Suchergebnisse - "Dahan, Karin"

PubPharm (143)

1

A step-by-step, multidisciplinary strategy to maximize the yield of genetic testing in pediatric patients with chronic kidney diseases

enthalten in: Pediatric nephrology (Berlin, Germany) | 2024

von Caliment, A. | Van Reeth, O. | Hougardy, C. | +2

2

Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease

enthalten in: Kidney international | 2023

von Claus, L. | Chen, C. | Stallworth, J. | +102

3

Severe parental phenotype associates with hypertension in children with ADPKD

enthalten in: Pediatric nephrology (Berlin, Germany) | 2023

von Demoulin, N. | Van Regemorter, E. | Dahan, K. | +5

4

The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

enthalten in: Kidney international | 2023

von Petzold, F. | Billot, K. | Chen, X. | +120

5

Retraction Note : Hypermethylation of the 5' CpG island of the p14ARF flanking exon 1β in human colorectal cancer displaying a restricted pattern of p53 overexpression concomitant with increased MDM2 expression

enthalten in: Clinical epigenetics | 2023

von Nyiraneza, C. | Sempoux, C. | Detry, R. | +2

RetractionOf: Clin Epigenetics. 2012 Jun 15;4(1):9. - PMID 22703554

6

Nephrolithiasis and Multicystic Kidneys in a Young Patient : A Quiz

enthalten in: American journal of kidney diseases : the official journal of the National Kidney Foundation | 2023

von Gillion, V. | Dahan, K. | Dragean, C. | +1

7

Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies

enthalten in: Clinical journal of the American Society of Nephrology : CJASN | 2023

von Werion, A. | Storms, P. | Zizi, Y. | +53

8

Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency

enthalten in: Gastroenterology | 2023

von Gallon, R. | Phelps, R. | Hayes, C. | +44

9

Lessons for the clinical nephrologist : lumasiran as the future cornerstone treatment for patients with primary hyperoxaluria type 1?

enthalten in: Journal of nephrology | 2023

von Gillion, V. | Dahan, K. | Scohy, A. | +2

10

Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes : a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes

enthalten in: The Lancet. Oncology | 2023

von Garcia-Pelaez, J. | Barbosa-Matos, R. | Lobo, S. | +66

ErratumIn: Lancet Oncol. 2023 Jan;24(1):e10. - PMID 36603924

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