المؤلفون: Jacopo Taurino, Emanuele Micaglio, Annalisa Russo Raucci, Monica Zanussi, Massimo Chessa, Nathasha Samali Udugampolage, Paola Carrera, Carlo Pappone, Alessandro Pini

المصدر: Frontiers in Cardiovascular Medicine, Vol 10 (2023)

مصطلحات موضوعية: COL3A1, vascular ehlers danlos syndrome, aneurysm - dissecting, pneumothorax, atypical onset, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fcvm.2023.1110392/full; https://doaj.org/toc/2297-055X

URL الوصول: https://doaj.org/article/0499b8e8fb24455795629233378b49f3

المؤلفون: Federica Barzaghi, Maria Pia Cicalese, Matteo Zoccolillo, Immacolata Brigida, Matteo Barcella, Ivan Merelli, Claudia Sartirana, Monica Zanussi, Valeria Calbi, Maria Ester Bernardo, Francesca Tucci, Maddalena Migliavacca, Fabio Giglio, Matteo Doglio, Daniele Canarutto, Francesca Ferrua, Giulia Consiglieri, Giulia Prunotto, Francesco Saettini, Sonia Bonanomi, Patrizia Rovere-Querini, Giulia Di Colo, Tatiana Jofra, Georgia Fousteri, Federica Penco, Marco Gattorno, Michael S. Hershfield, Lucia Bongiovanni, Maurilio Ponzoni, Sarah Marktel, Raffaella Milani, Jacopo Peccatori, Fabio Ciceri, Alessandra Mortellaro, Alessandro Aiuti

المصدر: Frontiers in Immunology, Vol 13 (2022)

مصطلحات موضوعية: ADA2, adenosine deaminase 2 deficiency, neutropenia, T large granular lymphocytes, TLGL, HSCT, Immunologic diseases. Allergy, RC581-607

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fimmu.2022.910021/full; https://doaj.org/toc/1664-3224

URL الوصول: https://doaj.org/article/90dfc8d0b666457dafde9ab89f41de11

المؤلفون: Mattia Pozzato, Emanuele Micaglio, Chiara Starvaggi Cucuzza, Alessandro Cagol, Daniela Galimberti, Daniela Calandrella, Claudia Cinnante, Carlo Pappone, Monica Zanussi, Giovanni Meola, Elio Scarpini, Nereo Bresolin, Filippo Martinelli Boneschi

المصدر: Frontiers in Neurology, Vol 11 (2021)

مصطلحات موضوعية: multiple sclerosis, rituximab, hepatotoxicity, case report, familal mediterranean fever, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fneur.2020.591395/full; https://doaj.org/toc/1664-2295

URL الوصول: https://doaj.org/article/7f93f91c898e4da1b7875a87f5f2acd1

المؤلفون: Anna Villa, Paola Carrera, Marita Bosticardo, Elena Fontana, Maria Carmina Castiello, Sara Penna, Monica Zanussi, Lucia Sergi Sergi, Elena Draghici, Luigi Poliani, Nicolò Sacchetti, Gerard Wagemaker, Valentina Capo, Barbara Cassani, Luigi D. Notarangelo, Niek P. van Til, Kerry Dobbs, Rosita Rigoni, Paolo Uva

المساهمون: İç Hastalıkları, Hematology, Capo, V, Castiello, M, Fontana, E, Penna, S, Bosticardo, M, Draghici, E, Poliani, L, Sergi Sergi, L, Rigoni, R, Cassani, B, Zanussi, M, Carrera, P, Uva, P, Dobbs, K, Sacchetti, N, Notarangelo, L, van Til, N, Wagemaker, G, Villa, A

المصدر: Journal of Allergy and Clinical Immunology, 142(3), 928-941.e8. Mosby Inc.
Journal of Allergy and Clinical Immunology

مصطلحات موضوعية: Male, 0301 basic medicine, Rag gene, Allergy, T-Lymphocytes, Genetic enhancement, Immunology, Autoimmunity, Mice, Transgenic, Article, Gene therapy, Lentiviral vector, Omenn syndrome, Rag genes, Immunology and Allergy, 03 medical and health sciences, RAG2, medicine, Animals, Lymphocyte Count, Immunodeficiency, Inflammation, B-Lymphocytes, Severe combined immunodeficiency, business.industry, Lentivirus, Genetic Therapy, medicine.disease, Autoimmune regulator, 3. Good health, DNA-Binding Proteins, Mice, Inbred C57BL, Transplantation, Disease Models, Animal, 030104 developmental biology, Primary immunodeficiency, Female, Severe Combined Immunodeficiency, business

وصف الملف: text/plain; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99001dcbbd04c3d9ef22f1392f528c92
http://hdl.handle.net/11655/15017

المؤلفون: Alberto Cappelletti, Alberto Margonato, Giliola Calori, Cosmo Godino, Monica Mazzavillani, Valeria Magni, Monica Zanussi, Maurizio Ferrari

المساهمون: Cappelletti, A, Zanussi, M, Mazzavillani, M, Magni, V, Calori, G, Godino, C, Ferrari, Maurizio, Margonato, Alberto

المصدر: Journal of Cardiovascular Medicine. 15:391-396

مصطلحات موضوعية: Male, medicine.medical_specialty, Population, Coronary Angiography, Polymorphism, Single Nucleotide, Severity of Illness Index, Coronary artery disease, Gene Frequency, Predictive Value of Tests, Risk Factors, Polymorphism (computer science), Diabetes mellitus, Internal medicine, Diabetes Mellitus, medicine, OLR1, Humans, Genetic Predisposition to Disease, education, Aged, Dyslipidemias, education.field_of_study, business.industry, Smoking, Coronary Stenosis, General Medicine, Middle Aged, Scavenger Receptors, Class E, medicine.disease, Pedigree, Stenosis, Phenotype, medicine.anatomical_structure, Italy, Case-Control Studies, Hypertension, Cardiology, Female, Cardiology and Cardiovascular Medicine, business, Dyslipidemia, Artery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dc8801a2eb866fd72fa3eeec30aa957
https://doi.org/10.2459/jcm.0b013e3283624251

المؤلفون: Monica Zanussi, Alessia Moiana, Emanuela Castiglioni, Maurizio Gramegna, Maurizio Ferrari

المصدر: Clinical Chemistry and Laboratory Medicine (CCLM). 51:e133-e136

مصطلحات موضوعية: medicine.diagnostic_test, business.industry, Biochemistry (medical), Clinical Biochemistry, MEDLINE, DNA, General Medicine, Computational biology, Molecular biology, stat, chemistry.chemical_compound, Molecular Diagnostic Techniques, Dna genetics, chemistry, Nat, medicine, Humans, Molecular diagnostic techniques, Genetic Testing, Reagent Kits, Diagnostic, business, Genetic testing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bef5516997728f89f6efcd101f14772
https://doi.org/10.1515/cclm-2012-0514

المؤلفون: Monica Zanussi, Maria Grazia Roncarolo, Luca Vago, Federica Torri, Benedetta Mazzi, Chiara Bonini, Fabio Ciceri, Massimo Bernardi, Claudio Bordignon, Maurizio Ferrari, Monica Casucci, Silvano Rossini, Andrea Angius, Cristina Barlassina, Consuelo Corti, Attilio Bondanza, Serena K. Perna, Nicola Flavio Perrelli, Cristian Cosentino, Barbara Forno, Jacopo Peccatori, Katharina Fleischhauer, Maria Teresa Lupo Stanghellini

المساهمون: Vago, L, Perna, S. K, Zanussi, M, Mazzi, B, Barlassina, C, LUPO STANGHELLINI, Mt, Perrelli, N. F, Cosentino, C, Torri, F, Angius, A, Forno, B, Casucci, M, Bernardi, M, Peccatori, J, Corti, C, Bondanza, Attilio, Ferrari, Maurizio, Rossini, S, Roncarolo, MARIA GRAZIA, Bordignon, Claudio, Bonini, MARIA CHIARA, Ciceri, Fabio, Fleischhauer, K.

المصدر: New England Journal of Medicine. 361:478-488

مصطلحات موضوعية: Adult, Myeloid, T-Lymphocytes, medicine.medical_treatment, Graft vs Leukemia Effect, Human leukocyte antigen, Transplantation Chimera, Hematopoietic stem cell transplantation, Major Histocompatibility Complex, HLA Antigens, Recurrence, medicine, Humans, Cells, Cultured, Retrospective Studies, business.industry, Histocompatibility Testing, Hematopoietic Stem Cell Transplantation, General Medicine, medicine.disease, Transplantation, Leukemia, Myeloid, Acute, Leukemia, medicine.anatomical_structure, Haplotypes, Myelodysplastic Syndromes, Mutation, Immunology, Chromosomes, Human, Pair 6, Bone marrow, Stem cell, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::130dfa03abc5d61a530e58472ba9a438
https://doi.org/10.1056/nejmoa0811036

المؤلفون: Cecilia Gelfi, Monica Zanussi, Pier Giorgio Righetti, Antonia Orsi, Maurizio Ferrari, Paola Carrera

المصدر: Journal of Chromatography B: Biomedical Sciences and Applications. 657:201-205

مصطلحات موضوعية: Chromatography, Adrenal Hyperplasia, Congenital, Base Sequence, Polymers, Oligonucleotide, Base pair, Molecular Sequence Data, Polyacrylamide, Intercalation (chemistry), Oligonucleotides, DNA, General Chemistry, Polymerase Chain Reaction, Matrix (chemical analysis), chemistry.chemical_compound, Electrophoresis, Capillary electrophoresis, chemistry, Ethidium, Humans, Electrophoresis, Polyacrylamide Gel, Steroid 21-Hydroxylase, Ethidium bromide, Capillary Action, Gene Deletion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dd223662936acdb0474ffe0b2eeb713
https://doi.org/10.1016/0378-4347(94)80088-x

المؤلفون: Monica Zanussi, Isabella Neri, Maurizio Ferrari, Antonio Percesepe, Maurizio Travi, Antonino Forabosco, Domenico A. Coviello, Marina Castagni, Silvana Tedeschi

المساهمون: Percesepe, A, Ferrari, Maurizio, Coviello, D, Zanussi, M, Castagni, M, Neri, I, Travi, M, Forabosco, A, Tedeschi, S.

مصطلحات موضوعية: Male, Heterozygote, Genetic Linkage, Duchenne muscular dystrophy, DNA Mutational Analysis, Prenatal diagnosis, Biology, medicine.disease_cause, law.invention, Dystrophin, Exon, Pregnancy, law, Genetic linkage, Prenatal Diagnosis, medicine, Humans, Gene, reproductive and urinary physiology, Genetics (clinical), Polymerase chain reaction, Recombination, Genetic, Genetics, Mutation, Haplotype, Infant, Newborn, Obstetrics and Gynecology, Exons, medicine.disease, Molecular biology, Pedigree, Muscular Dystrophy, Duchenne, Fetal Diseases, Haplotypes, embryonic structures, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43155f7735123cc2cc5ef5449ab76193
http://hdl.handle.net/11567/540304

المؤلفون: N. Greggio, F. Braggion, Maurizio Ferrari, Monica Zanussi, F. Rigon, Franco Zacchello, Ivana Spiga, Paola Carrera, F. Beccaro

المصدر: Human heredity. 43(3)

مصطلحات موضوعية: Male, Genotype, Pseudogene, Molecular Sequence Data, Restriction Mapping, Gene Conversion, Biology, medicine.disease_cause, Restriction map, Gene Frequency, Gene duplication, Genetics, medicine, Humans, Gene conversion, Amino Acid Sequence, Gene, Genetics (clinical), Mutation, Adrenal Hyperplasia, Congenital, Base Sequence, Genetic heterogeneity, C4A, DNA, Blotting, Southern, Phenotype, Italy, Multigene Family, Female, Chromosome Deletion, Pseudogenes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48f0232e764a1f60b71dace02bea4e9f
https://pubmed.ncbi.nlm.nih.gov/8330883