UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 185

Sortiert nach

Alport syndrome: its effects on the glomerular filtration barrier and implications for future treatment

The Journal of physiology, 2014-09, Vol.592 (18), p.4013-4023

Savige, Judy

2014

Link zum Volltext

Verfügbarkeit prüfen

Retinal small vessel dilatation in the systemic inflammatory response to surgery

Scientific reports, 2022-08, Vol.12 (1), p.13291-13291, Article 13291

2022

Link zum Volltext

Verfügbarkeit prüfen

Alport Syndrome in Women and Girls

Clinical journal of the American Society of Nephrology, 2016-09, Vol.11 (9), p.1713-1720

2016

Link zum Volltext

Verfügbarkeit prüfen

Tips for Testing Adults With Suspected Genetic Kidney Disease

American journal of kidney diseases, 2023-12

Savige, Judy

2023

Link zum Volltext

Verfügbarkeit prüfen

Obstructive sleep apnea, chronic obstructive pulmonary disease and hypertensive microvascular disease: a cross-sectional observational cohort study

Scientific reports, 2022-08, Vol.12 (1), p.13350-13350, Article 13350

2022

Link zum Volltext

Verfügbarkeit prüfen

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

European journal of human genetics : EJHG, 2021-08, Vol.29 (8), p.1186-1197

2021

Link zum Volltext

Verfügbarkeit prüfen

What patients want to know about genetic testing for kidney disease

Frontiers in medicine, 2023-06, Vol.10, p.1201712-1201712

2023

Link zum Volltext

Verfügbarkeit prüfen

Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review

American journal of kidney diseases, 2021-12, Vol.78 (6), p.857-864

2021

Link zum Volltext

Verfügbarkeit prüfen

Increased retinal drusen in IgA glomerulonephritis are further evidence for complement activation in disease pathogenesis

Scientific reports, 2022-10, Vol.12 (1), p.18301-18301, Article 18301

2022

Link zum Volltext

Verfügbarkeit prüfen

Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members

Pediatric nephrology (Berlin, West), 2020, Vol.35 (1), p.59-66

Savige, Judy

2020

Link zum Volltext

Verfügbarkeit prüfen

Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement activation in disease pathogenesis

Scientific reports, 2022-05, Vol.12 (1), p.8234-8234, Article 8234

2022

Link zum Volltext

Verfügbarkeit prüfen

Genotype-Phenotype Correlations for Pathogenic COL4A3-COL4A5 Variants in X-Linked, Autosomal Recessive, and Autosomal Dominant Alport Syndrome

Frontiers in medicine, 2022-05, Vol.9, p.865034-865034

2022

Link zum Volltext

Verfügbarkeit prüfen

Microvascular retinopathy and angiographically-demonstrated coronary artery disease: A cross-sectional, observational study

PloS one, 2018-05, Vol.13 (5), p.e0192350-e0192350

2018

Link zum Volltext

Verfügbarkeit prüfen

The 2019 and 2021 International Workshops on Alport Syndrome

European journal of human genetics : EJHG, 2022-05, Vol.30 (5), p.507-516

2022

Link zum Volltext

Verfügbarkeit prüfen

Increased retinal venular calibre in acute infections

Scientific reports, 2021-08, Vol.11 (1), p.17280-17280, Article 17280

2021

Link zum Volltext

Verfügbarkeit prüfen

Alport Syndrome With Kidney Cysts Is Still Alport Syndrome

Kidney international reports, 2022-02, Vol.7 (2), p.339-342

2022

Link zum Volltext

Verfügbarkeit prüfen

Microvascular narrowing and BP monitoring: A single centre observational study

PloS one, 2019-03, Vol.14 (3), p.e0210625-e0210625

2019

Link zum Volltext

Verfügbarkeit prüfen

Editorial: Collagen IV nephropathies: Alport syndrome and beyond

Frontiers in medicine, 2022-09, Vol.9, p.1039949-1039949

2022

Link zum Volltext

Verfügbarkeit prüfen

Retinal small vessel narrowing in women with gestational diabetes, pregnancy-associated hypertension, or small-for-gestational age babies

Frontiers in medicine, 2023-10, Vol.10, p.1265555-1265555

2023

Link zum Volltext

Verfügbarkeit prüfen

Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?

Kidney international reports, 2018-11, Vol.3 (6), p.1239-1241

Savige, Judy

2018

Link zum Volltext

Verfügbarkeit prüfen

A further genetic cause of thin basement membrane nephropathy

Nephrology, dialysis, transplantation, 2016-11, Vol.31 (11), p.1758-1760

Savige, Judy

2016

Link zum Volltext

Verfügbarkeit prüfen

Clinical and genetic features in autosomal recessive and X-linked Alport syndrome

Pediatric nephrology (Berlin, West), 2014-03, Vol.29 (3), p.391-396

2014

Link zum Volltext

Verfügbarkeit prüfen

Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice

Genes, 2023-08, Vol.14 (9), p.1686

2023

Link zum Volltext

Verfügbarkeit prüfen

Retinal Basement Membrane Abnormalities and the Retinopathy of Alport Syndrome

Investigative ophthalmology & visual science, 2010-03, Vol.51 (3), p.1621

2010

Link zum Volltext

Verfügbarkeit prüfen

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Polycystic Liver Disease

Seminars in nephrology, 2015-11, Vol.35 (6), p.618-622.e5

2015

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 185

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(167)
Mit Volltextzugriff
(161)

Publikationsform

Sprache

Englisch
(185)
Japanisch
(22)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Alport syndrome: its effects on the glomerular filtration barrier and implications for future treatment

Retinal small vessel dilatation in the systemic inflammatory response to surgery

Alport Syndrome in Women and Girls

Tips for Testing Adults With Suspected Genetic Kidney Disease

Obstructive sleep apnea, chronic obstructive pulmonary disease and hypertensive microvascular disease: a cross-sectional observational cohort study

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

What patients want to know about genetic testing for kidney disease

Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review

Increased retinal drusen in IgA glomerulonephritis are further evidence for complement activation in disease pathogenesis

Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members

Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement activation in disease pathogenesis

Genotype-Phenotype Correlations for Pathogenic COL4A3-COL4A5 Variants in X-Linked, Autosomal Recessive, and Autosomal Dominant Alport Syndrome

Microvascular retinopathy and angiographically-demonstrated coronary artery disease: A cross-sectional, observational study

The 2019 and 2021 International Workshops on Alport Syndrome

Increased retinal venular calibre in acute infections

Alport Syndrome With Kidney Cysts Is Still Alport Syndrome

Microvascular narrowing and BP monitoring: A single centre observational study

Editorial: Collagen IV nephropathies: Alport syndrome and beyond

Retinal small vessel narrowing in women with gestational diabetes, pregnancy-associated hypertension, or small-for-gestational age babies

Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?

A further genetic cause of thin basement membrane nephropathy

Clinical and genetic features in autosomal recessive and X-linked Alport syndrome

Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice

Retinal Basement Membrane Abnormalities and the Retinopathy of Alport Syndrome

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Polycystic Liver Disease

Suchergebnisse filtern