المؤلفون: Wilson, H, Dervenoulas, G, Pagano, G, Koros, C, Yousaf, T, Picillo, M, Polychronis, S, Simitsi, A, Giordano, B, Chappell, Z, Corcoran, B, Stamelou, M, Gunn, RN, Pellecchia, MT, Rabiner, EA, Barone, P, Stefanis, L, Politis, M

المصدر: 759 ; 748

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, COGNITIVE IMPAIRMENT, BRAIN PATHOLOGY, TRANSPORTER, MUTATION, FEATURES, PD, Adult, Aged, Brain, Cross-Sectional Studies, Female, Humans, Male, Middle Aged, Parkinsonian Disorders, Serotonin, Serotonin Plasma Membrane Transport Proteins, Severity of Illness Index, alpha-Synuclein, Neurology & Neurosurgery, 1103 Clinical Sciences, 1109 Neurosciences

جغرافية الموضوع: England

العلاقة: Lancet Neurology; http://hdl.handle.net/10044/1/71499Test

الإتاحة: https://doi.org/10.1016/S1474-4422Test(19)30140-1
http://hdl.handle.net/10044/1/71499Test

المؤلفون: Marongiu R, Ferraris A, Ialongo T, Michiorri S, Soleti F, Ferrari F, Elia AE, Ghezzi D, Albanese A, Altavista MC, Antonini A, Barone P, Brusa L, Cortelli P, Martinelli P, Pellecchia MT, Pezzoli G, Scaglione C, Stanzione P, Tinazzi M, Zecchinelli A, Zeviani M, Cassetta E, Garavaglia B, Dallapiccola B, Bentivoglio AR, Valente E

المساهمون: Marongiu, R, Ferraris, A, Ialongo, T, Michiorri, S, Soleti, F, Ferrari, F, Elia, Ae, Ghezzi, D, Albanese, A, Altavista, Mc, Antonini, A, Barone, P, Brusa, L, Cortelli, P, Martinelli, P, Pellecchia, Mt, Pezzoli, G, Scaglione, C, Stanzione, P, Tinazzi, M, Zecchinelli, A, Zeviani, M, Cassetta, E, Garavaglia, B, Dallapiccola, B, Bentivoglio, Ar, Valente, E

مصطلحات موضوعية: Autosomal recessive parkinsonism, Heterozygous rare variant, Parkinson disease, PINK1, Adult, Aged, 80 and over, Amino Acid Sequence, Case-Control Studie, Female, Gene Frequency, Genes, Recessive, Heterozygote, Human, Italy, Male, Middle Aged, Molecular Sequence Data, Phenotype, Protein Kinase, Retrospective Studie, Sequence Homology, Amino Acid, Genetic Variation, Genetic, Genetics (clinical)

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/18330912; info:eu-repo/semantics/altIdentifier/wos/WOS:000254800400016; volume:29; firstpage:565; lastpage:565; numberofpages:1; journal:HUMAN MUTATION; http://hdl.handle.net/11386/4679651Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-42049102405; http://onlinelibrary.wiley.com/journal/10.1002Test/(ISSN)1098-1004

الإتاحة: https://doi.org/10.1002/humu.20719Test
http://hdl.handle.net/11386/4679651Test

المؤلفون: Marongiu R., Ferraris A., Ialongo T., Michiorri S., Soleti F., Ferrari F., Elia A. E., Ghezzi D., Albanese A., Altavista M. C., Antonini A., Barone P., Brusa L., Pellecchia M. T., Pezzoli G., Stanzione P., Tinazzi M., Zecchinelli A., Zeviani M., Cassetta E., Garavaglia B., Dallapiccola B., Bentivoglio A. R., Valente E. M., Italian PD Study Group, CORTELLI, PIETRO, MARTINELLI, PAOLO, SCAGLIONE, CESA LORELLA MARIA

المساهمون: Marongiu R., Ferraris A., Ialongo T., Michiorri S., Soleti F., Ferrari F., Elia A.E., Ghezzi D., Albanese A., Altavista M.C., Antonini A., Barone P., Brusa L., Cortelli P., Martinelli P., Pellecchia M.T., Pezzoli G., Scaglione C., Stanzione P., Tinazzi M., Zecchinelli A., Zeviani M., Cassetta E., Garavaglia B., Dallapiccola B., Bentivoglio A.R., Valente E.M., Italian PD Study Group., Marongiu, R, Ferraris, A, Ialongo, T, Michiorri, S, Soleti, F, Ferrari, F, Elia, Ae, Ghezzi, D, Albanese, A, Altavista, Mc, Antonini, A, Barone, Paolo, Brusa, L, Cortelli, P, Martinelli, P, Pellecchia, Mt, Pezzoli, G, Scaglione, C, Stanzione, P, Tinazzi, M, Zecchinelli, A, Zeviani, M, Cassetta, E, Garavaglia, B, Dallapiccola, B, Bentivoglio, Ar, Valente, Em, Italian PD Study, G. r. o. u. p.

المصدر: Scopus-Elsevier

مصطلحات موضوعية: Adult, Male, Heterozygote, Autosomal recessive parkinsonism, Heterozygous rare variants, Parkinson disease, PINK1, Aged, Aged, 80 and over, Amino Acid Sequence, Case-Control Studies, Female, Gene Frequency, Genes, Recessive, Humans, Italy, Middle Aged, Molecular Sequence Data, Parkinson Disease, Phenotype, Protein Kinases, Retrospective Studies, Sequence Homology, Amino Acid, Genetic Variation, Genetics, Genetics (clinical), Sequence Homology, Context (language use), Biology, Compound heterozygosity, symbols.namesake, Genetic variation, 80 and over, medicine, Recessive, Allele frequency, Parkinsonism, heterozygous rare variants, Case-control study, Odds ratio, medicine.disease, Amino Acid, autosomal recessive parkinsonism, Genes, Immunology, Mendelian inheritance, symbols, Settore MED/26 - Neurologia

وصف الملف: ELETTRONICO; STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9889f96673ea4fff14a5f116e0d1d4e5Test
https://doi.org/10.1002/humu.20719Test