نتائج البحث - "E. Favaron"

1

دورية أكاديمية

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2

Negative ion treatment increases positive emotional processing in seasonal affective disorder

المؤلفون: E. Favaron, Catherine J. Harmer, S.F.B. McTavish, M. Charles, P J Cowen

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a5dd6d012d2ddeb01613075055295d
https://ora.ox.ac.uk/objects/uuid:3851e84f-325d-475b-afae-b7ce56fba64d

Find this article in full text from ProQuest

3

دورية أكاديمية

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

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4

Constructivism and Active Didactics

المؤلفون: P. M. Pumilia Gnarini, E. Favaron, E. Pacetti, J. Bishop, GUERRA, LUIGI

المساهمون: Guerra, Luigi, P.M.Pumilia-Gnarini, E.Favaron, E.Pacetti, J.Bishop, L.Guerra, P.M.Pumilia-Gnarini, E.Favaron, E.Pacetti, J.Bishop, L.Guerra

مصطلحات موضوعية: SCHOOLS, INNOVATION, VIRTUAL COMMUNITIES, ACTIVE CITIZENSHIP, ASSISTIVE TECHNOLOGY, LIFELONG LEARNING, TEACHER TRAINING, Interdisciplinary Learning, COLLABORATIVE LEARNING, DIDACTICS, Classroom 2.0

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______4094::9b11b2dd4a2afddb25e22ed4c11099ea
http://hdl.handle.net/11585/399061

5

Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature

المساهمون: Garavelli L., Zollino M., Cerruti Mainardi P., Gurrieri F., Rivieri F., Soli F., Verri R., Albertini E., Favaron E., Zignani M., Orteschi D., Bianchi P., Faravelli F., Forzano F., Seri M., Wischmeijer A., Turchetti D., Pompilii E., Gnoli M., Cocchi G., Mazzanti L., Bergamaschi R., De Brasi D., Sperandeo M.P., Mari F., Uliana V., Mostardini R., Cecconi M., Grasso M., Sassi S., Sebastio G., Renieri A., Silengo M., Bernasconi S., Wakamatsu N., Neri G.

مصطلحات موضوعية: Male, Pediatrics, Aging, Chromosomes, Artificial, Bacterial, Indoles, Hirschsprung disease, facial phenotype, Disease, medicine.disease_cause, Polymerase Chain Reaction, Craniofacial Abnormalities, Epilepsy, ZEB2 GENE, Mowat-Wilson syndrome, Young adult, Agenesis of the corpus callosum, Child, Genetics (clinical), In Situ Hybridization, Fluorescence, Oligonucleotide Array Sequence Analysis, ZEB2, Mutation, Nucleic Acid Hybridization, Dextrans, Syndrome, 2Q21-Q23 MICRODELETIONS, Phenotype, Italy, Child, Preschool, Female, medicine.medical_specialty, Heterozygote, Adolescent, Mowat–Wilson syndrome, Young Adult, Intellectual Disability, Genetics, medicine, Humans, Abnormalities, Multiple, Fluorescent Dyes, Zinc Finger E-box Binding Homeobox 2, Homeodomain Proteins, business.industry, Infant, medicine.disease, Repressor Proteins, Hypospadias, business