Works matching AU Infante, Jon

Results: 92

CMT1A duplication: refining the minimal adult phenotype.

Published in:

2008

By:

Berciano, José;
Gallardo, Elena;
García, Antonio;
Ramón, César;
Mateo, Ignacio;
Infante, Jon;
Rodríguez-Rodríguez, Eloy;
Combarros, Onofre

Publication type:

Letter

Cholesteryl ester transfer protein (CETP) polymorphism modifies the Alzheimer's disease risk associated with APOE ε4 allele.

Published in:

Journal of Neurology, 2006, v. 253, n. 2, p. 181, doi. 10.1007/s00415-005-0945-2

By:

Rodríguez, Eloy;
Mateo, Ignacio;
Infante, Jon;
Llorca, Javier;
Berciano, José;
Combarros, Onofre

Publication type:

Article

Interaction between interleukin-6 and intercellular adhesion molecule-1 genes and Alzheimer’s disease risk.

Published in:

Journal of Neurology, 2005, v. 252, n. 4, p. 485, doi. 10.1007/s00415-005-0658-6

By:

Combarros, Onofre;
Infante, Jon;
Llorca, Javier;
Peña, Nicolás;
Fernández-Viadero, Carlos;
Berciano, José

Publication type:

Article

Gene-gene interaction between interleukin-1A and interleukin-8 increases Alzheimer’s disease risk.

Published in:

Journal of Neurology, 2004, v. 251, n. 4, p. 482, doi. 10.1007/s00415-004-0375-6

By:

Infante, Jon;
Sanz, Cristina;
Fernández-Luna, José Luis;
Llorca, Javier;
Berciano, José;
Combarros, Onofre

Publication type:

Article

Age-dependent association between interleukin-1A (-889) genetic polymorphism and sporadic Alzheimer’s disease: A meta-analysis.

Published in:

Journal of Neurology, 2003, v. 250, n. 8, p. 987, doi. 10.1007/s00415-003-1136-7

By:

Combarros, Onofre;
Llorca, Javier;
Sánchez-Guerra, Marisa;
Infante, Jon;
Berciano, José

Publication type:

Article

Gene dose-dependent association of interleukin-1A [-889] allele 2 polymorphism with Alzheimer's disease.

Published in:

Journal of Neurology, 2002, v. 249, n. 9, p. 1242, doi. 10.1007/s00415-002-0819-9

By:

Combarros, Onofre;
Sánchez-Guerra, Marisa;
Infante, Jon;
Llorca, Javier;
Berciano, José

Publication type:

Article

Akinetic mutism from frontal lobe damage responding to levodopa.

Published in:

Journal of Neurology, 2000, v. 247, n. 7, p. 568, doi. 10.1007/s004150070161

By:

Combarros, Onofre;
Infante, Jon;
Berciano, José

Publication type:

Article

Lrrk2 R1441G-related Parkinson’s disease: evidence of a common founding event in the seventh century in Northern Spain.

Published in:

Neurogenetics, 2009, v. 10, n. 4, p. 347, doi. 10.1007/s10048-009-0187-z

By:

Mata, Ignacio F.;
Hutter, Carolyn M.;
González-Fernández, María C.;
de Pancorbo, Marian M.;
Lezcano, Elena;
Huerta, Cecilia;
Blazquez, Marta;
Ribacoba, Renee;
Guisasola, Luis M.;
Salvador, Carlos;
Gómez-Esteban, Juan C.;
Zarranz, Juan J.;
Infante, Jon;
Jankovic, Joseph;
Deng, Hao;
Edwards, Karen L.;
Alvarez, Victoria;
Zabetian, Cyrus P.

Publication type:

Article

HTT, ATXN1 and ATXN2 CAG triplet repeat sizes: exploring their role in the disease risk and cancer comorbidity in Parkinson's disease.

Published in:

Brain Communications, 2025, v. 7, n. 1, p. 1, doi. 10.1093/braincomms/fcaf060

By:

Pérez-Oliveira, Sergio;
Álvarez, Ignacio;
Menéndez-González, Manuel;
Duarte-Herrera, Israel David;
Blázquez-Estrada, Marta;
Castilla-Silgado, Juan;
Suárez, Esther;
García-Fernández, Ciara;
Siso-García, Pablo;
García-González, Pablo;
Rosende-Roca, Maitee;
Boada, Mercè;
Ruiz, Agustín;
Infante, Jon;
Casa-Fages, Beatriz De la;
González-Aramburu, Isabel;
Álvarez, Victoria;
Pastor, Pau

Publication type:

Article

Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene.

Published in:

Movement Disorders Clinical Practice, 2021, v. 8, n. 6, p. 969, doi. 10.1002/mdc3.13260

By:

Manrique, Leire;
Sánchez‐Rodríguez, Antonio;
Pelayo‐Negro, Ana L.;
Corral‐Juan, Marc;
Matilla‐Dueñas, Antoni;
Infante, Jon

Publication type:

Article

Oculomandibular Tremor and Bilateral Hypertrophic Olivary Degeneration.

Published in:

Movement Disorders Clinical Practice, 2017, v. 4, n. 1, p. 152, doi. 10.1002/mdc3.12366

By:

Fernández, Jennifer;
García‐García, Antonio;
Valle, Natalia;
Infante, Jon

Publication type:

Article

History of Ataxias and Paraplegias with an Annotation on the First Description of Striatonigral Degeneration.

Published in:

Cerebellum, 2022, v. 21, n. 4, p. 531, doi. 10.1007/s12311-021-01328-6

By:

Berciano, José;
Gazulla, José;
Infante, Jon

Publication type:

Article

Social Cognition in Chiari Malformation Type I: a Preliminary Characterization.

Published in:

Cerebellum, 2020, v. 19, n. 3, p. 392, doi. 10.1007/s12311-020-01117-7

By:

García, Maitane;
Amayra, Imanol;
López-Paz, Juan Francisco;
Martínez, Oscar;
Lázaro, Esther;
Pérez, Manuel;
Berrocoso, Sarah;
Al-Rashaida, Mohammad;
Infante, Jon

Publication type:

Article

Analysis of Visuospatial Abilities in Chiari Malformation Type I.

Published in:

Cerebellum, 2020, v. 19, n. 1, p. 6, doi. 10.1007/s12311-019-01056-y

By:

García, Maitane;
Lázaro, Esther;
Amayra, Imanol;
López-Paz, Juan Francisco;
Martínez, Oscar;
Pérez, Manuel;
Berrocoso, Sarah;
Al-Rashaida, Mohammad;
Infante, Jon

Publication type:

Article

Substantia Nigra Echogenicity in Friedreich's Ataxia Patients.

Published in:

Cerebellum, 2013, v. 12, n. 4, p. 437, doi. 10.1007/s12311-012-0434-y

By:

Sierra, María;
Infante, Jon;
Berciano, José

Publication type:

Article

Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings.

Published in:

Cerebellum, 2012, v. 11, n. 1, p. 155, doi. 10.1007/s12311-011-0292-z

By:

Jacobi, Heike;
Hauser, Till-Karsten;
Giunti, Paola;
Globas, Christoph;
Bauer, Peter;
Schmitz-Hübsch, Tanja;
Baliko, László;
Filla, Alessandro;
Mariotti, Caterina;
Rakowicz, Maria;
Charles, Perine;
Ribai, Pascale;
Szymanski, Sandra;
Infante, Jon;
Warrenburg, Bart;
Dürr, Alexandra;
Timmann, Dagmar;
Boesch, Sylvia;
Fancellu, Roberto;
Rola, Rafal

Publication type:

Article

Accuracy of plasma Aβ40, Aβ42, and p-tau181 to detect CSF Alzheimer's pathological changes in cognitively unimpaired subjects using the Lumipulse automated platform.

Published in:

Alzheimer's Research & Therapy, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13195-023-01319-1

By:

Martínez-Dubarbie, Francisco;
Guerra-Ruiz, Armando;
López-García, Sara;
Lage, Carmen;
Fernández-Matarrubia, Marta;
Infante, Jon;
Pozueta-Cantudo, Ana;
García-Martínez, María;
Corrales-Pardo, Andrea;
Bravo, María;
López-Hoyos, Marcos;
Irure-Ventura, Juan;
Sánchez-Juan, Pascual;
García-Unzueta, María Teresa;
Rodríguez-Rodríguez, Eloy

Publication type:

Article

Genetic Interaction between Tau and the Apolipoprotein E Receptor LRP1 Increases Alzheimer’s Disease Risk.

Published in:

Dementia & Geriatric Cognitive Disorders, 2009, v. 28, n. 2, p. 116, doi. 10.1159/000234913

By:

Vázquez-Higuera, José Luis;
Mateo, Ignacio;
Sánchez-Juan, Pascual;
Rodríguez-Rodríguez, Eloy;
Pozueta, Ana;
Infante, Jon;
Berciano, José;
Combarros, Onofre

Publication type:

Article

Synergistic Effect of Heme Oxygenase-1 and Tau Genetic Variants on Alzheimer’s Disease Risk.

Published in:

Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 4, p. 339, doi. 10.1159/000161059

By:

Mateo, Ignacio;
Sánchez-Juan, Pascual;
Rodríguez-Rodríguez, Eloy;
Infante, Jon;
Vázquez-Higuera, José Luis;
García-Gorostiaga, Inés;
Berciano, José;
Combarros, Onofre

Publication type:

Article

14-3-3 Zeta and Tau Genes Interactively Decrease Alzheimer’s Disease Risk.

Published in:

Dementia & Geriatric Cognitive Disorders, 2008, v. 25, n. 4, p. 317, doi. 10.1159/000119123

By:

Mateo, Ignacio;
Sánchez-Juan, Pascual;
Rodríguez-Rodríguez, Eloy;
Infante, Jon;
Fernández-Viadero, Carlos;
Peña, Nicolás;
Berciano, José;
Combarros, Onofre

Publication type:

Article

Interaction between Poly(ADP-Ribose) Polymerase 1 and Interleukin 1A Genes Is Associated with Alzheimer’s Disease Risk.

Published in:

Dementia & Geriatric Cognitive Disorders, 2007, v. 23, n. 4, p. 215, doi. 10.1159/000099471

By:

Infante, Jon;
Llorca, Javier;
Mateo, Ignacio;
Rodríguez-Rodríguez, Eloy;
Sánchez-Quintana, Coro;
Sánchez-Juan, Pascual;
Fernández-Viadero, Carlos;
Peña, Nicolás;
Berciano, José;
Combarros, Onofre

Publication type:

Article

Association between Glycogen Synthase Kinase-3β Genetic Polymorphism and Late-Onset Alzheimer’s Disease.

Published in:

Dementia & Geriatric Cognitive Disorders, 2006, v. 21, n. 4, p. 228, doi. 10.1159/000091044

By:

Mateo, Ignacio;
Infante, Jon;
Llorca, Javier;
Rodríguez, Eloy;
Berciano, José;
Combarros, Onofre

Publication type:

Article

Interaction between CYP19 Aromatase and Butyrylcholinesterase Genes Increases Alzheimer’s Disease Risk.

Published in:

Dementia & Geriatric Cognitive Disorders, 2005, v. 20, n. 2/3, p. 153, doi. 10.1159/000087065

By:

Combarros, Onofre;
Riancho, José A.;
Infante, Jon;
Sañudo, Carolina;
Llorca, Javier;
Zarrabeitia, María T.;
Berciano, José

Publication type:

Article

Horizontal Pendular Nystagmus and Ataxia Secondary to Severe Hypomagnesemia.

Published in:

2024

By:

Polanco, Marcos;
Rivera, María;
Manrique, Leire;
Lage, Carmen;
Infante, Jon

Publication type:

Case Study

Oculomotor Dysfunction in Idiopathic and LRRK2-Parkinson's Disease and At-Risk Individuals.

Published in:

Journal of Parkinson's Disease, 2024, v. 14, n. 4, p. 797, doi. 10.3233/JPD-230416

By:

Lage, Carmen;
Sánchez-Rodríguez, Antonio;
Rivera-Sánchez, María;
Sierra, María;
González-Aramburu, Isabel;
Madera, Jorge;
Delgado-Alvarado, Manuel;
López-García, Sara;
Martínez-Dubarbie, Francisco;
Fernández-Matarrubia, Marta;
Martínez-Amador, Néstor;
Martínez-Rodríguez, Isabel;
Calvo-Córdoba, Alberto;
Rodríguez-Rodríguez, Eloy;
García-Cena, Cecilia;
Sánchez-Juan, Pascual;
Infante, Jon

Publication type:

Article

A unicenter, prospective study of Guillain‐Barré syndrome in Spain.

Published in:

Acta Neurologica Scandinavica, 2019, v. 139, n. 6, p. 546, doi. 10.1111/ane.13092

By:

Sedano, María J.;
Orizaola, Pedro;
Gallardo, Elena;
García, Antonio;
Pelayo‐Negro, Ana L.;
Sánchez‐Juan, Pascual;
Infante, Jon;
Berciano, José

Publication type:

Article

Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1.

Published in:

2016

By:

Peeters, Kristien;
Palaima, Paulius;
Pelayo‐Negro, Ana L.;
García, Antonio;
Gallardo, Elena;
García‐Barredo, Rosario;
Mateiu, Ligia;
Baets, Jonathan;
Menten, Björn;
Vriendt, Els;
Jonghe, Peter;
Timmerman, Vincent;
Infante, Jon;
Berciano, José;
Jordanova, Albena

Publication type:

journal article

Glycogen synthase kinase-3 beta and tau genes interact in Parkinson's and Alzheimer's diseases.

Published in:

2009

By:

García-Gorostiaga I;
Sánchez-Juan P;
Mateo I;
Rodríguez-Rodríguez E;
Sánchez-Quintana C;
del Olmo SC;
Vázquez-Higuera JL;
Berciano J;
Combarros O;
Infante J;
García-Gorostiaga, Inés;
Sánchez-Juan, Pascual;
Mateo, Ignacio;
Rodríguez-Rodríguez, Eloy;
Sánchez-Quintana, Coro;
del Olmo, Soraya Curiel;
Vázquez-Higuera, José Luis;
Berciano, José;
Combarros, Onofre;
Infante, Jon

Publication type:

Letter

Glycogen synthase kinase-3β and tau genes interact in Parkinson's and Alzheimer's diseases.

Published in:

Annals of Neurology, 2009, v. 65, n. 6, p. 759, doi. 10.1002/ana.21687

By:

García-Gorostiaga, Inés;
Sánchez-Juan, Pascual;
Mateo, Ignacio;
Rodríguez-Rodríguez, Eloy;
Sánchez-Quintana, Coro;
Curiel del Olmo, Soraya;
Vázquez-Higuera, José Luis;
Berciano, José;
Combarros, Onofre;
Infante, Jon

Publication type:

Article

Influence of Physiological Variables and Comorbidities on Plasma Aβ40, Aβ42, and p-tau181 Levels in Cognitively Unimpaired Individuals.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 3, p. 1481, doi. 10.3390/ijms25031481

By:

Martínez-Dubarbie, Francisco;
Guerra-Ruiz, Armando;
López-García, Sara;
Irure-Ventura, Juan;
Lage, Carmen;
Fernández-Matarrubia, Marta;
Pozueta-Cantudo, Ana;
García-Martínez, María;
Corrales-Pardo, Andrea;
Bravo, María;
Martín-Arroyo, Juan;
Infante, Jon;
López-Hoyos, Marcos;
García-Unzueta, María Teresa;
Sánchez-Juan, Pascual;
Rodríguez-Rodríguez, Eloy

Publication type:

Article

Correction to: The frequency of non‑motor symptoms in SCA3 and their association with disease severity and lifestyle factors.

Published in:

2024

By:

Hengel, Holger;
Martus, Peter;
Faber, Jennifer;
Giunti, Paola;
Garcia-Moreno, Hector;
Solanky, Nita;
Klockgether, Thomas;
Reetz, Kathrin;
van de Warrenburg, Bart P.;
Santana, Magda M.;
Silva, Patrick;
Cunha, Inês;
de Almeida, Luís Pereira;
Timmann, Dagmar;
Infante, Jon;
de Vries, Jeroen;
Lima, Manuela;
Pires, Paula;
Bushara, Khalaf;
Jacobi, Heike

Publication type:

Correction Notice

The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors.

Published in:

Journal of Neurology, 2023, v. 270, n. 2, p. 944, doi. 10.1007/s00415-022-11441-z

By:

Hengel, Holger;
Martus, Peter;
Faber, Jennifer;
Giunit, Paola;
Garcia-Moreno, Hector;
Solanky, Nita;
Klockgether, Thomas;
Reetz, Kathrin;
van de Warrenburg, Bart P.;
Santana, Magda M.;
Silva, Patrick;
Cunha, Inês;
de Almeida, Luís Pereira;
Timmann, Dagmar;
Infante, Jon;
de Vries, Jeroen;
Lima, Manuela;
Pires, Paula;
Bushara, Khalaf;
Jacobi, Heike

Publication type:

Article

POLR3A-related spastic ataxia: new mutations and a look into the phenotype.

Published in:

Journal of Neurology, 2020, v. 267, n. 2, p. 324, doi. 10.1007/s00415-019-09574-9

By:

Infante, Jon;
Serrano-Cárdenas, Karla M.;
Corral‐Juan, Marc;
Farré, Xavier;
Sánchez, Ivelisse;
de Lucas, Enrique M.;
García, Antonio;
Martín-Gurpegui, José Luis;
Berciano, José;
Matilla-Dueñas, Antoni

Publication type:

Article

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) with chronic cough and preserved muscle stretch reflexes: evidence for selective sparing of afferent Ia fibres.

Published in:

Journal of Neurology, 2018, v. 265, n. 6, p. 1454, doi. 10.1007/s00415-018-8872-1

By:

Infante, Jon;
García, Antonio;
Serrano-Cárdenas, Karla M.;
González-Aguado, Rocío;
Gazulla, José;
de Lucas, Enrique M.;
Berciano, José

Publication type:

Article

Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.

Published in:

Journal of Neurology, 2017, v. 264, n. 8, p. 1655, doi. 10.1007/s00415-017-8474-3

By:

Berciano, José;
García, Antonio;
Gallardo, Elena;
Peeters, Kristien;
Pelayo-Negro, Ana;
Álvarez-Paradelo, Silvia;
Gazulla, José;
Martínez-Tames, Miriam;
Infante, Jon;
Jordanova, Albena

Publication type:

Article

NEFL N98S mutation: another cause of dominant intermediate Charcot-Marie-Tooth disease with heterogeneous early-onset phenotype.

Published in:

Journal of Neurology, 2016, v. 263, n. 2, p. 361, doi. 10.1007/s00415-015-7985-z

By:

Berciano, José;
Peeters, Kristien;
García, Antonio;
López-Alburquerque, Tomás;
Gallardo, Elena;
Hernández-Fabián, Arantxa;
Pelayo-Negro, Ana;
Vriendt, Els;
Infante, Jon;
Jordanova, Albena

Publication type:

Article

NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.

Published in:

Journal of Neurology, 2015, v. 262, n. 5, p. 1289, doi. 10.1007/s00415-015-7709-4

By:

Berciano, José;
García, Antonio;
Peeters, Kristien;
Gallardo, Elena;
Vriendt, Els;
Pelayo-Negro, Ana;
Infante, Jon;
Jordanova, Albena

Publication type:

Article

Evolution of Charcot-Marie-Tooth disease type 1A duplication: a 2-year clinico-electrophysiological and lower-limb muscle MRI longitudinal study.

Published in:

Journal of Neurology, 2014, v. 261, n. 4, p. 675, doi. 10.1007/s00415-014-7248-4

By:

Pelayo-Negro, Ana;
Gallardo, Elena;
García, Antonio;
Sánchez-Juan, Pascual;
Infante, Jon;
Berciano, José

Publication type:

Article

Hereditary neuropathy with liability to pressure palsy: fulminant radicular dysfunction during anterolateral lumbar interbody fusion.

Published in:

2013

By:

Berciano, José;
Martínez-Agüeros, José;
Gallardo, Elena;
Martínez-Martínez, M.;
Infante, Jon;
García, Antonio;
Fernández-Torre, José;
Combarros, Onofre

Publication type:

Letter

Magnetic resonance imaging of lower limb musculature in acute motor axonal neuropathy.

Published in:

Journal of Neurology, 2012, v. 259, n. 6, p. 1111, doi. 10.1007/s00415-011-6309-1

By:

Berciano, José;
Gallardo, Elena;
Fernández-Torre, José;
González-Quintanilla, Vicente;
Infante, Jon

Publication type:

Article

Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia.

Published in:

Journal of Neurology, 2012, v. 259, n. 2, p. 246, doi. 10.1007/s00415-011-6155-1

By:

Sánchez-Ferrero, Elena;
Coto, Eliecer;
Corao, Ana;
Díaz, Marta;
Gámez, Josep;
Esteban, Jesús;
Gonzalo, Juan;
Pascual-Pascual, Samuel;
Munaín, Adolfo;
Morís, Germán;
Infante, Jon;
Castillo, Emilia;
Márquez, Celedonio;
Álvarez, Victoria

Publication type:

Article

New insights into the pathophysiology of pes cavus in Charcot-Marie-Tooth disease type 1A duplication.

Published in:

Journal of Neurology, 2011, v. 258, n. 9, p. 1594, doi. 10.1007/s00415-011-6094-x

By:

Berciano, José;
Gallardo, Elena;
García, Antonio;
Pelayo-Negro, Ana L.;
Infante, Jon;
Combarros, Onofre

Publication type:

Article

Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation.

Published in:

Journal of Neurology, 2011, v. 258, n. 8, p. 1413, doi. 10.1007/s00415-011-5947-7

By:

Berciano, José;
Baets, Jonathan;
Gallardo, Elena;
Zimoń, Magdalena;
García, Antonio;
López-Laso, Eduardo;
Combarros, Onofre;
Infante, Jon;
Timmerman, Vincent;
Jordanova, Albena;
De Jonghe, Peter

Publication type:

Article

Striatal dopamine function in a family with multiple SCA-3 phenotypes.

Published in:

Journal of Neurology, 2011, v. 258, n. 2, p. 308, doi. 10.1007/s00415-010-5724-z

By:

Cubo, Esther;
López, Mateo;
Ceberio, Jon Infante;
Alfonso, Isabel Lanchas;
Martinez, Begoña;
Berciano, José Miguel;
Iglesias, Fernando;
Obeso, José

Publication type:

Article

Clinical progression in Charcot-Marie-Tooth disease type 1A duplication: clinico-electrophysiological and MRI longitudinal study of a family.

Published in:

Journal of Neurology, 2010, v. 257, n. 10, p. 1633, doi. 10.1007/s00415-010-5580-x

By:

Berciano, José;
Gallardo, Elena;
García, Antonio;
Ramón, César;
Infante, Jon;
Combarros, Onofre

Publication type:

Article

Charcot–Marie–Tooth disease type 2J with MPZ Thr124Met mutation: clinico-electrophysiological and MRI study of a family.

Published in:

Journal of Neurology, 2009, v. 256, n. 12, p. 2061, doi. 10.1007/s00415-009-5251-y

By:

Gallardo, Elena;
García, Antonio;
Ramón, César;
Maraví, Elías;
Infante, Jon;
Gastón, Itziar;
Alonso, Ángel;
Combarros, Onofre;
De Jonghe, Peter;
Berciano, José

Publication type:

Article

Interaction between estrogen receptor-α and butyrylcholinesterase genes modulates Alzheimer's disease risk.

Published in:

Journal of Neurology, 2007, v. 254, n. 9, p. 1290, doi. 10.1007/s00415-006-0502-7

By:

Combarros, Onofre;
Riancho, José Antonio;
Arozamena, Jana;
Mateo, Ignacio;
Llorca, Javier;
Infante, Jon;
Sánchez-Juan, Pascual;
Zarrabeitia, María Teresa;
Berciano, José

Publication type:

Article

Interaction between prion protein and interleukin-1A genes increases early-onset Alzheimer’s disease risk.

Published in:

Journal of Neurology, 2007, v. 254, n. 1, p. 115, doi. 10.1007/s00415-006-0291-z

By:

Combarros, Onofre;
Llorca, Javier;
Sánchez-Juan, Pascual;
Mateo, Ignacio;
Infante, Jon;
Rodríguez, Eloy;
Sánchez-Quintana, Coro;
Berciano, José

Publication type:

Article

Genetic interaction between two apolipoprotein E receptors increases Alzheimer's disease risk.

Published in:

Journal of Neurology, 2006, v. 253, n. 6, p. 801, doi. 10.1007/s00415-005-0063-1

By:

Rodríguez, Eloy;
Mateo, Ignacio;
Llorca, Javier;
Sánchez-Quintana, Coro;
Infante, Jon;
Berciano, José;
Combarros, Onofre

Publication type:

Article

Masseter reflex in the study of spinocerebellar ataxia type 2 and type 3.

Published in:

Muscle & Nerve, 2009, v. 40, n. 4, p. 640, doi. 10.1002/mus.21334

By:

García, Antonio;
Alvarez, Silvia;
Infante, Jon;
Berciano, José

Publication type:

Article