المؤلفون: Ana Šmaguc, Danijela Petković Ramadža, Vladimir Sarnavka, Vjekoslav Krželj, Bernarda Lozić, Silvija Pušeljić, Valentina Rahelić, Nikola Mesarić, Marina Grubić, Ana Bogdanić, Anita Špehar Uroić, Tamara Žigman, Ruža Grizelj, Jurica Vuković, Duško Mardešić, Ildiko Szatmari, Isabel Rivera, Ksenija Fumić, Ivo Barić

المصدر: Liječnički vjesnik, Vol 145, Iss 1-2, Pp 1-11 (2023)

مصطلحات موضوعية: galactosemias – complications, diagnosis, genetics, galactose – blood, utp-hexose-1-phosphate uridylyltransferase – deficiency, udp glucose 4-epimerase – deficiency, galactokinase – deficiency, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://lijecnicki-vjesnik.hlz.hr/pdf/1-2-2023/01_smaguc.pdf; https://doaj.org/toc/0024-3477; https://doaj.org/toc/1849-2177

URL الوصول: https://doaj.org/article/172aeb75c94342c59411f163b00e629a

المؤلفون: Šmaguc, Ana, Ramadža, Danijela Petković, Sarnavka, Vladimir, Krželj, Vjekoslav, Lozić, Bernarda, Pušeljić, Silvija, Rahelić, Valentina, Mesarić, Nikola, Grubić, Marina, Bogdanić, Ana, Uroić, Anita Špehar, Žigman, Tamara, Grizelj, Ruža, Vuković, Jurica, Mardešić, Duško, Szatmari, Ildiko, Rivera, Isabel, Fumić, Ksenija, Barić, Ivo

المصدر: Liječnički vjesnik
Volume 145
Issue 1-2

مصطلحات موضوعية: GALACTOSEMIAS – complications, diagnosis, genetics, GALACTOSE – blood, UTP-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE – deficiency, genetics, UDP GLUCOSE 4-EPIMERASE – deficiency, genetics, GALACTOKINASE – deficiency, genetics, MUTATION, PHENOTYPE, NEONATAL SCREENING, CROATIA, Deskriptori GALAKTOZEMIJA – dijagnoza, genetika, komplikacije, GALAKTOZA – u krvi, GALAKTOZA-1-FOSFAT URIDIL TRANSFERAZA – genetika, nedostatak, URIDIN DIFOSFAT GALAKTOZA 4-EPIMERAZA – genetika, nedostatak, GALAKTOKINAZA – genetika, nedostatak, MUTACIJA, FENOTIP, NOVOROĐENAČKI PROBIR, HRVATSKA, GALAKTOZEMIJA – dijagnoza, genetika, komplikacije

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2810e5ec76630a5348344fd768c11311
https://www.bib.irb.hr/1263470

عناروين إضافية: Experiences with galactosemia in Croatia

المصدر: Liječnički vjesnik; ISSN 0024-3477 (Print); ISSN 1849-2177 (Online); Volume 145; Issue 1-2

مصطلحات الفهرس: Deskriptori GALAKTOZEMIJA – dijagnoza, genetika, komplikacije; GALAKTOZA – u krvi; GALAKTOZA-1-FOSFAT URIDIL TRANSFERAZA – genetika, nedostatak; URIDIN DIFOSFAT GALAKTOZA 4-EPIMERAZA – genetika, nedostatak; GALAKTOKINAZA – genetika, nedostatak; MUTACIJA; FENOTIP; NOVOROĐENAČKI PROBIR; HRVATSKA, GALACTOSEMIAS – complications, diagnosis, genetics; GALACTOSE – blood; UTP-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE – deficiency, genetics; UDP GLUCOSE 4-EPIMERASE – deficiency, genetics; GALACTOKINASE – deficiency, genetics; MUTATION; PHENOTYPE; NEONATAL SCREENING; CROATIA, text, info:eu-repo/semantics/article, info:eu-repo/semantics/publishedVersion

URL: https://hrcak.srce.hr/294579
https://hrcak.srce.hr/file/433204
info:eu-repo/semantics/altIdentifier/doi/10.26800/LV-145-1-2-1