biomedicina slovenica


"HEMOCHROMATOSIS" : 48

  1. 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
  2. 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
  3. Požek Kity; Novak Katja; Karas Kuželički Nataša
    Dedna hemokromatoza
    [Hereditary hemocromatosis]
    2017
  4. Grošelj Urh; Oražem Miha; Kanič Maja; Vidmar Gaj; Grosek Štefan
    Experiences of slovene ICU physicians with end-of-life decision making
    2014
  5. 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
  6. Štepec Srečko; Makuc Jana; Markovič Saša; Medica Igor; Peterlin Borut
    Distribution of HFE gene mutations in Slovenian patients with hereditary hemochromatosis
    2008
  7. 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
  8. 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
  9. 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
  10. 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
  11. 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
  12. Terzić Rifet; Šehić Amela; Teran Nataša; Terzić Ibrahim; Peterlin Borut
    Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina
    2006
  13. 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
  14. 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
  15. 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
  16. 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
  17. Gobec Lidija
    Presnova železa in laboratorijski testi za oceno
    2003
  18. Štabuc Borut
    Posthepatic cirrhosis and liver tumors
    2004
  19. Markovič Saša
    Patološki jetrni testi: kažipot prepoznavanja in zdravljenja
    2004
  20. 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
  21. Cukjati Marko; Domanovič Dragoslav
    Vključevanje bolnikov z dedno hemokromatozo med krvodajalce
    [Recruitment of patients with hereditary haemochromatosis as blood donors]
    2004
  22. 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
  23. 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
  24. Weirich Gregor; von Bubnoff Nikolas; Langer Rupert; Rudelius Martina; Peschl Christian; Hoefler Heinz
    Molecular diagnosis of hereditary hemochromatosis
    2003
  25. Osredkar Joško
    Stopenjska laboratorijska diagnostika kardiovaskularnih bolezni
    [Stes in laboratory diagnostic of cardiovascular diseases]
    2003
  26. Makuc Jana
    Analiza mutacij gena za hemokromatozo v slovenski populaciji
    [Mutation analysis of the hemochromatosis gene in the Slovenian population]
    2001
  27. 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
  28. Gobec Lidija
    Železo
    2000
  29. Zagradišnik Boris; Kokalj-Vokač Nadja
    Molekularna genetika hemokromatoze
    2002
  30. Pernat Cvetka
    Etiologija in sodobno zdravljenje jetrne ciroze
    [Etiology and modern treatment of liver cirrhosis]
    2001
  31. Kocijan Irena
    Molekularna dijagnostika i terapija bolesti jetre
    [Molecular diagnosis and therapy of liver diseases]
    1998
  32. 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
  33. 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
  34. Domanovič Dragoslav
    Hemokromatoza v tansfuzijski praksi
    [Hemochromatosis in transfusion practice]
    2000
  35. Markovič Saša
    Hemokromatoza
    [Hemochromatosis]
    2000
  36. Zagradišnik B; Kokalj-Vokač N
    Frequency of common HFE gene mutations in 200 healthy individuals
    2000
  37. Berger Jelena
    Zgodnje odkrivanje genetske hemokromatoze
    [Early diagnosis in genetic hemochromatosis]
    1999
  38. Scheuer Peter J
    The role of the pathologist in the diagnosis of metabolic liver disease
    1997
  39. 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
  40. Markovič Saša
    Hemokromatoza
    1998
  41. Pietrangelo A
    Hemochromatosis
    1995
  42. Markovič S
    Hemokromatoza
    1993
  43. Trotovšek B
    Histomorfološko odkrivanje onkogeneze v jetrih
    [A histomorphological study of liver oncogenesis]
    1992
  44. Bosnić D
    Bolesti uz koje se često pojavljuje artropatija
    1991
  45. Hadžić N
    Metaboličke i infiltrativne bolesti jetre
    1991
  46. 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
  47. 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
  48. 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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