Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Trpinac, Dušan"'
Autor:
Minić, Snežana1,2 (AUTHOR) danijela_dobrosavljevic@yahoo.co.uk, Trpinac, Dušan3 (AUTHOR) dusantrpinac@gmail.com, Novaković, Ivana4 (AUTHOR) tetaana61@yahoo.com, Cerovac, Nataša2,5 (AUTHOR), Dobrosavljević Vukojević, Danijela1,2 (AUTHOR), Rosain, Jérémie6,7 (AUTHOR) jeremie.rosain@institutimagine.org
Publikováno v:
Diagnostics (2075-4418). Jul2022, Vol. 12 Issue 7, pN.PAG-N.PAG. 12p.
Autor:
Marković Olivera, Martinović Tamara, Ćirić Darko, Trpinac Dušan, Čemerikić-Martinović Vesna, Bumbaširević Vladimir, Bila Jelena, Marisavljević Dragomir, Kravić-Stevović Tamara
Publikováno v:
Vojnosanitetski Pregled, Vol 76, Iss 7, Pp 740-744 (2019)
Introduction. Congenital asplenia is an extremely rare condition that can be separate entity due to a specific defect of spleen development or may occur in the context of a malformation syndrome. The patients with asplenia have thrombocytosis and sus
Externí odkaz:
https://doaj.org/article/a15499406aaf49349fd654d39ab4d463
Akademický článek
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Publikováno v:
In Medical Hypotheses October 2013 81(4):671-674
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
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:
Jovanović Nataša, Žunić-Božinovski Snežana, Trpinac Dušan, Laušević Željko, Krstić Slobodan, Oprić Dejan, Trbojević-Stanković Jasna, Stojimirović Biljana
Publikováno v:
Vojnosanitetski Pregled, Vol 70, Iss 11, Pp 1023-1028 (2013)
Background/Aim. The number of patients with end-stage renal diseases treated with chronic dialysis is increasing over the last years. Long-term peritoneal dialysis is associated with progressive development of structural and functional alterations of
Externí odkaz:
https://doaj.org/article/508b3053c885478fbcef991e39a51d35
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