Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Obradović Miljana"'
Publikováno v:
Acta Veterinaria, Vol 64, Iss 1, Pp 52-60 (2014)
It has been shown in electrophysiological studies that the ligand L-655,708 possesses a binding selectivity and a moderate inverse agonist functional selectivity for α5-containing GABA-A receptors. The present study is aimed to investigate the antid
Externí odkaz:
https://doaj.org/article/c47ebc8ad75a4e6da813ff26e0368f99
Publikováno v:
In Medical Hypotheses October 2013 81(4):671-674
Autor:
Samardžić, Janko a, ⁎, Štrac, Dubravka Švob b, Obradović, Miljana c, Oprić, Dejan d, Obradović, Dragan I. a
Publikováno v:
In Behavioural Brain Research 1 December 2012 235(2):195-199
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 141, Iss 7-8, Pp 490-494 (2013)
Introduction. Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis. Mutations of the IKBKG gene are the only known cause of IP. The presence of other than skin changes is important in the diagnosis of atypical IP cases when skin cha
Externí odkaz:
https://doaj.org/article/5ab0362dd4e74aee90a8c56881e8087c
Autor:
Samardžić Janko, Savić Kristina, Stefanović Nemanja, Matunović Radomir, Baltezarević Dragana, Obradović Miljana, Jančić Jasna, Oprić Dejan, Obradović Dragan
Publikováno v:
Vojnosanitetski Pregled, Vol 70, Iss 4, Pp 391-395 (2013)
Background/Aim. Zinc is an essential element which has considerable interaction with gamma-aminobutyric acid A type receptors (GABAA) and glutamate receptors in the central nervous system (CNS). It is believed that zinc acts as a potent inhibitor of
Externí odkaz:
https://doaj.org/article/58e8b466466e4b72b6ce36ccb924a0d6
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 143, Iss 11-12, Pp 752-754 (2015)
Introduction. Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis. Mutations of the IKBKG gene are responsible for IP. A deletion of exons 4-10 can be found in 80% of patients with IP. There are 69 different mutations of the IKB
Externí odkaz:
https://doaj.org/article/666fcefd632a46629da6656c4f9faffa
Autor:
Samardžić Janko, Savić Kristina, Baltezarević Dragana, Matunović Radomir, Obradović Miljana, Jančić Jasna, Obradović Dragan I.
Publikováno v:
Veterinarski Glasnik, Vol 65, Iss 5-6, Pp 323-332 (2011)
Magnesium (Mg) is an essential element that catalyses more than 300 enzyme systems. Its effects on the central nervous system are exhibited through the blocking of activity of N-methyl D-aspartat (NMDA) receptors and potentiating of GABA-ergic neu
Externí odkaz:
https://doaj.org/article/1318c4f9484a444492c0b8e14a8327fd
Autor:
Trbojević-Stanković Jasna, Obradović Miljana, Čemerikić-Martinović Vesna, Trpinac Dušan, Laušević Željko, Stojimirović Biljana
Publikováno v:
Vojnosanitetski Pregled, Vol 68, Iss 7, Pp 556-560 (2011)
Background/Aim. During peritoneal dialysis (PD) an exchange of substances between blood and dialysate takes place through specific histological structures of peritoneum. Peritoneal double-layered serous membrane has, so far, mostly been studied with
Externí odkaz:
https://doaj.org/article/8a99d8586e484430a08572249f340329
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 138, Iss 3-4, Pp 150-153 (2010)
Introduction. Incontinentia pigmenti (IP) is a rare complex X-linked genodermatosis in which skin changes are combined with anomalies of other organs. Mutations of the NEMO gene localized on chromosome Xq28 are responsible for IP. Clinical manifestat
Externí odkaz:
https://doaj.org/article/9688ae238cb542df9b9d4d19dde551fa
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 138, Iss 7-8, Pp 408-413 (2010)
Introduction. Incontinentia pigmenti (IP) is an X-linked genodermatosis in which skin changes are combined with dental, eye and central nervous system anomalies. Objective. The goal of the study was to analyze ocular findings, IP minor criteria in av
Externí odkaz:
https://doaj.org/article/b0a2c95c7ef245a6b881826efeb80ff1