المؤلفون: DS Lynch, SH Loh, J Harley, AJ Noyce, LM Martins, NW Wood, H Houlden, H Plun-Favreau

مصطلحات موضوعية: Uncategorized, Parkinson disease, mitophagy, autosomal dominant optic atrophy

Relation: 2381/45343; https://figshare.com/articles/journal_contribution/Nonsyndromic_Parkinson_disease_in_a_family_with_autosomal_dominant_optic_atrophy_due_to_OPA1_mutations/10203935

الاتاحة: https://figshare.com/articles/journal_contribution/Nonsyndromic_Parkinson_disease_in_a_family_with_autosomal_dominant_optic_atrophy_due_to_OPA1_mutations/10203935

المؤلفون: Nw Wood, Marina Frontali, Elide Mantuano, Paola Giunti, Mb Davis, Liana Veneziano, G. Sabbadini, R Plasmati, MG Sweeney, Antonio Federico

المصدر: Brain. 121:459-467

مصطلحات موضوعية: Adult, Male, Aging, Spinocerebellar Ataxia Type 1, Adolescent, Cerebellar Ataxia, Biology, Gene Frequency, Trinucleotide Repeats, Autosomal dominant cerebellar ataxia, medicine, Humans, Allele, Genes, Dominant, Spinocerebellar Degenerations, Genetics, Sex Characteristics, Cerebellar ataxia, Haplotype, Middle Aged, medicine.disease, Haplotypes, Mutation, Spinocerebellar ataxia, Female, Neurology (clinical), medicine.symptom, Trinucleotide repeat expansion, Machado–Joseph disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed176beba55722bf9eb7ff6748e0b924
https://doi.org/10.1093/brain/121.3.459

المؤلفون: Matthew McKenzie, D Liolitsa, N Akinshina, M Campanella, S Sisodiya, I Hargreaves, N Nirmalananthan, MG Sweeney, PM Abou-Sleiman, NW Wood, MG Hanna, MR Duchen

مصطلحات موضوعية: Uncategorised value

Relation: http://hdl.handle.net/10536/DRO/DU:30112467; https://figshare.com/articles/journal_contribution/Mitochondrial_ND5_gene_variation_associated_with_encephalomyopathy_and_mitochondrial_ATP_consumption/20798476

الاتاحة: http://hdl.handle.net/10536/DRO/DU:30112467
https://figshare.com/articles/journal_contribution/Mitochondrial_ND5_gene_variation_associated_with_encephalomyopathy_and_mitochondrial_ATP_consumption/20798476

المؤلفون: PF Worth, NW Wood

مصطلحات موضوعية: World Wide Web, Genetics, Spinocerebellar ataxia, medicine, Biology, Genotype to phenotype, medicine.disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::069b52e3dc724bf92126f865d03a598b
https://doi.org/10.4324/9780203450420-10

المؤلفون: Wood-Kaczmar A, Gandhi S, Yao Z, Ay, Abramov, Ea, Miljan, Keen G, Stanyer L, Hargreaves I, Klupsch K, Deas E, Downward J, Mansfield L, Jat P, Taylor J, Heales S, Duchen MR, Latchman D, Sarah Tabrizi, Nw, Wood

المصدر: Europe PubMed Central

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::066cae5c6534b1298336c08583190315
http://europepmc.org/abstract/PMC/PMC2651652

المؤلفون: Mh, Horrocks, Sf, Lee, Gandhi S, Nk, Magdalinou, Sw, Chen, Mj, Devine, Tosatto L, Magnus Kjaergaard, Js, Beckwith, Zetterberg H, Iljina M, Cremades N, Cm, Dobson, Nw, Wood, Klenerman D

المصدر: Europe PubMed Central

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c30d30323137b12993b0e6b591186780
http://europepmc.org/abstract/med/26800462

المؤلفون: Kamm C, Healy DG, Quinn NP, Wüllner U, Moller JC, Schols L, Geser F, Burk K, Børglum AD, Maria Teresa Pellecchia, Tolosa E, del Sorbo F, Nilsson C, Bandmann O, Sharma M, Mayer P, Gasteiger M, Haworth A, Ozawa T, Lees AJ, Short J, Giunti P, Holinski-Feder E, Illig T, Wichmann HE, Wenning GK, Wood NW, Gasser T

المساهمون: C, Kamm, Dg, Healy, Np, Quinn, U, Wüllner, Jc, Moller, L, Schol, F, Geser, K, Burk, Ad, Børglum, Pellecchia, Maria Teresa, E, Tolosa, F, del Sorbo, C, Nilsson, O, Bandmann, M, Sharma, P, Mayer, M, Gasteiger, A, Haworth, T, Ozawa, Aj, Lee, J, Short, P, Giunti, E, Holinski-Feder, T, Illig, He, Wichmann, Gk, Wenning, Nw, Wood, T, Gasser

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000230724500013; firstpage:1855; lastpage:1860; numberofpages:6; journal:BRAIN; http://hdl.handle.net/11386/3099254; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-23444442557

الاتاحة: http://hdl.handle.net/11386/3099254

المؤلفون: Healy DG, Abou-Sleiman PM, Quinn N, Ahmadi KR, Ozawa T, Kamm C, Wullner U, Oertel WH, Burk K, Dupont E, Maria Teresa Pellecchia, Tolosa E, Gasser T, Holton JL, Revesz T, Goldstein DB, Lees AJ, Wood NW

المساهمون: Dg, Healy, Pm, Abou-Sleiman, N, Quinn, Kr, Ahmadi, T, Ozawa, C, Kamm, U, Wullner, Wh, Oertel, K, Burk, E, Dupont, Pellecchia, Maria Teresa, E, Tolosa, T, Gasser, Jl, Holton, T, Revesz, Db, Goldstein, Aj, Lee, Nw, Wood

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000232749300011; firstpage:1338; lastpage:1343; numberofpages:6; journal:MOVEMENT DISORDERS; http://hdl.handle.net/11386/3099255; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-27844507620

الاتاحة: http://hdl.handle.net/11386/3099255