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1دورية أكاديمية
المؤلفون: Rosa Camerlingo, Roberta Miceli, Laura Marra, Giuseppina Rea, Igea D'Agnano, Marta Nardella, Roberta Montella, Alessandro Morabito, Nicola Normanno, Virginia Tirino, Gaetano Rocco
المصدر: PLoS ONE, Vol 14, Iss 7, p e0219597 (2019)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1932-6203
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2دورية أكاديمية
المؤلفون: Loredana Guglielmi, Marta Nardella, Carla Musa, Ingrid Cifola, Manuela Porru, Beatrice Cardinali, Ilaria Iannetti, Chiara Di Pietro, Giulia Bolasco, Valentina Palmieri, Laura Vilardo, Nicolò Panini, Fabrizio Bonaventura, Massimiliano Papi, Ferdinando Scavizzi, Marcello Raspa, Carlo Leonetti, Germana Falcone, Armando Felsani, Igea D’Agnano
المصدر: Cancers, Vol 12, Iss 6, p 1635 (2020)
مصطلحات موضوعية: melanoma, circulating miRNAs, small extracellular vesicles, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Giovanna Maresca, Manuela Natoli, Marta Nardella, Ivan Arisi, Daniela Trisciuoglio, Marianna Desideri, Rossella Brandi, Simona D'Aguanno, Maria Rita Nicotra, Mara D'Onofrio, Andrea Urbani, Pier Giorgio Natali, Donatella Del Bufalo, Armando Felsani, Igea D'Agnano
المصدر: PLoS ONE, Vol 7, Iss 9, p e45513 (2012)
وصف الملف: electronic resource
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4
المؤلفون: Francesco Nicita, Elena Panzeri, Cristina Maghini, Fabrizia Stregapede, Antonio Pizzuti, Maria Teresa Bassi, Guja Astrea, Piotr Gasperowicz, Melissa Barghigiani, Guido Primiano, Enrico Bertini, Ginevra Zanni, Marta Nardella, Aleksandra Jezela-Stanek, Luciana Losito, Rafał Płoski, Alessandra Tessa, Lorena Travaglini, Serenella Servidei, Filippo M. Santorelli
المصدر: Journal of Neurology. 266:2657-2664
مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Adolescent, Genotype, Hereditary spastic paraplegia, Hereditary spastic paraparesis, HSP, Leukodystrophy, SPG54, Thin corpus callosum, Brain, Child, Female, Humans, Middle Aged, Phenotype, Phospholipases, Spastic Paraplegia, Hereditary, Young Adult, Gene mutation, Corpus callosum, Compound heterozygosity, 03 medical and health sciences, 0302 clinical medicine, medicine, Spastic Paraplegia, 030212 general & internal medicine, Spasticity, Cerebellar ataxia, business.industry, medicine.disease, Settore MED/26 - NEUROLOGIA, Hereditary, Neurology, Neurology (clinical), medicine.symptom, Differential diagnosis, business, 030217 neurology & neurosurgery
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5
المؤلفون: Carlo Leonetti, Germana Falcone, Igea D'Agnano, Valentina Palmieri, Nicolò Panini, Carla Musa, Ingrid Cifola, Laura Vilardo, Ferdinando Scavizzi, Armando Felsani, Fabrizio Bonaventura, Ilaria Iannetti, Marta Nardella, Giulia Bolasco, Marcello Raspa, Beatrice Cardinali, Chiara Di Pietro, Loredana Guglielmi, Manuela Porru, Massimiliano Papi
المصدر: Cancers
Cancers, Vol 12, Iss 1635, p 1635 (2020)
Volume 12
Issue 6مصطلحات موضوعية: Circulating mirnas, Cancer Research, Melanoma, Biology, small extracellular vesicles, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, medicine.disease, lcsh:RC254-282, Extracellular vesicles, Article, Oncology, Downregulation and upregulation, Tumor progression, microRNA, medicine, Cancer research, melanoma, circulating miRNAs, Human melanoma, Brain metastasis
وصف الملف: application/pdf
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6
المؤلفون: Guido, Primiano, Ginevra, Zanni, Marta, Nardella, Serenella, Servidei
المصدر: Neurology. 94(19)
مصطلحات موضوعية: Mutation, Palatal Muscles, Tremor, Olivopontocerebellar Atrophies, ATPases Associated with Diverse Cellular Activities, Humans, Metalloendopeptidases, Ataxia, Female, Middle Aged
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::ee669a5b32d77b88246fc5517ddade1a
https://pubmed.ncbi.nlm.nih.gov/32317346 -
7
المؤلفون: Loredana Guglielmi 1, Marta Nardella 2, Carla Musa 3, Ingrid Cifola 1, Manuela Porru 4, Beatrice Cardinali 3, Ilaria Iannetti 3, Chiara Di Pietro 3, Giulia Bolasco 5, Valentina Palmieri 6, 7, Laura Vilardo 1, Nicolò Panini 8, Fabrizio Bonaventura 3, Massimiliano Papi 6, Ferdinando Scavizzi 3, Marcello Raspa 3, Carlo Leonetti 4, Germana Falcone 3, Armando Felsani 9, and Igea D'Agnano 1
المصدر: Cancers (Basel) (2020).
info:cnr-pdr/source/autori:Loredana Guglielmi 1,+, Marta Nardella 2,+, Carla Musa 3,+, Ingrid Cifola 1,+, Manuela Porru 4, Beatrice Cardinali 3, Ilaria Iannetti 3, Chiara Di Pietro 3, Giulia Bolasco 5, Valentina Palmieri 6,7, Laura Vilardo 1, Nicolò Panini 8, Fabrizio Bonaventura 3, Massimiliano Papi 6,7, Ferdinando Scavizzi 3, Marcello Raspa 3, Carlo Leonetti 4,?, Germana Falcone 3,?, Armando Felsani 9,? and Igea D'Agnano 1,*,?/titolo:Circulating miRNAs in Small Extracellular Vesicles Secreted by a Human Melanoma Xenograft in Mouse Brains/doi:/rivista:Cancers (Basel)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volumeمصطلحات موضوعية: melanoma, circulating miRNAs, small extracellular vesicles
URL الوصول: https://explore.openaire.eu/search/publication?articleId=cnr_________::1fb15bb01db7349a35718b84ae406547
http://www.cnr.it/prodotto/i/424284 -
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المؤلفون: Ginevra Zanni, Alberto Danieli, Enrico Bertini, Francesca Pantaleoni, Marta Nardella, Marco Tartaglia, Giancarlo Iarossi, Emanuele Bellacchio, Marco Cappa, Alessandro Bruselles, Maria Lisa Dentici, Paolo Alfieri, Sabina Barresi
المصدر: Gene
مصطلحات موضوعية: Adult, 0301 basic medicine, Ataxia, Cerebellar Ataxia, Short Communication, InsP3, Inositol 1,4,5 tri-phosphate receptor, DNA Mutational Analysis, Intellectual disability, Mutation, Missense, Gene mutation, Biology, Gillespie syndrome, 03 medical and health sciences, Partial aniridia, NPCA, Nonprogressive congenital ataxia, ERG, Electroretinography, WAIS-IV, Wechsler Adult Intelligence Scale–Fourth Edition, SCA, Spinocerebellar ataxia, Inositol 1,4,5 tri-phosphate receptor (InsP3) type 1 (ITPR1), Genetics, medicine, PMCA, Plasma membrane Ca2 + ATPase, Humans, Inositol 1,4,5-Trisphosphate Receptors, Missense mutation, VEP, Flash visual evoked potential, GRM1, Metabotropic glutamate receptor, Aniridia, Cerebellar ataxia, CARP, Carbonic anhydrase-related protein VIII, General Medicine, medicine.disease, IRBIT, InsP3-binding domain, Hypoplasia, GS, Gillespie syndrome, 030104 developmental biology, Child, Preschool, Cerebellar atrophy, Mutation, Female, medicine.symptom, Gene Deletion
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9
المؤلفون: Marta Nardella, Adele D'Amico, Matteo Di Capua, Marina Trivisano, Nicola Specchio, Roberto Frusciante, Ginevra Zanni, José M. Fernández-Fernández, Lorena Travaglini, Emanuele Bellacchio, Raffaella Cusmai, Federico Vigevano, Massimiliano Valeriani, Enrico Bertini, Sabina Barresi, Alessandro Capuano, Silvia Morlino
المصدر: European Journal of Paediatric Neurology. 21:450-456
مصطلحات موضوعية: Male, 0301 basic medicine, Cerebellum, Pathology, medicine.medical_specialty, Ataxia, Migraine Disorders, Mutation, Missense, Neuroimaging, Biology, 03 medical and health sciences, Calcium Channels, N-Type, 0302 clinical medicine, Atrophy, medicine, Humans, Missense mutation, Child, Gene, Genetics, General Medicine, medicine.disease, Magnetic Resonance Imaging, Phenotype, Pedigree, 030104 developmental biology, medicine.anatomical_structure, Migraine, Child, Preschool, Pediatrics, Perinatology and Child Health, Female, Cerebellar atrophy, Neurology (clinical), medicine.symptom, 030217 neurology & neurosurgery
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المؤلفون: Marta Nardella, Ginevra Zanni, Guido Primiano, Serenella Servidei
المصدر: Neurology. 94:e2074-e2075
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Ataxia, Neuroferritinopathy, SPG7, ataxia, palatal myoclonus, Cerebrotendinous Xanthomatosis, SPG7, 03 medical and health sciences, Dysarthria, 0302 clinical medicine, medicine, 030212 general & internal medicine, Spasticity, Soft palate, business.industry, ataxia, palatal myoclonus, medicine.disease, nervous system diseases, Settore MED/26 - NEUROLOGIA, medicine.anatomical_structure, Cerebellar atrophy, Neurology (clinical), medicine.symptom, business, Spastic paraplegia type 7, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9a04a0d15797ae97dd3e8450ce4996c
https://doi.org/10.1212/wnl.0000000000009409