23 results on '"Sertić, Jadranka"'
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2. Genetic and Clinical Characterization of Patients with HNF1B-Related MODY in Croatia
3. Total tau in cerebrospinal fluid detects treatment responders among spinal muscular atrophy types 1–3 patients treated with nusinersen
4. 209 Are kindey malformations possible feature of men2b syndrome? – report of a patient with men2b, type 1 diabetes, situs viscerum inversus and kidney malformations
5. Association of methylenetetrahydrofolate reductase C677T CT gene polymorphism with a non-dipping blood pressure pattern in morbidly obese patients
6. Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness
7. Association of gene polymorphism methylenetetrahydrofolate reductase cytosine-to-thymidine substitution at nucleotide 677 with cardiovascular and metabolic risk in morbidly obese patients
8. Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics
9. ATP7B Gene Mutations in Croatian Patients with Wilson Disease
10. Estrogen receptor 1 gene (TA)n polymorphism is associated with lone atrial fibrillation in men
11. Interaction of Genetic Risk Factors Confers Increased Risk for Metabolic Syndrome: The Role of Peroxisome Proliferator-Activated Receptor γ
12. Signal Hyperintensities on Brain Magnetic Resonance Imaging in Patients with Primary Sjögren Syndrome and Frequent Episodic Tension-type Headache: Relation to Platelet Serotonin Level and Disease Activity
13. Mutation detection in Croatian patients with Familial Hypercholesterolemia
14. Adiponectin Level and Gene Variability Are Obesity and Metabolic Syndrome Markers in a Young Population
15. Metabolic syndrome and serum homocysteine in patients with bipolar disorder and schizophrenia treated with second generation antipsychotics
16. Angiotensin-Converting Enzyme Gene Polymorphism and N-Acetyl-β-D-Glucosaminidase Excretion in Endemic Nephropathy
17. Ethylene glycol poisoning
18. Cytogenetic analysis of azoospermic patients: karyotype comparison of peripheral blood lymphocytes and testicular tissue
19. A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness
20. Incidence of Chromosomopathies and Cystic Fibrosis Mutations in Second Trimester Fetuses with Isolated Hyperechoic Bowel
21. Molecular Analysis and Electromyoneurographic Abnormalities in Croatian Children with Proximal Spinal Muscular Atrophies
22. Association between Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Cerebral Atherosclerosis
23. Characterization ofH-2 congenic strains using DNA markers
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