Human Genome Epidemiology Literature Finder
|
Records 1 - 15 (of 15 Records) |
| Query Trace: Tremor and MAPT[original query] |
|---|
| H1-MAPT and the risk for familial essential tremor. PloS one 2012 7 (7): e41581. García-Martín Elena, Martínez Carmen, Alonso-Navarro Hortensia, Benito-León Julián, Lorenzo-Betancor Oswaldo, Pastor Pau, López-Alburquerque Tomás, Samaranch Lluis, Lorenzo Elena, Agúndez José A G, Jiménez-Jiménez Félix Javi |
| The CamPaIGN study of Parkinson's disease: 10-year outlook in an incident population-based cohort. Journal of neurology, neurosurgery, and psychiatry 2013 Nov 84 (11): 1258-64. Williams-Gray Caroline H, Mason Sarah L, Evans Jonathan R, Foltynie Thomas, Brayne Carol, Robbins Trevor W, Barker Roger |
| Clinical subtypes in Parkinson's disease: the impact of MAPT haplotypes. Journal of neural transmission (Vienna, Austria : 1996) 2013 Nov . Di Battista ME, Pascale E, Purcaro C, Passarelli F, Passarelli E, Guglielmi R, Vanacore N, Meco G |
| Association of Parkinson disease risk loci with mild parkinsonian signs in older persons. JAMA neurology 2014 Apr 71 (4): 429-35. Shulman Joshua M, Yu Lei, Buchman Aron S, Evans Denis A, Schneider Julie A, Bennett David A, De Jager Philip |
| The microtubule associated protein tau H1 haplotype and risk of essential tremor. European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 Jul 21 (7): 1044-8. Clark L N, Liu X, Parmalee N L, Hernandez N, Louis E |
| CSF tau and tau/A?42 predict cognitive decline in Parkinson's disease. Parkinsonism & related disorders 2015 1 21 (3): 271-6. Liu Changqin, Cholerton Brenna, Shi Min, Ginghina Carmen, Cain Kevin C, Auinger Peggy, , Zhang Ji |
| A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor. Neurological research 2016 Oct 38 (10): 880-7. Jiménez-Jiménez Félix Javier, García-Martín Elena, Alonso-Navarro Hortensia, Lorenzo-Betancor Oswaldo, Ortega-Cubero Sara, Pastor Pau, Calleja Marisol, Agúndez José A |
| H1/H2 MAPT haplotype and Parkinson's disease in Mexican mestizo population. Neuroscience letters 2019 01 690 210-213. Miranda-Morales Ernesto G, Sandoval-Carrillo Ada, Castellanos-Juárez Francisco X, Méndez-Hernández Edna M, La Llave-León Osmel, Quiñones-Canales Gerardo, Ruano-Calderón Luis A, Arias-Carrión Oscar, Salas-Pacheco Jose |
| Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients. Neuro-degenerative diseases 2019 Mar 18 (5-6): 310-314. Origone Paola, Geroldi Alessandro, Lamp Merit, Sanguineri Francesca, Caponnetto Claudia, Cabona Corrado, Gotta Fabio, Trevisan Lucia, Bellone Emilia, Manganelli Fiore, Devigili Grazia, Mandich Pao |
| Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
| Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. EBioMedicine 2022 10 85 104290. Clark Lorraine N, Gao Yizhe, Wang Gao T, Hernandez Nora, Ashley-Koch Allison, Jankovic Joseph, Ottman Ruth, Leal Suzanne M, Rodriguez Sandra M Barral, Louis Elan |
| Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients. Journal of molecular neuroscience : MN 2023 5 . Imane Smaili, Houyam Tibar, Mounia Rahmani, Najlaa Machkour, Rachid Razine, Hajar Naciri Darai, Naima Bouslam, Ali Benomar, Wafa Regragui, Ahmed Bouhouc |
| Cognitive Performance as a Function of MAPT Haplotype: A Prospective Longitudinal Study of an Essential Tremor Cohort. Tremor and other hyperkinetic movements (New York, N.Y.) 2023 5 13 19. Ali Ghanem, Diane S Berry, Kurt Farrell, Stephanie Cosentino, John F Crary, Elan D Lou |
| Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
| Clinical and molecular predictors of survival among atypical parkinsonian syndromes in a North African tertiary referral center. Journal of the neurological sciences 2024 8 464 123155. Ikram Sghaier, Amina Nasri, Amal Atrous, Youssef Abida, Alya Gharbi, Amira Souissi, Saloua Mrabet, Mouna Ben Djebara, Imen Kacem, Amina Gargouri-Berrechid, Riadh Gouid |
- Page last reviewed:Feb 1, 2024
- Content source: