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Autor:
Di Candia S. 1, Gessi A. 2, Pepe G. 3, Sogno Valin P. 1, Mangano E. 2, Chiumello G. 1, Gianolli L. 3, Proverbio M.C. 2, Mora S. 4
Publikováno v:
European journal of endocrinology 160 (2009): 1019–1023.
info:cnr-pdr/source/autori:Di Candia S. 1, Gessi A. 2, Pepe G. 3, Sogno Valin P. 1, Mangano E. 2, Chiumello G. 1, Gianolli L. 3, Proverbio M.C. 2, Mora S. 4/titolo:Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography%2FCT in a patient carrying a novel mutation of the HADH gene./doi:/rivista:European journal of endocrinology/anno:2009/pagina_da:1019/pagina_a:1023/intervallo_pagine:1019–1023/volume:160
info:cnr-pdr/source/autori:Di Candia S. 1, Gessi A. 2, Pepe G. 3, Sogno Valin P. 1, Mangano E. 2, Chiumello G. 1, Gianolli L. 3, Proverbio M.C. 2, Mora S. 4/titolo:Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography%2FCT in a patient carrying a novel mutation of the HADH gene./doi:/rivista:European journal of endocrinology/anno:2009/pagina_da:1019/pagina_a:1023/intervallo_pagine:1019–1023/volume:160
OBJECTIVE: Congenital hyperinsulinism is the most common cause of persistent hypoglycemia in infancy (HI), leading to severe neurologic disabilities if not promptly treated. The recent application of positron emission tomography (PET)/computed tomogr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::2e9ffe722237b4715fe0c5bbdf0d6ea7
https://publications.cnr.it/doc/10464
https://publications.cnr.it/doc/10464