Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Z. Sabol"'
Autor:
Goran Krakar, M Meštrović, Sanja Delin, Filip Sabol, Z. Sabol, Goran Tešović, Vlasta Đuranović, I Mrkić Kobal, R. Gjergja Juraški, Kovač Šižgorić, Svjetlana Bela Klancir
Publikováno v:
Abstracts.
Autor:
Sanja Delin, Vlasta Đuranović, Goran Krakar, S Bela Klancir, M Meštrović, I Mrkić Kobal, Goran Tešović, R. Gjergja Juraški, Z. Sabol, Filip Sabol, M Kovač Šižgorić
Publikováno v:
Abstracts.
Autor:
M L Nelson, Sue Z. Sabol, Dean H. Hamer, Leo A. Sirota, S E Marcus, Gunzerath L, Craig Fisher, Dennis L. Murphy, Benjamin D. Greenberg, Cindy L. Brody, Hu S
Publikováno v:
Molecular Psychiatry. 5:181-188
Cigarette smoking behavior is influenced by both personality traits and inherited factors. Previous research showed that neuroticism-a broad personality domain that includes anxiety, depression, impulsiveness and vulnerability-increases the risk of b
Autor:
Issar Smith, Shengwei Yu, Manuel Gómez, William R. Jacobs, Sue Z. Sabol, Olivier Dussurget, Randall K. Holmes, Juliano Timm, Ben Gold
Publikováno v:
Manuel J Gómez
Publons
Europe PubMed Central
Publons
Europe PubMed Central
Exochelin is the primary extracellular siderophore of Mycobacterium smegmatis , and the iron-regulated fxbA gene encodes a putative formyltransferase, an essential enzyme in the exochelin biosynthetic pathway (E. H. Fiss, Y. Yu, and W. R. Jacobs, Jr.
Autor:
Sue Z. Sabol, Mark L. Nelson, Craig Fisher, Lorraine Gunzerath, Cindy L. Brody, Stella Hu, Leo A. Sirota, Stephen E. Marcus, Benjamin D. Greenberg, Frank R. Lucas, Jonathan Benjamin, Dennis L. Murphy, Dean H. Hamer
Publikováno v:
Health Psychology. 18:7-13
Autor:
Sue Z. Sabol, Dean H. Hamer
Publikováno v:
Behavior Genetics. 29:257-261
Pianezza et al. (1998) reported an association between the CYP2A6 gene, which codes for the enzyme that metabolizes nicotine to cotinine, and cigarette smoking behavior. We attempted to replicate their findings by analyzing the CYP2A6 gene in a popul
Publikováno v:
European Journal of Paediatric Neurology. 19:S90-S91
Objective Neurofibromatosis 1 (NF1) is autosomal dominant inherited disorder often difficult to diagnose in children besause of its age-dependent presentation. The early diagnosis using National Intitutes of Health (so called NIH-criteria) cannot be
Autor:
Ana Radica, Vesna Plavšić, Z. Sabol, Lj Brkljačić, Vladimir Sarnavka, Miroslav Dumić, Jurica Vuković
Publikováno v:
European Journal of Pediatrics. 150:696-699
Five children with adrenocorticotropic hormone (ACTH) insensitivity associated with autonomic nervous system disorders are described. A t the time of diagnosis, four of them had osteoporosis. The fifth p a t i e n t died and skeletal roentgenograms w
Autor:
Z. Sabol
Publikováno v:
Paediatria Croatica
Volume 51
Issue 4
Volume 51
Issue 4
Paroksizmalni nekonvulzivni (neepileptički) poremećaji su česti u dječjoj populaciji (procjenjuju se na oko 10%). Oko 25-% djece s normalnim psihomotornim razvojem i čak 60% dojenčadi koja se upućuju na procjenu paroksizmalnih poremećaja imaj
Autor:
T. Gojmerac, M. Kovac Sizgoric, Z. Sabol, L. Lujic, Vlatka Mejaški-Bošnjak, Vlasta Duranovic, Z. Plesa Premilovac, I. Djakovic, J. Lenicek Krleza, Goran Krakar
Publikováno v:
European Journal of Paediatric Neurology. 19:S44
Objective Moyamoya is progressive occlusive cerebral arteriopathy of unknown etiology, a common cause of cerebral ischemic stroke in children. It is characterized by progressive constriction (and finally, occlusion) of the terminal part of internal c