UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Kidney international, 2017-01, Vol.91 (1), p.24-33

2017

Volltextzugriff (PDF)

Urinary Exosomes Contain MicroRNAs Capable of Paracrine Modulation of Tubular Transporters in Kidney

Scientific reports, 2017-01, Vol.7 (1), p.40601, Article 40601

2017

Volltextzugriff (PDF)

Pregnancy, Primary Aldosteronism, and Adrenal CTNNB1 Mutations

The New England journal of medicine, 2015-10, Vol.373 (15), p.1429-1436

2015

Volltextzugriff (PDF)

Neutrophil extracellular traps protect the kidney from ascending infection and are required for a positive leukocyte dipstick test

Science translational medicine, 2024-09, Vol.16 (766), p.eadh5090

2024

Volltextzugriff (PDF)

Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype

Proceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (34), p.13775-13780

2012

Volltextzugriff (PDF)

The importance of being rare

The Lancet (British edition), 2016-08, Vol.388 (10044), p.632-632

Frankl, Fiona E Karet, Prof

2016

Volltextzugriff (PDF)

PDLIM5 links kidney anion exchanger 1 (kAE1) to ILK and is required for membrane targeting of kAE1

Scientific reports, 2017-01, Vol.7 (1), p.39701-39701, Article 39701

2017

Volltextzugriff (PDF)

Excretory-secretory products from the brown stomach worm, Teladorsagia circumcincta, exert antimicrobial activity in in vitro growth assays

Parasites & vectors, 2022-10, Vol.15 (1), p.1-354, Article 354

2022

Volltextzugriff (PDF)

HYDROchlorothiazide versus placebo to PROTECT polycystic kidney disease patients and improve their quality of life: study protocol and rationale for the HYDRO-PROTECT randomized controlled trial

Trials, 2024-02, Vol.25 (1), p.120-120, Article 120

2024

Volltextzugriff (PDF)

Mutation Conferring Apical-Targeting Motif on AE1 Exchanger Causes Autosomal Dominant Distal RTA

Journal of the American Society of Nephrology, 2012-07, Vol.23 (7), p.1238-1249

2012

Volltextzugriff (PDF)

Human Urinary Exosomes as Innate Immune Effectors

Journal of the American Society of Nephrology, 2014-09, Vol.25 (9), p.2017-2027

2014

Volltextzugriff (PDF)

Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause

Nature genetics, 2021-09, Vol.53 (9), p.1360-1372

2021

Volltextzugriff (PDF)

Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear

Disease models & mechanisms, 2013-03, Vol.6 (2), p.434-442

2013

Volltextzugriff (PDF)

Magnesium lactate in the treatment of Gitelman syndrome: patient-reported outcomes

Nephrology, dialysis, transplantation, 2017-03, Vol.32 (3), p.508-512

2017

Volltextzugriff (PDF)

Characterization of a Recurrent In-frame UMOD Indel Mutation Causing Late-onset Autosomal Dominant End-Stage Renal Failure

Clinical journal of the American Society of Nephrology, 2011-12, Vol.6 (12), p.2766-2774

2011

Volltextzugriff (PDF)

Unexpected clinical sequelae of Gitelman syndrome: hypertension in adulthood is common and females have higher potassium requirements

Nephrology, dialysis, transplantation, 2013-06, Vol.28 (6), p.1533-1542

2013

Volltextzugriff (PDF)

Size-Exclusion Chromatography Separation Reveals That Vesicular and Non-Vesicular Small RNA Profiles Differ in Cell Free Urine

International journal of molecular sciences, 2021-05, Vol.22 (9), p.4881

2021

Volltextzugriff (PDF)

Point-of-care and self-testing for potassium: recent advances

Sensors & diagnostics, 2022-07, Vol.1 (4), p.614-626

2022

Volltextzugriff (PDF)

Renal peroxiredoxin 6 interacts with anion exchanger 1 and plays a novel role in pH homeostasis

Kidney international, 2016-01, Vol.89 (1), p.105-112

2016

Volltextzugriff (PDF)

To be or not to be

Postgraduate medical journal, 2016-10, Vol.92 (1092), p.569-570

Karet Frankl, Fiona E

2016

Volltextzugriff (PDF)

Developing a patient-centred tool for pain measurement and evaluation in autosomal dominant polycystic kidney disease

Clinical kidney journal, 2021-11, Vol.14 (11), p.2338-2348

2021

Volltextzugriff (PDF)

Randomised controlled trial of high versus ad libitum water intake in patients with autosomal dominant polycystic kidney disease: rationale and design of the DRINK feasibility trial

BMJ open, 2018-05, Vol.8 (5), p.e022859-e022859

2018

Volltextzugriff (PDF)

Accuracy of urine pH testing in a regional metabolic renal clinic: is the dipstick accurate enough?

Urolithiasis, 2013-04, Vol.41 (2), p.129-132

2013

Volltextzugriff (PDF)

Clinical utility of PKD2 mutation testing in a polycystic kidney disease cohort attending a specialist nephrology out-patient clinic

BMC nephrology, 2012-08, Vol.13 (1), p.79-79, Article 79

2012

Volltextzugriff (PDF)

1 – 25 von 39

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(31)

Publikationsform

Artikel
(39)

Sprache

Englisch
(39)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Urinary Exosomes Contain MicroRNAs Capable of Paracrine Modulation of Tubular Transporters in Kidney

Pregnancy, Primary Aldosteronism, and Adrenal CTNNB1 Mutations

Neutrophil extracellular traps protect the kidney from ascending infection and are required for a positive leukocyte dipstick test

Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype

The importance of being rare

PDLIM5 links kidney anion exchanger 1 (kAE1) to ILK and is required for membrane targeting of kAE1

Excretory-secretory products from the brown stomach worm, Teladorsagia circumcincta, exert antimicrobial activity in in vitro growth assays

HYDROchlorothiazide versus placebo to PROTECT polycystic kidney disease patients and improve their quality of life: study protocol and rationale for the HYDRO-PROTECT randomized controlled trial

Mutation Conferring Apical-Targeting Motif on AE1 Exchanger Causes Autosomal Dominant Distal RTA

Human Urinary Exosomes as Innate Immune Effectors

Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause

Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear

Magnesium lactate in the treatment of Gitelman syndrome: patient-reported outcomes

Characterization of a Recurrent In-frame UMOD Indel Mutation Causing Late-onset Autosomal Dominant End-Stage Renal Failure

Unexpected clinical sequelae of Gitelman syndrome: hypertension in adulthood is common and females have higher potassium requirements

Size-Exclusion Chromatography Separation Reveals That Vesicular and Non-Vesicular Small RNA Profiles Differ in Cell Free Urine

Point-of-care and self-testing for potassium: recent advances

Renal peroxiredoxin 6 interacts with anion exchanger 1 and plays a novel role in pH homeostasis

To be or not to be

Developing a patient-centred tool for pain measurement and evaluation in autosomal dominant polycystic kidney disease

Randomised controlled trial of high versus ad libitum water intake in patients with autosomal dominant polycystic kidney disease: rationale and design of the DRINK feasibility trial

Accuracy of urine pH testing in a regional metabolic renal clinic: is the dipstick accurate enough?

Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism

Clinical utility of PKD2 mutation testing in a polycystic kidney disease cohort attending a specialist nephrology out-patient clinic

Suchergebnisse filtern