Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Jamie Willows"'
Autor:
Sheikh B. Khalid, Rachel Hung, William Andres Vasquez Espinosa, Nayan Arora, Joel M. Topf, Jamie Willows
Publikováno v:
Kidney Medicine, Vol 5, Iss 4, Pp 100615- (2023)
Externí odkaz:
https://doaj.org/article/232ef76bee3e41288bfd0e868363ae0f
Autor:
Anoushka Krishnan, Cristina Popa, Priyadarshini John, Swapnil Hiremath, Jamie Willows, Jade Teakell
Publikováno v:
Kidney Medicine, Vol 4, Iss 10, Pp 100541- (2022)
Externí odkaz:
https://doaj.org/article/66f6dd8462034882badbfbc025d02458
Autor:
Priyadarshini John, Cristina Popa, Momen Abbasi, Jade Teakell, Swapnil Hiremath, Jamie Willows
Publikováno v:
Kidney Medicine, Vol 4, Iss 8, Pp 100515- (2022)
Externí odkaz:
https://doaj.org/article/372a932f77674d558a79e5678a445136
Publikováno v:
Kidney Medicine, Vol 4, Iss 1, Pp 100352- (2022)
Externí odkaz:
https://doaj.org/article/33e547b8a6dd46bb9001b315da1a7ae3
Autor:
Jamie Willows, Maryam Al Badi, Chloe Richardson, Aisha Al Sinani, Noel Edwards, Sarah Rice, John A. Sayer
Publikováno v:
F1000Research, Vol 8 (2019)
Genetic mutations causing familial hypomagnesaemia syndromes are well-recognised. Affected patients can present with severe symptoms of hypomagnesaemia, such as seizures or cardiac arrhythmia. We report an affected child, from a consanguineous family
Externí odkaz:
https://doaj.org/article/46fce2fed8144670a8b9ebcc9b078149
Publikováno v:
F1000Research, Vol 8 (2019)
Genetic mutations causing familial hypomagnesaemia syndromes are well-recognised. Affected patients can present with severe symptoms of hypomagnesaemia, such as seizures or cardiac arrhythmia. We report an affected child, from a consanguineous family
Externí odkaz:
https://doaj.org/article/7bdc5824a0364e3f841f3d6a90418d5b
Publikováno v:
Kidney Medicine
Kidney Medicine, Vol 4, Iss 1, Pp 100352-(2022)
Kidney Medicine, Vol 4, Iss 1, Pp 100352-(2022)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b175ee92ef3bbba64163806c1c6cbf07
https://pubmed.ncbi.nlm.nih.gov/35072039
https://pubmed.ncbi.nlm.nih.gov/35072039
Publikováno v:
Clinical Kidney Journal
Biopsy-proven acute interstitial nephritis (AIN) secondary to sodium-glucose co-transporter 2 (SGLT2) inhibitors has not been described previously. Here, we report on the management of a patient with severe acute kidney injury that developed 6 weeks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04681ad6ce46d65c59983c45be2b16da
http://europepmc.org/articles/PMC7986450
http://europepmc.org/articles/PMC7986450
Publikováno v:
Clinical Endocrinology. 92:3-10
Gitelman syndrome is an inherited tubulopathy characterized by renal salt wasting from the distal convoluted tubule. Defects in the sodium chloride cotransporter (encoded by SLC12A3) underlie this autosomal recessive condition. This article focuses o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc3d508de5a838e33900a93305506fe
https://doi.org/10.1111/cen.14104
https://doi.org/10.1111/cen.14104
Publikováno v:
Nephrology Dialysis Transplantation. 36
Introduction Acute uric acid nephropathy (UAN) is characterized by acute kidney injury (AKI) due to uric acid crystal precipitation within the distal tubules and collecting ducts. We present a young woman, with a history of hyperuricaemia, who was tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1afb831be0dbcb098a99ff8a88856bd2
https://doi.org/10.1093/ndt/gfab083.0019
https://doi.org/10.1093/ndt/gfab083.0019