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المؤلفون: Frequin, H.L., Schouten, J., Verschuur, C.V., Suwijn, S.R., Boel, J.A., Post, B., Bloem, B.R., Hilten, J.J. van, Laar, T. van, Tissingh, G., Munts, A.G., Dijk, J.M.C. van, Deuschl, G., Lang, A., Dijkgraaf, M.G.W., Haan, R.J. den, Bie, R.M. de
المصدر: Neurology, 100, 4, pp. e367-e376
Neurology, 100, e367-e376مصطلحات موضوعية: All institutes and research themes of the Radboud University Medical Center, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3]
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9c91be06e00e180b70d18bad8f603622
https://hdl.handle.net/2066/290895 -
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المؤلفون: Contarino, M.F., Hilten, J.J. van, Kuijper, E.J.
المصدر: Movement Disorders Clinical Practice. WILEY
Movement Disorders Clinical Practiceمصطلحات موضوعية: Neurology, gut-brain axis, Parkinson's disease, microbiota, gastrointestinal system, fecal microbiota transplantation, Neurology (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0fdbaa012b3c02be49e764c9e99a76e
https://hdl.handle.net/1887/3505375 -
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المؤلفون: Hienen, M.M. van, Kuiper, R., Middelkoop, H.A.M., Hilten, J.J. van, Contarino, M.F., Geraedts, V.J.
المصدر: Journal of Parkinson's Disease, 12(4), 1285-1293. IOS PRESS
Journal of Parkinson's Disease, 12(4), 1285-1293. IOS Pressمصطلحات موضوعية: Male, Cellular and Molecular Neuroscience, caregiver burden, Caregivers, quality of life, Parkinson's disease, Humans, Female, Parkinson Disease, epidemiology, Neurology (clinical), Aged, deep brain stimulation
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b80892bc3a28f58196c733f0b790f5b
http://hdl.handle.net/1887/3495927 -
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المؤلفون: Iwaki, H., Blauwendraat, C., Leonard, H.L., Kim, J.J., Liu, G.Q., Maple-Grodem, J., Corvol, J.C., Pihlstrom, L., Nimwegen, M. van, Hutten, S.J., Nguyen, K.D.H., Rick, J., Eberly, S., Faghri, F., Auinger, P., Scott, K.M., Wijeyekoon, R., Deerlin, V.M. van, Hernandez, D.G., Gibbs, J.R., Chitrala, K.N., Day-Williams, A.G., Brice, A., Alves, G., Noyce, A.J., Tysnes, O.B., Evans, J.R., Breen, D.P., Estrada, K., Wegel, C.E., Danjou, F., Simon, D.K., Andreassen, O., Ravina, B., Toft, M., Heutink, P., Bloem, B.R., Weintraub, D., Barker, R.A., Williams-Gray, C.H., Warrenburg, B.P. van de, Hilten, J.J. van, Scherzer, C.R., Singleton, A.B., Nalls, M.A., Int Parkinson's Dis Genomics Cons
مصطلحات موضوعية: Parkinson's disease, GBA, Apolipoprotein E, genomewide association study
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_____10693::116c9c4f2bbfd874bfac1410727ec42d
https://hdl.handle.net/1887/120796 -
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المؤلفون: Reynolds, R.H., Botia, J., Nalls, M.A., Hardy, J., Taliun, S.A.G., Ryten, M., Noyce, A.J., Nicolas, A., Cookson, M.R., Bandres-Ciga, S., Gibbs, J.R., Hernandez, D.G., Singleton, A.B., Reed, X., Leonard, H., Blauwendraat, C., Faghri, F., Bras, J., Guerreiro, R., Tucci, A., Kia, D.A., Houlden, H., Plun-Favreau, H., Mok, K.Y., Wood, N.W., Lovering, R., R'Bibo, L., Rizig, M., Chelban, V., Trabzuni, D., Tan, M., Morris, H.R., Middlehurst, B., Quinn, J., Billingsley, K., Holmans, P., Kinghorn, K.J., Lewis, P., Escott-Price, V., Williams, N., Foltynie, T., Brice, A., Danjou, F., Lesage, S., Corvol, J.C., Martinez, M., Giri, A., Schulte, C., Brockmann, K., Simon-Sanchez, J., Heutink, P., Gasser, T., Rizzu, P., Sharma, M., Shulman, J.M., Robak, L., Lubbe, S., Mencacci, N.E., Finkbeiner, S., Lungu, C., Scholz, S.W., Gan-Or, Z., Rouleau, G.A., Krohan, L., Hilten, J.J. van, Marinus, J., Adarmes-Gomez, A.D., Bernal-Bernal, I., Bonilla-Toribio, M., Buiza-Rueda, D., Carrillo, F., Carrion-Claro, M., Mir, P., Gomez-Garre, P., Jesus, S., Labrador-Espinosa, M.A., Macias, D., Vargas-Gonzalez, L., Mendez-del-Barrio, C., Perinan-Tocino, T., Tejera-Parrado, C., Diez-Fairen, M., Aguilar, M., Alvarez, I., Boungiorno, M.T., Carcel, M., Pastor, P., Tartari, J.P., Alvarez, V., Gonzalez, M.M., Blazquez, M., Garcia, C., Suarez-Sanmartin, E., Barrero, F.J., Rezola, E.M., Yarza, J.A.B., Pagola, A.G., Arregui, A.L.D., Ruiz-Martinez, J., Cerdan, D., Duarte, J., Clarimon, J., Dols-Icardo, O., Infante, J., Marin, J., Kulisevsky, J., Pagonabarraga, J., Gonzalez-Aramburu, I., Rodriguez, A.S., Sierra, M., Duran, R., Ruz, C., Vives, F., Escamilla-Sevilla, F., Minguez, A., Camara, A., Compta, Y., Ezquerra, M., Marti, M.J., Fernandez, M., Munoz, E., Fernandez-Santiago, R., Tolosa, E., Valldeoriola, F., Garcia-Ruiz, P., Heredia, M.J.G., Errazquin, F.P., Hoenicka, J., Jimenez-Escrig, A., Martinez-Castrillo, J.C., Lopez-Sendon, J.L., Torres, I.M., Tabernero, C., Vela, L., Zimprich, A., Pihlstrom, L., Koks, S., Taba, P., Majamaa, K., Siitonen, A., Okubadejo, N.U., Ojo, O.O., Pitcher, T., Anderson, T., Bentley, S., Fowdar, J., Mellick, G., Dalrymple-Alford, J., Henders, A.K., Kassam, I., Montgomery, G., Sidorenko, J., Zhang, F.T., Xue, A.L., Vallerga, C.L., Wallace, L., Wray, N.R., Yang, J., Visscher, P.M., Gratten, J., Silburn, P.A., Halliday, G., Hickie, I., Kwok, J., Lewis, S., Kennedy, M., Pearson, J., Int Parkinsons Dis Genomics, Syst Genomics Parkinsons Dis
المصدر: npj Parkinson's Disease, 5
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::15558a829cd2ccd32d8196e2ff7c4991
https://hdl.handle.net/1887/120798 -
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المؤلفون: Fernandez-Santiago, R., Martin-Flores, N., Antonelli, F., Cerquera, C., Moreno, V., Bandres-Ciga, S., Manduchi, E., Tolosa, E., Singleton, A.B., Moore, J.H., Noyce, A.J., Kaiyrzhanov, R., Middlehurst, B., Kia, D.A., Tan, M., Houlden, H., Morris, H.R., Plun-Favreau, H., Holmans, P., Hardy, J., Trabzuni, D., Bras, J., Quinn, J., Mok, K.Y., Kinghorn, K.J., Billingsley, K., Wood, N.W., Lewis, P., Schreglmann, S., Guerreiro, R., Lovering, R., R'Bibo, L., Manzoni, C., Rizig, M., Ryten, M., Guelfi, S., Escott-Price, V., Chelban, V., Foltynie, T., Williams, N., Morrison, K.E., Clarke, C., Brice, A., Danjou, F., Lesage, S., Corvol, J.C., Martinez, M., Schulte, C., Brockmann, K., Simoon-Saanchez, J., Heutink, P., Rizzu, P., Sharma, M., Gasser, T., Nicolas, A., Cookson, M.R., Blauwendraat, C., Craig, D.W., Faghri, F., Gibbs, J.R., Hernandez, D.G., Keuren-Jensen, K. van, Shulman, J.M., Iwaki, H., Leonard, H.L., Nalls, M.A., Robak, L., Lubbe, S., Finkbeiner, S., Mencacci, N.E., Lungu, C., Scholz, S.W., Reed, X., Alcalay, R.N., Gan-Or, Z., Rouleau, G.A., Krohn, L., Hilten, J.J. van, Marinus, J., Adarmes-Goomez, A.D., Aguilar, I., Alvarez, I., Alvarez, V., Barrero, F.J., Yarza, J.A.B., Bernal-Bernal, I., Blazquez, M., Bonilla-Toribio, M., Botia, J.A., Boungiorno, M.T., Buiza-Rueda, D., Camara, A., Carrillo, F., Carrion-Claro, M., Cerdan, D., Clarimon, J., Compta, Y., Casa, B. de la, Diez-Fairen, M., Dols-Icardo, O., Duarte, J., Duran, R., Escamilla-Sevilla, F., Ezquerra, M., Feliz, C., Fernandez, M., Garcia, C., Garcia-Ruiz, P., Gomez-Garre, P., Heredia, M.J.G., Gonzalez-Aramburu, I., Pagola, A.G., Hoenicka, J., Infante, J., Jesus, S., Jimenez-Escrig, A., Kulisevsky, J., Labrador-Espinosa, M.A., Lopez-Sendon, J.L., Arregui, A.L.D., Macias, D., Torres, I.M., Marin, J., Marti, M.J., Martinez-Castrillo, C., Mendez-del-Barrio, C., Gonzalez, M.M., Mata, M., Minguez, A., Mir, P., Rezola, E.M., Munoz, E., Pagonabarraga, J., Pascual-Sedano, B., Pastor, P., Errazquin, F.P., Perinan-Tocino, T., Ruiz-Martinez, J., Ruz, C., Rodriguez, A.S., Sierra, M., Suarez-Sanmartin, E., Tabernero, C., Tartari, J.P., Tejera-Parrado, C., Valldeoriola, F., Vargas-Gonzalez, L., Vela, L., Vives, F., Zimprich, A., Pihlstrom, L., Toft, M., Koks, S., Taba, P., Hassin-Baer, S., Malagelada, C., Int Parkinson's Dis Genomics Conso
المساهمون: Fundació La Marató de TV3, Michael J. Fox Foundation for Parkinson's Research, National Institutes of Health (US), Ministerio de Economía y Competitividad (España), Agencia Estatal de Investigación (España), Ministerio de Ciencia, Innovación y Universidades (España)
المصدر: Mov Disord
Movement disorders 34(9), 1333-1344 (2019). doi:10.1002/mds.27770
Digital.CSIC. Repositorio Institucional del CSIC
instname
Movement Disorders, 34(9), 1333-1344
MOVEMENT DISORDERS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pauمصطلحات موضوعية: 0301 basic medicine, epistasis, Male, Parkinson's disease, very elderly, alpha-synuclein, Alpha‐synuclein, regulatory associated protein of mTOR, Cohort Studies, 0302 clinical medicine, single nucleotide polymorphism, genetics, Age of Onset, Genetics, Aged, 80 and over, Polymorphism, Single Nucleoti, biology, TOR Serine-Threonine Kinases, target of rapamycin kinase, fchsd1 gene, Age at onset, Chromosome Mapping, glycogen synthase kinase 3beta, Parkinson Disease, Middle Aged, cohort analysis, LRRK2, priority journal, Neurology, chromosomal mapping, neuromodulation, mTOR, alpha-Synuclein, Female, age at onset, Signal Transduction, onset age, Adult, MTOR protein, human, protein kinase LKB1, gene locus, Genotype, multifactor dimensionality reduction, SNP, Single-nucleotide polymorphism, rps6ka2 gene, Polymorphism, Single Nucleotide, Risk Assessment, Article, brain function, 03 medical and health sciences, alpha synuclein, medicine, Humans, controlled study, Genetic Predisposition to Disease, human, ddc:610, SNCA protein, human, gene, Mechanistic target of rapamycin, PI3K/AKT/mTOR pathway, mammalian target of rapamycin, Aged, RPTOR, Epistasis, Genetic, Odds ratio, medicine.disease, major clinical study, nervous system diseases, 030104 developmental biology, mTOR signaling, biology.protein, Epistasis, pathology, Neurology (clinical), genetic predisposition, 030217 neurology & neurosurgery
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المؤلفون: Baatt, C. de, Stiphout, M.A.E. van, Marinus, J., Hilten, J.J. van
المصدر: Parkinsonism and Related Disorders, 46, E13-E13
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::55f275b1747c05a9ea9b92f221e48e13
https://hdl.handle.net/1887/96509 -
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المؤلفون: Marinus, J., Hilten, J.J. van
المصدر: Movement Disorders, 30(3), 379-385
مصطلحات موضوعية: Male, medicine.medical_specialty, Parkinson's disease, motor distribution pattern, Excessive daytime sleepiness, Disease, Motor Activity, Audiology, Severity of Illness Index, Functional Laterality, Cohort Studies, Disease severity, cohort study, medicine, Humans, Aged, symmetry, Confounding, Parkinson Disease, Cognition, Middle Aged, medicine.disease, Neurology, Potential change, Disease Progression, Physical therapy, Female, Neurology (clinical), medicine.symptom, Psychology, Cohort study
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المؤلفون: Egmond, M.E. van, Lugtenberg, C.H.A., Brouwer, O.F., Contarino, M.F., Fung, V.S.C., Heiner-Fokkema, M.R., Hilten, J.J. van, Hout, A.H. van der, Peall, K.J., Sinke, R.J., Roze, E., Verschuuren-Bemelmans, C.C., Willemsen, M.A., Wolf, N.I., Tijssen, M.A., Koning, T.J. de
المصدر: Movement Disorders, 32, 4, pp. 569-575
Movement Disorders, 32, 569-575
Movement Disorders, 32(4), 569-575مصطلحات موضوعية: gene panel analysis, diagnostic yield, cost, next-generation sequencing, dystonia, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3]
وصف الملف: application/pdf
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المؤلفون: Bank, P.J.M., Marinus, J., Groot, J.H. de, Meskers, C.G.M., Hilten, J.J. van
المصدر: Movement Disorders, 31, S505-S505
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d45e3d0432fe97248dc584dda977e353
http://hdl.handle.net/1887/113084