Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Šoštarko, Marija"'
Autor:
Žagar, Marija, Vranješ, Davorka, Šoštarko, Marija, Vogrinc, Željka, Bilić, Ervina, Trbojević Čepe, Milica
Publikováno v:
Collegium antropologicum
Volume 33
Issue 4
Volume 33
Issue 4
In myasthenia gravis (MG) patients without detectable anti-acetylcholine receptor (anti-AChR) antibody, referred to as seronegative myasthenia gravis patients, there is a variable proportion of patients with antibodies against the muscle- specific ki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::12799b333baa4073b81b096757c5a77f
https://pubmed.ncbi.nlm.nih.gov/20102061
https://pubmed.ncbi.nlm.nih.gov/20102061
Autor:
Žagar, Marija, Vranješ, Davorka, Šoštarko, Marija, Vogrinc, Željka, Bilić, Ervina, Trbojević Čepe, Milica
In myasthenia gravis (MG) patients without detectable anti-acetylcholine receptor (anti-AChR) antibody, referred to as seronegative myasthenia gravis patients, there is a variable proportion of patients with antibodies against the muscle specific kin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______579::0605033a4792682dc308e651af269d75
https://hrcak.srce.hr/51480
https://hrcak.srce.hr/51480
Autor:
Bilić, Ervina:Bilić, Ernest, Šoštarko, Marija, Vranješ, Davorka, Jurenić, Dubravka, Žagar, Marija, Rajić, Ljubica, Femenić, Ranka, Dekleva, Vanja
Nasljedna neuropatija sa sklonošću parezi zbog pritiska (HNPP) pripada u grupu senzomotornih neuropatija sa pridruženim kliničkim znacima motoričkog i senzornog deficita. U vrlo blagih kliničkih slučajeva može biti neprepoznata. U ovom radu p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::1abc73a26c2192f1eec34c44536c2a86
https://www.bib.irb.hr/335450
https://www.bib.irb.hr/335450
Autor:
Vranješ, Davorka, Bilić, Ervina, Zurak, Niko, Bilić, Ernest, Žagar, Marija, Šoštarko, Marija, Kušec, Vesna
Uvod: Neurotrofički učinci hormona rasta (HR) na središnji živčani sustav postaju sve češće predmet znanstvenog interesa, posebice unatrag desetak godina. Stimulacijski i neuroprotektivni učinci HR na proliferaciju cerebrokortikalnih stanica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::179337c2d1818e83706fa4f90888ae7c
https://www.bib.irb.hr/220209
https://www.bib.irb.hr/220209
Autor:
Bauer, Vladimir, Mitrović, Zoran, Sertić, Jadranka, Canki-Klain, Nina, Hećimović, Silva, Jurenić, Dubravka, Vranješ, Davorka, Žagar, Marija, Šoštarko, Marija
Unatoč tipičnim neurološkim ispadima, miotonična distrofija (DM1, M.Steinert)je bolest, koja još uvijek godinama prolazi nedijagnosticirana. Jednim dijelom vjerojatno zbog slabije informiranosti liječnika, drugim zbog varijabilne ekspresije bol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::651f6e3efff2e8dfc6ac282241cbe1e5
https://www.bib.irb.hr/179631
https://www.bib.irb.hr/179631
Autor:
Vranješ, Davorka, Mitrović, Zoran, Canki-Klain, Nina, Bilić, Ervina, Jurenić, Dubravka, Žagar, Marija, Šoštarko, Marija
Facioskapulohumeralna mišićna distrofija je relativno česta primarna bolest mišića s prevalencijom 1: 20 000. Nasljeđuje se autosomno dominantno, a uzrokovana je patološkom genskom promjenom na krajnjem dijelu dugog kraka kromosoma 4. Kliničk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::8bf3a125c529d55adc6710ea67edf4e3
https://www.bib.irb.hr/179479
https://www.bib.irb.hr/179479
Autor:
Malojčić, Branko, Šoštarko, Marija, Jurenić, Dubravka, Žagar, Marija, Mitrović, Zoran, Vranješ, Davorka
Causes of death other than related to myasthenic crisis or thymoma are rarely reported in myasthenia gravis (MG) patients. We reviewed records of 580 patients observed at our Department over the 30 years period from 1972 to 2001. We analysed data on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::9928c14f1866bb21e073dd044404e29b
https://www.bib.irb.hr/178058
https://www.bib.irb.hr/178058
Prikazan je rijedak slučaj multisistemne bolesti koji uključuje polineuropatiju, organomegaliju, endokrinopatiju i gamapatiju.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7d3f6f6d044437b9f75db6749fcf0b0b
https://www.bib.irb.hr/139859
https://www.bib.irb.hr/139859
Autor:
Hećimović, Silva, Bago , R., Čulić, V, Baraba, R, Bauer, Vladimir, Bučuk, Mira, Kovač, Biserka, Žagar, Marija, Mitrović , Zoran, Šoštarko, Marija, Pavelić, K, Canki-Klain , Nina
Rad ukazuje na pouzdanost molekularne analize ponavljajućih CTG tripleta u DMPG genu u postavljanju dijagnoze u obiteljima s kliničkom slikom miotoničke distrofije.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::8472a0d989036855527d928eb83a0f3d
https://www.bib.irb.hr/1111240
https://www.bib.irb.hr/1111240
Autor:
Canki-Klain, Nina, Šoštarko, Marija, Vranješ, Davorka, Urtizberea Jan Andoni 2 Richard Pascale, Zurak, Niksa
Oculopharyngeal musular dystrophy (OPMD) (MIM 164 300) is an autosomal dominant generalised myopathy caused by short (GCG)8-13 coding triplet repeat expansions in the polyadenylation binding protein 2 (PABP2) gene. First described in French Canadians
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::cc18611fd8c1391d28197e313425a37b
https://www.bib.irb.hr/70010
https://www.bib.irb.hr/70010