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Page 1
Status of the neuromyelitis optica spectrum disorder in Latin America.
Rivera VM, Hamuy F, Rivas V, Gracia F, Rojas JI, Bichuetti DB, Villa AM, Marques VD, Soto A, Bertado B, Frenk IT, Galleguillos L, Quiñones J, Ramirez DA, Caparó-Zamalloa C, Ciampi E, Lana-Peixoto MA, Rodríguez E, Zarco L, Sinay V, Armas E, Becker J, Benzadón A, Lopez E, Carnero Contentti E, Correa-Diaz EP, Diaz A, Fleitas CV, Playas G, Molina O, Rojas E, Sato D, Soto I, Céspedes JV, Correale J, Barboza A, Monterrey P, Candelario A, Tavolini DR, Parajeles A, Pujol BS, Diaz de la Fe A, Alonso R, Bolaña C, Guzman MK, Carrá A, Gamarra OG, Raggio JV, Rodriguez LC, Ramirez NE, Ordoñez L, Skromne E, Portillo LL, Canabal AP, Weiser R, Sirias V, Calderón RF, Cornejo EA, Hernández M, Quiroz JCD, Garcia LA, Cedeño CO, Martínez J, Abad-Herrera P. Rivera VM, et al. Among authors: weiser r. Mult Scler Relat Disord. 2021 Aug;53:103083. doi: 10.1016/j.msard.2021.103083. Epub 2021 Jun 15. Mult Scler Relat Disord. 2021. PMID: 34171682 Free article.
COVID-19 in multiple sclerosis and neuromyelitis optica spectrum disorder patients in Latin America: COVID-19 in MS and NMOSD patients in LATAM.
Alonso R, Silva B, Garcea O, Diaz PEC, Dos Passos GR, Navarro DAR, Valle LAG, Salinas LCR, Negrotto L, Luetic G, Tkachuk VA, Míguez J, de Bedoya FHD, Goiry LG, Sánchez NER, Burgos M, Steinberg J, Balbuena ME, Alvarez PM, López PA, Ysrraelit MC, León RA, Cohen AB, Gracia F, Molina O, Casas M, Deri NH, Pappolla A, Patrucco L, Cristiano E, Tavolini D, Nadur D, Granda AMT, Weiser R, Cassará FP, Sinay V, Rodríguez CC, Lazaro LG, Menichini ML, Piedrabuena R, Escobar GO, Carrá A, Chertcoff A, Pujols BS, Vrech C, Tarulla A, Carvajal R, Mainella C, Becker J, Peeters LM, Walton C, Serena MA, Nuñez S, Rojas JI. Alonso R, et al. Among authors: weiser r. Mult Scler Relat Disord. 2021 Jun;51:102886. doi: 10.1016/j.msard.2021.102886. Epub 2021 Mar 7. Mult Scler Relat Disord. 2021. PMID: 33744758 Free PMC article.
Neuromyelitis Optica Spectrum Disorder in Central America and the Caribbean: A Multinational Clinical Characterization Study.
Gracia F, Ramírez D, Parajeles-Vindas A, Díaz A, Díaz de la Fé A, Sánchez NER, Escobar RC, Valle LAG, Weiser R, Santos B, Candelario A, Benzadon A, Araujo P, Valderrama C, Larreategui M, Carrillo G, Gracia K, Vázquez-Céspedes J, Monterrey-Alvarez P, Carazo-Céspedes K, Sanabria-Castro A, Miranda-Loria G, Balmaceda-Meza A, Rivera LIP, Leal IO, Salinas LCR, Thompson A, Torres EL, Pereira DE, Zepeda C, López CA, Valse EAC, Urbina KZC, Urrutia MA, Van Sijtveld I, Armien B, Rivera VM. Gracia F, et al. Among authors: weiser r. Neurol Int. 2022 Mar 17;14(1):284-293. doi: 10.3390/neurolint14010023. Neurol Int. 2022. PMID: 35324579 Free PMC article.
Care of patients with Huntington's disease in South America: a survey.
Maciel RO, Cardoso FE, Chaná-Cuevas P, Cosentino C, Fernández W, Rieder CR, Serrano-Dueñas M, Weiser R. Maciel RO, et al. Among authors: weiser r. Arq Neuropsiquiatr. 2013 Jun;71(6):368-70. doi: 10.1590/0004-282X20130040. Arq Neuropsiquiatr. 2013. PMID: 23828534 Free article.
Américo Negrette and Huntington's disease.
Moscovich M, Munhoz RP, Becker N, Barbosa ER, Espay AJ, Weiser R, Teive HA. Moscovich M, et al. Among authors: weiser r. Arq Neuropsiquiatr. 2011 Aug;69(4):711-3. doi: 10.1590/s0004-282x2011000500025. Arq Neuropsiquiatr. 2011. PMID: 21877046 Free article.
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies.
Johnson J, Hague SM, Hanson M, Gibson A, Wilson KE, Evans EW, Singleton AA, McInerney-Leo A, Nussbaum RL, Hernandez DG, Gallardo M, McKeith IG, Burn DJ, Ryu M, Hellstrom O, Ravina B, Eerola J, Perry RH, Jaros E, Tienari P, Weiser R, Gwinn-Hardy K, Morris CM, Hardy J, Singleton AB. Johnson J, et al. Among authors: weiser r. Neurology. 2004 Aug 10;63(3):554-6. doi: 10.1212/01.wnl.0000133401.09043.44. Neurology. 2004. PMID: 15304594
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
Hague S, Rogaeva E, Hernandez D, Gulick C, Singleton A, Hanson M, Johnson J, Weiser R, Gallardo M, Ravina B, Gwinn-Hardy K, Crawley A, St George-Hyslop PH, Lang AE, Heutink P, Bonifati V, Hardy J, Singleton A. Hague S, et al. Among authors: weiser r. Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685
Mutation at the SCA17 locus is not a common cause of parkinsonism.
Hernandez D, Hanson M, Singleton A, Gwinn-Hardy K, Freeman J, Ravina B, Doheny D, Gallardo M, Weiser R, Hardy J, Singleton A. Hernandez D, et al. Among authors: weiser r. Parkinsonism Relat Disord. 2003 Aug;9(6):317-20. doi: 10.1016/s1353-8020(03)00027-0. Parkinsonism Relat Disord. 2003. PMID: 12853230
Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease.
Simon-Sanchez J, Hanson M, Singleton A, Hernandez D, McInerney A, Nussbaum R, Werner J, Gallardo M, Weiser R, Gwinn-Hardy K, Singleton AB, Clarimon J. Simon-Sanchez J, et al. Among authors: weiser r. Neurosci Lett. 2005 Jul 1-8;382(1-2):191-4. doi: 10.1016/j.neulet.2005.03.015. Epub 2005 Apr 1. Neurosci Lett. 2005. PMID: 15911147
191 results