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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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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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Pregnancy, Primary Aldosteronism, and Adrenal CTNNB1 Mutations

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

2015

Volltextzugriff (PDF)

Physical and functional links between anion exchanger-1 and sodium pump

Journal of the American Society of Nephrology, 2015-02, Vol.26 (2), p.400-409

2015

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Human Urinary Exosomes as Innate Immune Effectors

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

2014

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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

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Use of HbA1c in the diagnosis of diabetes mellitus in the UK. The implementation of World Health Organization guidance 2011

Diabetic medicine, 2012-11, Vol.29 (11), p.1350-1357

John, W. G.

2012

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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

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Gitelman syndrome

BMJ. British medical journal (International ed.), 2012-08, Vol.345 (7868), p.46

International edition, 2012

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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)

Developing a strategy for the management of rare diseases

BMJ. British medical journal (International ed.), 2012-06, Vol.344 (7859), p.7

International edition, 2012

Volltextzugriff (PDF)

Gitelman syndrome

BMJ (Online), 2012-05, Vol.344, p.e3590

2012

Volltextzugriff (PDF)

Developing a strategy for the management of rare diseases

BMJ (Online), 2012-04, Vol.344, p.e2417

2012

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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

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

Pregnancy, Primary Aldosteronism, and Adrenal CTNNB1 Mutations

Physical and functional links between anion exchanger-1 and sodium pump

Human Urinary Exosomes as Innate Immune Effectors

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

Use of HbA1c in the diagnosis of diabetes mellitus in the UK. The implementation of World Health Organization guidance 2011

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

Gitelman syndrome

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

Developing a strategy for the management of rare diseases

Gitelman syndrome

Developing a strategy for the management of rare diseases

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