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1Academic Journal
المؤلفون: Anita Špehar Uroić, Nataša Rojnić Putarek, Lucija Kolega Mrkić, Sanja Kusačić-Kuna, Ana Merkler Šorgić, Jadranka Sertić, Sanja Perić, Nevena Krnić
المصدر: Liječnički vjesnik, Vol 145, Iss 5-6, Pp 212-215 (2023)
مصطلحات موضوعية: MULTIPLA ENDOKRINA NEOPLAZIJA TIPA 2B – dijagnoza, genetika, PROTOONKOGEN RET – genetika, MUTACIJA, BUBREG – anomalije, MOKRAĆNI SUSTAV – anomalije, DULARNI KARCINOM – dijagnoza, kirurgija, Medicine (General), R5-920
وصف الملف: electronic resource
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2Academic Journal
المؤلفون: Dorian Tješić-Drinković, Ivan Bambir, Duška Tješić-Drinković, Andrea Vukić Dugac, Ivan Bambiar, Maja Baretić, Latinka Basara, Ana Bogdanić, Dolores Bzik, Fedža Džubur, Vesna Elveđi Gašparović, Nataša Firis, Sanda Huljev Frković, Nevena Krnić, Ivana Kuhtić, Ana Kunović, Tatjana Jalušić Glunčić, Mateja Janković Makek, Agata Ladić, Ivana Lalić, Gorana Levačić, Ivona Markelić, Jasna Markušić, Ana Merkler, Iveta Merčep, Petra Mihelčić, Tomislava Milinković, Tihana Odobašić Palković, Lana Omerza, Eva Pavić, Sanja Perić, Sanja Pleško, Gorazd Poje, Ivana Rako, Ivana Todorić, Katarina Vuković Đurić, Zrinka Šmuljić
المصدر: Liječnički vjesnik, Vol 145, Iss Supp 5, Pp 121-130 (2023)
مصطلحات موضوعية: CISTIČNA FIBROZA, CFTR, MODULATOR, LUMAKAFTOR/ IVAKAFTOR, ELEKSAKAFTOR/TEZAKAFTOR/IVAKAFTOR, HRVATSKA, Medicine (General), R5-920
وصف الملف: electronic resource
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3Academic Journal
المؤلفون: Monika Logara Klarić, Lucija Žunić, Tihana Marić, Lovro Trgovec-Greif, Filip Rokić, Ana Merkler, Robert Belužić, Oliver Vugrek, Ana Katušić Bojanac, Maja Barbalić
المصدر: Genetics & Applications, Vol 7, Iss 1 (2023)
وصف الملف: electronic resource
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4Academic Journal
المؤلفون: Ivana Karmelić, Jasna Lovrić, Tamara Božina, Ana Merkler, Nada Božina, Jadranka Sertić
المصدر: Annals of Human Biology, Vol 44, Iss 3, Pp 287-294 (2017)
مصطلحات موضوعية: obesity, apoe polymorphism, metabolic syndrome, mediterranean diet, young population, Biology (General), QH301-705.5, Human anatomy, QM1-695, Physiology, QP1-981
وصف الملف: electronic resource
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5Academic Journal
المؤلفون: Monika Logara Klarić, Tihana Marić, Lucija Žunić, Lovro Trgovec-Greif, Filip Rokić, Ana Fiolić, Ana Merkler Šorgić, Davor Ježek, Oliver Vugrek, Antonia Jakovčević, Maja Barbalić, Robert Belužić, Ana Katušić Bojanac
المصدر: Genes, Vol 15, Iss 6, p 707 (2024)
مصطلحات موضوعية: non-obstructive azoospermia, male infertility, SCOS syndrome, FANCM, astrocytoma, cancer, Genetics, QH426-470
Relation: https://www.mdpi.com/2073-4425/15/6/707; https://doaj.org/toc/2073-4425; https://doaj.org/article/de4284f94a324658a97ca3abec03e1af
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6Academic Journal
المؤلفون: Klarić, Monika Logara, Marić, Tihana, Žunić, Lucija, Trgovec-Greif, Lovro, Rokić, Filip, Fiolić, Ana, Šorgić, Ana Merkler, Ježek, Davor, Vugrek, Oliver, Jakovčević, Antonia, Barbalić, Maja, Belužić, Robert, Katušić Bojanac, Ana
المصدر: Genes; Jun2024, Vol. 15 Issue 6, p707, 12p
مصطلحات موضوعية: GENETIC variation, ASTROCYTOMAS, MALE infertility, AZOOSPERMIA, MISSENSE mutation, SPERMATOGENESIS, DYSPLASIA
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7
المؤلفون: Goran Šimić, Vana Vukić, Marija Babić, Maria Banović, Ivana Berečić, Ena Španić, Klara Zubčić, Anja Tea Golubić, Marija Barišić Kutija, Ana Merkler Šorgić, Željka Vogrinc, Ivan Lehman, Patrick R. Hof, Jadranka Sertić, Nina Barišić
المصدر: CNS Neuroscience & Therapeutics.
مصطلحات موضوعية: Pharmacology, Psychiatry and Mental health, Physiology (medical), Pharmacology (medical)
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8Academic Journal
Alternate Title: Are kidney malformations an additional feature of MEN2B syndrome? – Case report and literature review. (English)
المؤلفون: Uroić, Anita Špehar, Putarek, Nataša Rojnić, Mrkić, Lucija Kolega, Kusačić-Kuna, Sanja, Šorgić, Ana Merkler, Sertić, Jadranka, Perić, Sanja, Krnić, Nevena
المصدر: Lijecnicki Vjesnik; 2023, Vol. 145 Issue 5/6, p212-215, 4p
مصطلحات موضوعية: SITUS inversus, TYPE 1 diabetes, URINARY organs, MEDULLARY thyroid carcinoma, KIDNEY development
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9
المؤلفون: I. Ćelić, K. Starčević, Dubravka Kalinić, Ivana Karmelić, Ana Merkler, M. Šimić, Zdravka Poljaković, Jadranka Sertić, A. Bazina Martinović
المصدر: Gene. 809
مصطلحات موضوعية: Male, medicine.medical_specialty, Genotype, Peroxisome proliferator-activated receptor, chemistry.chemical_compound, Internal medicine, Genetics, medicine, Humans, In patient, Ischemic Stroke, chemistry.chemical_classification, biology, Cholesterol, C-reactive protein, Protein level, ishemic stroke, serum CRP level, PPAG CC genotype, General Medicine, Middle Aged, PPAR gamma, Endocrinology, C-Reactive Protein, chemistry, Case-Control Studies, Ischemic stroke, biology.protein, lipids (amino acids, peptides, and proteins), Female, Body mass index
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10
المؤلفون: Jasna Lovrić, Livija Šimičević, Jadranka Sertić, Mislav Božina, Ana Merkler, Bojan Jelaković, Tamara Božina
المصدر: Gene. 679:291-296
مصطلحات موضوعية: Male, 0301 basic medicine, Genotype, Croatia, Physiology, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, Receptor, Angiotensin, Type 1, Nutrigenetics, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Genetics, medicine, Humans, Genetic Predisposition to Disease, Prospective Studies, Gene, Genotyping, Triglycerides, Metabolic Syndrome, gene-diet interactions, nutrigenetics, metabolic syndrome, AT1R polymorphism, 030109 nutrition & dietetics, General Medicine, Middle Aged, medicine.disease, Angiotensin II, Diet, 3. Good health, Case-Control Studies, Female, Gene polymorphism, Restriction fragment length polymorphism, Metabolic syndrome
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11
المؤلفون: A. Bazina Martinović, Hana Ljubić, M. Šimić, Željko Reiner, Jadranka Sertić, S. Kaštelan, Ivan Pećin, I. Miličić, Jasenka Markeljević, Livija Šimičević, Domagoj Caban, Ana Merkler, T. Križ
مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Genotype, Gastroenterology, Brain Ischemia, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Stroke, Carotid atherosclerotic lesions, Hp2-2 genotype, Internal medicine, Genetics, medicine, Humans, In patient, Carotid Stenosis, Stroke, Polymorphism, Genetic, biology, Haptoglobins, business.industry, Haptoglobin, Carotid atherosclerotic lesions, Hp2-2 genotype, General Medicine, Middle Aged, medicine.disease, Atherosclerosis, Plaque, Atherosclerotic, Stenosis, 030104 developmental biology, 030220 oncology & carcinogenesis, Ischemic stroke, biology.protein, Biomarker (medicine), Female, Personalized medicine, business
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12
المؤلفون: Ana, Merkler
المساهمون: Sertić, Jadranka
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13
المؤلفون: Ana, Merkler
المساهمون: Sertić, Jadranka
مصطلحات موضوعية: Biološke znanosti. Fizička antropologija. Bioraznolikost, Charcot-Marie-Tooth, PRIRODNE ZNANOSTI. Biologija, udc:57(043.3), PMP22, gene sequencing, GJB1, sekvenciranje gena, NATURAL SCIENCES. Biology, MPZ, Biological sciences. Physical anthropology. Biodiversity
وصف الملف: application/pdf
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14
المؤلفون: Jasna Lovrić, Jadranka Sertić, Ivana Karmelić, Nada Božina, Tamara Božina, Ana Merkler
المصدر: Annals of human biology. 44(3)
مصطلحات موضوعية: Apolipoprotein E, Adult, Male, Aging, medicine.medical_specialty, Mediterranean diet, Genotype, Physiology, Epidemiology, Croatia, APOE polymorphism, metabolic syndrome, obesity, young population, 030209 endocrinology & metabolism, 030204 cardiovascular system & hematology, Biology, Real-Time Polymerase Chain Reaction, Apolipoproteins E, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Internal medicine, Genetics, medicine, Humans, Young adult, Allele, Metabolic Syndrome, Polymorphism, Genetic, Public Health, Environmental and Occupational Health, medicine.disease, Obesity, Diet, Endocrinology, lipids (amino acids, peptides, and proteins), Female, Metabolic syndrome
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15Dissertation/ Thesis
المؤلفون: Ana, Merkler
المساهمون: Sertić, Jadranka
مصطلحات موضوعية: Charcot-Marie-Tooth, PMP22, GJB1, MPZ, sekvenciranje gena, gene sequencing, PRIRODNE ZNANOSTI. Biologija, NATURAL SCIENCES. Biology, Biološke znanosti. Fizička antropologija. Bioraznolikost, Biological sciences. Physical anthropology. Biodiversity, info:eu-repo/classification/udc/57(043.3)
وصف الملف: application/pdf
Relation: https://dr.nsk.hr/islandora/object/pmf:2042; https://urn.nsk.hr/urn:nbn:hr:217:713405; https://repozitorij.unizg.hr/islandora/object/pmf:2042; https://repozitorij.unizg.hr/islandora/object/pmf:2042/datastream/PDF
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16
المؤلفون: Srđana Telarović, Marina Premužić, Jadranka Sertić, Peter Ferenci, Katja Grubelić Ravić, Rajko Ostojić, Mirjana Kalauz, Irena Hrstić, Maria Cristina Noli, Davor Radić, B. Vucelić, Maria Barbara Lepori, Jurica Vuković, Georgios Loudianos, Hana Ljubić, Ana Merkler, Ana Barišić
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Sequence analysis, Croatia, education, DNA Mutational Analysis, Biology, medicine.disease_cause, Wilson disease, genetics, 03 medical and health sciences, symbols.namesake, Exon, 0302 clinical medicine, Hepatolenticular Degeneration, Genotype, medicine, Wilson disease, ATP7B, Sanger sequencing, Humans, Allele, Cation Transport Proteins, Genetics (clinical), Alleles, Genetic Association Studies, Croatian, Genetics, Adenosine Triphosphatases, Mutation, Polymorphism, Genetic, General Medicine, Exons, Middle Aged, language.human_language, 030104 developmental biology, Copper-Transporting ATPases, language, symbols, 030211 gastroenterology & hepatology, Female, Polymorphism, Restriction Fragment Length
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17
المؤلفون: Diana Muačević Katanec, Marijan Merkler, Ana Merkler, Ksenija Fumić, Ivo Barić, Željko Reiner
المصدر: Paediatria Croatica
Volume 58
Issue 3مصطلحات موضوعية: homocystinuria, cystatione beta-synthase, delayed diagnosis, neonatal screening, homocistinurija, cistationin beta-sintaza, zakašnjela dijagnoza, novorođenački probir, Pediatrics, Perinatology and Child Health
وصف الملف: application/pdf