Acute renal failure from contrast medium: Beware patients taking metformin...

od Sayer, John A
Izdano 2006

Progress in Understanding the Genetics of Calcium-Containing Nephrolithiasis

od Sayer, John A.
Izdano u J Am Soc Nephrol (2017)

Multiple thyroid cysts as an extra-renal manifestation of ADPKD

od Alejmi, Abdulfattah, Sayer, John A.
Izdano u NDT Plus (2008)

Nephronophthisis

od Srivastava, Shalabh, Sayer, John A.
Izdano u J Pediatr Genet (2014)

Case Report: Making a diagnosis of familial renal disease – clinical and patient perspectives

od Iqbal, Zahra, Sayer, John A.
Izdano u F1000Res (2017)

Precision medicine in renal stone-formers

od Hill, Fay, Sayer, John A.
Izdano u Urolithiasis (2018)

CYP24A1 mutations and hypervitaminosis D

od Willows, Jamie, Sayer, John A
Izdano u Clin Med (Lond) (2019)

The Molecular Genetics of Gordon Syndrome

od Mabillard, Holly, Sayer, John A.
Izdano u Genes (Basel) (2019)

Disease Modeling To Understand the Pathomechanisms of Human Genetic Kidney Disorders

od Molinari, Elisa, Sayer, John A.
Izdano u Clin J Am Soc Nephrol (2020)

Electrolyte Disturbances in SARS-CoV-2 Infection

od Mabillard, Holly, Sayer, John A.
Izdano u F1000Res (2020)

Nephrocalcinosis: A Review of Monogenic Causes and Insights They Provide into This Heterogeneous Condition

od Dickson, Fay J., Sayer, John A.
Izdano u Int J Mol Sci (2020)

Case Report: Cervical chondrocalcinosis as a complication of Gitelman syndrome

od Iqbal, Zahra, Mead, Paul, Sayer, John A.
Izdano u F1000Res (2016)

Nephronophthisis

od Simms, Roslyn J, Eley, Lorraine, Sayer, John A
Izdano 2009

Sarcoidosis presenting with hypercalcaemia following withdrawal of long-term immunosuppression in renal transplantation

od Wong, Edwin K.S., Husain, Akhtar, Sayer, John A.
Izdano u Oxf Med Case Reports (2014)

Practical approaches to the management of autosomal dominant polycystic kidney disease patients in the era of tolvaptan

od Müller, Roman-Ulrich, Haas, Christian S, Sayer, John A
Izdano u Clin Kidney J (2018)

Variable phenotypic presentations of renal involvement in Fabry disease: a case series

od McCloskey, Sarah, Brennan, Paul, Sayer, John A
Izdano u F1000Res (2018)

Many Genes—One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders

od Srivastava, Shalabh, Molinari, Elisa, Raman, Shreya, Sayer, John A.
Izdano u Front Pediatr (2018)

From disease modelling to personalised therapy in patients with CEP290 mutations

od Molinari, Elisa, Srivastava, Shalabh, Sayer, John A., Ramsbottom, Simon A.
Izdano u F1000Res (2017)

Use of patient derived urine renal epithelial cells to confirm pathogenicity of PKHD1 alleles

od Molinari, Elisa, Srivastava, Shalabh, Dewhurst, Rebecca M., Sayer, John A.
Izdano u BMC Nephrol (2020)

ARL3, a small GTPase with a functionally conserved role in primary cilia and immune synapses

od Powell, Laura, Samarakoon, Youhani H., Ismail, Shehab, Sayer, John A.
Izdano u Small GTPases (2019)