UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Autosomal Dominant Polycystic Kidney Disease: From Pathophysiology of Cystogenesis to Advances in the Treatment

International journal of molecular sciences, 2022-03, Vol.23 (6), p.3317

2022

Link zum Volltext

Verfügbarkeit prüfen

Current and Future Therapeutical Options in Alport Syndrome

International journal of molecular sciences, 2023-03, Vol.24 (6), p.5522

2023

Link zum Volltext

Verfügbarkeit prüfen

Severity in polycystic liver disease is associated with aetiology and female gender: Results of the International PLD Registry

Liver international, 2019-03, Vol.39 (3), p.575-582

2019

Link zum Volltext

Verfügbarkeit prüfen

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele

BMC nephrology, 2013-03, Vol.14 (1), p.59-59, Article 59

2013

Link zum Volltext

Verfügbarkeit prüfen

Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis

PloS one, 2020-06, Vol.15 (6), p.e0235071-e0235071

2020

Link zum Volltext

Verfügbarkeit prüfen

SP015NEW TECHNOLOGIES IN DNA ANALYSIS OF POLYCYSTIC KIDNEY DISEASES

Nephrology, dialysis, transplantation, 2017-05, Vol.32 (suppl_3), p.iii107-iii107

2017

Link zum Volltext

Verfügbarkeit prüfen

The coincidence of IgA nephropathy and Fabry disease

BMC nephrology, 2013-01, Vol.14 (1), p.6-6, Article 6

2013

Link zum Volltext

Verfügbarkeit prüfen

Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic

BMC medical genetics, 2018-08, Vol.19 (1), p.147-147, Article 147

2018

Link zum Volltext

Verfügbarkeit prüfen

PKD2 mutations in a Czech population with autosomal dominant polycystic kidney disease

Nephrology, dialysis, transplantation, 2004-05, Vol.19 (5), p.1116-1122

2004

Link zum Volltext

Verfügbarkeit prüfen

SP032THE MUTATIONAL ANALYSIS OF THE INF2 GENE IN CZECH PATIENTS WITH FSGS AND MCD

Nephrology, dialysis, transplantation, 2015-05, Vol.30 (suppl_3), p.iii391-iii391

2015

Link zum Volltext

Verfügbarkeit prüfen

Unusual manifestation of AL amyloidosis—stenosis of inferior vena cava

Nephrology, dialysis, transplantation, 2006-05, Vol.21 (5), p.1430-1433

2006

Link zum Volltext

Verfügbarkeit prüfen

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report

BMC nephrology, 2018-07, Vol.19 (1), p.163-163, Article 163

2018

Link zum Volltext

Verfügbarkeit prüfen

Genetic Analysis of Gitelman Syndrome Patients from the Czech Republic and Slovakia – Three Novel Mutations Found

Kidney & blood pressure research, 2006-01, Vol.29 (6), p.360-365

2006

Link zum Volltext

Verfügbarkeit prüfen

Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia

Vnitřní lékar̆stvĭ, 2016, Vol.62 Suppl 6, p.78-83

2016

Link zum Volltext

Verfügbarkeit prüfen

IgA Nephropathy in Czech Patients - Are We Able Reliably Predict the Outcome?

Kidney & blood pressure research, 2014-01, Vol.39 (6), p.555-562

2014

Link zum Volltext

Verfügbarkeit prüfen

Endothelial Nitric Oxide Synthase Affects the Progression of Autosomal Dominant Polycystic Kidney Disease

Kidney & blood pressure research, 2002-01, Vol.25 (2), p.87-90

2002

Link zum Volltext

Verfügbarkeit prüfen

INFLUENCE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE POLYMORPHISM ON THE PROGRESSION OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND IgA NEPHROPATHY

Renal failure, 2002-01, Vol.24 (4), p.467-475

2002

Link zum Volltext

Verfügbarkeit prüfen

INFLUENCE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE POLYMORPHISM ON THE PROGRESSION OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND IgA NEPHROPATHY

Renal failure, 2002-01, Vol.24 (5), p.585-593

2002

Link zum Volltext

Verfügbarkeit prüfen

New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease

BMC medical genetics, 2009-08, Vol.10 (1), p.78-78, Article 78

2009

Link zum Volltext

Verfügbarkeit prüfen

MP037THE ROLE OF DNA ANALYSIS IN DIAGNOSIS OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE

Nephrology, dialysis, transplantation, 2016-05, Vol.31 (suppl_1), p.i355-i355

2016

Link zum Volltext

Verfügbarkeit prüfen

Nationwide biopsy survey of renal diseases in the Czech Republic during the years 1994–2011

Journal of nephrology, 2015-02, Vol.28 (1), p.39-49

2015

Link zum Volltext

Verfügbarkeit prüfen

Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease

BMC medical genetics, 2015-12, Vol.16 (1), p.116-116, Article 116

2015

Link zum Volltext

Verfügbarkeit prüfen

Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease

BMC medical genetics, 2014-04, Vol.15 (1), p.41-41, Article 41

2014

Link zum Volltext

Verfügbarkeit prüfen

SP875MOLECULAR GENETIC ANALYSIS IN FAMILIES WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE

Nephrology, dialysis, transplantation, 2015-05, Vol.30 (suppl_3), p.iii665-iii666

2015

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 40

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(40)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(33)
Life Sciences & Biomedicine
(32)
Humans
(31)
Female
(24)
Male
(22)
Adult
(20)
Middle Aged
(19)
Urology & Nephrology
(18)
Polycystic Kidney, Autosomal Dominant - Genetics
(13)
Aged
(11)
Mutation
(11)
Kidney Diseases
(10)
Biological And Medical Sciences
(8)
Czech Republic
(8)
Medical Sciences
(8)
Nephrology. Urinary Tract Diseases
(8)
Polycystic Kidney Disease
(8)
Cysts
(7)
Diagnosis
(7)
Genetic Aspects
(7)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Autosomal Dominant Polycystic Kidney Disease: From Pathophysiology of Cystogenesis to Advances in the Treatment

Current and Future Therapeutical Options in Alport Syndrome

Severity in polycystic liver disease is associated with aetiology and female gender: Results of the International PLD Registry

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele

The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood

Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis

SP015NEW TECHNOLOGIES IN DNA ANALYSIS OF POLYCYSTIC KIDNEY DISEASES

The coincidence of IgA nephropathy and Fabry disease

Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic

PKD2 mutations in a Czech population with autosomal dominant polycystic kidney disease

SP032THE MUTATIONAL ANALYSIS OF THE INF2 GENE IN CZECH PATIENTS WITH FSGS AND MCD

Unusual manifestation of AL amyloidosis—stenosis of inferior vena cava

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report

Genetic Analysis of Gitelman Syndrome Patients from the Czech Republic and Slovakia – Three Novel Mutations Found

Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia

IgA Nephropathy in Czech Patients - Are We Able Reliably Predict the Outcome?

Endothelial Nitric Oxide Synthase Affects the Progression of Autosomal Dominant Polycystic Kidney Disease

INFLUENCE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE POLYMORPHISM ON THE PROGRESSION OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND IgA NEPHROPATHY

INFLUENCE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE POLYMORPHISM ON THE PROGRESSION OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND IgA NEPHROPATHY

New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease

MP037THE ROLE OF DNA ANALYSIS IN DIAGNOSIS OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE

Nationwide biopsy survey of renal diseases in the Czech Republic during the years 1994–2011

Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease

Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease

SP875MOLECULAR GENETIC ANALYSIS IN FAMILIES WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE

Suchergebnisse filtern