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Javier Arpa

Observed names: Arpa, Javier, J Arpa, J Arpa Gutiérrez, J. Arpa, JAVIER ARPA
Observed institutions: Hospital Universitario La Paz, Hospital Clínico San Carlos, Research Institute Hospital 12 de Octubre, Hospital La Luz, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos, Hospital Universitario 12 De Octubre, Hospital La Paz Institute for Health Research, Hospital Clínic de Barcelona, Instituto de Microcirugía Ocular, Hospital de Cruces, Hospital Universitario Ramón y Cajal, Instituto Nacional de la Salud, University College London, Universidad Autónoma de Madrid, Universitat de Barcelona
ORCID: 0000-0002-0579-0801
Observed ORCID: 0000-0002-0579-0801
OpenAlex ID: A5020664290
Paraneoplastic Neurological Syndromes and Glutamic Acid Decarboxylase Antibodies
2015 · Helena Ariño, Romana Höftberger, et al. · JAMA Neurology · 230
Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data
2015 · Kathrin Reetz, Imis Dogan, et al. · The Lancet Neurology · 209
Autoantibodies to glutamic acid decarboxylase in three patients with cerebellar ataxia, late-onset insulin-dependent diabetes mellitus, and polyendocrine autoimmunity
1997 · A. Saiz, J. Arpa, et al. · Neurology · 202
Progression characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study
2016 · Kathrin Reetz, Imis Dogan, et al. · The Lancet Neurology · 154
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Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis
2002 · C Dobson-Stone, A Danek, et al. · European Journal of Human Genetics · 149
Deferiprone in F riedreich ataxia: A 6‐Month randomized controlled trial
2014 · Massimo Pandolfo, Javier Arpa, et al. · Annals of Neurology · 140
Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies
1997 · Sylvia Bort, E. Nelis, et al. · Human Genetics · 137
Peroneal neuropathy after weight loss
2000 · Antonio Cruz‐Martinez, Javier Arpa, et al. · Journal of the Peripheral Nervous System · 117
Neuralgic amyotrophy: variable expression in 40 patients
2002 · A. Cruz‐Martínez, M. Barrio, et al. · Journal of the Peripheral Nervous System · 105
Idebenone treatment in paediatric and adult patients with Friedreich ataxia: Long-term follow-up
2008 · Mercè Pineda, Javier Arpa, et al. · European Journal of Paediatric Neurology · 101
Guillain-Barré Syndrome: Natural history and prognostic factors: a retrospective review of 106 cases
2013 · Inés González-Suárez, Irene Sanz-Gallego, et al. · BMC Neurology · 100
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Nonataxia symptoms in Friedreich Ataxia
2018 · Kathrin Reetz, Imis Dogan, et al. · Neurology · 91
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Onset features and time to diagnosis in Friedreich’s Ataxia
2020 · Elisabetta Indelicato, Wolfgang Nachbauer, et al. · Orphanet Journal of Rare Diseases · 73
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Targeted screening for the detection of Pompe disease in patients with unclassified limb-girdle muscular dystrophy or asymptomatic hyperCKemia using dried blood: A Spanish cohort
2015 · E. Gutiérrez-Rivas, J. Bautista, et al. · Neuromuscular Disorders · 57
Association of Novel POLGMutations and Multiple Mitochondrial DNA Deletions With Variable Clinical Phenotypes in a Spanish Population
2006 · Emiliano González-Vioque, Alberto Blázquez, et al. · Archives of Neurology · 56
Prevalence and progression of mitochondrial diseases: A study of 50 patients
2003 · Javier Arpa, Antonio Cruz‐Martínez, et al. · Muscle & Nerve · 54
Ophthalmic features of Friedreich ataxia
2011 · S Noval, I Contreras, et al. · Eye · 50
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Triple therapy with deferiprone, idebenone and riboflavin in Friedreich's ataxia - open-label trial
2013 · J. Arpa, I. Sanz-Gallego, et al. · Acta Neurologica Scandinavica · 49
Letters to the editor
1995 · Richard T. Moxley, Kenneth Ricker, et al. · Muscle & Nerve · 49
Serum insulin‐like system alterations in patients with spinocerebellar ataxia type 3
2010 · Jonas Alex Morales Saute, Andrew Chaves Feitosa da Silva, et al. · Movement Disorders · 39
Migrainous Syndrome With CSF Pleocytosis. SPECT Findings
1997 · A.B. Caminero Rodriguez, J.A. Pareja, et al. · Headache The Journal of Head and Face Pain · 39
Subcutaneous insulin‐like growth factor‐1 treatment in spinocerebellar ataxias: An open label clinical trial
2010 · Javier Arpa, Irene Sanz‐Gallego, et al. · Movement Disorders · 38
Ophthalmic Features of Spinocerebellar Ataxia Type 7
2009 · Roslyn K Manrique, Susana Noval, et al. · Journal of Neuro-Ophthalmology · 38
Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 gene
2011 · María J. Mazón, Francisco Barros, et al. · Neuromuscular Disorders · 36
Leukoencephalopathy due to Oral Methotrexate
2013 · I. González-Suárez, M. J. Aguilar-Amat, et al. · The Cerebellum · 34
Works count: 107
Citation count: 3,173
H-index: 27
I10-index: 63
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