Compound heterozygous mutations in CC2D2A cause Meckel-Gruber syndrome: a case report and review of the literature. [PDF]
Liu L, Lv Y, Zhou X.
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Endocannabinoid System-Related Inflammation and Progression of Autosomal Dominant Polycystic Kidney Disease. [PDF]
Simankowicz P +5 more
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Linezolid as a potential alternative to glycopeptide in treating <i>Enterococcus faecium</i> suspected cyst infection in a hemodialysis patient with autosomal-dominant polycystic kidney disease: A case report. [PDF]
Inagaki T, Otsu M, Takuma A, Momo K.
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Prenatal Diagnosis of Renal Cysts and Diabetes Syndrome (RCAD): A Case Report. [PDF]
Manasar-Dyrbuś M +4 more
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Kidney organoids as models for hereditary kidney diseases: Toward precision medicine (Review). [PDF]
Cui S +6 more
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Five-year Incidence Trends and the Status of Major Rare Diseases in 2023 in the 「Annual Report on the Rare Disease Patients in Korea」. [PDF]
Park IS +7 more
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Social Reintegration and Associated Factors Among Patients Receiving Peritoneal Dialysis: A Cross-Sectional Study. [PDF]
Lin QQ +6 more
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From silos to synergy: the interdisciplinary discovery potential in redefining polyendocrine metabolic ovarian syndrome. [PDF]
Morhaus MM +2 more
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A cross-model single-cell atlas reveals conserved involvement of osteopontin in polycystic kidney disease. [PDF]
Miller SJ +27 more
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Timing Matters: Decoding the microRNA Landscape of Polycystic Kidney Disease. [PDF]
Nyimanu D, Yu ASL.
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