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miR-182, miR-221 and miR-222 are potential urinary extracellular vesicle biomarkers for canine urothelial carcinoma

Scientific reports, 2024-08, Vol.14 (1), p.17967-11, Article 17967

2024

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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

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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

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

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

2022

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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

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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

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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

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SO090EVALUATING PAIN IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

Nephrology, dialysis, transplantation, 2020-06, Vol.35 (Supplement_3)

2020

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SAT-224 Recurrent Co-Driver Mutation in CTNNB1-Mutant Aldosterone-producing Adenomas (APA), Causing Reversible Hypertension in Puberty, Pregnancy or Menopause

Journal of the Endocrine Society, 2020-05, Vol.4 (Supplement_1)

2020

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Making urinary extracellular vesicles a clinically tractable source of biomarkers for inherited tubulopathies using a small volume precipitation method: proof of concept

Journal of nephrology, 2020-04, Vol.33 (2), p.383-386

2020

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Correction to: Making urinary extracellular vesicles a clinically tractable source of biomarkers for inherited tubulopathies using a small volume precipitation method: proof of concept

Journal of nephrology, 2020-04, Vol.33 (2), p.391-391

2020

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FP049SELF-MONITORING OF URINE SPECIFIC GRAVITY USING STUDY SMARTPHONE APPLICATIONS PROMOTES ADHERENCE TO HIGH WATER THERAPY AND FACILITATES REMOTE DATA CAPTURE IN THE DRINK RANDOMISED TRIAL

Nephrology, dialysis, transplantation, 2019-06, Vol.34 (Supplement_1)

2019

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A renal genetics clinic – model for our times

Clinical medicine (London, England), 2019-03, Vol.19 (2), p.s140-s141

2019

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Evaluation of support events for individuals with Gitelman/Bartter syndromes and their families: participant feedback and reflections

Clinical medicine (London, England), 2019-03, Vol.19 (2), p.s142-s142

2019

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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

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FP059A RETROSPECTIVE STUDY ASSESSSING THE EFFECT OF HIGH WATER INTAKE ADVICE ON URINE SPECIFIC GRAVITY IN POLYCYSTIC KIDNEY DISEASE

Nephrology, dialysis, transplantation, 2018-05, Vol.33 (suppl_1), p.i67-i67

2018

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Patient Survey of current water Intake practices in autosomal dominant Polycystic kidney disease: the SIPs survey

Clinical kidney journal, 2017-06, Vol.10 (3), p.305-309

2017

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

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

2017

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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

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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

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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

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The importance of being rare

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

Frankl, Fiona E Karet, Prof

2016

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Extra-renal locations of the a4 subunit of H(+)ATPase

BMC cell biology, 2016-07, Vol.17 (1), p.27

2016

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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

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miR-182, miR-221 and miR-222 are potential urinary extracellular vesicle biomarkers for canine urothelial carcinoma

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

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

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

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

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

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

SO090EVALUATING PAIN IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

SAT-224 Recurrent Co-Driver Mutation in CTNNB1-Mutant Aldosterone-producing Adenomas (APA), Causing Reversible Hypertension in Puberty, Pregnancy or Menopause

Making urinary extracellular vesicles a clinically tractable source of biomarkers for inherited tubulopathies using a small volume precipitation method: proof of concept

Correction to: Making urinary extracellular vesicles a clinically tractable source of biomarkers for inherited tubulopathies using a small volume precipitation method: proof of concept

FP049SELF-MONITORING OF URINE SPECIFIC GRAVITY USING STUDY SMARTPHONE APPLICATIONS PROMOTES ADHERENCE TO HIGH WATER THERAPY AND FACILITATES REMOTE DATA CAPTURE IN THE DRINK RANDOMISED TRIAL

A renal genetics clinic – model for our times

Evaluation of support events for individuals with Gitelman/Bartter syndromes and their families: participant feedback and reflections

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

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

FP059A RETROSPECTIVE STUDY ASSESSSING THE EFFECT OF HIGH WATER INTAKE ADVICE ON URINE SPECIFIC GRAVITY IN POLYCYSTIC KIDNEY DISEASE

Patient Survey of current water Intake practices in autosomal dominant Polycystic kidney disease: the SIPs survey

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

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

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

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

The importance of being rare

Extra-renal locations of the a4 subunit of H(+)ATPase

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

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