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Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

Journal of the American Society of Nephrology, 2001-09, Vol.12 (9), p.1872-1881

2001

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The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect

Kidney international, 2007-03, Vol.71 (6), p.574-581

2007

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Deutsche Vergangenheiten - eine gemeinsame Herausforderung. Der schwierige Umgang mit der doppelten Nachkriegsgeschichte

1999

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Nephrocalcinosis in children : a retrospective survey

Pediatric nephrology (Berlin, West), 2000-09, Vol.14 (10-11), p.1016-1021

2000

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Mycophenolate Mofetil versus Cyclosporin A in Children with Frequently Relapsing Nephrotic Syndrome

Journal of the American Society of Nephrology, 2013-10, Vol.24 (10), p.1689-1697

2013

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Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen

Nature genetics, 1994-07, Vol.7 (3), p.429-432

1994

Volltextzugriff (PDF)

Mandat für Deutsche Einheit: Die 10. Volkskammer zwischen DDR-Verfassung und Grundgesetz

2000

Volltextzugriff (PDF)

Renal function in long-term survivors of stem cell transplantation in childhood. A prospective trial

Bone marrow transplantation (Basingstoke), 2001-02, Vol.27 (3), p.319-327

2001

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Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli—Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae

Clinical infectious diseases, 2012-05, Vol.54 (10), p.1413-1421

2012

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Efforts to establish an animal model of Fanconi syndrome after ifosfamide administration to rats

Journal of applied toxicology, 2007-07, Vol.27 (4), p.327-336

2007

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Two-Hour Postdose Concentration: A Reliable Marker for Cyclosporine Exposure in Adolescents With Stable Renal Transplants

Transplantation proceedings, 2005-04, Vol.37 (3), p.1608-1611

2005

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Growth in Very Young Children Undergoing Chronic Peritoneal Dialysis

Journal of the American Society of Nephrology, 2011-12, Vol.22 (12), p.2303-2312

2011

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Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender

Acta Paediatrica, 1996-04, Vol.85 (4), p.437-445

1996

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Management of anemia in children receiving chronic peritoneal dialysis

Journal of the American Society of Nephrology, 2013-03, Vol.24 (4), p.665-676

2013

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IMPACT OF GLOBAL ECONOMIC DISPARITIES ON PRACTICES AND OUTCOMES OF CHRONIC PERITONEAL DIALYSIS IN CHILDREN: INSIGHTS FROM THE INTERNATIONAL PEDIATRIC PERITONEAL DIALYSIS NETWORK REGISTRY

Peritoneal dialysis international, 2012-07, Vol.32 (4), p.399-409

2012

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Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

Kidney international, 2005-03, Vol.67 (3), p.829-848

2005

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Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

Journal of the American Society of Nephrology, 2008-02, Vol.19 (2), p.365-371

2008

Volltextzugriff (PDF)

STAR SIGN study: Evaluation of COVID-19 vaccine efficacy against the SARS-CoV-2 variants BQ.1.1 and XBB.1.5 in patients with inflammatory bowel disease

Alimentary pharmacology & therapeutics, 2023-10, Vol.58 (7), p.678-691

2023

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Day- and night-time blood pressure elevation in children with higher grades of renal scarring

The Journal of pediatrics, 2003-02, Vol.142 (2), p.117-122

2003

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Diagnostik bei konnatalen Dilatationen der Harnwege

Monatsschrift Kinderheilkunde, 2002, Vol.150 (1), p.76-84

2002

Volltextzugriff (PDF)

The Relevance of Urodynamic Studies for Urge Syndrome and Dysfunctional Voiding: A Multicenter Controlled Trial in Children

The Journal of urology, 2008-10, Vol.180 (4), p.1486-1495

2008

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Reduced systemic advanced glycation end products in children receiving peritoneal dialysis with low glucose degradation product content

Nephrology, dialysis, transplantation, 2007-07, Vol.22 (7), p.2038-2044

2007

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Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Nephrology, dialysis, transplantation, 2008-11, Vol.23 (11), p.3527-3533

2008

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Idiopathische Hyperkalziurie im Kindesalter

Monatsschrift für Kinderheilkunde, 1996, Vol.144 (10), p.1054-1062

1996

Volltextzugriff (PDF)

Comorbidities in Chronic Pediatric Peritoneal Dialysis Patients: A Report of the International Pediatric Peritoneal Dialysis Network

Peritoneal dialysis international, 2012-07, Vol.32 (4), p.410-418

2012

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Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect

Deutsche Vergangenheiten - eine gemeinsame Herausforderung. Der schwierige Umgang mit der doppelten Nachkriegsgeschichte

Nephrocalcinosis in children : a retrospective survey

Mycophenolate Mofetil versus Cyclosporin A in Children with Frequently Relapsing Nephrotic Syndrome

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen

Mandat für Deutsche Einheit: Die 10. Volkskammer zwischen DDR-Verfassung und Grundgesetz

Renal function in long-term survivors of stem cell transplantation in childhood. A prospective trial

Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli—Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae

Efforts to establish an animal model of Fanconi syndrome after ifosfamide administration to rats

Two-Hour Postdose Concentration: A Reliable Marker for Cyclosporine Exposure in Adolescents With Stable Renal Transplants

Growth in Very Young Children Undergoing Chronic Peritoneal Dialysis

Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender

Management of anemia in children receiving chronic peritoneal dialysis

IMPACT OF GLOBAL ECONOMIC DISPARITIES ON PRACTICES AND OUTCOMES OF CHRONIC PERITONEAL DIALYSIS IN CHILDREN: INSIGHTS FROM THE INTERNATIONAL PEDIATRIC PERITONEAL DIALYSIS NETWORK REGISTRY

Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

STAR SIGN study: Evaluation of COVID-19 vaccine efficacy against the SARS-CoV-2 variants BQ.1.1 and XBB.1.5 in patients with inflammatory bowel disease

Day- and night-time blood pressure elevation in children with higher grades of renal scarring

Diagnostik bei konnatalen Dilatationen der Harnwege

The Relevance of Urodynamic Studies for Urge Syndrome and Dysfunctional Voiding: A Multicenter Controlled Trial in Children

Reduced systemic advanced glycation end products in children receiving peritoneal dialysis with low glucose degradation product content

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Idiopathische Hyperkalziurie im Kindesalter

Comorbidities in Chronic Pediatric Peritoneal Dialysis Patients: A Report of the International Pediatric Peritoneal Dialysis Network

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