Zobrazeno 1 - 4
of 4
pro vyhledávání: '"L. E. Donovan"'
Publikováno v:
Case Reports in Endocrinology, Vol 2018 (2018)
Background. Classical Wolfram syndrome (WS) is a rare autosomal recessive disorder caused by mutations in WFS1, a gene implicated in endoplasmic reticulum (ER) and mitochondrial function. WS is characterized by insulin-requiring diabetes mellitus and
Externí odkaz:
https://doaj.org/article/dad2381656904fb99c057c9cf9bd4217
Publikováno v:
Case Reports in Endocrinology, Vol 2016 (2016)
Background. Primary hyperparathyroidism (PHPT) and Familial Hypocalciuric Hypercalcemia (FHH) result in different maternal and fetal complications in pregnancy. Calcium to creatinine clearance ratio (CCCR) is commonly used to help distinguish these t
Externí odkaz:
https://doaj.org/article/de5af527c88e485986b6e75ef5250c15
Publikováno v:
Case Reports in Endocrinology, Vol 2018 (2018)
Case Reports in Endocrinology
Case Reports in Endocrinology
Background.Classical Wolfram syndrome (WS) is a rare autosomal recessive disorder caused by mutations inWFS1,a gene implicated in endoplasmic reticulum (ER) and mitochondrial function. WS is characterized by insulin-requiring diabetes mellitus and op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c55f5e0be7f02eb185d34c28480d6b2
https://doaj.org/article/dad2381656904fb99c057c9cf9bd4217
https://doaj.org/article/dad2381656904fb99c057c9cf9bd4217
Autor:
L. E. Donovan
Publikováno v:
Archives of Internal Medicine. 155:181-183
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::111f6f4376df42f6c0256cb614528a24
https://doi.org/10.1001/archinte.155.2.181
https://doi.org/10.1001/archinte.155.2.181