Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Juliana C. Sarubi"'
Autor:
Eitan Friedman, Juliana C. Sarubi, Daniela R. Faria, Catarina B. D’Alva, Luiz De Marco, Bernardo Léo Wajchenberg, W. L. Boson
Publikováno v:
Clinical Endocrinology. 58:108-110
Familial neurohypophysial diabetes insipidus (FNDI) is a rare autosomal dominant syndrome stemming from the absence of arginine vasopressin (AVP). More than thirty-five different germline mutations in the arginine vasopressin-neurophysin II gene have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0aa524490ebd1f12fb2810d2af86c446
https://doi.org/10.1046/j.1365-2265.2003.01667.x
https://doi.org/10.1046/j.1365-2265.2003.01667.x
Autor:
Wolfanga L, Boson, Juliana C, Sarubi, Catarina B, d'Alva, Eitan, Friedman, Daniela, Faria, Luiz, De Marco, Bernardo, Wajchenberg
Publikováno v:
Clinical endocrinology. 58(1)
Familial neurohypophysial diabetes insipidus (FNDI) is a rare autosomal dominant syndrome stemming from the absence of arginine vasopressin (AVP). More than thirty-five different germline mutations in the arginine vasopressin-neurophysin II gene have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3851fb7eb2ef7ba360473c0548b4f33a
https://pubmed.ncbi.nlm.nih.gov/12519420
https://pubmed.ncbi.nlm.nih.gov/12519420