نتائج البحث - "Cihan Meral"

المساهمون: EuroEPINOMICS RES Consortium, ESF, European Science Foundation, WT089062, Wellcome Trust, 098051, Wellcome Trust, 261123, EC, European Commission, DFG, Deutsche Forschungsgemeinschaft [sponsor], Luxembourg Centre for Systems Biomedicine (LCSB): Chemical Biology (Crawford Group) [research center], Hendrickx, Rik, Holmgren, Philip, Stephani, Ulrich, Ulrich, Hiltrud, Pendiziwiat, Manuela, Appenzeller, Silke, Selmer, Kaja, Brilstra, Eva, Koeleman, Bobby, Rosenow, Felix, Leguern, Eric, Sterbova, Katalin, Magdalena, Budisteanu, Rodica, Gherghiceanu, Tarta Arsene, Oana, Diana, Barca, Guerrero-Lopez, Rosa, Ortega, Laura, Todorova, Albena P, Kirov, Andrey V, Robbiano, Angela, Arslan, Mutluay, Yiş, Uluç, Ivanović, Vanja

المصدر: Suls, A, Jaehn, J A, Kecskés, A, Weber, Y, Weckhuysen, S, Craiu, D C, Siekierska, A, Djémié, T, Afrikanova, T, Gormley, P, von Spiczak, S, Kluger, G, Iliescu, C M, Talvik, T, Talvik, I, Meral, C, Caglayan, H S, Giraldez, B G, Serratosa, J, Lemke, J R, Hoffman-Zacharska, D, Szczepanik, E, Barisic, N, Komarek, V, Hjalgrim, H, Møller, R S, Linnankivi, T, Dimova, P, Striano, P, Zara, F, Marini, C, Guerrini, R, Depienne, C, Baulac, S, Kuhlenbäumer, G, Crawford, A D, Lehesjoki, A-E, de Witte, P A M, Palotie, A, Lerche, H, Esguerra, C V, De Jonghe, P, Helbig, I & EuroEPINOMICS RES Consortium 2013, ' De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome ', American Journal of Human Genetics, vol. 93, no. 5, pp. 967-975 . https://doi.org/10.1016/j.ajhg.2013.09.017Test
The American journal of human genetics
American Journal of Human Genetics, 93(5), 967-975. (2013).
ResearcherID
The American Journal of Human Genetics; Vol 93

مصطلحات موضوعية: Male, Proband, Epilepsies, Myoclonic, Haploinsufficiency, medicine.disease_cause, Cohort Studies, 0302 clinical medicine, Intellectual disability, Genetics(clinical), Exome, Cognitive decline, Child, Multidisciplinary, general & others [D99] [Human health sciences], Zebrafish, Genetics (clinical), Genetics, 0303 health sciences, Mutation, 3. Good health, DNA-Binding Proteins, Phenotype, Gene Knockdown Techniques, Larva, Female, Multidisciplinaire, généralités & autres [D99] [Sciences de la santé humaine], Biology, Seizures, Febrile, Young Adult, 03 medical and health sciences, Dravet syndrome, Report, Intellectual Disability, medicine, Animals, Humans, 030304 developmental biology, Danio rerio, Dravet Syndrome, DNA fragment, medicine.disease, DNA binding protein, NAV1.1 Voltage-Gated Sodium Channel, CHD2, Immunology, Human medicine, Cognition Disorders, 030217 neurology & neurosurgery

وصف الملف: Print-Electronic; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e0e22ad1eaf15b4fd1ad1275cf9dca5Test
https://doi.org/10.1016/j.ajhg.2013.09.017Test

9

Comparison between daily supplementation doses of 200 versus 400 IU of vitamin D in infants

المؤلفون: Atilla Ersen, Cihan Meral, İsmail Göçmen, Selami Süleymanoğlu, Erman Ataş, Mustafa Gültepe, Ferhan Karademir, Secil Aydinoz

المصدر: European Journal of Pediatrics. 172:1039-1042

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::016e47a08dad9d15d6739e18fbdd4be5Test
https://doi.org/10.1007/s00431-013-1997-4Test

10

Assessment of Sleeping Positions of İnfants in Pediatric Outpatient Clinic

المؤلفون: Yalçın Çelik, Sevim Purisa, Bulent Ozturk, Cihan Meral

المصدر: Tuberculin Skin Test in Children. 10:179-182

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Supine position, business.industry, mental disorders, Health care, Prevalence, Medicine, Outpatient clinic, Grandparent, Sudden infant death syndrome, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d14e85fff4c63b7a73a605a2fd17d861Test
https://doi.org/10.5222/j.child.2010.179Test

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