4.4 Editorial Material

Atypical severe early-onset nephrotic syndrome: Answers

Related references

Note: Only part of the references are listed.
Article Urology & Nephrology

Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group

Olivia Boyer et al.

Summary: Congenital nephrotic syndrome is a group of disorders characterized by genetic defects in podocytes leading to nephrotic-range proteinuria, hypoalbuminemia, and edema. Managing this condition is challenging due to the high risk of severe complications.

NATURE REVIEWS NEPHROLOGY (2021)

Article Biochemistry & Molecular Biology

Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group

Beata Stefania Lipska-Zietkiewicz et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2020)

Article Transplantation

Treatment and outcome of congenital nephrotic syndrome

Sandra Berody et al.

NEPHROLOGY DIALYSIS TRANSPLANTATION (2019)

Article Pediatrics

Analysis of 14 Patients With Congenital Nephrotic Syndrome

Yan Chen et al.

FRONTIERS IN PEDIATRICS (2019)

Article Urology & Nephrology

The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε

Karolis Azukaitis et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2017)

Article Urology & Nephrology

Nephrotic-Range Proteinuria and Peripheral Edema in a Child: Not Only Idiopathic Nephrotic Syndrome

Valentina Dolcemascolo et al.

CASE REPORTS IN NEPHROLOGY AND DIALYSIS (2016)

Article Urology & Nephrology

Pneumococcal hemolytic uremic syndrome and steroid resistant nephrotic syndrome

Andrew P. Groves et al.

CLINICAL KIDNEY JOURNAL (2016)

Article Urology & Nephrology

Podocyte dysfunction in atypical haemolytic uraemic syndrome

Marina Noris et al.

NATURE REVIEWS NEPHROLOGY (2015)

Article Urology & Nephrology

A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome

Carolin E. Sadowski et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2015)

Article Urology & Nephrology

Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults

Veronique Fremeaux-Bacchi et al.

CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2013)

Article Genetics & Heredity

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

Mathieu Lemaire et al.

NATURE GENETICS (2013)

Article Biochemistry & Molecular Biology

WT1 Protein Directly Regulates Expression of Vascular Endothelial Growth Factor and Is a Mediator of Tumor Response to Hypoxia

Gregory McCarty et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2011)

Review Genetics & Heredity

Atypical hemolytic uremic syndrome

Chantal Loirat et al.

ORPHANET JOURNAL OF RARE DISEASES (2011)

Article Urology & Nephrology

Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Gil Chernin et al.

CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2010)

Review Biochemistry & Molecular Biology

Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology

Eduardo Machuca et al.

HUMAN MOLECULAR GENETICS (2009)

Article Transplantation

Thrombotic microangiopathy secondary to VEGF pathway inhibition by sunitinib

Guillaume Bollee et al.

NEPHROLOGY DIALYSIS TRANSPLANTATION (2009)

Article Urology & Nephrology

Impaired glomerular maturation and lack of VEGF165b in Denys-Drash syndrome

Valerie Anne Schumacher et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)

Article Oncology

Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period

T Kind et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2002)

Article Pediatrics

Hemolytic uremic syndrome associated with Denys-Drash syndrome

JR Sherbotie et al.

PEDIATRIC NEPHROLOGY (2000)