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Seite 7 für „kidney“ · Literaturverweise aus öffentlichen Artikeln
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Congenital anomalies of the kidney and urinary tract in children treated at a tertiary hospital in Northern Tanzania: assessment of coexisting congenital anomalies
pubmed · 42046783
Literaturverweis öffnenNovel somatic PBX1 mosaicism likely masking syndromic CAKUT in an adult with bilateral kidney hypoplasia
pubmed · 35756743
Literaturverweis öffnenMolecular and biochemical correlates of urinary composition in kidney stone pathogenesis
pubmed · 42320707
Literaturverweis öffnenPrevalence and Genetic Spectrum of Inherited Kidney Diseases: A Chinese Cohort Study
pubmed · 41920701
Literaturverweis öffnenKidney Morbidity in Pediatric Patients With Spina Bifida
pubmed · 42360745
Literaturverweis öffnenExstrophied Variant of Rectal Duplication Cyst with Supernumerary Kidney
pubmed · 39968262
Literaturverweis öffnenKetoanalogue-Supplemented Low-Protein Diet in Patients with Stage 4+ Chronic Kidney Disease in Italy: A Cost-Utility Analysis
pubmed · 41978192
Literaturverweis öffnenInfection risk mitigation with complement inhibitors in kidney disease
pubmed · 42175904
Literaturverweis öffnenClinical impact of genetic testing in inherited kidney diseases
pubmed · 42389199
Literaturverweis öffnenAutosomal dominant polycystic kidney disease
pubmed · 41771281
Literaturverweis öffnenTest accuracy of glomerular filtration rate estimation with creatinine and cystatin C in adults with moderate chronic kidney disease: prospective cohort study
pubmed · 41586348
Literaturverweis öffnenPrevalence of undiagnosed stage 3 chronic kidney disease in France, Germany, Italy, Japan and the USA: results from the multinational observational REVEAL-CKD study
pubmed · 37217263
Literaturverweis öffnenAutosomal dominant polycystic kidney disease: Current perspectives in 2026
pubmed · 42315404
Literaturverweis öffnenCongenital Alopecia, Hypoplastic Kidneys, Growth Restriction, Growth Hormone Resistance, and Liver Fibrosis: Confirmation of a New Syndrome Caused by Biallelic Variants in ZPR1
pubmed · 40776660
Literaturverweis öffnen[Dietary protein and kidney diseases]
pubmed · 3811569
Literaturverweis öffnenTiming Matters: Decoding the microRNA Landscape of Polycystic Kidney Disease
pubmed · 42348408
Literaturverweis öffnenDuplex kidney formation: developmental mechanisms and genetic predisposition
pubmed · 32030122
Literaturverweis öffnenDeletion of decay-accelerating factor in kidney tubular cells mitigates kidney fibrosis in aristolochic acid nephropathy
pubmed · 42412640
Literaturverweis öffnenTailored Kidney Stone Prevention Improves Metabolic Risk Factors and Reduces Renal Colic Rate
pubmed · 41584268
Literaturverweis öffnenPrimary Alveolar Echinococcosis of the Kidney
pubmed · 41670084
Literaturverweis öffnenFibrinogen-like protein 2-complement C3 interaction exacerbates tubular inflammation in acute kidney injury by elevating complement C3a levels
pubmed · 42473685
Literaturverweis öffnenPost-Transplant Bone Disease in Kidney Transplant Recipients: Diagnosis and Management
pubmed · 38339137
Literaturverweis öffnenSuccessful Kidney Transplantation for Bilateral Renal Hypoplasia With Ebstein Disease
pubmed · 39688353
Literaturverweis öffnenEffectiveness and mechanistic effects of green mamba related peptide MQ232 in an orthologous mouse model of autosomal dominant polycystic kidney disease
pubmed · 42176774
Literaturverweis öffnenVascular pathologies in chronic kidney disease: pathophysiological mechanisms and novel therapeutic approaches
pubmed · 33481059
Literaturverweis öffnenDrug-Induced Kidney Stones and Crystalline Nephropathy: Pathophysiology, Prevention and Treatment
pubmed · 29264783
Literaturverweis öffnenMapping Genetic Susceptibility to Urinary Tract Infection from Kidney Papilla to Bladder
doi · 10.64898/2026.07.07.26357417
Literaturverweis öffnenKDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease
guideline · KDIGO-2024-CKD
Literaturverweis öffnenAnti-Polyamine Therapy Restrains Kidney Cyst Growth in an Orthologous Mouse Model of Autosomal Dominant Polycystic Kidney Disease
doi · 10.64898/2026.06.02.729335
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