UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 65

Sortiert nach

Membranous lupus nephritis secondary to secukinumab therapy: A case report and literature review

Lupus, 2024-05, Vol.33 (6), p.644-649

2024

Link zum Volltext

Verfügbarkeit prüfen

Systematic review and meta-analysis of the clinical features of MGRS

BMC nephrology, 2024-01, Vol.25 (1), p.22-22, Article 22

2024

Link zum Volltext

Verfügbarkeit prüfen

The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T＞C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Journal of Atherosclerosis and Thrombosis, 2018/08/01, Vol.25(8), pp.733-740

2018

Link zum Volltext

Verfügbarkeit prüfen

Reverse complete heart block using transcutaneous pacing and repeated plasmapheresis in a neonate with lupus: a case report

Pediatric rheumatology online journal, 2023-11, Vol.21 (1), p.135-135, Article 135

2023

Link zum Volltext

Verfügbarkeit prüfen

Pembrolizumab induced-C3 glomerulonephritis and RBC cast nephropathy: a case report

BMC nephrology, 2023-05, Vol.24 (1), p.145-145, Article 145

2023

Link zum Volltext

Verfügbarkeit prüfen

Integration of multiomics analysis to reveal the major pathways of vitamin A deficiency aggravates acute respiratory distress syndrome in neonatal rats

Scientific reports, 2023-12, Vol.13 (1), p.22643-22643, Article 22643

2023

Link zum Volltext

Verfügbarkeit prüfen

Discovery of a Chinese Tibetan patient with lipoprotein glomerulopathy due to APOE Osaka/Kurashiki variant

Zhonghua yi xue yi chuan xue za zhi, 2020-02, Vol.37 (2), p.166

2020

Link zum Volltext

Verfügbarkeit prüfen

Regulation of Cholesterol Homeostasis by a Novel Long Non-coding RNA LASER

Scientific reports, 2019-05, Vol.9 (1), p.7693, Article 7693

2019

Link zum Volltext

Verfügbarkeit prüfen

Lipoprotein glomerulopathy induced by ApoE Kyoto mutation in ApoE-deficient mice

Journal of translational medicine, 2021-03, Vol.19 (1), p.97-97, Article 97

2021

Link zum Volltext

Verfügbarkeit prüfen

The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T>C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Journal of Atherosclerosis and Thrombosis, 2018, Vol.25 (8), p.733-740

2018

Link zum Volltext

Verfügbarkeit prüfen

Study of a family affected with focal segmental glomerulosclerosis due to mutation of COL4A5 gene

Zhonghua yi xue yi chuan xue za zhi, 2017-06, Vol.34 (3), p.373

2017

Link zum Volltext

Verfügbarkeit prüfen

Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome

Scientific reports, 2015-11, Vol.5 (1), p.17317-17317, Article 17317

2015

Link zum Volltext

Verfügbarkeit prüfen

Cholesteryl ester transfer protein inhibitors in the treatment of dyslipidemia: a systematic review and meta-analysis

PloS one, 2013-10, Vol.8 (10), p.e77049

2013

Link zum Volltext

Verfügbarkeit prüfen

Myoglobin clearance by continuous venous-venous haemofiltration in rhabdomyolysis with acute kidney injury: A case series

Injury, 2012-05, Vol.43 (5), p.619-623

2012

Link zum Volltext

Verfügbarkeit prüfen

Glycochenodeoxycholate induces rat alveolar epithelial type II cell death and inhibits surfactant secretion in vitro

Free radical biology & medicine, 2012-07, Vol.53 (1), p.122-128

2012

Link zum Volltext

Verfügbarkeit prüfen

Dendritic cells transduced with TEM8 recombinant adenovirus prevents hepatocellular carcinoma angiogenesis and inhibits cells growth

Vaccine, 2010-10, Vol.28 (43), p.7130-7135

2010

Link zum Volltext

Verfügbarkeit prüfen

Mammalian target of rapamycin complex 1 activation in podocytes promotes cellular crescent formation

American journal of physiology. Renal physiology, 2014-11, Vol.307 (9), p.F1023-F1032

2014

Link zum Volltext

Verfügbarkeit prüfen

Unique imaging findings in fibromuscular dysplasia of renal arteries: A case report

Medicine (Baltimore), 2018-11, Vol.97 (46), p.e12815-e12815

2018

Link zum Volltext

Verfügbarkeit prüfen

A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy

Biochemical and biophysical research communications, 2018-11, Vol.506 (3), p.444-449

2018

Link zum Volltext

Verfügbarkeit prüfen

Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease

BMC medical genetics, 2011-12, Vol.12 (1), p.164-164, Article 164

2011

Link zum Volltext

Verfügbarkeit prüfen

A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report

Medicine (Baltimore), 2020-07, Vol.99 (31), p.e21438-e21438

2020

Link zum Volltext

Verfügbarkeit prüfen

Infections in crush syndrome: a retrospective observational study after the Wenchuan earthquake

Emergency medicine journal : EMJ, 2011-01, Vol.28 (1), p.14-17

2011

Link zum Volltext

Verfügbarkeit prüfen

Activation of liver X receptor attenuates endothelin-1 expression in vascular endothelial cells

The international journal of biochemistry & cell biology, 2012-12, Vol.44 (12), p.2299-2307

2012

Link zum Volltext

Verfügbarkeit prüfen

A case of malignant hypertension with thrombotic microangiopathy

Internal medicine journal, 2018-03, Vol.48 (3), p.361-362

2018

Link zum Volltext

Verfügbarkeit prüfen

CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice

Molecular neurobiology, 2024-06

2024

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 65

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(59)

Publikationsform

Artikel
(64)
Berichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Membranous lupus nephritis secondary to secukinumab therapy: A case report and literature review

Systematic review and meta-analysis of the clinical features of MGRS

The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T＞C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Reverse complete heart block using transcutaneous pacing and repeated plasmapheresis in a neonate with lupus: a case report

Pembrolizumab induced-C3 glomerulonephritis and RBC cast nephropathy: a case report

Integration of multiomics analysis to reveal the major pathways of vitamin A deficiency aggravates acute respiratory distress syndrome in neonatal rats

Discovery of a Chinese Tibetan patient with lipoprotein glomerulopathy due to APOE Osaka/Kurashiki variant

Regulation of Cholesterol Homeostasis by a Novel Long Non-coding RNA LASER

Lipoprotein glomerulopathy induced by ApoE Kyoto mutation in ApoE-deficient mice

The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T>C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Study of a family affected with focal segmental glomerulosclerosis due to mutation of COL4A5 gene

Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome

Cholesteryl ester transfer protein inhibitors in the treatment of dyslipidemia: a systematic review and meta-analysis

Myoglobin clearance by continuous venous-venous haemofiltration in rhabdomyolysis with acute kidney injury: A case series

Glycochenodeoxycholate induces rat alveolar epithelial type II cell death and inhibits surfactant secretion in vitro

Dendritic cells transduced with TEM8 recombinant adenovirus prevents hepatocellular carcinoma angiogenesis and inhibits cells growth

Mammalian target of rapamycin complex 1 activation in podocytes promotes cellular crescent formation

Unique imaging findings in fibromuscular dysplasia of renal arteries: A case report

A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy

Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease

A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report

Infections in crush syndrome: a retrospective observational study after the Wenchuan earthquake

Activation of liver X receptor attenuates endothelin-1 expression in vascular endothelial cells

A case of malignant hypertension with thrombotic microangiopathy

CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice

Suchergebnisse filtern