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Eliana Marisa Ramos

Showing results (1-10 of 85) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2011
Intergenerational instability in Huntington disease: extreme repeat changes among 134 transmissionsEliana Marisa Ramos, Joana Cerqueira, Carolina Lemos, et al.
Archives of Neurology|April 14, 2010
Evidence of syntaxin 1A involvement in migraine susceptibility: a Portuguese studyCarolina Lemos, José Pereira-Monteiro, Denisa Mendonça, et al.
Plos One|June 26, 2008
Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancerBo Eskerod Madsen, Eliana Marisa Ramos, Mathieu Boulard, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 14, 2009
Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2)Eliana Marisa Ramos, Sandra Martins, Isabel Alonso, et al.
Frontiers in Neurology|July 11, 2022
Case Report: Novel <i>CSF1R</i> Variant in a Patient With Behavioral Variant Frontotemporal Dementia Syndrome With Prodromal Repetitive Scratching BehaviorAdit Friedberg, Eliana Marisa Ramos, Zhongan Yang, et al.
Neurogenetics|March 22, 2019
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian familyEliana Marisa Ramos, Alessandro Roca, Noravit Chumchim, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 4, 2015
Chromosome substitution strain assessment of a Huntington's disease modifier locusEliana Marisa Ramos, Marina Kovalenko, Jolene R Guide, et al.
Neurology|July 24, 2020
Familial language network vulnerability in primary progressive aphasiaSandra Weintraub, Benjamin Rader, Christina Coventry, et al.
Bipolar Disorders|March 3, 2015
Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorderEliana Marisa Ramos, Tammy Gillis, Jayalakshmi S Mysore, et al.
Plos One|February 24, 2009
Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)Teresa Almeida, Isabel Alonso, Sandra Martins, et al.
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2011
Intergenerational instability in Huntington disease: extreme repeat changes among 134 transmissionsEliana Marisa Ramos, Joana Cerqueira, Carolina Lemos, et al.
Archives of Neurology|April 14, 2010
Evidence of syntaxin 1A involvement in migraine susceptibility: a Portuguese studyCarolina Lemos, José Pereira-Monteiro, Denisa Mendonça, et al.
Plos One|June 26, 2008
Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancerBo Eskerod Madsen, Eliana Marisa Ramos, Mathieu Boulard, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 14, 2009
Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2)Eliana Marisa Ramos, Sandra Martins, Isabel Alonso, et al.
Frontiers in Neurology|July 11, 2022
Case Report: Novel <i>CSF1R</i> Variant in a Patient With Behavioral Variant Frontotemporal Dementia Syndrome With Prodromal Repetitive Scratching BehaviorAdit Friedberg, Eliana Marisa Ramos, Zhongan Yang, et al.
Neurogenetics|March 22, 2019
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian familyEliana Marisa Ramos, Alessandro Roca, Noravit Chumchim, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 4, 2015
Chromosome substitution strain assessment of a Huntington's disease modifier locusEliana Marisa Ramos, Marina Kovalenko, Jolene R Guide, et al.
Neurology|July 24, 2020
Familial language network vulnerability in primary progressive aphasiaSandra Weintraub, Benjamin Rader, Christina Coventry, et al.
Bipolar Disorders|March 3, 2015
Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorderEliana Marisa Ramos, Tammy Gillis, Jayalakshmi S Mysore, et al.
Plos One|February 24, 2009
Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)Teresa Almeida, Isabel Alonso, Sandra Martins, et al.
Pageof 9