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biomedicina slovenica |
"HEMOCHROMATOSIS" : 48
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Kristan Aleša; Gašperšič Jernej; Režen Tadeja; Kunej Tanja; Količ Rok; Vuga Andrej; Fink Martina; Žula Špela; Anžej Doma Saša; Preložnik-Zupan Irena; Pajič Tadej; Podgornik Helena; Debeljak Nataša
Genetic analysis of 39 erythrocytosis and hereditary hemochromatosis-associated genes in the Slovenian family with idiopathic erythrocytosis
2021 ►
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Herga Primož; Mlakar Gorazd; Urlep Žužej Darja; Brecelj Jernej; Fister Petja; Ponikvar Rafael; Ranković Branislava; Plut Domen; Bonanomi Enzio; D'Antiga Lorenzo; Grosek Štefan
Liver magnetic resonance imaging and the histological and clinical picture of a neonatal near-miss case of a term newborn with gestational alloimmune liver disease treated with extracorporeal membrane oxygenation, plasmapheresis, and liver transplantation
2020 ►
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Požek Kity; Novak Katja; Karas Kuželički Nataša
Dedna hemokromatoza
[Hereditary hemocromatosis]
2017 ►
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Grošelj Urh; Oražem Miha; Kanič Maja; Vidmar Gaj; Grosek Štefan
Experiences of slovene ICU physicians with end-of-life decision making
2014 ►
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Ramagopalan Sreeram V; Cukjati Marko; Černilec Maja; DeLuca Gabriele C; Dyment David A; Degenhardt Alexandra; Sadovnick A Dessa; Čurin-Šerbec Vladka; Ebers George C; Duquette Pierre
Mutations in the hemochromatosis gene and the clinical outcome of multiple sclerosis
2008 ►
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Štepec Srečko; Makuc Jana; Markovič Saša; Medica Igor; Peterlin Borut
Distribution of HFE gene mutations in Slovenian patients with hereditary hemochromatosis
2008 ►
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Cukjati M; Vaupotič T; Rupreht R; Čurin-Šerbec V
Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay
2007 ►
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Koren Simon; Cukjati Marko; Černilec Maja; Vidan-Jeras Blanka; Rupreht Ruth; Čurin-Šerbec Vladka
First case of a homozygous frameshift deletion in HFE associated with hemochromatosis
2007 ►
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Cukjati M; Koren S; Čurin Šerbec V; Vidan-Jeras B; Rupreht R
A novel homozygous frameshift deletion c.471del of HFE associated with hemochromatosis
2007 ►
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Globočnik-Petrovič Mojca
Vpliv genetskih in biokemičnih dejavnikov na napredovanje in zdravljenje diabetične retinopatije pri diabetesu tipa 2
[The influence of genetical and biochemical factors for the progression and treatment of diabetic retinopathy in type 2 diabetes]
2007 ►
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Starčevič-Čizmarevič Nada; Štepec S; Ristić S; Milić S; Brajenović-Milić B; Štimac D; Kapović M; Peterlin B
Hemochromatosis gene mutations in patients with alcoholic cirrhosis
2006 ►
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Terzić Rifet; Šehić Amela; Teran Nataša; Terzić Ibrahim; Peterlin Borut
Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina
2006 ►
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Starčević-Čizmarević N; Štepec S; Ristič S; Milić S; Brajenović-Milić B; Štimac D; Kapović M; Peterlin B
C282Y, H63D and S65C mutations of the hemochromatosis gene (HFE) in patients with alcoholic cirrhosis
2005 ►
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Ristić S; Lovrecic L; Brajenović-Milić B; Starčević-Čizmarević N; Šega-Jazbec S; Sepčič J; Kapović M; Peterlin B
Mutations in the hemochromatosis gene (HFE) and multiple sclerosis
2005 ►
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Hruškovičova Helena; Milanez Tomaž; Kobal Jan; Peterlin-Potisk Karmen; Petrovič Danijel; Peterlin Borut
Hemochromatosis-causing mutations C282Y and H63D are not risk factors for atherothrombotic cerebral infarction
2005 ►
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Ristić Smiljana; Lovrecic Luca; Brajenović-Milić Bojana; Starčević-Čizmarević Nada; Šega-Jazbec Saša; Sepčić Juraj; Kapović Miljenko; Peterlin Borut
Mutations in the hemochromatosis gene (HFE) and multiple sclerosis
2005 ►
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Gobec Lidija
Presnova železa in laboratorijski testi za oceno
2003 ►
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Štabuc Borut
Posthepatic cirrhosis and liver tumors
2004 ►
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Markovič Saša
Patološki jetrni testi: kažipot prepoznavanja in zdravljenja
2004 ►
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Zorc M; Hruškovičova H; Globočnik-Petrovič M; Milčič M; Peterlin B; Petrovič D
Haemochromatosis-causing mutations C282Y and H63D are not risk factors for coronary artery disease in Caucasians with type 2 diabetes
2004 ►
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Cukjati Marko; Domanovič Dragoslav
Vključevanje bolnikov z dedno hemokromatozo med krvodajalce
[Recruitment of patients with hereditary haemochromatosis as blood donors]
2004 ►
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Ristić S; Makuc J; Starčević N; Logar N; Brajenović-Milić B; Stepec S; Pleša I; Kapović M; Milić S; Štimac D; Crnić-Martinović M; Peterlin B
Hemochromatosis gene mutations in the Croatian and Slovenian populations
2003 ►
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Peterlin Borut; Globočnik-Petrovič Mojca; Makuc Jana; Hawlina Marko; Petrovič Daniel
A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes
2003 ►
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Weirich Gregor; von Bubnoff Nikolas; Langer Rupert; Rudelius Martina; Peschl Christian; Hoefler Heinz
Molecular diagnosis of hereditary hemochromatosis
2003 ►
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Osredkar Joško
Stopenjska laboratorijska diagnostika kardiovaskularnih bolezni
[Stes in laboratory diagnostic of cardiovascular diseases]
2003 ►
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Makuc Jana
Analiza mutacij gena za hemokromatozo v slovenski populaciji
[Mutation analysis of the hemochromatosis gene in the Slovenian population]
2001 ►
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Rupreht RR; Cukjati M; Vaupotič M; Galvani V; Lukič L; Čurin-Šerbec V
Simultaneous high-throughput genotyping of 193A>T (S65C), I87C>G (H63D) and 845G>A (C282Y) mutations in hfe gene using novel MGB probes
2003 ►
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Gobec Lidija
Železo
2000 ►
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Zagradišnik Boris; Kokalj-Vokač Nadja
Molekularna genetika hemokromatoze
2002 ►
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Pernat Cvetka
Etiologija in sodobno zdravljenje jetrne ciroze
[Etiology and modern treatment of liver cirrhosis]
2001 ►
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Kocijan Irena
Molekularna dijagnostika i terapija bolesti jetre
[Molecular diagnosis and therapy of liver diseases]
1998 ►
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Zagradišnik Boris; Kokalj-Vokač Nadja
Pogostnost mutacij C282Y In H63D v genu HFE pri 200 zdravih osebah
[C282Y and H63D mutation of HFE gene in 200 healthy subjects]
2000 ►
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Tonejc Miha; Zukanovič Melisa; Vuksan Melanija; Domanovič Dragoslav
Terapevtski odvzemi krvi pri bonikih s hemokromatozo na zavodu RS za tansfuzijo krvi v letih 1997-2000
[Therapeutic blood removal in patients with hemochromatosis at the Slovenian centre for transfusion in the period 1997-2000]
2000 ►
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Domanovič Dragoslav
Hemokromatoza v tansfuzijski praksi
[Hemochromatosis in transfusion practice]
2000 ►
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Markovič Saša
Hemokromatoza
[Hemochromatosis]
2000 ►
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Zagradišnik B; Kokalj-Vokač N
Frequency of common HFE gene mutations in 200 healthy individuals
2000 ►
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Berger Jelena
Zgodnje odkrivanje genetske hemokromatoze
[Early diagnosis in genetic hemochromatosis]
1999 ►
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Scheuer Peter J
The role of the pathologist in the diagnosis of metabolic liver disease
1997 ►
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Ferlan-Marolt Vera
Ali so protokoli lahko merilo za kakovostno ravnanje v patohistološki diagnostiki
[Could diagnostic protocols contribute to quality control in pathohistological diagnosis]
1998 ►
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Markovič Saša
Hemokromatoza
1998 ►
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Pietrangelo A
Hemochromatosis
1995 ►
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Markovič S
Hemokromatoza
1993 ►
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Trotovšek B
Histomorfološko odkrivanje onkogeneze v jetrih
[A histomorphological study of liver oncogenesis]
1992 ►
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Bosnić D
Bolesti uz koje se često pojavljuje artropatija
1991 ►
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Hadžić N
Metaboličke i infiltrativne bolesti jetre
1991 ►
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Kendereški A; Žarković M; Stojanović R; Ćirić S; Ćirić J; Mićić J
Hipotalamo-hipofizni poremećaji u bolesnika sa primarnom hemohromatozom
[Abnormalities of hypothalamic-pituitary control in patients with primary haemochromatosis]
1989 ►
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Nešović M; Ćirić J; Popović V; Kendereški A; Micić D; Mićić J
Reverzibilnost poremečaja u idiopatskoj hemohromatozi tretiranoj flebotomijama
[Reversibility of disorders in idiopathic hemochromatosis treated by phlebotomies]
1988 ►
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Nešović M; Micić D; Popović V; Kendereški A; Subotić Z; Manojlović D; Mićić J
LH pulsatilnost u bolesnice sa hereditarnom hemohromatozom
[LH pulsatility in female patient with hereditary hemochromatosis]
1987 ►
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Institute for Biostatistics and Medical Informatics