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1. Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

2. The Applied Genomics Development Strategy by the Croatian Academy of Sciences and Arts paves the way for the future development of applied genomics in Croatia.

3. Total tau in cerebrospinal fluid detects treatment responders among spinal muscular atrophy types 1–3 patients treated with nusinersen.

6. Jesu li bubrežne malformacije jedno od obilježja sindroma MEN2B? – prikaz bolesnika i pregled literature

8. S100 calcium-binding protein B in cerebrospinal fluid of spinal atrophy patients patients treated with nusinersen

9. Change of total tau protein in cerebrospinal fluid of patients with spinal muscular atrophy after nusinersen treatment

10. Total tau in cerebrospinal fluid detects treatment responders among spinal muscular atrophy types 1–3 patients treated with nusinersen

14. Jesu li bubrežne malformacije jedno od obilježja sindroma MEN2B? – prikaz bolesnika i pregled literature.

17. The first report on MODY testing in children in Croatia

21. genetic diagnosis; limb-girdle weakness; neuromuscular disease; next-generation sequencing; targeted exome analysisweakness

24. Association of gene polymorphism methylenetetrahydrofolate reductase cytosine- to-thymidine substitution at nucleotide 677 with cardiovascular and metabolic risk in morbidly obese patients

25. GCK mutations in Croatian MODY patients

26. Mutations in the Hepatocyte Nuclear Factor 1 Alpha (HNF1A), 4 Alpha (HNF4A) and 1 Beta (HNF1B) in Maturity-Onset Diabetes of the Young in Croatia

27. Genski i biokemijski biljezi monogenskog dijabetesa

29. Molekularna laboratorijska dijagnostika cistične fibroze od 1991.-2018. u Kliničkom bolničkom centru Zagreb

30. Bolesnik s MEN 2b, inverznim položajem organa, ureterohidronefrozom i dijabetesom melitusom tip 1 - skriva li se među različitim entitetima novo fenotipsko svojstvo sindroma MEN 2b

31. Real life practice of sweat testing in Europe

32. Određivanje broja tripleta CTG u molekularnoj dijagnostici miotonične distrofije tipa 1 kapilarnom elektroforezom

33. Molekularna dijagnostika monogenskog dijabetesa u Hrvatskoj - preliminarni rezultati

34. Molekularna ekstenzijska analiza mikrodelecija kromosoma Y u neplodnih muških ispitanika u Kliničkom bolničkom centru Zagreb

35. Iskustva u liječenju bolesnika sa spinalnom mišićnom atrofi jom u Hrvatskoj -- pozitivni rezultati praćenja iz nacionalnog registra i novi izazovi.

36. PREHYPERTENSION AND SINGLE NUCLEOTIDE POLYMORPHISM RS13333226 OF THE UROMODULIN (UMOD) GENE

37. Shwachman-Diamondov sindrom - nova mutacija gena SBDS

38. Association of adiponectin gene polymorphisms with blood pressure and hypertension

39. Metabolički moždani udar u sindromu MELAS – prikaz bolesnika i preporuke za liječenje

40. Molecular diagnostics of Duchenne-Becker muscular distrophy by MLPA method in University hospital centre Zagreb

41. Molekularna dijagnostika genetičkih bolesti - Klinički bolnički centar Zagreb

42. Metode molekularne biologije u medicini

43. Biokemijski i genski biljezi ateroskleroze

45. Nutrigenetika i razvoj metaboličkog sindroma: uloga polimorfizma AT1R

46. APOLIPOPROTEIN E GENE (APOE) VARIANTS, AND GENE-ENVIRONMENT INTERACTIONS AS PREDICTORS OF EARLY METABOLIC SYNDROME AND ITS TRAITS IN A YOUNG CROATIAN POPULATION

47. PREDICTIVE VALUE OF LEPTIN AND ADIPONECTIN-TO- LEPTIN RATIO FOR HYPERTENSION AND INSULIN RESISTANCE IN SUBJECTS WITH LOW CARDIOVASCULAR RISK

48. Prediktivna vrijednost leptina i omjera adiponektina i leptina za hipertenziju i inzulinsku rezistenciju u osoba s niskim kardiovaskularnim rizikom

49. PPARγ and IL-6 - 174G>C gene variants in Croatian patients with ischemic stroke

50. MERRF syndrome

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