UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 31

Sortiert nach

Macrothrombocytopenia, renal dysfunction and nephrotic syndrome in a young male patient: a case report of MYH9-related disease

Brazilian Journal of Nephrology, 2018-04, Vol.40 (2), p.198-200

2018

Volltextzugriff (PDF)

A case of aquaporin 2 R85X mutation in a boy with congenital nephrogenic diabetes insipidus

Pediatric nephrology (Berlin, West), 2008-04, Vol.23 (4), p.663-665

2008

Volltextzugriff (PDF)

Burosumab treatment in adults with X-linked hypophosphataemia: 96-week patient-reported outcomes and ambulatory function from a randomised phase 3 trial and open-label extension

Rheumatic & musculoskeletal diseases open, 2021-09, Vol.7 (3), p.e001714

2021

Volltextzugriff (PDF)

Features of Autosomal Recessive Alport Syndrome: A Systematic Review

Journal of clinical medicine, 2019-02, Vol.8 (2), p.178

2019

Volltextzugriff (PDF)

Hepatorenal fibrocystic diseases in children

Pediatric nephrology (Berlin, West), 2016-01, Vol.31 (1), p.113-119

2016

Volltextzugriff (PDF)

Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature

Jornal Brasileiro de nefrologia, 2020-10, Vol.42 (4), p.494-497

2020

Volltextzugriff (PDF)

Acute Kidney Injury in Pediatric Cancer Patients

The Journal of pediatrics, 2019-05, Vol.208, p.243-250.e3

2019

Volltextzugriff (PDF)

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

Journal of the American Society of Nephrology, 2017-10, Vol.28 (10), p.3066-3075

2017

Volltextzugriff (PDF)

Dent-2 Disease: A Mild Variant of Lowe Syndrome

The Journal of pediatrics, 2009-07, Vol.155 (1), p.94-99

2009

Volltextzugriff (PDF)

Early recurrent nephrotic syndrome after renal transplantation in children with focal segmental glomerulosclerosis

Nephrology, dialysis, transplantation, 2000-01, Vol.15 (1), p.78-81

2000

Volltextzugriff (PDF)

Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature

Brazilian Journal of Nephrology, 2020-12, Vol.42 (4), p.494-497

2020

Volltextzugriff (PDF)

Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature

Brazilian Journal of Nephrology, 2020-12

2020

Volltextzugriff (PDF)

Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period

JBMR plus, 2024, Vol.8 (1), p.ziad001-ziad001

2024

Volltextzugriff (PDF)

Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney

Pediatric nephrology (Berlin, West), 2015-09, Vol.30 (9), p.1451-1458

2015

Volltextzugriff (PDF)

Clinical Features of Anti-Factor H Autoantibody-Associated Hemolytic Uremic Syndrome

Journal of the American Society of Nephrology, 2010-12, Vol.21 (12), p.2180-2187

2010

Volltextzugriff (PDF)

Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome

Journal of clinical medicine, 2019-04, Vol.8 (4), p.491

2019

Volltextzugriff (PDF)

Translational read-through of a nonsense mutation causing Bartter syndrome

Journal of Korean Medical Science, 2013, 28(6), 177, pp.821-826

2013

Volltextzugriff (PDF)

Clinical features of anti-FH auto antibodies-associated HUS: A typical onset but an atypical outcome

Molecular immunology, 2010-08, Vol.47 (13), p.2214-2214

2010

Volltextzugriff (PDF)

Can liver–kidney transplantation cure aHUS?

Nature reviews. Nephrology, 2009-10, Vol.5 (10), p.556-557

Cheong, Hae Il

2009

Volltextzugriff (PDF)

Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation

Pediatric nephrology (Berlin, West), 1999-08, Vol.13 (6), p.477-480

1999

Volltextzugriff (PDF)

Differential Diagnosis of Hereditary Nephrogenic Diabetes Insipidus with Desmopressin Infusion Test

Indian journal of pediatrics, 2010-11, Vol.77 (11), p.1329-1331

2010

Volltextzugriff (PDF)

Role of Anti-Endothelial Cell Antibody in the Development of Coronary Arterial Lesions in Kawasaki Disease

Korean circulation journal, 2006, Vol.36 (11), p.723

2006

Volltextzugriff (PDF)

A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H

Pediatric nephrology (Berlin, West), 2006-02, Vol.21 (2), p.295-298

2006

Volltextzugriff (PDF)

Glucocorticoid diminishes vascular endothelial growth factor and exacerbates proteinuria in rats with mesangial proliferative glomerulonephritis

American journal of kidney diseases, 2002-05, Vol.39 (5), p.1001-1010

2002

Volltextzugriff (PDF)

1 – 25 von 31

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(31)
Mit Volltextzugriff
(29)

Publikationsform

Artikel
(31)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Macrothrombocytopenia, renal dysfunction and nephrotic syndrome in a young male patient: a case report of MYH9-related disease

A case of aquaporin 2 R85X mutation in a boy with congenital nephrogenic diabetes insipidus

Burosumab treatment in adults with X-linked hypophosphataemia: 96-week patient-reported outcomes and ambulatory function from a randomised phase 3 trial and open-label extension

Features of Autosomal Recessive Alport Syndrome: A Systematic Review

Hepatorenal fibrocystic diseases in children

Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature

Acute Kidney Injury in Pediatric Cancer Patients

Continued Beneficial Effects of Burosumab in Adults with X-Linked Hypophosphatemia: Results from a 24-Week Treatment Continuation Period After a 24-Week Double-Blind Placebo-Controlled Period

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

Dent-2 Disease: A Mild Variant of Lowe Syndrome

Early recurrent nephrotic syndrome after renal transplantation in children with focal segmental glomerulosclerosis

Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature

Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature

Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period

Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney

Clinical Features of Anti-Factor H Autoantibody-Associated Hemolytic Uremic Syndrome

Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome

Translational read-through of a nonsense mutation causing Bartter syndrome

Clinical features of anti-FH auto antibodies-associated HUS: A typical onset but an atypical outcome

Can liver–kidney transplantation cure aHUS?

Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation

Differential Diagnosis of Hereditary Nephrogenic Diabetes Insipidus with Desmopressin Infusion Test

Role of Anti-Endothelial Cell Antibody in the Development of Coronary Arterial Lesions in Kawasaki Disease

A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H

Glucocorticoid diminishes vascular endothelial growth factor and exacerbates proteinuria in rats with mesangial proliferative glomerulonephritis

Suchergebnisse filtern