Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Counseling and LRRK2[original query] |
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| A novel P755L mutation in LRRK2 gene associated with Parkinson's disease. Neuroreport 2006 Dec 17 (18): 1859-62. Wu Ting, Zeng Yanying, Ding Xinsheng, Li Xiaobo, Li Wenlei, Dong Hairong, Chen Senqing, Zhang Xiaomei, Ma Guojian, Yao Juan, Deng Xiaoxu |
| Genetic analysis of LRRK2 mutations in patients with Parkinson disease. Journal of the neurological sciences 2006 Dec 251 (1-2): 102-6. Deng Hao, Le WeiDong, Guo Yi, Hunter Christine B, Xie WenJie, Huang MaoSheng, Jankovic Jose |
| Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's disease. Genetic testing 2006 10 (3): 221-7. Kay Denise M, Bird Tom D, Zabetian Cyrus P, Factor Stewart A, Samii Ali, Higgins Donald S, Nutt John, Roberts John W, Griffith Alida, Leis Berta C, Montimurro Jennifer S, Philpott Sean, Payami Hayd |
| Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients. Neuroscience letters 2006 Dec 409 (2): 83-8. Punia Sohan, Behari Madhuri, Govindappa Shyla T, Swaminath Pazhayannur V, Jayaram Sachi, Goyal Vinay, Muthane Uday B, Juyal R C, Thelma B |
| High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal. Movement disorders : official journal of the Movement Disorder Society 2007 Jun 22 (8): 1194-201. Ferreira Joaquim J, Guedes Leonor Correia, Rosa Mário Miguel, Coelho Miguel, van Doeselaar Marina, Schweiger Dorothea, Di Fonzo Alessio, Oostra Ben A, Sampaio Cristina, Bonifati Vincen |
| A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia. European journal of neurology : the official journal of the European Federation of Neurological Societies 2007 Apr 14 (4): 413-7. Illarioshkin S N, Shadrina M I, Slominsky P A, Bespalova E V, Zagorovskaya T B, Bagyeva G Kh, Markova E D, Limborska S A, Ivanova-Smolenskaya I |
| Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects. Genetic testing 2008 Sep 12 (3): 333-9. Change Nathalie, Mercier Géraldine, Lucotte Géra |
| Is the G2019S LRRK2 mutation common in all southern European populations? Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2008 Sep 15 (9): 1027-30. Papapetropoulos Spiridon, Adi Nikhil, Shehadeh Lina, Bishopric Nanette, Singer Carlos, Argyriou Andreas A, Chroni Elizabe |
| [A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2007 107 (3): 46-50. Shadrina M I, Illarioshkin S N, Bagyeva G Kh, Bespalova E V, Zagorodskaia T B, Slominski? P A, Markova E D, Kliushnikov S A, Limborskaia S A, Ivanova-Smolenskaia I |
| Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2. BMC neurology 2008 8 (1): 1. Bras Jose, Guerreiro Rita, Ribeiro Maria, Morgadinho Ana, Januario Cristina, Dias Margarida, Calado Ana, Semedo Cristina, Oliveira Catarina, Hardy John, Singleton Andr |
| Absence of commonly reported leucine-rich repeat kinase 2 mutations in Eastern Indian Parkinson's disease patients. Genetic testing and molecular biomarkers 2010 Oct 14 (5): 691-4. Sanyal Jaya, Sarkar Biswanath, Ojha Sabyasachi, Banerjee Tapas Kumar, Ray Bidhan Chandra, Rao Vadlam Raghavend |
| Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain). Movement disorders : official journal of the Movement Disorder Society 2010 Oct 25 (14): 2340-5. Ruiz-Martínez Javier, Gorostidi Ana, Ibañez Berta, Alzualde Ainhoa, Otaegui David, Moreno Fermin, López de Munain Adolfo, Bergareche Alberto, Gómez-Esteban Juan Carlos, Martí Massó José |
| High frequency and reduced penetrance of LRRK2 G2019S mutation among Parkinson's disease patients in Cantabria (Spain). Movement disorders : official journal of the Movement Disorder Society 2011 Nov 26 (13): 2343-6. Sierra María, González-Aramburu Isabel, Sánchez-Juan Pascual, Sánchez-Quintana Coro, Polo José Miguel, Berciano José, Combarros Onofre, Infante J |
| Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease. Journal of the neurological sciences 2011 Jun . Giladi N, Mirelman A, Thaler A, Bar-Shira A, Gurevich T, Orr-Urtreger A |
| Comprehensive LRRK2 and GBA screening in Portuguese patients with Parkinson's disease: identification of a new family with the LRRK2 p.Arg1441His mutation and novel missense variants. Parkinsonism & related disorders 2013 Oct 19 (10): 897-900. Zhang Lei, Quadri Marialuisa, Guedes Leonor Correia, Coelho Miguel, Valadas Anabela, Mestre Tiago, Lobo Patrícia Pita, Rosa Mário Miguel, Simons Erik, Oostra Ben A, Ferreira Joaquim J, Bonifati Vincen |
| Genetic screening for the LRRK2 R1441C and G2019S mutations in Parkinsonian patients from Campania. Journal of Parkinson's disease 2014 4 (1): 123-8. De Rosa Anna, De Michele Giuseppe, Guacci Anna, Carbone Rosa, Lieto Maria, Peluso Silvio, Picillo Marina, Barone Paolo, Salemi Fabrizio, Laiso Antonio, Saccà Francesco, Tessitore Alessandro, Pellecchia Maria Teresa, Bonifati Vincenzo, Criscuolo Chia |
| Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population. Journal of the neurological sciences 2015 Jun 353 (1-2): 59-62. Jankovi? Milena Z, Kresojevi? Nikola D, Dobri?i? Valerija S, Markovi? Vladana V, Petrovi? Igor N, Novakovi? Ivana V, Kosti? Vladimir |
| A genetic analysis of a Spanish population with early onset Parkinson's disease. PloS one 2020 15 (9): e0238098. Cristina Tejera-Parrado, Pablo Mir, Teresa Periñán María, Lydia Vela-Desojo, Irene Abreu-Rodríguez, Araceli Alonso-Cánovas, Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, Dolores Buiza-Rueda, José Catalán-Alonso María, Rocío García-Ramos, José García-Ruiz Pedro, Ismael Huertas-Fernández, Silvia Jesús, Labrador Miguel A-Espinosa, Lydia López-Manzanares, Carlos Martínez-Castrillo Juan, Posada Ignacio J, Ana Rojo-Sebastián, Cristina Ruiz-Huete, Javier Del Val, Gómez-Garre Pil |
| When does postural instability appear in monogenic parkinsonisms? An individual-patient meta-analysis. Journal of neurology 2020 5 268 (9): 3203-3211. Marsili Luca, Vizcarra Joaquin A, Sturchio Andrea, Dwivedi Alok K, Keeling Elizabeth G, Patel Dhiren, Mishra Murli, Farooqi Ashar, Merola Aristide, Fasano Alfonso, Mata Ignacio F, Kauffman Marcelo A, Espay Alberto |
| Genetics of Parkinson's disease in Brazil: a systematic review of monogenic forms. Arquivos de neuro-psiquiatria 2021 9 79 (7): 612-623. Santos-Lobato Bruno L, Schumacher-Schuh Artur, Mata Ignacio F, Letro Grace H, Braga-Neto Pedro, Brandão Pedro R P, Godeiro-Junior Clécio O, Coletta Marcus V Della, Camargos Sarah T, Borges Vanderci, Rieder Carlos R M, Tumas Vit |
| Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey. Parkinsonism & related disorders 2021 11 93 35-39. Emekli Inci, Tepgeç Fatih, Samanc? Bedia, Toksoy Güven, Hasano?ullar? K?na Gizem, Tüfekçio?lu Zeynep, Ba?aran Seher, Bilgiç Ba?ar, Gürvit I Hakan, Emre Murat, Uyguner Zehra Oya, Hanagasi Hasmet |
| Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis. Movement disorders : official journal of the Movement Disorder Society 2023 11 . Paula Saffie Awad, Daniel Teixeira-Dos-Santos, Bruno Lopes Santos-Lobato, Sarah Camargos, Mario Cornejo-Olivas, Carlos Roberto de Mello Rieder, Ignacio F Mata, Pedro Chaná-Cuevas, Christine Klein, Artur F Schumacher Sch |
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