المؤلفون: Diana Miclea, Sergiu Osan, Simona Bucerzan, Delia Stefan, Radu Popp, Monica Mager, Maria Puiu, Cristian Zimbru, Adela Chirita-Emandi, Camelia Alkhzouz

المصدر: Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-7 (2022)

مصطلحات موضوعية: Global developmental delay, Intellectual disability, Chromosomal microarray analysis, Copy number variants, Etiology, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1824-7288

URL الوصول: https://doaj.org/article/bee18013fc23455d845c0666f2a8a93d

المؤلفون: Cristina Hotoleanu, Daniela Fodor, Adrian Trifa, Radu Popp

المصدر: Balkan Medical Journal, Vol 30, Iss 2, Pp 197-203 (2013)

مصطلحات موضوعية: Medicine

وصف الملف: electronic resource

Relation: http://balkanmedicaljournal.org/text.php?lang=en&id=395; https://doaj.org/toc/2146-3123; https://doaj.org/toc/2146-3131

URL الوصول: https://doaj.org/article/c873dc19e55143fbaf5f958167a64389

المؤلفون: Florin STAMATIAN, Gabriela CARACOSTEA, Cristina BUTUZA, Radu POPP, Daniel MUREŞAN, Sorana D. BOLBOACĂ, Ioana ROTAR, Felicia PETRIŞOR, Marius FĂRCAŞ

المصدر: Applied Medical Informatics, Vol 27, Iss 3, Pp 43-52 (2010)

مصطلحات موضوعية: Genetic polymorphism, Restriction fragment length polymorphism (RFLP), Polymerase chain reaction (PCR), Interleukin-4 (IL4), Cervical intraepithelial neoplasia (CIN), Human papiloma virus (HPV) infection, Human papiloma virus high risk (HPV-HR), Negative for intraepithelial lesion (NILM), Computer applications to medicine. Medical informatics, R858-859.7

وصف الملف: electronic resource

Relation: http://ami.info.umfcluj.ro/Full-text/AMI_27_2010/AMI(27)_043_052.pdf; https://doaj.org/toc/1224-5593

URL الوصول: https://doaj.org/article/1bfb35e137d3452298e3a8af40399f76

المؤلفون: Anca-Lelia Riza, Camelia Alkhzouz, Marius Farcaș, Andrei Pîrvu, Diana Miclea, Gheorghe Mihuț, Răzvan-Mihail Pleșea, Delia Ștefan, Mihaela Drodar, Călin Lazăr, on behalf of the HINT Study, on behalf of the FUSE Study, Mihai Ioana, Radu Popp

المصدر: Genes, Vol 14, Iss 69, p 69 (2022)

مصطلحات موضوعية: GJB2 (gap-junction protein β 2), connexin 26, autosomal recessive non-syndromic hearing loss, deafness, Genetics, QH426-470

Relation: https://www.mdpi.com/2073-4425/14/1/69; https://doaj.org/toc/2073-4425; https://doaj.org/article/dc8118aa06e442daab7f1e9d7d3d206f

الاتاحة: https://doi.org/10.3390/genes14010069
https://doaj.org/article/dc8118aa06e442daab7f1e9d7d3d206f

المؤلفون: Vasile Ťibre, Radu Popp, Cătălina Crišan, Ramona Moldovan

المصدر: Cognition, Brain, Behavior. An Interdisciplinary Journal. 21:203-209

مصطلحات موضوعية: medicine.medical_specialty, Genetic Medicine, medicine.diagnostic_test, business.industry, Experimental and Cognitive Psychology, Disease, Private practice, Health care, Medicine, Outpatient clinic, Apathy, medicine.symptom, Cognitive decline, business, Psychiatry, Genetic testing, Clinical psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e1c2e93508a7e8dcc4e53d529f3d05d5
https://doi.org/10.24193/cbb.2017.21.12

المؤلفون: Daniela, Fodor, Cosmina, Bondor, Adriana, Albu, Radu, Popp, Ioan Victor, Pop, Laura, Poanta

المصدر: The Indian Journal of Medical Research

مصطلحات موضوعية: Male, Atherosclerotic plaque, carotid intima-media thickness, Middle Aged, Polymorphism, Single Nucleotide, osteoporosis, VKORC1, Carotid Arteries, vitamin K epoxide, Bone Density, Vitamin K Epoxide Reductases, reductase, Humans, Female, Original Article, bone mineral density, gene, Genetic Association Studies, Aged

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::d5ba34b1858b8544c5ee9d6a510334dc
https://pubmed.ncbi.nlm.nih.gov/23703341