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José Berciano
José Berciano
Professor of Neurology, University of Cantabria
Verified email at unican.es
Title
Cited by
Cited by
Year
Scale for the assessment and rating of ataxia: development of a new clinical scale
T Schmitz-Hubsch, ST Du Montcel, L Baliko, J Berciano, S Boesch, ...
Neurology 66 (11), 1717-1720, 2006
18502006
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ...
The Lancet Neurology 7 (7), 583-590, 2008
16462008
Multiple-system atrophy
A Fanciulli, GK Wenning
New England Journal of Medicine 372 (3), 249-263, 2015
6662015
Neurofascin IgG4 antibodies in CIDP associate with disabling tremor and poor response to IVIg
L Querol, G Nogales-Gadea, R Rojas-Garcia, J Diaz-Manera, J Pardo, ...
Neurology 82 (10), 879-886, 2014
3562014
Cough, exertional, and sexual headaches: an analysis of 72 benign and symptomatic cases
J Pascual, F Iglesias, A Oterino, A Vazquez-Barquero, J Berciano
Neurology 46 (6), 1520-1524, 1996
3131996
Olivopontocerebellar atrophy: a review of 117 cases
J Berciano
Journal of the Neurological Sciences 53 (2), 253-272, 1982
2921982
Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry
M Köllensperger, F Geser, JP Ndayisaba, S Boesch, K Seppi, ...
Movement Disorders 25 (15), 2604-2612, 2010
2892010
Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study
H Jacobi, ST du Montcel, P Bauer, P Giunti, A Cook, R Labrum, ...
The Lancet Neurology 14 (11), 1101-1108, 2015
2632015
Hereditary ataxias and paraplegias in Cantabria, Spain: an epidemiological and clinical study
JM Polo, J Calleja, O Combarros, J Berciano
Brain 114 (2), 855-866, 1991
2561991
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study
H Jacobi, P Bauer, P Giunti, R Labrum, MG Sweeney, P Charles, A Duerr, ...
Neurology 77 (11), 1035-1041, 2011
2242011
Basichondrocranium anomalies in adult Chiari type I malformation: a morphometric study
A Vega, F Quintana, J Berciano
Journal of the neurological sciences 99 (2-3), 137-145, 1990
2121990
Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect
R Claramunt, L Pedrola, T Sevilla, AL De Munain, J Berciano, A Cuesta, ...
Journal of medical genetics 42 (4), 358-365, 2005
1972005
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes
S Tezenas du Montcel, A Durr, P Bauer, KP Figueroa, Y Ichikawa, ...
Brain 137 (9), 2444-2455, 2014
1862014
Headache in type I Chiari malformation
J Pascual, A Oterino, J Berciano
Neurology 42 (8), 1519-1519, 1992
1811992
Livedo reticularis and cerebrovascular lesions (Sneddon's syndrome) Clinical, radiological and pathological features in eight cases
M Rebollo, JF Val, F Garijo, F Quintana, J Berciano
Brain 106 (4), 965-979, 1983
1791983
Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases
MA Pujana, J Corral, M Gratacòs, O Combarros, J Berciano, D Genís, ...
Human genetics 104, 516-522, 1999
1771999
Charcot–Marie–Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles
E Gallardo, A García, O Combarros, J Berciano
Brain 129 (2), 426-437, 2006
1582006
Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study
A García, O Combarros, J Calleja, J Berciano
Neurology 50 (4), 1061-1067, 1998
1531998
The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q
J M. Serratosa, A V. Delgado-Escueta, I Posada, S Shih, I Drury, ...
Human molecular genetics 4 (9), 1657-1663, 1995
1531995
A prospective study of stroke in young adults in Cantabria, Spain.
C Leno, J Berciano, O Combarros, JM Polo, J Pascual, F Quintana, ...
Stroke 24 (6), 792-795, 1993
1531993
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