Tim Lynch - Publications

Affiliations: 
Neurology University College Dublin, Dublin, County Dublin, Ireland 
Area:
genetics of Parkinson’s disease, neurodegeneration and other movement disorders
Website:
http://www.neurologicalinstitute.ie/about-the-neurological-institute/prof-tim-lynch-consultant-neurologist

129 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Olszewska DA, Lynch T. Lysosomal Storage Disorders and Parkinson's Disease: New Susceptibility Loci Identified. Movement Disorders Clinical Practice. 5: 404-405. PMID 30838294 DOI: 10.1002/mdc3.12625  0.44
2018 Paramanandam V, Hadjivassiliou M, Olszewska DA, Munteanu T, Williams L, Magennis B, Fearon C, O'Connell M, Sarrigiannis P, Lynch T. Reversible Corticobasal Syndrome due to Coeliac Disease. Movement Disorders Clinical Practice. 5: 551-554. PMID 30637273 DOI: 10.1002/mdc3.12659  0.44
2018 Olszewska DA, McVeigh T, Fallon EM, Pastores GM, Lynch T. The benefits of a Neurogenetics clinic in an adult Academic Teaching Hospital. Irish Journal of Medical Science. PMID 29524103 DOI: 10.1007/s11845-018-1784-3  0.44
2017 Olszewska DA, McCarthy A, Murray B, Magennis B, Connolly S, Lynch T. A Wolf in Sheep's Clothing: An "Alien Leg" in Corticobasal Syndrome. Tremor and Other Hyperkinetic Movements (New York, N.Y.). 7: 455. PMID 28469972 DOI: 10.7916/D86D5ZT8  0.44
2017 Olszewska DA, Lynch T. Nature's Parkin experiment: Nix-a novel protective mechanism in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28432765 DOI: 10.1002/mds.27015  0.44
2016 Olszewska DA, Walsh R, Lynch T. SCA 6 with Writer's Cramp: The Phenotype Expanded. Movement Disorders Clinical Practice. 3: 83-86. PMID 30713900 DOI: 10.1002/mdc3.12222  0.44
2016 Olszewska DA, Lynch T. New Light Shed on Leucine-Rich Repeat Kinase 2 (LRRK2) Kinase Inhibitors in Parkinson's Disease. Movement Disorders Clinical Practice. 3: 241-242. PMID 30363548 DOI: 10.1002/mdc3.12333  0.44
2016 Olszewska DA, Fearon C, Lynch T. Loss of visual feedback revealing motor impairment - an early symptom of Parkinson's disease in two Irish farmers. Journal of Clinical Movement Disorders. 3: 12. PMID 28035288 DOI: 10.1186/s40734-016-0040-0  0.44
2016 Olszewska DA, Lonergan R, Fallon EM, Lynch T. Genetics of Frontotemporal Dementia. Current Neurology and Neuroscience Reports. 16: 107. PMID 27878525 DOI: 10.1007/s11910-016-0707-9  0.44
2016 Olszewska DA, Fearon C, Lynch T. Novel gene (TMEM230) linked to Parkinson's disease. Journal of Clinical Movement Disorders. 3: 17. PMID 27872751 DOI: 10.1186/s40734-016-0046-7  0.44
2016 Olszewska DA, Lynch T. PINK1, parkin, and autophagy receptors: A new model of mitophagy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27709687 DOI: 10.1002/mds.26812  0.44
2016 Olszewska DA, McCarthy A, Lynch T. Commentary: Parkinson's Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein. Frontiers in Neuroscience. 10: 162. PMID 27147954 DOI: 10.3389/fnins.2016.00162  0.44
2016 Fearon C, Vijayashankar P, Olszewska DA, Goggin C, Magennis B, Quigley G, Lynch T. Micrographia following bilateral subthalamic nucleus deep brain stimulation. Parkinsonism & Related Disorders. PMID 27132462 DOI: 10.1016/j.parkreldis.2016.04.004  0.44
2016 Olszewska DA, Lynch T. MUL1-A new potential for a therapeutic target for Parkinson's disease a commentary on "MUL1 acts in parallel to the PINK1/parkin pathway in regulating mitofusin and compensates for loss of PINK1/parkin" by Yun and colleagues (eLife 2014; 3: 1-26). Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27126246 DOI: 10.1002/mds.26652  0.44
2016 Olszewska DA, Lynch T. Is PARK10 a Locus for Familial PD? Yes or Not? Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27090980 DOI: 10.1002/mds.26612  0.44
2015 Olszewska DA, Lynch T. Lewy Bodies' absence in grafted dopaminergic transplants in Parkinson's Disease. Movement Disorders Clinical Practice. 2: 369-370. PMID 30363538 DOI: 10.1002/mdc3.12180  0.44
2015 Butler JS, Beiser IM, Williams L, McGovern E, Molloy F, Lynch T, Healy DG, Moore H, Walsh R, Reilly RB, O'Riordan S, Walsh C, Hutchinson M. Age-Related Sexual Dimorphism in Temporal Discrimination and in Adult-Onset Dystonia Suggests GABAergic Mechanisms. Frontiers in Neurology. 6: 258. PMID 26696957 DOI: 10.3389/fneur.2015.00258  0.48
2015 Ogaki K, Koga S, Heckman MG, Fiesel FC, Ando M, Labbé C, Lorenzo-Betancor O, Moussaud-Lamodière EL, Soto-Ortolaza AI, Walton RL, Strongosky AJ, Uitti RJ, McCarthy A, Lynch T, Siuda J, et al. Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders. Neurology. PMID 26561290 DOI: 10.1212/WNL.0000000000002170  0.48
2015 Fearon C, Butler JS, Newman L, Lynch T, Reilly RB. Audiovisual Processing is Abnormal in Parkinson's Disease and Correlates with Freezing of Gait and Disease Duration. Journal of Parkinson's Disease. PMID 26485427 DOI: 10.3233/JPD-150655  0.48
2015 Killane I, Fearon C, Newman L, McDonnell C, Waechter SM, Sons K, Lynch T, Reilly RB. Dual Motor-Cognitive Virtual Reality Training Impacts Dual-Task Performance in Freezing of Gait. Ieee Journal of Biomedical and Health Informatics. 19: 1855-61. PMID 26394439 DOI: 10.1109/JBHI.2015.2479625  0.48
2015 Wang L, Aasly JO, Annesi G, Bardien S, Bozi M, Brice A, Carr J, Chung SJ, Clarke C, Crosiers D, Deutschländer A, Eckstein G, Farrer MJ, Goldwurm S, Garraux G, ... ... Lynch T, et al. Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. Neurology. PMID 26354989 DOI: 10.1212/WNL.0000000000002016  0.48
2015 Labbé C, Ogaki K, Lorenzo-Betancor O, Soto-Ortolaza AI, Walton RL, Rayaprolu S, Fujioka S, Murray ME, Heckman MG, McCarthy A, Lynch T, Siuda J, Opala G, Rudzinska M, Krygowska-Wajs A, et al. Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies. Neurology. PMID 26333800 DOI: 10.1212/WNL.0000000000001946  0.48
2015 McCarthy A, Lonergan R, Olszewska DA, O'Dowd S, Cummins G, Magennis B, Fallon EM, Pender N, Huey ED, Cosentino S, O'Rourke K, Kelly BD, O'Connell M, Delon I, Farrell M, ... ... Lynch T, et al. Closing the tau loop: the missing tau mutation. Brain : a Journal of Neurology. PMID 26297556 DOI: 10.1093/brain/awv234  0.48
2015 Iovino M, Agathou S, González-Rueda A, Del Castillo Velasco-Herrera M, Borroni B, Alberici A, Lynch T, O'Dowd S, Geti I, Gaffney D, Vallier L, Paulsen O, Káradóttir RT, Spillantini MG. Early maturation and distinct tau pathology in induced pluripotent stem cell-derived neurons from patients with MAPT mutations. Brain : a Journal of Neurology. PMID 26220942 DOI: 10.1093/brain/awv222  0.48
2015 Labbé C, Ogaki K, Lorenzo-Betancor O, Carrasquillo MM, Heckman MG, McCarthy A, Soto-Ortolaza AI, Walton RL, Lynch T, Siuda J, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Dickson DW, et al. Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus. Plos One. 10: e0128586. PMID 26090850 DOI: 10.1371/journal.pone.0128586  0.48
2015 Govern EM, Judge EP, Kavanagh E, Gaine S, Lynch T. Interferon beta related pulmonary arterial hypertension; an emerging worrying entity? Multiple Sclerosis and Related Disorders. 4: 284-6. PMID 26008947 DOI: 10.1016/j.msard.2015.03.008  0.48
2015 Olszewska DA, Chalissery AJ, Williams J, Lynch T, Smyth S. Speech myoclonus due to probable pregabalin adverse drug-reaction. Parkinsonism & Related Disorders. 21: 823-4. PMID 25956204 DOI: 10.1016/j.parkreldis.2015.04.026  0.44
2015 Olszewska DA, Lynch T. Will crystal parkin help in understanding the future of Parkinson's disease? Frontiers in Neurology. 6: 35. PMID 25759682 DOI: 10.3389/fneur.2015.00035  0.48
2015 O'Toole O, Murphy O, O'Dwyer J, Lonergan R, Keogh B, Tubridy N, Lynch T, Farrell M. Paraneoplastic dentate ganglionopathy: clinical and neuroimmunologic studies. Clinical Neuropathology. 34: 34-38. PMID 25074875 DOI: 10.5414/NP300754  0.48
2015 Molloy A, Kimmich O, Williams L, Butler JS, Byrne N, Molloy F, Moore H, Healy DG, Lynch T, Edwards MJ, Walsh C, Reilly RB, O'Riordan S, Hutchinson M. An evaluation of the role of environmental factors in the disease penetrance of cervical dystonia. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 331-5. PMID 24963124 DOI: 10.1136/jnnp-2014-307699  0.48
2015 Lorenzo-Betancor O, Ogaki K, Soto-Ortolaza AI, Labbe C, Walton RL, Strongosky AJ, van Gerpen JA, Uitti RJ, Mclean PJ, Springer W, Siuda J, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, ... ... Lynch T, et al. DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients European Journal of Neurology. 22: 1323-1325. DOI: 10.1111/ene.12770  0.48
2015 Waechter SM, Fearon C, McDonnell C, Gallego J, Quinlivan B, Killane I, Butler JS, Lynch T, Reilly RB. The impact of dual tasking on cognitive performance in a Parkinson's disease cohort with and without freezing of gait: An EEG and behavioral based approach International Ieee/Embs Conference On Neural Engineering, Ner. 2015: 1072-1075. DOI: 10.1109/NER.2015.7146813  0.48
2014 Olszewska DA, Fearon C, Lynch T. New Perception of Mitochondrial Regulatory Pathway in Parkinsonism - Ubiquitin, PINK1, and Parkin. Frontiers in Neurology. 5: 247. PMID 25505445 DOI: 10.3389/fneur.2014.00247  0.48
2014 Peall KJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine PE, Lynch B, Kirov G, O'Riordan S, ... ... Lynch T, et al. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. Journal of Neurology. 261: 2296-304. PMID 25209853 DOI: 10.1007/s00415-014-7488-3  0.48
2014 McKinley J, O'Connell M, Farrell M, Lynch T. Normal dopamine transporter imaging does not exclude multiple system atrophy. Parkinsonism & Related Disorders. 20: 933-4. PMID 24861660 DOI: 10.1016/j.parkreldis.2014.04.022  0.48
2014 Hutchinson M, Isa T, Molloy A, Kimmich O, Williams L, Molloy F, Moore H, Healy DG, Lynch T, Walsh C, Butler J, Reilly RB, Walsh R, O'Riordan S. Cervical dystonia: a disorder of the midbrain network for covert attentional orienting. Frontiers in Neurology. 5: 54. PMID 24803911 DOI: 10.3389/fneur.2014.00054  0.48
2014 Pfeffer G, Gorman GS, Griffin H, Kurzawa-Akanbi M, Blakely EL, Wilson I, Sitarz K, Moore D, Murphy JL, Alston CL, Pyle A, Coxhead J, Payne B, Gorrie GH, Longman C, ... ... Lynch T, et al. Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance. Brain : a Journal of Neurology. 137: 1323-36. PMID 24727571 DOI: 10.1093/brain/awu060  0.48
2014 Shannon B, Soto-Ortolaza A, Rayaprolu S, Cannon HD, Labbé C, Benitez BA, Choi J, Lynch T, Boczarska-Jedynak M, Opala G, Krygowska-Wajs A, Barcikowska M, Van Gerpen JA, Uitti RJ, Springer W, et al. Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease. Neurobiology of Aging. 35: 1958.e1-2. PMID 24684791 DOI: 10.1016/j.neurobiolaging.2014.03.004  0.48
2014 Kimmich O, Molloy A, Whelan R, Williams L, Bradley D, Balsters J, Molloy F, Lynch T, Healy DG, Walsh C, O'Riordan S, Reilly RB, Hutchinson M. Temporal discrimination, a cervical dystonia endophenotype: penetrance and functional correlates. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 804-11. PMID 24482092 DOI: 10.1002/mds.25822  0.48
2014 Mulroy E, McCarthy A, Lynch T, Costello D, Ross OA. Asymmetrical leg atrophy in levodopa-responsive dystonia due to a novel GTP cyclohydrolase mutation. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 425-6. PMID 24474670 DOI: 10.1002/mds.25813  0.48
2014 McCarthy A, McKinley J, Lynch T. Putting the downstream breaks on neurodegeneration? Movement Disorders : Official Journal of the Movement Disorder Society. 29: 186. PMID 24375885 DOI: 10.1002/mds.25744  0.48
2014 Allen NM, Lin JP, Lynch T, King MD. Status dystonicus: a practice guide. Developmental Medicine and Child Neurology. 56: 105-12. PMID 24304390 DOI: 10.1111/dmcn.12339  0.48
2014 Salomone S, Robertson IH, Lynch T, Balsters JH, Fearon C, Marnane M, Pender NP, Dockree PM. The effects of immunologic brainstem encephalopathy on cognitive function following awakening from a progressive autoimmune coma. Neurocase. 20: 569-80. PMID 23998396 DOI: 10.1080/13554794.2013.826688  0.48
2014 Heckman MG, Elbaz A, Soto-Ortolaza AI, Serie DJ, Aasly JO, Annesi G, Auburger G, Bacon JA, Boczarska-Jedynak M, Bozi M, Brighina L, Chartier-Harlin MC, Dardiotis E, Destée A, Ferrarese C, ... ... Lynch T, et al. Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants. Neurobiology of Aging. 35: 266.e5-14. PMID 23962496 DOI: 10.1016/j.neurobiolaging.2013.07.013  0.48
2014 McKinley JJ, McCarthy A, Kavanagh E, Lynch T. Neurological picture. Neurological ornithology. Journal of Neurology, Neurosurgery, and Psychiatry. 85: 239-40. PMID 23946417 DOI: 10.1136/jnnp-2013-305845  0.48
2013 McKinley J, McCarthy A, Lynch T. Don'T lose sleep over neurodegeneration-it helps clear amyloid Beta. Frontiers in Neurology. 4: 206. PMID 24391624 DOI: 10.3389/fneur.2013.00206  0.48
2013 An K, Klyubin I, Kim Y, Jung JH, Mably AJ, O'Dowd ST, Lynch T, Kanmert D, Lemere CA, Finan GM, Park JW, Kim TW, Walsh DM, Rowan MJ, Kim JH. Exosomes neutralize synaptic-plasticity-disrupting activity of Aβ assemblies in vivo. Molecular Brain. 6: 47. PMID 24284042 DOI: 10.1186/1756-6606-6-47  0.48
2013 Cummins G, Jawad T, Taylor M, Lynch T. Myoclonic head jerks and extensor axial dystonia in the variant form of ataxia telangiectasia. Parkinsonism & Related Disorders. 19: 1173-4. PMID 24120321 DOI: 10.1016/j.parkreldis.2013.08.013  0.48
2013 Hutchinson M, Kimmich O, Molloy A, Whelan R, Molloy F, Lynch T, Healy DG, Walsh C, Edwards MJ, Ozelius L, Reilly RB, O'Riordan S. The endophenotype and the phenotype: temporal discrimination and adult-onset dystonia. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1766-74. PMID 24108447 DOI: 10.1002/mds.25676  0.48
2013 McKinley J, McCarthy A, Lynch T. Pathogenic LRRK2 mutations in nuclear ageing--a new organelle to study in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1344-5. PMID 24078329 DOI: 10.1002/mds.25595  0.48
2013 McKinley J, McCarthy A, Lynch T. In vivo Photometry during Movement Changes Our Understanding of the Direct and Indirect Pathways. Frontiers in Neurology. 4: 118. PMID 23966975 DOI: 10.3389/fneur.2013.00118  0.48
2013 Heckman MG, Soto-Ortolaza AI, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, ... ... Lynch T, et al. Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1740-4. PMID 23913756 DOI: 10.1002/mds.25600  0.48
2013 Joyce E, Mulroy E, Scott J, Melling J, Goggin C, McGorrian C, O'Rourke K, Lynch T, Mahon N. Subclinical myocardial dysfunction in multiple sclerosis patients remotely treated with mitoxantrone: evidence of persistent diastolic dysfunction. Journal of Cardiac Failure. 19: 571-6. PMID 23910587 DOI: 10.1016/j.cardfail.2013.06.003  0.48
2013 Elhassan Y, Kiernan D, Lynch T, O'Brien T. Bilateral knee extensor disruption in severe crouch gait. Bmj Case Reports. 2013. PMID 23814213 DOI: 10.1136/bcr-2013-010337  0.48
2013 Rayaprolu S, Mullen B, Baker M, Lynch T, Finger E, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C, Kertesz A, Bigio EH, Lippa C, Josephs KA, Knopman DS, White CL, Caselli R, et al. TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease. Molecular Neurodegeneration. 8: 19. PMID 23800361 DOI: 10.1186/1750-1326-8-19  0.48
2013 Volpe D, Signorini M, Marchetto A, Lynch T, Morris ME. A comparison of Irish set dancing and exercises for people with Parkinson's disease: a phase II feasibility study. Bmc Geriatrics. 13: 54. PMID 23731986 DOI: 10.1186/1471-2318-13-54  0.48
2013 Graham D, McCarthy A, Kavanagh E, O'Rourke K, Lynch T. Teaching NeuroImages: longitudinally extensive transverse myelitis in neuro-Behcet disease. Neurology. 80: e189-90. PMID 23628935 DOI: 10.1212/WNL.0b013e3182904d2e  0.48
2013 McCarthy A, Farrell M, Hedley-Whyte T, McGuone D, Kavanagh E, McNally S, Keogan M, Horgan N, Lynch T, O'Rourke K. Granulomatosis with polyangiitis masquerading as giant cell arteritis Journal of Neurology. 260: 1661-1663. PMID 23579235 DOI: 10.1007/s00415-013-6913-3  0.48
2013 Doherty KM, Silveira-Moriyama L, Parkkinen L, Healy DG, Farrell M, Mencacci NE, Ahmed Z, Brett FM, Hardy J, Quinn N, Counihan TJ, Lynch T, Fox ZV, Revesz T, Lees AJ, et al. Parkin disease: a clinicopathologic entity? Jama Neurology. 70: 571-9. PMID 23459986 DOI: 10.1001/jamaneurol.2013.172  0.48
2013 Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, ... ... Lynch T, et al. SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain : a Journal of Neurology. 136: 294-303. PMID 23365103 DOI: 10.1093/brain/aws308  0.48
2013 O'Dowd ST, Ardah MT, Johansson P, Lomakin A, Benedek GB, Roberts KA, Cummins G, El Agnaf OM, Svensson J, Zetterberg H, Lynch T, Walsh DM. The ELISA-measured increase in cerebrospinal fluid tau that discriminates Alzheimer's disease from other neurodegenerative disorders is not attributable to differential recognition of tau assembly forms. Journal of Alzheimer's Disease : Jad. 33: 923-8. PMID 23034520 DOI: 10.3233/JAD-2012-121393  0.48
2013 McCarthy A, McKinley J, Lynch T. The inherent susceptibility of dorsal motor nucleus cholinergic neurons to the neurodegenerative process in parkinson's disease Frontiers in Neurology. 3. DOI: 10.3389/fneur.2012.00189  0.48
2012 Mulroy E, Quigley G, Roberts K, Cummins G, Magennis B, Fortune G, O'Brien D, Blunnie WP, Harrington E, Gillivan-Murphy P, Kavanagh E, Gilligan P, Reilly R, Scolaí PO, Kelly S, ... ... Lynch T, et al. Deep brain stimulation in ireland for Parkinson's disease and essential tremor. Irish Medical Journal. 105: 278-80. PMID 23155918  0.48
2012 Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Bertram L, Bozi M, Barcikowska M, Crosiers D, Clarke CE, Facheris MF, Farrer M, Garraux G, Gispert S, Auburger G, ... ... Lynch T, et al. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics. 49: 721-6. PMID 23125461 DOI: 10.1136/jmedgenet-2012-101155  0.48
2012 O'Dowd S, Curtin D, Waite AJ, Roberts K, Pender N, Reid V, O'Connell M, Williams NM, Morris HR, Traynor BJ, Lynch T. C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1072-4. PMID 22807188 DOI: 10.1002/mds.25022  0.48
2012 Lynch T. Commentary on "Cluster of partial motor seizures heralding the onset of hemi-myoclonic SSPE". Movement Disorders : Official Journal of the Movement Disorder Society. 27: 960-1. PMID 22807185 DOI: 10.1002/mds.25069  0.48
2012 Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Van Broeckhoven C, Bertram L, Bozi M, Crosiers D, Clarke C, Facheris M, Farrer M, Garraux G, Gispert S, Auburger G, ... ... Lynch T, et al. Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology. 79: 659-67. PMID 22786590 DOI: 10.1212/WNL.0b013e318264e353  0.48
2012 McCarthy A, Dineen J, McKenna P, Keogan M, Sheehan J, Lynch T, O'Rourke K. Anti-NMDA receptor encephalitis with associated catatonia during pregnancy Journal of Neurology. 259: 2632-2635. PMID 22752087 DOI: 10.1007/s00415-012-6561-z  0.48
2012 O'Dowd S, Murray B, Roberts K, Cummins G, Magennis B, Lynch T. Pallidopontonigral degeneration: a deceptive familial tauopathy. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 817-9. PMID 22729984 DOI: 10.1002/mds.24052  0.48
2012 Yssel J, Casey E, O'Rourke K, Magennis B, Lynch T. The role of a movement disorders clinic Irish Medical Journal. 105: 57-59. PMID 22455244  0.48
2012 Walsh RA, Gillivan-Murphy P, Murphy C, Colreavy M, O'Rourke K, Lynch T. Bilateral cerebellar stroke presenting with acute dysphonia and late palatal tremor. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 346-8. PMID 22411846 DOI: 10.1002/mds.24055  0.48
2012 Kearney H, O'Dowd S, Murray B, Kavanagh E, O'Connell M, Lynch T. Re-emergence of artistic traits in a patient with frontotemporal dementia. Clinical Neurology and Neurosurgery. 114: 417-20. PMID 22169065 DOI: 10.1016/j.clineuro.2011.11.010  0.48
2012 Mulroy E, Joyce E, Scott J, Melling J, Goggin C, Mahon N, O'Rourke K, Lynch T. Long-term risk of leukaemia or cardiomyopathy after mitoxantrone therapy for multiple sclerosis. European Neurology. 67: 45-7. PMID 22156316 DOI: 10.1159/000334101  0.48
2012 Roberts K, Lynch T. Movement disorders following non-metal intoxications Movement Disorders in Neurologic and Systemic Disease. 234-246. DOI: 10.1017/CBO9781139175845.017  0.48
2012 O'Dowd S, Lynch T. Does secretion of aberrant tau underlie lesion spread in tauopathies? Movement Disorders. 27: 201-201. DOI: 10.1002/mds.24895  0.48
2011 Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, ... ... Lynch T, et al. Translation initiator EIF4G1 mutations in familial Parkinson disease. American Journal of Human Genetics. 89: 398-406. PMID 21907011 DOI: 10.1016/j.ajhg.2011.08.009  0.48
2011 Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, ... ... Lynch T, et al. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. The Lancet. Neurology. 10: 898-908. PMID 21885347 DOI: 10.1016/S1474-4422(11)70175-2  0.48
2011 Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, ... ... Lynch T, et al. Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Neurobiology of Aging. 32: 2108.e1-5. PMID 21782285 DOI: 10.1016/j.neurobiolaging.2011.05.024  0.48
2011 Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, ... ... Lynch T, et al. VPS35 mutations in Parkinson disease. American Journal of Human Genetics. 89: 162-7. PMID 21763482 DOI: 10.1016/j.ajhg.2011.06.001  0.48
2011 Dachsel JC, Wider C, Vilariño-Güell C, Aasly JO, Rajput A, Rajput AH, Lynch T, Craig D, Krygowska-Wajs A, Jasinska-Myga B, Opala G, Barcikowska M, Czyzewski K, Wu RM, Heckman MG, et al. Death-associated protein kinase 1 variation and Parkinson's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 18: 1090-3. PMID 21749573 DOI: 10.1111/j.1468-1331.2010.03255.x  0.48
2011 Mulroy E, Murphy S, Lynch T. Alexia without agraphia Irish Medical Journal. 104. PMID 21675099  0.48
2011 Puschmann A, Verbeeck C, Heckman MG, Soto-Ortolaza AI, Lynch T, Jasinska-Myga B, Opala G, Krygowska-Wajs A, Barcikowska M, Uitti RJ, Wszolek ZK, Ross OA. Human leukocyte antigen variation and Parkinson's disease. Parkinsonism & Related Disorders. 17: 376-8. PMID 21482477 DOI: 10.1016/j.parkreldis.2011.03.008  0.48
2011 Elbaz A, Ross OA, Ioannidis JP, Soto-Ortolaza AI, Moisan F, Aasly J, Annesi G, Bozi M, Brighina L, Chartier-Harlin MC, Destée A, Ferrarese C, Ferraris A, Gibson JM, Gispert S, ... ... Lynch T, et al. Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Annals of Neurology. 69: 778-92. PMID 21391235 DOI: 10.1002/ana.22321  0.48
2011 Walsh RA, Duggan J, Lynch T. Localisation of the applause sign in a patient with acute bilateral lenticular infarction. Journal of Neurology. 258: 1180-2. PMID 21267592 DOI: 10.1007/s00415-011-5904-5  0.48
2011 Cummins G, O'Hare A, Dunne R, Connolly S, O'Rourke K, Lynch T. "sixteen and a half": A novel pontine neuro-ophthalmological syndrome Journal of Neurology. 258: 1347-1348. PMID 21210137 DOI: 10.1007/s00415-010-5890-z  0.48
2011 Wider C, Vilariño-Güell C, Heckman MG, Jasinska-Myga B, Ortolaza-Soto AI, Diehl NN, Crook JE, Cobb SA, Bacon JA, Aasly JO, Gibson JM, Lynch T, Uitti RJ, Wszolek ZK, Farrer MJ, et al. SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 18: 876-81. PMID 21159074 DOI: 10.1111/j.1468-1331.2010.03297.x  0.48
2011 Kearney H, Murray B, Kavanagh E, O'Rourke K, Kelly P, Lynch T. Autoimmune encephalopathy presenting as a 'posterior circulation stroke'. Journal of Neurology. 258: 330-2. PMID 20865284 DOI: 10.1007/s00415-010-5749-3  0.48
2011 Burgunder JM, Schöls L, Baets J, Andersen P, Gasser T, Szolnoki Z, Fontaine B, Van Broeckhoven C, Di Donato S, De Jonghe P, Lynch T, Mariotti C, Spinazzola A, Tabrizi SJ, Tallaksen C, et al. EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 18: 207-17. PMID 20500522 DOI: 10.1111/j.1468-1331.2010.03069.x  0.48
2011 Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, ... ... Lynch T, et al. A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. Neurobiology of Aging. 32: 548.e9-18. PMID 20036034 DOI: 10.1016/j.neurobiolaging.2009.11.021  0.48
2011 Burgunder JM, Schöls L, Baets J, Andersen P, Gasser T, Szolnoki Z, Fontaine B, Van Broeckhoven C, Di Donato S, De Jonghe P, Lynch T, Mariotti C, Spinazzola A, Tabrizi SJ, Tallaksen C, et al. Molecular Diagnosis of Neurogenetic Disorders: Motoneuron, Peripheral Nerve and Muscle Disorders European Handbook of Neurological Management. 2: 97-109. DOI: 10.1002/9781444346268.ch8  0.48
2011 Burgunder JM, Finsterer J, Szolnoki Z, Fontaine B, Baets J, Van Broeckhoven C, Di Donato S, De Jonghe P, Lynch T, Mariotti C, Schöls L, Spinazzola A, Tabrizi SJ, Tallaksen C, Zeviani M, et al. Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias European Handbook of Neurological Management. 2: 87-96. DOI: 10.1002/9781444346268.ch7  0.48
2011 Gasser T, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen CME, et al. Molecular Diagnosis of Ataxias and Spastic Paraplegias European Handbook of Neurological Management. 2: 73-85. DOI: 10.1002/9781444346268.ch6  0.48
2011 Finsterer J, Harbo HF, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen C, et al. Molecular Diagnosis of Mitochondrial Disorders European Handbook of Neurological Management. 2: 61-72. DOI: 10.1002/9781444346268.ch5  0.48
2011 Harbo HF, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen C, et al. Molecular Diagnosis of Neurogenetic Disorders: General Issues, Huntington's Disease, Parkinson's Disease and Dystonias European Handbook of Neurological Management. 2: 51-60. DOI: 10.1002/9781444346268.ch4  0.48
2010 Vilariño-Güell C, Ross OA, Aasly JO, White LR, Rajput A, Rajput AH, Lynch T, Krygowska-Wajs A, Jasinska-Myga B, Opala G, Barcikowska M, Lee MC, Hentati F, Uitti RJ, Wszolek ZK, et al. An independent replication of PARK16 in Asian samples. Neurology. 75: 2248-9. PMID 21172849 DOI: 10.1212/WNL.0b013e318202031f  0.48
2010 Behrouz B, Vilariño-Güell C, Heckman MG, Soto-Ortolaza AI, Aasly JO, Sando S, Lynch T, Craig D, Uitti RJ, Wszolek ZK, Ross OA, Farrer MJ. Mitochondrial translation initiation factor 3 polymorphism and Parkinson's disease. Neuroscience Letters. 486: 228-30. PMID 20887776 DOI: 10.1016/j.neulet.2010.09.059  0.48
2010 Vilariño-Güell C, Wider C, Aasly JO, White LR, Rajput A, Rajput AH, Lynch T, Krygowska-Wajs A, Jasinska-Myga B, Opala G, Barcikowska M, Czyzewski K, Wu RM, Uitti RJ, Wszolek ZK, et al. Association of pyridoxal kinase and Parkinson disease. Annals of Neurology. 67: 409-11. PMID 20373354 DOI: 10.1002/ana.21962  0.48
2010 Burgunder JM, Finsterer J, Szolnoki Z, Fontaine B, Baets J, Van Broeckhoven C, Di Donato S, De Jonghe P, Lynch T, Mariotti C, Schöls L, Spinazzola A, Tabrizi SJ, Tallaksen C, Zeviani M, et al. EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 641-8. PMID 20298421 DOI: 10.1111/j.1468-1331.2010.02985.x  0.48
2010 Gasser T, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen CM, et al. EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 179-88. PMID 20050888 DOI: 10.1111/j.1468-1331.2009.02873.x  0.48
2010 Wider C, Vilariño-Güell C, Jasinska-Myga B, Heckman MG, Soto-Ortolaza AI, Cobb SA, Aasly JO, Gibson JM, Lynch T, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA. Association of the MAPT locus with Parkinson's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 483-6. PMID 19912324 DOI: 10.1111/j.1468-1331.2009.02847.x  0.48
2010 Soto-Ortolaza AI, Behrouz B, Wider C, Vilariño-Güell C, Heckman MG, Aasly JO, Mark Gibson J, Lynch T, Jasinska-Myga B, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, Wszolek ZK, et al. Calbindin-1 association and Parkinson's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 208-11. PMID 19674066 DOI: 10.1111/j.1468-1331.2009.02769.x  0.48
2009 Finsterer J, Harbo HF, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen CM, et al. EFNS guidelines on the molecular diagnosis of mitochondrial disorders. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 16: 1255-64. PMID 19950421 DOI: 10.1111/j.1468-1331.2009.02811.x  0.48
2009 Cobb SA, Wider C, Ross OA, Mata IF, Adler CH, Rajput A, Rajput AH, Wu RM, Hauser R, Josephs KA, Carr J, Gwinn K, Heckman MG, Aasly JO, Lynch T, et al. GCH1 in early-onset Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 2070-5. PMID 19735094 DOI: 10.1002/mds.22729  0.48
2009 Vilariño-Güell C, Chai H, Keeling BH, Young JE, Rajput A, Lynch T, Aasly JO, Uitti RJ, Wszolek ZK, Farrer MJ, Lin SC. MEIS1 p.R272H in familial restless legs syndrome. Neurology. 73: 243-5. PMID 19620614 DOI: 10.1212/WNL.0b013e3181ae7c79  0.48
2009 Harbo HF, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen C, et al. EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 16: 777-85. PMID 19469830 DOI: 10.1111/j.1468-1331.2009.02646.x  0.48
2009 Wider C, Lincoln SJ, Heckman MG, Diehl NN, Stone JT, Haugarvoll K, Aasly JO, Gibson JM, Lynch T, Rajput A, Rajput ML, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA. Phactr2 and Parkinson's disease. Neuroscience Letters. 453: 9-11. PMID 19429005 DOI: 10.1016/j.neulet.2009.02.009  0.48
2009 Marnane M, Lynch T, Scott J, Stack J, Kelly PJ. Steroid-unresponsive neurosarcoidosis successfully treated with adalimumab. Journal of Neurology. 256: 139-40. PMID 19219574 DOI: 10.1007/s00415-009-0077-1  0.48
2009 Wider C, Dachsel JC, Soto AI, Heckman MG, Diehl NN, Yue M, Lincoln S, Aasly JO, Haugarvoll K, Trojanowski JQ, Papapetropoulos S, Mash D, Rajput A, Rajput AH, Gibson JM, ... Lynch T, et al. FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 455-9. PMID 19133659 DOI: 10.1002/mds.22442  0.48
2009 Asmus F, Langseth A, Doherty E, Nestor T, Munz M, Gasser T, Lynch T, King MD. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 702-9. PMID 19117362 DOI: 10.1002/mds.22426  0.48
2009 Haugarvoll K, Toft M, Skipper L, Heckman MG, Crook JE, Soto A, Ross OA, Hulihan MM, Kachergus JM, Sando SB, White LR, Lynch T, Gibson JM, Uitti RJ, Wszolek ZK, et al. Fine-mapping and candidate gene investigation within the PARK10 locus. European Journal of Human Genetics : Ejhg. 17: 336-43. PMID 18854859 DOI: 10.1038/ejhg.2008.187  0.48
2008 Ross OA, Soto AI, Vilariño-Güell C, Heckman MG, Diehl NN, Hulihan MM, Aasly JO, Sando S, Gibson JM, Lynch T, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, et al. Genetic variation of Omi/HtrA2 and Parkinson's disease. Parkinsonism & Related Disorders. 14: 539-43. PMID 18790661 DOI: 10.1016/j.parkreldis.2008.08.003  0.48
2008 Ross OA, Heckman MG, Soto AI, Diehl NN, Haugarvoll K, Vilariño-Güell C, Aasly JO, Sando S, Gibson JM, Lynch T, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, et al. Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease. Parkinsonism & Related Disorders. 14: 544-7. PMID 18722802 DOI: 10.1016/j.parkreldis.2008.07.002  0.48
2007 Walsh R, O'Dwyer JP, Sheikh IH, O'Riordan S, Lynch T, Hutchinson M. Sporadic adult onset dystonia: sensory abnormalities as an endophenotype in unaffected relatives. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 980-3. PMID 17702779 DOI: 10.1136/jnnp.2006.105585  0.48
2006 Ryan A, Mullins G, Scott J, Connolly S, Hardiman O, Yilmaz E, Vincent A, Lynch T. A 45-year history of acquired autoimmune neuromyotonia. Journal of Neurology. 253: 1243-5. PMID 16998651 DOI: 10.1007/s00415-006-0172-5  0.48
2004 Gordon PH, Fahn S, Chin S, Golbe LI, Lynch T, Eidelberg D. Woman with a 26-year history of parkinsonism, supranuclear ophthalmoplegia, and loss of postural reflexes. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 950-61. PMID 15300663 DOI: 10.1002/mds.20139  0.48
2004 Ross OA, O'Neill C, Rea IM, Lynch T, Gosal D, Wallace A, Curran MD, Middleton D, Gibson JM. Functional promoter region polymorphism of the proinflammatory chemokine IL-8 gene associates with Parkinson's disease in the Irish. Human Immunology. 65: 340-6. PMID 15120188 DOI: 10.1016/j.humimm.2004.01.015  0.48
2002 Hedrich K, Marder K, Harris J, Kann M, Lynch T, Meija-Santana H, Pramstaller PP, Schwinger E, Bressman SB, Fahn S, Klein C. Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations. Neurology. 58: 1239-46. PMID 11971093  0.68
2001 Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S, Mayeux R, Rowland LP, Wilhelmsen KC. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994. Neurology. 57: S39-45. PMID 11775599  0.48
2000 Thyagarajan D, Bressman S, Bruno C, Przedborski S, Shanske S, Lynch T, Fahn S, DiMauro S. A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy. Annals of Neurology. 48: 730-6. PMID 11079536 DOI: 10.1002/1531-8249(200011)48:5<730::AID-ANA6>3.0.CO;2-0  0.48
1998 Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, ... ... Lynch T, et al. Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. Nature. 393: 702-5. PMID 9641683 DOI: 10.1038/31508  0.48
1997 Lynch T, Fahn S, Louis ED, Odel JG. Oculofacial-skeletal myorhythmia in Whipple's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 12: 625-6. PMID 9251096  0.68
1997 Lynch T, Odel J, Fredericks DN, Louis ED, Forman S, Rotterdam H, Fahn S, Relman DA. Polymerase chain reaction-based detection of Tropheryma whippelii in central nervous system Whipple's disease. Annals of Neurology. 42: 120-4. PMID 9225695 DOI: 10.1002/ana.410420120  0.48
1996 Louis ED, Lynch T, Kaufmann P, Fahn S, Odel J. Diagnostic guidelines in central nervous system Whipple's disease. Annals of Neurology. 40: 561-8. PMID 8871574 DOI: 10.1002/ana.410400404  0.68
1996 Louis ED, Lynch T, Marder K, Fahn S. Reliability of patient completion of the historical section of the Unified Parkinson's Disease Rating Scale. Movement Disorders : Official Journal of the Movement Disorder Society. 11: 185-92. PMID 8684390 DOI: 10.1002/mds.870110212  0.68
1996 Louis ED, Lynch T, Ford B, Greene P, Bressman SB, Fahn S. Delayed-onset cerebellar syndrome. Archives of Neurology. 53: 450-4. PMID 8624221  0.68
1996 Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Annals of Neurology. 39: 507-20. PMID 8619529 DOI: 10.1002/ana.410390413  0.48
1995 Louis ED, Lynch T, Cargan AL, Fahn S. Generalized chorea in an infant with semilobar holoprosencephaly. Pediatric Neurology. 13: 355-7. PMID 8771177  0.68
1994 Lynch T, Burke RE, Fahn S. Progress in psychiatry. The New England Journal of Medicine. 330: 285-6. PMID 8272093  0.68
1994 Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology. 44: 1878-84. PMID 7936241  0.48
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