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Polycystic liver disease
Ursodeoxycholic Acid in Advanced Polycystic Liver Disease: a Phase 2 Multicenter Randomized Controlled Trial
Article Pansomatostatin Agonist Pasireotide Long-Acting Release
Instelling Naam Expertise Centrum Cluster Van / Specifieke Aandoening Toelichting Erkenning
International Consensus Statement on the Diagnosis and Management of Autosomal Dominant Polycystic Kidney Disease in Children and Young People
Statistical Analysis Plan
Successful Aspiration and Ethanol Sclerosis of a Large, Symptomatic, Simple Liver Cyst: Case Presentation and Review of the Literature
Whole Exome Sequencing Gene Package Skeletal Dysplasia, Version 2.1, 31-1-2020
Current Treatment Status of Polycystic Liver Disease in Japan
Autosomal Dominant Polycystic Kidney Disease; ARPKD Ϭ Autosomal Recessive Polycystic Kidney Disease; RCAD Ϭ Renal Cysts and Diabetes Syndrome
WES Gene Package Multiple Congenital Anomalie.Xlsx
Clinical Characteristics of Individual Organ System Disease in Non-Motile Ciliopathies
WES Gene Package Multiple Congenital Anomalie.Xlsx
An Approach to Cystic Kidney Diseases: the Clinician's View
Update on Mapping the Landscape of Genetic Tests for Non-Cancer
CTGT Req Form 07302018.Pdf
Clinical Application of a Phenotype-Based NGS Panel for Differential Diagnosis of Inherited Kidney Disease and the Beyond
Osteopetrosis Precision Panel Overview Indications
The Liver and Polycystic Kidney Disease
Top View
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
Statistical Analysis Plan
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Polycystin-1: a Master Regulator of Intersecting Cystic Pathways
Next Generation Sequencing (NGS)
Genetic Analyses for Kidney Diseases
Genetic Diagnostics Test(S)/Gene(S)/Panel(S)
Mendeliome Panel Versie V3 (4362 Genen) Centrum Voor Medische Genetica Gent
Inherited Thrombocytopenia Precision Panel Overview Indications
1 Supplementary Material Appendix 1 Read Codes to Identify a Child With
On Clinical Renal Genetics
Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing
Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
Long‑Term Results of Liver Transplantation for Polycystic Liver Disease: Single‑Center Experience in China
WES Gene Package Multiple Congenital Anomalie
Liver & Pancreas
Autosomal Dominant Pseudohypoaldosteronism Type 1: Mechanisms, Evidence for Neonatal Lethality, and Phenotypic Expression in Adults
(Pasireotide LAR) in Severe Polycystic Liver Disease. NCT# NCT0167011