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99951 - 99960 von 3687907

	99951	Mutation Analysis of PKD1 and PKD2 Genes in a Large Italian Cohort Reveals Novel Pathogenic Variants Including a Novel Complex Rearrangement Enthalten in Nephron Bd. 148, 2024, Nr. 5: 273-291. 19 S.
	99952	Suspected Autosomal Recessive Polycystic Kidney Disease but Cerebellar Vermis Hypoplasia, Oligophrenia Ataxia, Coloboma, and Hepatic Fibrosis (COACH) Syndrome in Retrospect, A Delayed Diagnosis Aided by Genotyping and Reverse Phenotyping: A Case Report and A Review of the Literature Enthalten in Nephron Bd. 148, 2024, Nr. 4: 264-272. 9 S.
	99953	LncRNA CASC2 Alleviates Renal Interstitial Inflammation and Fibrosis through MEF2C Downregulation-Induced Hinderance of M1 Macrophage Polarization Enthalten in Nephron Bd. 148, 2024, Nr. 4: 245-263. 19 S.
	99954	Transcription Factor ATF3 Mediating SOCS3 Expression Aggravates Renal Ischemia-Reperfusion Injury by Activating Mitophagy Enthalten in Nephron Bd. 148, 2024, Nr. 4: 230-244. 15 S.
	99955	Acceptance of Illness, Satisfaction with Life, and Emotional Control in the Early Stage of Autosomal Dominant Polycystic Kidney Disease Enthalten in Nephron Bd. 148, 2024, Nr. 4: 224-229. 6 S.
	99956	The Pathophysiology of Left Ventricular Hypertrophy, beyond Hypertension, in Autosomal Dominant Polycystic Kidney Disease Enthalten in Nephron Bd. 148, 2024, Nr. 4: 215-223. 9 S.
	99957	Tubulointerstitial Nephritis and Uveitis Syndrome: A Report of 6 Cases with Renal Biopsy and Electron Microscopy Evaluation Enthalten in Nephron Bd. 148, 2024, Nr. 4: 204-214. 11 S.
	99958	Long-Term Renal Function in Adult Patients with Phenylketonuria Enthalten in Nephron Bd. 148, 2024, Nr. 4: 195-203. 9 S.
	99959	Hospitalizations after Renal Transplantation in Children: Risk Factors, Causes, and Outcomes Enthalten in Nephron Bd. 148, 2024, Nr. 3: 185-194. 9 S.
	99960	Association of Familial Hyperkalemia and Hypertension with Proximal Renal Tubular Acidosis and Epileptic Seizures Enthalten in Nephron Bd. 148, 2024, Nr. 3: 179-184. 6 S.

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