Max C. Liebau

Germany

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Articles (14)

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2025

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2025

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (12)

Oliver Semler

head of department

University Hospital

GERMANY

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Ronald D. Perrone

Tufts University School of Medicine

UNITED STATES

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Joost P Schanstra

INSERM Délégation régionale Midi-Pyrenees Limousin

FRANCE

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Ann Raes

Administrative and medical head of department of pediatric nephrology

Ghent University

BELGIUM

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David Stephens

University of Bristol

UNITED KINGDOM

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Rita Cascão

Gulbenkian Institute for Molecular Medicine

PORTUGAL

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Mirko Rehberg

GERMANY

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Claudia Faria

Invited Assistant Professor

Universidade do Porto Faculdade de Medicina

PORTUGAL

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Franz Schaefer

Heidelberg University

GERMANY

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Gisela Slaats

assistant professor

University Medical Center Utrecht, Utrecht University

NETHERLANDS

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Michiel Schreuder

Professor Pediatric Nephrology

Radboudumc

NETHERLANDS

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Susanna Negrisolo

University of Padova

ITALY

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Max C. Liebau

Research Interests

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Articles (14)

The nephronophthisis protein GLIS2/NPHP7 is required for the DNA damage response in kidney tubular epithelial cells

Anti-nephrin antibodies guide living donor kidney transplantation in a pediatric patient with primary focal segmental glomerular sclerosis

TAPT1-at the crossroads of extracellular matrix and signaling in Osteogenesis imperfecta

Fetal and Perinatal Nephrology: Small but Mighty

Fetal and Perinatal Nephrology: Small but Mighty

Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease

Autosomal Recessive Polycystic Kidney Disease: Diagnosis, Prognosis, and Management

Primary cilia contribute to the aggressiveness of atypical teratoid/rhabdoid tumors

Definition, diagnosis, and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet working group on Kidney Malformations

Refining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis.

Perspectives on Drug Development in Autosomal Recessive Polycystic Kidney Disease

Correction to: Impact of coronavirus disease-2019 on pediatric nephrology practice and education: an ESPN survey.

Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney Disease.

Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseases.

Collaborators (12)

Oliver Semler

Ronald D. Perrone

Joost P Schanstra

Ann Raes

David Stephens

Rita Cascão

Mirko Rehberg

Claudia Faria

Franz Schaefer

Gisela Slaats

Michiel Schreuder

Susanna Negrisolo

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