Search filters

List of works by Max Christoph Liebau

A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome

A molecular mechanism explaining albuminuria in kidney disease

scientific article published on 11 May 2020

AATF/Che-1 acts as a phosphorylation-dependent molecular modulator to repress p53-driven apoptosis

scientific article

ADPedKD: A Global Online Platform on the Management of Children With ADPKD

scientific article published on 29 May 2019

Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt, Germany. 27-28 October 2016.

scientific article

Altered molecular signatures during kidney development after intrauterine growth restriction of different origins

scientific article published on 01 February 2020

An emerging molecular understanding and novel targeted treatment approaches in pediatric kidney diseases

scientific article

Atypical Alport syndrome associated with a novel COL4A5 mutation

scientific article published in March 2009

Bicarbonate buffered peritoneal dialysis fluid upregulates angiopoietin-1 and promotes vessel maturation

scientific article published on 18 December 2017

Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations

scientific article published on 31 March 2017

Ciliopathies - from rare inherited cystic kidney diseases to basic cellular function

scientific article published on 19 May 2015

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD).

scientific article published on 28 May 2019

Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease

scientific article published on 29 September 2017

Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT).

scientific article published on 24 January 2013

Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference

scientific article

Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing

scientific article published on 7 August 2015

Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities

scientific article published on 12 January 2017

Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development

Dysregulated autophagy contributes to podocyte damage in Fabry's disease

scientific article

Editorial: Genetic Kidney Diseases of Childhood

scientific article published on 19 December 2018

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

scientific article

Expanding the role of vasopressin antagonism in polycystic kidney diseases: From adults to children?

scientific article published on 28 April 2017

Functional expression of the renin-angiotensin system in human podocytes

scientific article published on 27 September 2005

Gastrostomy Tube Insertion in Pediatric Patients With Autosomal Recessive Polycystic Kidney Disease (ARPKD): Current Practice.

scientific article

IL-6/Smad2 signaling mediates acute kidney injury and regeneration in a murine model of neonatal hyperoxia

scientific article published on 05 February 2019

Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus Statement

Implications of early diagnosis of autosomal dominant polycystic kidney disease: A post hoc analysis of the TEMPO 3:4 trial

scientific article published on 09 March 2020

Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4.

scientific article

International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people

scientific article published on 01 November 2019

L1CAM mutation in a boy with hydrocephalus and duplex kidneys

scientific article published on 10 February 2007

Looking at the (w)hole: magnet resonance imaging in polycystic kidney disease

scientific article published on 14 December 2012

Maintenance Peritoneal Dialysis in Children With Autosomal Recessive Polycystic Kidney Disease: A Comparative Cohort Study of the International Pediatric Peritoneal Dialysis Network Registry

scientific article published on 23 January 2020

Metabolic Changes in Polycystic Kidney Disease as a Potential Target for Systemic Treatment

scientific article published on 24 August 2020

Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics

scientific article

Mycophenolate Mofetil Therapy in Children With Idiopathic Nephrotic Syndrome: Does Therapeutic Drug Monitoring Make a Difference?

scientific article published on 20 October 2015

Mycophenolate mofetil following glucocorticoid treatment in Henoch-Schönlein purpura nephritis: the role of early initiation and therapeutic drug monitoring

scientific article published on 25 November 2017

NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway

scientific article

Nephrocystin-4 regulates Pyk2-induced tyrosine phosphorylation of nephrocystin-1 to control targeting to monocilia

scientific article published on 28 February 2011

No general treatment recommendation for nephrectomy in prenatal suspicion of ARPKD

scientific article published in November 2017

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

scientific article

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.

scientific article

Perinatal Diagnosis, Management, and Follow-up of Cystic Renal Diseases: A Clinical Practice Recommendation With Systematic Literature Reviews

scientific article

Polycystic Kidney Disease: ADPKD and ARPKD

Protection of human podocytes from shiga toxin 2-induced phosphorylation of mitogen-activated protein kinases and apoptosis by human serum amyloid P component

scientific article published on 24 February 2014

Proteinurie und Hämaturie

Quiz Page December 2016: Anuria on the Second Day Following Kidney Transplantation

scientific article published in December 2016

Rationale, design and objectives of ARegPKD, a European ARPKD registry study

scientific article

Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease

scientific article published on 16 February 2017

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease.

scientific article published on 9 May 2018

Single nephron proteomes connect morphology and function in proteinuric kidney disease.

scientific article published on 9 March 2018

Syndromale und ziliäre Erkrankungen1

Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus.

scientific article published on 28 June 2018

The carboxy-terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC-activation

scientific article published on 28 October 2020

The centrosomal kinase Plk1 localizes to the transition zone of primary cilia and induces phosphorylation of nephrocystin-1

scientific article

The ciliary protein nephrocystin-4 translocates the canonical Wnt regulator Jade-1 to the nucleus to negatively regulate β-catenin signaling

scientific journal article

Unmet needs and challenges for follow-up and treatment of autosomal dominant polycystic kidney disease: the paediatric perspective

Upregulation of Id-1 via BMP-2 receptors induces reactive oxygen species in podocytes

scientific article published on 18 April 2006

Paulina is supported by:

About Paulina

Help