UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision

Journal of inherited metabolic disease, 2019-11, Vol.42 (6), p.1192-1230

2019

Link zum Volltext

Verfügbarkeit prüfen

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

Clinical journal of the American Society of Nephrology, 2013-04, Vol.8 (4), p.554-562

2013

Link zum Volltext

Verfügbarkeit prüfen

Suggested guidelines for the diagnosis and management of urea cycle disorders

Orphanet journal of rare diseases, 2012-05, Vol.7 (1), p.32-32

2012

Link zum Volltext

Verfügbarkeit prüfen

Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation

Clinical journal of the American Society of Nephrology, 2017-01, Vol.12 (1), p.50-59

2017

Link zum Volltext

Verfügbarkeit prüfen

Preemptive rituximab infusions after remission efficiently prevent relapses in acquired thrombotic thrombocytopenic purpura

Blood, 2014-07, Vol.124 (2), p.204-210

2014

Link zum Volltext

Verfügbarkeit prüfen

Complement receptor CD46 co-stimulates optimal human CD8 + T cell effector function via fatty acid metabolism

Nature communications, 2018-10, Vol.9 (1), p.4186-15, Article 4186

2018

Link zum Volltext

Verfügbarkeit prüfen

Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults

Kidney international, 2012-01, Vol.81 (2), p.179-189

2012

Link zum Volltext

Verfügbarkeit prüfen

Clinical and histological differences between adults and children in new onset IgA nephropathy

Pediatric nephrology (Berlin, West), 2020-10, Vol.35 (10), p.1897-1905

2020

Link zum Volltext

Verfügbarkeit prüfen

Increased risk of solid renal tumors in lithium-treated patients

Kidney international, 2014-07, Vol.86 (1), p.184-190

2014

Link zum Volltext

Verfügbarkeit prüfen

Long-term renal outcome in methylmalonic acidemia in adolescents and adults

Orphanet journal of rare diseases, 2021-05, Vol.16 (1), p.220-220, Article 220

2021

Link zum Volltext

Verfügbarkeit prüfen

Cystinosis: a rare multisystem disease

Polskie archiwum medycyny wewne̦trznej, 2022-11, Vol.132 (11)

Servais, Aude

2022

Link zum Volltext

Verfügbarkeit prüfen

Risk Factors for Autoimmune Diseases Development After Thrombotic Thrombocytopenic Purpura

Medicine (Baltimore), 2015-10, Vol.94 (42), p.e1598-e1598

2015

Link zum Volltext

Verfügbarkeit prüfen

Hemodialysis without systemic anticoagulation: a prospective randomized trial to evaluate 3 strategies in patients at risk of bleeding

PloS one, 2014-05, Vol.9 (5), p.e97187-e97187

2014

Link zum Volltext

Verfügbarkeit prüfen

Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients

Orphanet journal of rare diseases, 2015-05, Vol.10 (1), p.58-58, Article 58

2015

Link zum Volltext

Verfügbarkeit prüfen

Central Nervous System Complications in Cystinosis: The Role of Neuroimaging

Cells (Basel, Switzerland), 2022-02, Vol.11 (4), p.682

2022

Link zum Volltext

Verfügbarkeit prüfen

Predictive features of chronic kidney disease in atypical haemolytic uremic syndrome

PloS one, 2017-05, Vol.12 (5), p.e0177894-e0177894

2017

Link zum Volltext

Verfügbarkeit prüfen

Intravenous administration of a branched-chain amino-acid-free solution in children and adults with acute decompensation of maple syrup urine disease: a prospective multicentre observational study

Orphanet journal of rare diseases, 2022-05, Vol.17 (1), p.202-202, Article 202

2022

Link zum Volltext

Verfügbarkeit prüfen

Biopsy-proven kidney involvement in hypocomplementemic urticarial vasculitis

BMC nephrology, 2022-02, Vol.23 (1), p.67-67, Article 67

2022

Link zum Volltext

Verfügbarkeit prüfen

Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort

Molecular genetics and metabolism reports, 2020-06, Vol.23, p.100581, Article 100581

2020

Link zum Volltext

Verfügbarkeit prüfen

Response to Cysteamine in Osteoclasts Obtained from Patients with Nephropathic Cystinosis: A Genotype/Phenotype Correlation

Cells (Basel, Switzerland), 2021-09, Vol.10 (9), p.2498

2021

Link zum Volltext

Verfügbarkeit prüfen

Is Serum Cystatin-C a Reliable Marker for Metabolic Syndrome?

The American journal of medicine, 2008-05, Vol.121 (5), p.426-432

2008

Link zum Volltext

Verfügbarkeit prüfen

Hereditary Podocytopathies in Adults: The Next Generation

Kidney diseases, 2017-07, Vol.3 (2), p.50-56

2017

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 173

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(161)
Mit Volltextzugriff
(156)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision

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

Suggested guidelines for the diagnosis and management of urea cycle disorders

Preemptive rituximab prevents long-term relapses in immune-mediated thrombotic thrombocytopenic purpura

Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation

Preemptive rituximab infusions after remission efficiently prevent relapses in acquired thrombotic thrombocytopenic purpura

Complement receptor CD46 co-stimulates optimal human CD8 + T cell effector function via fatty acid metabolism

Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults

Immune thrombotic thrombocytopenic purpura in older patients: prognosis and long-term survival

Clinical and histological differences between adults and children in new onset IgA nephropathy

Increased risk of solid renal tumors in lithium-treated patients

Long-term renal outcome in methylmalonic acidemia in adolescents and adults

Cystinosis: a rare multisystem disease

Risk Factors for Autoimmune Diseases Development After Thrombotic Thrombocytopenic Purpura

Hemodialysis without systemic anticoagulation: a prospective randomized trial to evaluate 3 strategies in patients at risk of bleeding

Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients

Insights From the Use in Clinical Practice of Eculizumab in Adult Patients With Atypical Hemolytic Uremic Syndrome Affecting the Native Kidneys: An Analysis of 19 Cases

Central Nervous System Complications in Cystinosis: The Role of Neuroimaging

Predictive features of chronic kidney disease in atypical haemolytic uremic syndrome

Intravenous administration of a branched-chain amino-acid-free solution in children and adults with acute decompensation of maple syrup urine disease: a prospective multicentre observational study

Biopsy-proven kidney involvement in hypocomplementemic urticarial vasculitis

Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort

Response to Cysteamine in Osteoclasts Obtained from Patients with Nephropathic Cystinosis: A Genotype/Phenotype Correlation

Is Serum Cystatin-C a Reliable Marker for Metabolic Syndrome?

Hereditary Podocytopathies in Adults: The Next Generation

Suchergebnisse filtern