.   JOURNAL OF PEDIATRIC SURGERY

A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling

(2017) Asaf Vivante et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Incidence and Risks of Congenital Anomalies of Kidney and Urinary Tract in Newborns

(2016) You-Lin Tain et al.   MEDICINE

Heterozygous p.S811F RET gene mutation associated with renal agenesis, oligomeganephronia and total colonic aganglionosis: a case report

(2016) Keisuke Sugimoto et al.   BMC Nephrology

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

(2015) Asaf Vivante et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Urinary Tract Infections in Children: EAU/ESPU Guidelines

(2015) Raimund Stein et al.   EUROPEAN UROLOGY

Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung’s disease: a systematic review

(2014) Alejandro D. Hofmann et al.   PEDIATRIC SURGERY INTERNATIONAL

Mutations in DSTYK and Dominant Urinary Tract Malformations

(2013) S. Sanna-Cherchi et al.   NEW ENGLAND JOURNAL OF MEDICINE

A prospective observational study of associated anomalies in Hirschsprung’s disease

(2013) Alessio Pini Prato et al.   Orphanet Journal of Rare Diseases

Timing and Outcome of Renal Replacement Therapy in Patients with Congenital Malformations of the Kidney and Urinary Tract

(2012) E. Wuhl et al.   Clinical Journal of the American Society of Nephrology

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

(2011) C. Jeanpierre et al.   JOURNAL OF MEDICAL GENETICS

Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease

(2010) Matthew G. Sampson et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Development of a standardized definition for Hirschsprung's-associated enterocolitis: a Delphi analysis

(2009) Aimee C. Pastor et al.   JOURNAL OF PEDIATRIC SURGERY

Renal outcome in patients with congenital anomalies of the kidney and urinary tract

(2009) Simone Sanna-Cherchi et al.   KIDNEY INTERNATIONAL

Hirschsprung Disease and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)

(2009) Alessio Pini Prato et al.   MEDICINE