FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Adriana Ochoa

Research Profile

Disorders

Geographic Areas

Mexico

Concepts & Ideas

Physiology

Anatomy

Chromosomes, Human, Pair 6

Procedures

Chemicals & Drugs

Calcium Binding Proteins

Co-author Network

Publications

TOP 3
Aurelio Jara-Prado; Minerva López-Ruiz; Iris E Martínez-Juárez; Marco T Medina; Adriana Ochoa; Julia N Bailey; Antonio V Delgado-Escueta; María Del Carmen Fernández-González-Aragón; Víctor M González; María Elisa Alonso
Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsy.
Jose Flores; Silvia González; Ximena Morales; Adriana Ochoa; Petra Yescas; Teresa Corona
Absence of Multiple Sclerosis and Demyelinating Diseases among Lacandonians, a Pure Amerindian Ethnic Group in Mexico.
Petra Yescas; Marisol López; Nancy Monroy; Marie-Catherine Boll; Mayela Rodríguez-Violante; Ulises Rodríguez; Adriana Ochoa; Maria E Alonso
Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Adriana Ochoa (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Aurelio Jara-Prado; Minerva López-Ruiz; Iris E Martínez-Juárez; Marco T Medina; Adriana Ochoa; Julia N Bailey; Antonio V Delgado-Escueta; María Del Carmen Fernández-González-Aragón; Víctor M González; María Elisa Alonso
Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsy.
Seizure : the journal of the British Epilepsy Association 2012;21(7):550-4.
2012: Jose Flores; Silvia González; Ximena Morales; Adriana Ochoa; Petra Yescas; Teresa Corona
Absence of Multiple Sclerosis and Demyelinating Diseases among Lacandonians, a Pure Amerindian Ethnic Group in Mexico.
Multiple sclerosis international 2012;2012():292631.
2010: Petra Yescas; Marisol López; Nancy Monroy; Marie-Catherine Boll; Mayela Rodríguez-Violante; Ulises Rodríguez; Adriana Ochoa; Maria E Alonso
Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease.
Neuroscience letters 2010;485(2):79-82.
2010: Astrid Rasmussen; Elisa Alonso; Adriana Ochoa; Irene De Biase; Itziar Familiar; Petra Yescas; Ana-Luisa Sosa; Yaneth Rodríguez; Mireya Chávez; Marisol López-López; Sanjay I Bidichandani
Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease.
BMC medical genetics 2010;11():4.
2009: Maria Elisa Alonso; Adriana Ochoa; Ana Luisa Sosa; Yaneth Rodríguez; Mireya Chávez; Catherine Boll; Petra Yescas; Rosario Macías; Astrid Rasmussen
Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
Genetic testing and molecular biomarkers 2009;13(6):717-20.
2009: Maria E Alonso; Adriana Ochoa; Marie-Catherine Boll; Ana Luisa Sosa; Petra Yescas; Marisol López; Rosario Macias; Itziar Familiar; Astrid Rasmussen
Clinical and genetic characteristics of Mexican Huntington's disease patients.
Movement disorders : official journal of the Movement Disorder Society 2009;24(13):2012-5.
2009: Dongsheng Bai; Julia N Bailey; Reyna M Durón; Maria E Alonso; Marco T Medina; Iris E Martínez-Juárez; Toshimitsu Suzuki; Jesús Machado-Salas; Ricardo Ramos-Ramírez; Miyabi Tanaka; Ramón H Castro Ortega; Minerva López-Ruiz; Astrid Rasmussen; Adriana Ochoa; Aurelio Jara-Prado; Kazuhiro Yamakawa; Antonio V Delgado-Escueta
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
Epilepsia 2009;50(5):1184-90.
2008: Miyabi Tanaka; Richard W Olsen; Marco T Medina; Emily Schwartz; Maria E Alonso; Reyna M Duron; Ramon Castro-Ortega; Iris E Martinez-Juarez; Ignacio Pascual-Castroviejo; Jesús Machado-Salas; Rene Silva; Julia N Bailey; Dongsheng Bai; Adriana Ochoa; Aurelio Jara-Prado; Gregorio Pineda; Robert L Macdonald; Antonio V Delgado-Escueta
Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.
American journal of human genetics 2008;82(6):1249-61.
2007: Astrid Rasmussen; Irene De Biase; Marcela Fragoso-Benítez; Marco Antonio Macías-Flores; Petra Yescas; Adriana Ochoa; Tetsuo Ashizawa; Maria E Alonso; Sanjay I Bidichandani
Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
Annals of neurology 2007;61(6):607-10.
2007: Elisa Alonso; Leticia Martínez-Ruano; Irene De Biase; Christopher Mader; Adriana Ochoa; Petra Yescas; Roxana Gutiérrez; Misti White; Luís Ruano; Marcela Fragoso-Benítez; Tetsuo Ashizawa; Sanjay I Bidichandani; Astrid Rasmussen
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
Movement disorders : official journal of the Movement Disorder Society 2007;22(7):1050-3.
2007: Marisol López; Jorge Guerrero; Petra Yescas; Marie-Catherine Boll; Itziar Familiar; Adriana Ochoa; Astrid Rasmussen; Maria E Alonso
Apolipoprotein E epsilon4 allele is associated with Parkinson disease risk in a Mexican Mestizo population.
Movement disorders : official journal of the Movement Disorder Society 2007;22(3):417-20.
2006: Toshimitsu Suzuki; Antonio V Delgado-Escueta; Maria E Alonso; Ryoji Morita; Nami Okamura; Yoshihisa Sugimoto; Dongsheng Bai; Marco T Medina; Julia N Bailey; Astrid Rasmussen; Jaime Ramos-Peek; Sergio Cordova; Francisco Rubio-Donnadieu; Adriana Ochoa; Aurelio Jara-Prado; Johji Inazawa; Kazuhiro Yamakawa
Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.
Neuroscience letters 2006;405(1-2):126-31.
2005: Araceli Trejo; Marie-Catherine Boll; Maria E Alonso; Adriana Ochoa; Leora Velásquez
Use of oral nutritional supplements in patients with Huntington's disease.
Nutrition (Burbank, Los Angeles County, Calif.) 2005;21(9):889-94.
2004: Toshimitsu Suzuki; Antonio V Delgado-Escueta; Kripamoy Aguan; Maria E Alonso; Jun Shi; Yuji Hara; Motohiro Nishida; Tomohiro Numata; Marco T Medina; Tamaki Takeuchi; Ryoji Morita; Dongsheng Bai; Subramaniam Ganesh; Yoshihisa Sugimoto; Johji Inazawa; Julia N Bailey; Adriana Ochoa; Aurelio Jara-Prado; Astrid Rasmussen; Jaime Ramos-Peek; Sergio Cordova; Francisco Rubio-Donnadieu; Yushi Inoue; Makiko Osawa; Sunao Kaneko; Hirokazu Oguni; Yasuo Mori; Kazuhiro Yamakawa
Mutations in EFHC1 cause juvenile myoclonic epilepsy.
Nature genetics 2004;36(8):842-9.
2004: Araceli Trejo; Rosa María Tarrats; Maria E Alonso; Marie-Catherine Boll; Adriana Ochoa; Leora Velásquez
Assessment of the nutrition status of patients with Huntington's disease.
Nutrition (Burbank, Los Angeles County, Calif.) 2004;20(2):192-6.
2003: Juan Fernandez-Ruiz; Rosalinda Diaz; Cynthia Hall-Haro; Patricia Vergara; J Mischner; L Nuñez; René Drucker-Colin; Adriana Ochoa; Maria E Alonso
Normal prism adaptation but reduced after-effect in basal ganglia disorders using a throwing task.
The European journal of neuroscience 2003;18(3):689-94.
2003: Juan Fernandez-Ruiz; Rosalinda Díaz; Cynthia Hall-Haro; Patricia Vergara; Aldo Fiorentini; Lilia Nuñez; René Drucker-Colín; Adriana Ochoa; Petra Yescas; Astrid Rasmussen; Maria E Alonso
Olfactory dysfunction in hereditary ataxia and basal ganglia disorders.
Neuroreport 2003;14(10):1339-41.
2003: Antonio V Delgado-Escueta; Katerina B Perez-Gosiengfiao; Dongsheng Bai; Julia Bailey; Marco T Medina; Ryoji Morita; Toshimitsu Suzuki; Subramaniam Ganesh; Toshihisa Sugimoto; Kazuhiro Yamakawa; Adriana Ochoa; Aurelio Jara-Prado; Astrid Rasmussen; Jaime Ramos-Peek; Sergio Cordova; Francisco Rubio-Donnadieu; Maria E Alonso
Recent developments in the quest for myoclonic epilepsy genes.
Epilepsia 2003;44 Suppl 11():13-26.
2002: Dongsheng Bai; Maria E Alonso; Marco T Medina; Julia N Bailey; Ryoji Morita; Sergio Cordova; Astrid Rasmussen; Jaime Ramos-Peek; Adriana Ochoa; Aurelio Jara; Francisco R Donnadieu; Gilbert Cadena; Kazuhiro Yamakawa; Antonio V Delgado-Escueta
Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.
American journal of medical genetics 2002;113(3):268-74.
2002: Toshimitsu Suzuki; Ryoji Morita; Yoshihisa Sugimoto; Takashi Sugawara; Dong-Sheng Bai; Maria E Alonso; Marco T Medina; Julia N Bailey; Astrid Rasmussen; Jaime Ramos-Peek; Sergio Cordova; Francisco Rubio-Donnadieu; Adriana Ochoa; Aurelio Jara-Prado; Johji Inazawa; Antonio V Delgado-Escueta; Kazuhiro Yamakawa
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.
Epilepsy research 2002;50(3):265-75.
2002: Antonio V Delgado-Escueta; Dongsheng Bai; Julia Bailey; Marco T Medina; Maria E Alonso; Ryoji Morita; Toshimitsu Suzuki; Subramaniam Ganesh; T Sugimoto; Kazuhiro Yamakawa; Adriana Ochoa; Aurelio Jara-Prado; Astrid Rasmussen; M Ramos-Peek; Sergio Cordova; Francisco Rubio-Donnadieu
[Juvenile myoclonic epilepsy in chromosome 6p12: clinical and genetic advances].
Revista de neurologia 2002;35(1):82-6.
2002: Maria E Alonso; Petra Yescas; Astrid Rasmussen; Adriana Ochoa; R Macías; I Ruiz; R Suástegui
Homozygosity in Huntington's disease: new ethical dilemma caused by molecular diagnosis.
Clinical genetics 2002;61(6):437-42.
2002: Subramaniam Ganesh; Antonio V Delgado-Escueta; Toshimitsu Suzuki; Silvana Francheschetti; Concetta Riggio; Giuliano Avanzini; Adrian Rabinowicz; Saeed Bohlega; Julia Bailey; Maria E Alonso; Astrid Rasmussen; Alfredo E Thomson; Adriana Ochoa; Aurelio J Prado; Marco T Medina; Kazuhiro Yamakawa
Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype.
Human molecular genetics 2002;11(11):1263-71.
2001: Astrid Rasmussen; T Matsuura; L Ruano; Petra Yescas; Adriana Ochoa; Tetsuo Ashizawa; Elisa Alonso
Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.
Annals of neurology 2001;50(2):234-9.
2000: Astrid Rasmussen; R Macias; Petra Yescas; Adriana Ochoa; G Davila; Elisa Alonso
Huntington disease in children: genotype-phenotype correlation.
Neuropediatrics 2000;31(4):190-4.
1997: Maria E Alonso; Petra Yescas; Bulmaro Cisneros; C Martínez; G Silva; Adriana Ochoa; Cecilia Montañez
Analysis of the (CAG)n repeat causing Huntington's disease in a Mexican population.
Clinical genetics 1997;51(4):225-30.
1997: C Garcia de la Cadena; Maria E Alonso; Adriana Ochoa; C Martinez
Attitudes regarding molecular diagnosis in Mexican families at risk of inheriting Huntington's disease.
Archives of medical research 1997;28(4):513-6.