Verfasser Suchresultate

Normdaten (Quelle GND / Entity Facts )

Carsten Bergmann

geboren 1972 in Mönchengladbach
Facharzt für Humangenetik

Weiterführende Links

Gemeinsame Normdatei (GND) im Katalog der Deutschen Nationalbibliothek

Virtual International Authority File (VIAF)

Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort

Wong, Katie (Verfasser)

Freiburg : Universität, 2025

E-Book

Description and cross-sectional analyses of 25,880 adults and children in the UK National Registry of Rare Kidney Diseases Cohort

Wong, Katie (Verfasser)

Freiburg : Universität, 2025

E-Book

Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendations

Dollfus, Helene (Verfasser)

Freiburg : Universität, 2024

E-Book

Renal and extrarenal phenotypes in patients with HNF1B variants and chromosome 17q12 microdeletions

Buffin-Meyer, Bénédicte (Verfasser)

Freiburg : Universität, 2024

E-Book

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Köttgen, Anna (Verfasser)

Freiburg : Universität, 2022

E-Book

Collagen IVα345 dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture’s and Alport diseases

Pokidysheva, Elena N. (Verfasser)

Freiburg : Universität, 2021

E-Book

Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practice

Knoers, Nine V. A. M. (Verfasser)

Accepted manuscript

Freiburg : Universität, 2021

E-Book

Long-term follow-up of retinal function and structure in TRPM1-associated complete congenital stationary night blindness

Al-Hujaili, Haneen (Verfasser)

Freiburg : Universität, 2020

E-Book

Management of bone disease in cystinosis: Statement from an international conference

Hohenfellner, Katharina (Verfasser)

Freiburg : Universität, 2019

E-Book

Kif21a deficiency leads to impaired glomerular filtration barrier function

Riedmann, Hanna Valentina (Verfasser)

Freiburg : Universität, 2023

E-Book

Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Bergmann, Carsten (Verfasser)

Freiburg : Universität, 2019

E-Book

Refining kidney survival in 383 genetically characterized patients with nephronophthisis

König, Jens (Verfasser)

Freiburg : Universität, 2022

E-Book

A SEC61A1 variant is associated with autosomal dominant polycystic liver disease

Schlevogt, Bernhard (Verfasser)

Freiburg : Universität, 2022

E-Book

PATJ deficiency leads to cystic kidney disease and related ciliopathies

Epting, Daniel (Verfasser)

Freiburg : Universität, 2025

E-Book

Correction: Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesis

Epting, Daniel (Verfasser)

Freiburg : Universität, 2026

E-Book

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

Epting, Daniel (Verfasser)

Freiburg : Universität, 2020

E-Book

Non-invasive screening for liver fibrosis by acoustic radiation force impulse in patients with ciliopathies

Bresch, Johanna (Verfasser)

Freiburg : Universität, 2025

E-Book

Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesis

Epting, Daniel (Verfasser)

Freiburg : Universität, 2025

E-Book

Membranoproliferative glomerulonephritis and C3 glomerulopathy in children: change in treatment modality? : : a report of a case series

Spartà, Giuseppina (Verfasser)

Freiburg : Universität, 2023

E-Book

A novel role for the chloride intracellular channel protein Clic5 in ciliary function

Ott, Elisabeth (Verfasser)

Freiburg : Universität, 2023

E-Book

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Carsten Bergmann

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