Browsing by Author Klein, Christine

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Showing results 1 to 15 of 15
Issue DateTitleAuthor(s)Citation
2012ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndromeSue, Carolyn; Arns, Bjorn; Grunewald, A; Klein, Christine; Munchau, Alexander; Rakovic, Aleksandar; Ramirez, Alfredo; Seibler, Philip; Northern Clinical School: MedicineATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome, Neurobiology of Aging, vol.33, 8, 2012,pp e1-e7
2012Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's diseaseKumar, Kishore; Bruggemann, Norbert; Buhmann, Carsten; Hagenah, Johann; Kasten, Meike; Kertelge, Lena; Klein, Christine; Lencer, Rebekka; Lohmann, Katja; Schmidt, Alexander; Siebner, Hartwig; Tadic, Vera; Van der Vegt, Joyce; Northern Clinical School: Kolling InstituteDepression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease, Movement Disorders, vol.27, 6, 2012,pp 754-759
2012Genetics of Parkinson disease and other movement disordersKumar, Kishore; Klein, Christine; Lohmann, Katja; Northern Clinical School: Kolling InstituteGenetics of Parkinson disease and other movement disorders, Current Opinion In Neurology, vol.25, 4, 2012,pp 466-474
2013Glucocerebrosidase mutations in a Serbian Parkinson's disease populationKumar, Kishore Raj; Sue, Carolyn; Alcalay, Roy N; Gobel, Anna; Grunewald, A; Klein, Christine; Kostic, Vladimir S; Krainc, Dimitri; Kresojevic, Nikola D; Lohmann, Katja; Mazzulli, Joseph R; Ramirez, Alfredo R; Rolfs, Arndt; Svetel, Marina; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineGlucocerebrosidase mutations in a Serbian Parkinson's disease population, European Journal of Neurology, vol.20, 2, 2013,pp 402-405
2008The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD studyCorbett, Alastair; Nicholson, Garth; et al, Not Known; Golbe, Lawrence I.; Growdon, J; Klein, Christine; Latourelle, J.C.; Lew, M.; Mark, Margery H.; Suchowersky, Oksana; Sun, Mei; Watts, Ray L; Wooten, Frederick; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteThe Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study, B M C Medicine, vol.6,(32),2008,pp 32-1-32-7
2008Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD studyCorbett, Alastair; Nicholson, Garth; et al, Not Known; Golbe, Lawrence I.; Growdon, J; Klein, Christine; Latourelle, J.C.; Lew, M.; MacDonald, M E; Mark, Margery H.; McNicoll, Christopher F; Suchowersky, Oksana; Wooten, G. F.; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteHuntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study, Movement Disorders, vol.23,(11),2008,pp 1596-1601
2006Influence of heterozygosity for Parkin mutation on onset age in familial Parkinson disease The GenePD study.Nicholson, Garth; et, al; Golbe, Lawrence I.; Klein, Christine; Latourelle, Jeanne C.; Lew, Mark F.; Mark, Margery H.; Racette, Brad A.; Shill, Holly A.; Sun, Mei; Wooten, Frederick; Concord Clinical School: ANZAC Research InstituteInfluence of heterozygosity for Parkin mutation on onset age in familial Parkinson disease The GenePD study., Archives of Neurology, February 2005, vol.63,(6),2006,pp 826-832
2010Mutant Parkin Impairs Mitochondrial Function and Morphology in Human FibroblastsGrunewald, Anne; Sue, Carolyn; Vandebona, Himesha; Hemmelmann, Claudia; Kasten, Meike; Klein, Christine; Lohmann - Hedrich, K.; Orolicki, Slobodanka; Pramstaller, Peter P; Rakovic, Aleksandar; Ramirez, Alfredo; Schapira, Anthony H V; Voges, Lisa; Northern Clinical School: Kolling Institute; Northern Clinical School: Medicine; Northern Clinical School: Kolling InstituteMutant Parkin Impairs Mitochondrial Function and Morphology in Human Fibroblasts, PLoS One, vol.5, 9,pp e12962-1-e12962-6
2013Phenomenology and classification of dystonia: a consensus updateFung, Victor; Albanese, Alberto; Bhatia, Kailash P; Bressman, Susan; DeLong, Mahlon; Fahn, Stanley; Hallett, Mark; Jancovic, Joseph; Jinnah, H. A.; Klein, Christine; Lang, Anthony; Mink, Jonathan; Teller, Jan K; Western Clinical School: Medicine (Westmead)Phenomenology and classification of dystonia: a consensus update, Movement Disorders, vol.28, 7, 2013,pp 863-873
2015Presenting symptoms of GBA-related Parkinson's diseaseKumar, Kishore Raj; Dobricic, Valerija; Dragasevic, Natasa; Jankovic, Milena; Klein, Christine; Kostic, Vladimir S; Kresojevic, Nikola D; Novakovic, Ivana; Pekmezovic, Tatjana; Petrovic, Igor; Svetel, Marina; Northern Clinical School: Kolling InstitutePresenting symptoms of GBA-related Parkinson's disease, Parkinsonism and Related Disorders, vol.21, 7, 2015,pp 804-807
2008Replication of association between ELAVL4 and Parkinson disease: the GenePD studyCorbett, Alastair; Nicholson, Garth; DeStefano, Anita; et al, Not Known; Golbe, L. I.; Growdon, J; Klein, Christine; Latourelle, J.C.; Lew, M.; Mark, Margery H.; Suchowersky, Oksana; Watts, Ray L; Wooten, G. F.; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteReplication of association between ELAVL4 and Parkinson disease: the GenePD study, Human Genetics, vol.124,(1),2008,pp 95-99
2017Screening study of TUBB4A in isolated dystoniaKumar, Kishore Raj; Bruggemann, Norbert; Chung, Sun Ju; Defazio, Giovanni; Domingo, Aloysius; Klein, Christine; Lohmann, Katja; Mir, Pablo; Ozelius, Laurie J.; Rakovic, Aleksandar; Schaake, Susen; Simonyan, Kristina; Vulinovic, Franca; Northern Clinical School: Kolling InstituteScreening study of TUBB4A in isolated dystonia, Parkinsonism and Related Disorders, vol.41, N/A, 2017,pp 118-120
2013Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegiaBlair, Nicholas; Kumar, Kishore; Liang, Christina; Ng, Karl; Sue, Carolyn; Vandebona, Himesha; Gölnitz, Uta; Grünewald, A.; Klein, Christine; Rolfs, Arndt; Saviouk, Viatcheslav; Sharpe, David; School of Public Health: Public Health; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Central Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Kolling InstituteTargeted next generation sequencing in SPAST-negative hereditary spastic paraplegia, Journal of Neurology, vol.260, 10, 2013,pp 2516-2522
2012Two Faces of the Same Coin: Benign Familial Infantile Seizures and Paroxysmal Kinesigenic Dyskinesia Caused by PRRT2 MutationsKumar, Kishore; Sue, Carolyn; Christen, Hans-Jurgen; Grunewald, A; Hagenah, Johann; Hartmann, Hans; Klein, Christine; Leben, Matthias; Lohmann, Katja; Munchau, Alexander; Redyk, Katharina; Schmidt, Alexander; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineTwo Faces of the Same Coin: Benign Familial Infantile Seizures and Paroxysmal Kinesigenic Dyskinesia Caused by PRRT2 Mutations, JAMA Neurology (formerly Archives of Neurology), vol.69, 5, 2012,pp 668-670
2015Unusual a-synuclein and cerebellar pathologies in a case of hereditary myoclonus-dystonia without SGCE mutationFung, Victor; Halliday, Glenda M.; Klein, Christine; McCann, Heather; Western Clinical School: Medicine (Westmead)Unusual a-synuclein and cerebellar pathologies in a case of hereditary myoclonus-dystonia without SGCE mutation, Neuropathology and applied neurobiology, vol.41, 6, 2015,pp 837-842