Molecular Diagnosis and Identification of a Novel Pathogenic Variant in Autosomal Dominant Polycystic Kidney Disease (ADPKD): A Case in Full Bloom. [PDF]
Pallas D +4 more
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Qualitative Analysis and Comparison of Externally Led Patient-Focused Drug Development Concepts for Autosomal Recessive Polycystic Kidney Disease Against SONG Initiatives. [PDF]
Soyfer B +9 more
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Efficacy and Safety Comparisons of Lingshu Granule versus Decoction in Polycystic Ovary Syndrome Patients with Insulin Resistance: A Multicenter Randomized Controlled Dose-Finding Trial Protocol. [PDF]
Feng Y, Wen X, Li X, Luo Y.
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Kidney Failure Risk Equation performance according to the etiology of chronic kidney disease in the CKD-CAREMEAU cohort. [PDF]
Prouvot J +8 more
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Diagnostic Value of Serum Periostin for Cyst Involution in Children with Multicystic Dysplastic Kidney. [PDF]
Szmigielska A +4 more
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Identification of Pathogenic <i>PKHD1</i> Variants in Infants with Autosomal Recessive Polycystic Kidney Disease from the Dhofar Region, Oman. [PDF]
Al Alawi I +8 more
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Polycystic Kidney/Liver Disease
Clinics in Liver Disease, 2022Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder that leads to chronic kidney disease and end-stage kidney disease (ESKD). Polycystic liver disease (PCLD) is the most common extrarenal manifestation of ADPKD. Though isolated PCLD and PCLD due to ADPKD are genetically distinct, they follow a similar clinical course of ...
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Reversing polycystic kidney disease
Nature Genetics, 2021A new study shows that re-expressing PKD genes early in the course of the disease can fully reverse polycystic kidney disease in mice. These results reveal an unexpected ability of the kidney to regenerate following genetic rescue of polycystin function.
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