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Max Christoph Liebau (1977-)

Hochschullehrer

Name	Max Christoph Liebau
Zeit	1977- (Lebensdaten)
Ort	Göttingen (Geburtsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Priv.-Doz. Dr. med.
Beruf	Hochschullehrer (charakteristischer Beruf) Arzt
Variante	Max Liebau M. Liebau M. C. Liebau
Beziehung	Klinik und Poliklinik für Kinder- und Jugendmedizin (Köln)
Weitere Angaben	Habil., Med. Fak. d. Univ. zu Köln, 31. März 2014 Leiter Experimentelle Pädiatrische Nephrologie Diss. Medizinische Fakultät
Datensatztyp	Person
GND-Nummer	130871842
Datensatz-ID	130871842
Beteiligt an alle anzeigen Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease Prävalenz und Komplikationen der hepatischen Manifestation bei Patienten mit ARPKD. Analyse anhand einer internationalen multizentrischen Kohorte Definition, diagnosis and management of fetal lower urinary tract obstruction: consensus of the ERKNet CAKUT-Obstructive Uropathy Work Group Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseases Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease - are patient-centered outcomes our blind spot? Translational research approaches to study pediatric polycystic kidney disease Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease—are patient-centered outcomes our blind spot? Early clinical management of autosomal recessive polycystic kidney disease Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD Long-term peritoneal dialysis in children with autosomal recessive polycystic kidney disease : a comparative cohort study of the international pediatric peritoneal dialysis network registry Nierenzysten und zystische Nierenerkrankungen bei Kindern (AWMF S2k-Leitlinie) Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD) International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus Charakterisierung des Angiotensin-II-AT1-Rezeptors in humanen differenzierten Podozyten

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Katalog der Deutschen Nationalbibliothek

Max Christoph Liebau (1977-)

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

Prävalenz und Komplikationen der hepatischen Manifestation bei Patienten mit ARPKD. Analyse anhand einer internationalen multizentrischen Kohorte

Definition, diagnosis and management of fetal lower urinary tract obstruction: consensus of the ERKNet CAKUT-Obstructive Uropathy Work Group

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

Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease - are patient-centered outcomes our blind spot?

Translational research approaches to study pediatric polycystic kidney disease

Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease—are patient-centered outcomes our blind spot?

Early clinical management of autosomal recessive polycystic kidney disease

Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality

Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD

Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD

Long-term peritoneal dialysis in children with autosomal recessive polycystic kidney disease : a comparative cohort study of the international pediatric peritoneal dialysis network registry

Nierenzysten und zystische Nierenerkrankungen bei Kindern (AWMF S2k-Leitlinie)

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

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

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

Charakterisierung des Angiotensin-II-AT1-Rezeptors in humanen differenzierten Podozyten