Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease. - Wikidata - awgldk - TriplyDB

Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease.

Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease.

http://www.wikidata.org/entity/Q34170317

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Drug Induced Liver Injury: Review with a Focus on Genetic Factors, Tissue Diagnosis, and Treatment Options Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy Telmisartan ameliorates fibrocystic liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease Whole exome sequencing identifies recessive PKHD1 mutations in a Chinese twin family with Caroli disease Changes in liver and spleen volumes after living liver donation: a report from the Adult-to-Adult Living Donor Liver Transplantation Cohort Study (A2ALL)Kidney and liver transplantation in children with fibrocystic liver-kidney disease: data from the US Scientific Registry of Transplant Recipients: 1990-2010.Factors associated with the platelet count in patients with chronic hepatitis C.Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference.Rationale, design and objectives of ARegPKD, a European ARPKD registry study Magnetic resonance microscopy of renal and biliary abnormalities in excised tissues from a mouse model of autosomal recessive polycystic kidney disease Growth in Children with Autosomal Recessive Polycystic Kidney Disease in the CKiD Cohort Study Pediatric living donor liver transplantation for congenital hepatic fibrosis using a mother's graft with von Meyenburg complex: A case report.Balancing and communicating the risks and benefits of biologics in pediatric inflammatory bowel disease Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes.Clinical implications of ageing for the management of IBD.Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?Tumor necrosis factor-alpha antagonists twenty years later: what do Cochrane reviews tell us?Tesevatinib ameliorates progression of polycystic kidney disease in rodent models of autosomal recessive polycystic kidney disease.Emerging Therapies for Childhood Polycystic Kidney Disease.Long-term pulmonary function in children with recessive polycystic kidney disease.Combined and sequential liver-kidney transplantation in children.Characteristics of Liver Disease in 100 Individuals With Joubert Syndrome Prospectively Evaluated At A Single Center.Compound heterozygous PKHD1 variants cause a wide spectrum of ductal plate malformations.Severe Polycystic Liver Disease Is Not Caused by Large Deletions of the PRKCSH Gene.Congenital abnormalities and hepatoblastoma: a report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB).Congenital hepatic fibrosis in a 9-year-old female patient - a case report Clinical characteristics and mutation analysis of three Chinese children with autosomal recessive polycystic kidney disease

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P2860

Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease.

http://www.wikidata.org/entity/Q34170317

description

2012 nî lūn-bûn

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2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2012 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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Annelys Roque

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P2860

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

Liver and kidney disease in ciliopathies

New equations to estimate GFR in children with CKD

Body Length and Organ Weights of Infants and Children: A Study of the Body Length and Normal Weights of the More Important Vital Organs of the Body between Birth and Twelve Years of Age

Diseases of the intrahepatic biliary tree

Normal values for renal length and volume as measured by magnetic resonance imaging.

PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis.

Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.

Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference

Ludwig symposium on biliary disorders--part I. Pathogenesis of ductal plate abnormalities.

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