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

Por Sayer, John A
Publicado em 2006

Progress in Understanding the Genetics of Calcium-Containing Nephrolithiasis

Por Sayer, John A.
Publicado no J Am Soc Nephrol (2017)

Multiple thyroid cysts as an extra-renal manifestation of ADPKD

Por Alejmi, Abdulfattah, Sayer, John A.
Publicado no NDT Plus (2008)

Nephronophthisis

Por Srivastava, Shalabh, Sayer, John A.
Publicado no J Pediatr Genet (2014)

Case Report: Cervical chondrocalcinosis as a complication of Gitelman syndrome

Por Iqbal, Zahra, Mead, Paul, Sayer, John A.
Publicado no F1000Res (2016)

Nephronophthisis

Por Simms, Roslyn J, Eley, Lorraine, Sayer, John A
Publicado em 2009

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

Por Wong, Edwin K.S., Husain, Akhtar, Sayer, John A.
Publicado no Oxf Med Case Reports (2014)

Nephronophthisis: A Genetically Diverse Ciliopathy

Por Simms, Roslyn J., Hynes, Ann Marie, Eley, Lorraine, Sayer, John A.
Publicado em 2011

Emphysematous pyelonephritis leading to end-stage renal failure

Por Simms, Roslyn, Torpey, Nicholas, Kanagasundaram, Nigel S., Baines, Laura, Sayer, John A.
Publicado no NDT Plus (2008)

Yersinia pseudotuberculosis aortitis in a patient with diverticulosis and polycystic kidney disease

Por McCloskey, Sarah, Haslam, Philip, Price, David A., Sayer, John A.
Publicado no Oxf Med Case Reports (2015)

A novel mutation in NPHS2 causing nephrotic syndrome in a Saudi Arabian family

Por Al-Hamed, Mohamed, Sayer, John A., Al-Hassoun, Ibrahim, Aldahmesh, Mohamed A., Meyer, Brian
Publicado no NDT Plus (2010)

A novel CLDN16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis

Por Deeb, Asma, Abood, Salima Atia, Simon, Job, Dastoor, Hormazdiar, Pearce, Simon HS, Sayer, John A
Publicado em 2013

A wide spectrum of phenotypes in a family with renal coloboma syndrome caused by a PAX2 mutation

Por Adam, Jennifer, Browning, Andrew C., Vaideanu, Daniela, Heidet, Laurence, Goodship, Judith A., Sayer, John A.
Publicado no Clin Kidney J (2013)

Renal tubular dysgenesis: antenatal ultrasound scanning and molecular investigations in a Saudi Arabian family

Por Al-Hamed, Mohamed H., Kurdi, Wesam, Alsahan, Nada, Ambosaidi, Qaamariya, Tulbah, Maha, Sayer, John A.
Publicado no Clin Kidney J (2016)

Successful treatment of hypercalcaemia associated with a CYP24A1 mutation with fluconazole

Por Sayers, Judith, Hynes, Ann Marie, Srivastava, Shalabh, Dowen, Frances, Quinton, Richard, Datta, Harish K., Sayer, John A.
Publicado no Clin Kidney J (2015)

Genetic testing can resolve diagnostic confusion in Alport syndrome

Por Adam, Jennifer, Connor, Thomas M. F., Wood, Katrina, Lewis, David, Naik, Ramesh, Gale, Daniel P., Sayer, John A.
Publicado em 2014

Senior-Loken syndrome secondary to NPHP5/IQCB1 mutation in an Iranian family

Por Haghighi, Alireza, Al-Hamed, Mohamed, Al-Hissi, Safa, Hynes, Ann-Marie, Sharifian, Maryam, Roozbeh, Jamshid, Saleh-Gohari, Nasrollah, Sayer, John A.
Publicado no NDT Plus (2011)

Clinical and Functional Characterization of URAT1 Variants

Por Tasic, Velibor, Hynes, Ann Marie, Kitamura, Kenichiro, Cheong, Hae Il, Lozanovski, Vladimir J., Gucev, Zoran, Jutabha, Promsuk, Anzai, Naohiko, Sayer, John A.
Publicado em 2011

Autosomal Dominant Mutation in the Signal Peptide of Renin in a Kindred with Anemia, Hyperuricemia, and CKD

Por Beck, Bodo B., Trachtman, Howard, Gitman, Michael, Miller, Ilene, Sayer, John A., Pannes, Andrea, Baasner, Anne, Hildebrandt, Friedhelm, Wolf, Matthias T.F.
Publicado em 2011

Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case report

Por Montgomery, Emma, Sayer, John A., Baines, Laura A., Hynes, Ann Marie, Vega-Warner, Virginia, Johnson, Sally, Goodship, Judith A., Otto, Edgar A.
Publicado no BMC Med Genet (2015)