Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis-Reference-Cited by-同舟云学术

Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis

Published:2020-09 Issue:1-2 Volume:131 Page:267-276
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Abdul Majeed Nehna,Font-Montgomery Esperanza,Lukose Linda,Bryant Joy,Veppumthara Peter,Choyke Peter L.,Turkbey Ismail B.,Heller Theo,Gahl William A.,Gunay-Aygun Meral

Funder

ARPKD/CHF

National Human Genome Research Institute

National Institutes of Health Clinical Center

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference30 articles.

1. Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender. Arbeitsgemeinschaft fur Padiatrische, Nephrologie;Zerres;Acta Paediatr.,1996

2. Autosomal recessive polycystic kidney disease: long-term outcome of neonatal survivors;Roy;Pediatr. Nephrol.,1997

3. Apn: clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD);Bergmann;Kidney Int.,2005

4. Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference;Gunay-Aygun;J. Pediatr.,2006

5. Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD);Adeva;Medicine (Baltimore),2006

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association of congenital hepatic fibrosis and Caroli's syndrome: Two illustrative cases;Clinics and Research in Hepatology and Gastroenterology;2024-10

2. Next generation sequencing identifies WNT signalling as a significant pathway in Autosomal Recessive Polycystic Kidney Disease (ARPKD) manifestation and may be linked to disease severity;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-10

3. Multi-Modal MRI Assessments of Kidney Disease Severity in Autosomal Recessive Polycystic Kidney Disease;Kidney International Reports;2024-09

4. Case report: Rare genetic liver disease - a case of congenital hepatic fibrosis in adults with autosomal dominant polycystic kidney disease;Frontiers in Medicine;2024-02-07

5. Developmental, Familial, and Metabolic Disorders;Atlas of Liver Pathology;2024