Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
346 14 |
Ultima descărcare din IBN: 2024-04-27 13:56 |
SM ISO690:2012 ŢÎBULEAC, Sava. Hiperbilirubinemiile ereditare: diagnosticul diferenţial, tratamentul. In: Curierul Medical, 2008, nr. 4(304), pp. 70-73. ISSN 1875-0666. |
EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
Curierul Medical | ||||||
Numărul 4(304) / 2008 / ISSN 1875-0666 | ||||||
|
||||||
Pag. 70-73 | ||||||
|
||||||
Descarcă PDF | ||||||
Rezumat | ||||||
The author presents bibliographic data on general description, diagnosis, differential diagnosis and treatment of hereditarily jaundice: CriglerNajjar syndrome type I, Crigler-Najjar syndrome type II, Jilbert syndrome, Dubin-Jhonson syndrome and Rotor syndrome. |
||||||
Cuvinte-cheie hereditary, hyperbilirubinemy, наследственные желтухи, диагностика, лечение |
||||||
|
Google Scholar Export
<meta name="citation_title" content="Hiperbilirubinemiile ereditare: diagnosticul diferenţial, tratamentul"> <meta name="citation_author" content="Ţîbuleac Sava"> <meta name="citation_publication_date" content="2008/08/01"> <meta name="citation_journal_title" content="Curierul Medical"> <meta name="citation_volume" content="304"> <meta name="citation_issue" content="4"> <meta name="citation_firstpage" content="70"> <meta name="citation_lastpage" content="73"> <meta name="citation_pdf_url" content="https://ibn.idsi.md/sites/default/files/imag_file/70_73_Hiperbilirubinemiile%20ereditare_diagnostic%20diferential%2C%20tratament.pdf">