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1دورية أكاديمية
المؤلفون: Giulia Pezzoni, Lidia Stercoli, Eleonora Pegoiani, Emiliana Brocchi
المصدر: Viruses, Vol 13, Iss 7, p 1385 (2021)
مصطلحات موضوعية: HEV, monoclonal antibodies, recombinant antigens, HEV ORF2, Microbiology, QR1-502
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Luisa Benussi, Roberta Ghidoni, Eleonora Pegoiani, Davide V. Moretti, Orazio Zanetti, Giuliano Binetti
المصدر: Neurobiology of Disease, Vol 33, Iss 3, Pp 379-385 (2009)
مصطلحات موضوعية: Frontotemporal dementia, Corticobasal syndrome, Progressive supranuclear palsy, Motorneuron disease, PGRN, MAPT haplotype, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
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3
المؤلفون: Lidia Stercoli, Eleonora Pegoiani, Giulia Pezzoni, Emiliana Brocchi
المصدر: Viruses, Vol 13, Iss 1385, p 1385 (2021)
Viruses
Volume 13
Issue 7مصطلحات موضوعية: 0301 basic medicine, Swine, medicine.drug_class, Recombinant antigen, animal diseases, viruses, Biology, Monoclonal antibody, medicine.disease_cause, Microbiology, Epitope, Article, Epitopes, Mice, Open Reading Frames, Viral Proteins, 03 medical and health sciences, 0302 clinical medicine, Antigen, Hepatitis E virus, Virology, Escherichia coli, medicine, Animals, Hepatitis Antibodies, Antigens, Viral, chemistry.chemical_classification, Mice, Inbred BALB C, HEV ORF2, Immunogenicity, virus diseases, recombinant antigens, QR1-502, Amino acid, Open reading frame, 030104 developmental biology, Infectious Diseases, chemistry, HEV, 030211 gastroenterology & hepatology, monoclonal antibodies, Baculoviridae
وصف الملف: application/pdf
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4
المؤلفون: Anna Paterlini, Chiara Fenoglio, Giuliano Binetti, Luisa Benussi, Giacomina Rossi, Michela Glionna, Elena Stoppani, Daniela Galimberti, Valentina Albertini, Eleonora Pegoiani, Elena Piccoli, Roberta Ghidoni, Elio Scarpini, Luigi F. Agnati, Michela Morbin, Fabrizio Tagliavini
المصدر: Neurodegenerative Diseases. 9:121-127
مصطلحات موضوعية: Adult, Male, Oncology, Heterozygote, medicine.medical_specialty, Pathology, medicine.disease_cause, Sensitivity and Specificity, Progranulins, Predictive Value of Tests, Internal medicine, mental disorders, medicine, Humans, Cutoff, Cognitive Dysfunction, Age of Onset, Aged, Aged, 80 and over, Mutation, Neurodegeneration, Null (mathematics), Neurodegenerative Diseases, Heterozygote advantage, Frontotemporal lobar degeneration, Middle Aged, medicine.disease, Italy, Neurology, Intercellular Signaling Peptides and Proteins, Biomarker (medicine), Female, Neurology (clinical), Age of onset, Psychology
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5
المؤلفون: Eleonora Pegoiani, Giuliano Binetti, Davide V. Moretti, Orazio Zanetti, Roberta Ghidoni, Luisa Benussi
المصدر: Neurobiology of Disease, Vol 33, Iss 3, Pp 379-385 (2009)
مصطلحات موضوعية: Oncology, Male, Pathology, DNA Mutational Analysis, medicine.disease_cause, Primary progressive aphasia, Cognition, Progranulins, Gene Frequency, Medicine, Language, Mutation, Motorneuron disease, Neurodegenerative Diseases, Frontotemporal lobar degeneration, MAPT haplotype, Middle Aged, Corticobasal syndrome, Neurology, Italy, Intercellular Signaling Peptides and Proteins, Female, Frontotemporal dementia, medicine.medical_specialty, tau Proteins, PGRN, Progressive supranuclear palsy, lcsh:RC321-571, Atrophy, Memory, Internal medicine, mental disorders, Aphasia, Humans, Family, Motor Neuron Disease, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, Aged, Behavior, business.industry, Dementia with Lewy bodies, Haplotype, nutritional and metabolic diseases, medicine.disease, nervous system diseases, Haplotypes, Dementia, business
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6
المؤلفون: Fotini D. Kavadas, Eleonora Pegoiani, Silvia Giliani, Andrea Bates, Chaim M. Roifman, Yiping Gu, Evelina Mazzolari, Luigi D. Notarangelo
المصدر: The Journal of allergy and clinical immunology. 122(6)
مصطلحات موضوعية: Male, Mitochondrial RNA processing, Cellular immunity, Heterozygote, Receptors, Antigen, T-Cell, alpha-beta, Immunology, Biology, Gene mutation, CD8-Positive T-Lymphocytes, medicine.disease_cause, Compound heterozygosity, Osteochondrodysplasias, Lymphopenia, Endoribonucleases, medicine, Cartilage–hair hypoplasia, Immunology and Allergy, Humans, Promoter Regions, Genetic, Retrospective Studies, Genetics, Mutation, Genetic heterogeneity, Genetic Diseases, Inborn, medicine.disease, Omenn syndrome, Female, Cartilage Diseases