يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"V189I"', وقت الاستعلام: 0.94s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene

    المؤلفون: Giuseppe Di Fede, Marcella Catania, Cristiana Atzori, Fabio Moda, Claudio Pasquali, Antonio Indaco, Marina Grisoli, Marta Zuffi, Maria Cristina Guaita, Roberto Testi, Stefano Taraglio, Maria Sessa, Graziano Gusmaroli, Mariacarmela Spinelli, Giulia Salzano, Giuseppe Legname, Roberto Tarletti, Laura Godi, Maurizio Pocchiari, Fabrizio Tagliavini, Daniele Imperiale, Giorgio Giaccone

    المصدر: Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-11 (2019)

    مصطلحات موضوعية: Creutzfeldt-Jakob disease, PRNP, Prion, V189I, CJD, PrP, Neurology. Diseases of the nervous system, RC346-429

    وصف الملف: electronic resource

    Relation: http://link.springer.com/article/10.1186/s40478-018-0656-4; https://doaj.org/toc/2051-5960

    URL الوصول: https://doaj.org/article/46afdf2fd23547ffa41d811b6d180715

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  2. 2
    دورية أكاديمية
    Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene

    المؤلفون: Di Fede, GiuseppeAff1, Catania, Marcella, Atzori, Cristiana, Moda, Fabio, Pasquali, Claudio, Indaco, Antonio, Grisoli, Marina, Zuffi, Marta, Guaita, Maria Cristina, Testi, Roberto, Taraglio, Stefano, Sessa, MariaAff6, Aff7, Gusmaroli, Graziano, Spinelli, Mariacarmela, Salzano, Giulia, Legname, Giuseppe, Tarletti, Roberto, Godi, Laura, Pocchiari, Maurizio, Tagliavini, Fabrizio, Imperiale, Daniele, Giaccone, Giorgio

    المصدر: Acta Neuropathologica Communications. 7(1)

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  3. 3
    Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene

    المؤلفون: Graziano Gusmaroli, Antonio Indaco, Maria Sessa, Fabrizio Tagliavini, Giorgio Giaccone, Claudio Pasquali, Marcella Catania, Giulia Salzano, Giuseppe Legname, Maria Cristina Guaita, Cristiana Atzori, Roberto Testi, Daniele Imperiale, Roberto Tarletti, Giuseppe Di Fede, Mariacarmela Spinelli, Fabio Moda, Marina Grisoli, Laura Godi, Maurizio Pocchiari, Marta Zuffi, Stefano Taraglio

    المصدر: Acta Neuropathologica Communications
    acta neuropathologica communications
    Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-11 (2019)

    مصطلحات موضوعية: 0301 basic medicine, Male, PrPSc Proteins, animal diseases, V189I, Scrapie, Disease, CJD, Creutzfeldt-Jakob disease, Dementia, Mutation, Prion, PRNP, PrP, 2734, Neurology (clinical), Cellular and Molecular Neuroscience, medicine.disease_cause, lcsh:RC346-429, Creutzfeldt-Jakob Syndrome, 0302 clinical medicine, Settore BIO/10 - Biochimica, Genetics, Aged, 80 and over, Brain, Phenotype, Pedigree, Female, medicine.symptom, Ataxia, Biology, Prion Proteins, Pathology and Forensic Medicine, 03 medical and health sciences, mental disorders, medicine, Humans, Gene, lcsh:Neurology. Diseases of the nervous system, Aged, Research, medicine.disease, nervous system diseases, 030104 developmental biology, 030217 neurology & neurosurgery

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::081bb9a20fb00bec1c79593bc816f36d
    https://pubmed.ncbi.nlm.nih.gov/30606247

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest
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