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Publications by Carsten Bergmann
Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype With ESRD
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Mutations in KIRREL1, a Slit Diaphragm Component, Cause Steroid-Resistant Nephrotic Syndrome
Kidney International
Nephrology
Clinical and Molecular Characterization of Patients With Heterozygous Mutations in Wilms Tumor Suppressor Gene 1
Clinical Journal of the American Society of Nephrology
Epidemiology
Nephrology
Critical Care
Transplantation
Intensive Care Medicine
Management of Bone Disease in Cystinosis: Statement From an International Conference
Journal of Inherited Metabolic Disease
Genetics
Genetic Characteristics of the Human Hepatic Stellate Cell Line LX-2
PLoS ONE
Multidisciplinary
Educational Paper
European Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Retrospective Genetic Analysis Illustrates the Spectrum of Autosomal Alport Syndrome in a Case of Living-Related Donor Kidney Transplantation
BMC Nephrology
Nephrology
Diagnostic Applications of Next Generation Sequencing: Working Towards Quality Standards/Diagnostische Anwendung Von Next Generation Sequencing: Auf Dem Weg Zu Qualitätsstandards
LaboratoriumsMedizin
Biochemistry
Medical Laboratory Technology
Clinical Biochemistry
Transient, Recurrent, White Matter Lesions in X-Linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation
Archives of Neurology
