José Miguel Laffita‐Mesa

Author

Also Known As

J Laffita‐Mesa, J. Laffita-Mesa, J.M. Laffita-Mesa, J.M. Laffita‐Mesa, Jose Laffita-Mesa, Jose Laffita‐Mesa, Jose M. Laffita-Mesa, Jose Miguel Laffita-Mesa, Jose Miguel Laffita‐Mesa, José Laffita-Mesa

Publications

963

Citations

H-Index

Concepts

All Affiliations

University of Holguín Karolinska University Hospital Karolinska Institutet Goethe University Frankfurt Universidad Nacional Autónoma de México

About

José Miguel Laffita‐Mesa is an author at University of Holguín specializing in medicine, neuroscience, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	492
2	Social Sciences	3	3	68
3	Public Health	2	2	71
4	Engineering	1	1	13
5	Health Sciences	1	1	83

José Miguel Laffita‐Mesa

Publications

707

Citations

H-Index

Page 1

	Year	Citations
Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study Luis Velázquez‐Pérez, Roberto Rodríguez‐Labrada, Nalia Canales‐Ochoa, The Lancet Neurology Early FeaturesNeurologyNeuroscienceMotor DisorderNeuropathology	2014	88
Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2 Luis Velázquez‐Pérez, Carola Seifried, Michael Abele, Clinical Neurophysiology Neurological DisorderNeuroanatomySaccade VelocityMotor ControlMotor Disorder	2009	83
Plasma biomarker profiles in autosomal dominant Alzheimer’s disease Charlotte Johansson, José Miguel Laffita‐Mesa, Elena Rodriguez‐Vieitez, Brain	2023	69
Comprehensive Study of Early Features in Spinocerebellar Ataxia 2: Delineating the Prodromal Stage of the Disease Luis Velázquez‐Pérez, Roberto Rodríguez‐Labrada, Edilia Cruz-Rivas, The Cerebellum Neurodegenerative DiseasesSpinocerebellar Ataxia 2Neurological DisorderDegenerative DiseaseEarly Features	2014	64
Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles José Miguel Laffita‐Mesa, Luis Velázquez‐Pérez, Nieves Santos Falcón, European Journal of Human Genetics Allelic VariantGenotype-phenotype AssociationMedicineGeneticsEvolutionary Biology	2011	59
Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis LE Almaguer‐Mederos, N Santos Falcón, Y Rodríguez Almira, Clinical Genetics	2009	59
Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications José Miguel Laffita‐Mesa, Peter Bauer, Vivian Kourí, Human Genetics ChromatinPathological ImplicationsSystems BiologyEpigenetic ChangeGenetics	2011	50
Subtle rapid eye movement sleep abnormalities in presymptomatic spinocerebellar ataxia type 2 gene carriers Roberto Rodríguez‐Labrada, Luis Velázquez‐Pérez, N Ochoa, Movement Disorders Sleep DisordersSleepRem Sleep PathologySleep DisorderOphthalmology	2010	45
Saccadic latency is prolonged in Spinocerebellar Ataxia type 2 and correlates with the frontal-executive dysfunctions Roberto Rodríguez‐Labrada, Luis Velázquez‐Pérez, Carola Seigfried, Journal of the Neurological Sciences Neuropsychological FunctioningNeuropsychologyBrain FunctionSaccadic LatencyNeuroanatomy	2011	35
Correlations Between Methionine Cycle Metabolism, COMT Genotype, and Polyneuropathy in L-Dopa Treated Parkinson’s Disease: A Preliminary Cross-Sectional Study Mattias Andréasson, Lovisa Brodin, José Miguel Laffita‐Mesa, Journal of Parkinson s Disease	2017	19

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