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Jon Infante Ceberio

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Jon Infante Ceberio

Presentación

Servicio de Neurología, Hospital Universitario Marqués de Valdecilla (Santander).

Másteres

Máster en Trastornos del Movimiento

Universidad de Murcia

Puesto de trabajo

 
Médico Adjunto del Servicio de Neurología
CSUR-Ataxias y Paraplejias hereditarias
Hospital Universitario Marqués de Valdecilla
Santander
 
Profesor Asociado Ciencias de la Salud
Universidad de Cantabria
 

Sociedades científicas

 
Miembro de la Sociedad Española de Neurología
Miembro de CIBERNED
Miembro de Ataxia Study Group (ASG) (ataxia-study-group.net)
 

Publicaciones científicas

 
1: Berciano J, García A, Infante J. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders. Handb Clin Neurol 2013;115:907-32.
 
 
2: Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M,  Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J,  Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T. Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data. Lancet Neurol 2013;12(7):650-8
 
 
3: Sierra M, Infante J, Berciano J. Substantia nigra echogenicity in Friedreich's ataxia patients. Cerebellum 2013;12(4):437-40
 
 
4: Pelayo-Negro AL, Sánchez-Quintana C, Rodríguez-Oroz MC, Volpini V, Zeviani M, Tola-Arribas MA, Berciano J, Infante J. Screening for POLG W748S and A467T mutations in ataxia patients from Spain. Mov Disord 2012;27(10):1326
 
 
5: Jacobi H, Bauer P, Giunti P, Labrum R, Sweeney MG, Charles P, Dürr A, Marelli C, Globas C, Linnemann C, Schöls L, Rakowicz M, Rola R, Zdzienicka E, Schmitz-Hübsch T, Fancellu R, Mariotti C, Tomasello C, Baliko L, Melegh B, Filla  A, Rinaldi C, van de Warrenburg BP, Verstappen CC, Szymanski S, Berciano J, Infante J, Timmann D, Boesch S, Hering S, Depondt C, Pandolfo M, Kang JS, Ratzka  S, Schulz J, Tezenas du Montcel S, Klockgether T. The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study. Neurology 2011;77(11):1035-41
 
6: Jacobi H, Hauser TK, Giunti P, Globas C, Bauer P, Schmitz-Hübsch T, Baliko L, Filla A, Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van
de Warrenburg BP, Dürr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C,
Schöls L, Zdzienicka E, Kang JS, Ratzka S, Kremer B, Stephenson DA, Melegh B,
Pandolfo M, Tezenas du Montcel S, Borkert J, Schulz JB, Klockgether T.
Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and
morphometric brainstem and cerebellar findings. Cerebellum 2012;11(1):155-66.
 
7: Schmitz-Hübsch T, Coudert M, Tezenas du Montcel S, Giunti P, Labrum R, Dürr A,
Ribai P, Charles P, Linnemann C, Schöls L, Rakowicz M, Rola R, Zdzienicka E,
Fancellu R, Mariotti C, Baliko L, Melegh B, Filla A, Salvatore E, van de
Warrenburg BP, Szymanski S, Infante J, Timmann D, Boesch S, Depondt C, Kang JS,
Schulz JB, Klopstock T, Lossnitzer N, Löwe B, Frick C, Rottländer D, Schlaepfer
TE, Klockgether T. Depression comorbidity in spinocerebellar ataxia. Mov Disord
2011;26(5):870-6
 
8: Álvarez-Paradelo S, García A, Infante J, Berciano J. Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias. Neurologia 2011;26(3):157-65
 
9: Schmitz-Hübsch T, Fimmers R, Rakowicz M, Rola R, Zdzienicka E, Fancellu R,
Mariotti C, Linnemann C, Schöls L, Timmann D, Filla A, Salvatore E, Infante J,
Giunti P, Labrum R, Kremer B, van de Warrenburg BP, Baliko L, Melegh B, Depondt
C, Schulz J, du Montcel ST, Klockgether T. Responsiveness of different rating
instruments in spinocerebellar ataxia patients. Neurology 2010;74(8):678-84
 
 
10: Schmitz-Hübsch T, Coudert M, Giunti P, Globas C, Baliko L, Fancellu R,
Mariotti C, Filla A, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van
de Warrenburg BP, Dürr A, Timmann D, Boesch S, Rola R, Depondt C, Schöls L,
Zdzienicka E, Kang JS, Ratzka S, Kremer B, Schulz JB, Klopstock T, Melegh B, du
Montcel ST, Klockgether T. Self-rated health status in spinocerebellar
ataxia--results from a European multicenter study. Mov Disord 2010;25(5):587-95
 
11: García A, Alvarez S, Infante J, Berciano J. Masseter reflex in the study of
spinocerebellar ataxia type 2 and type 3. Muscle Nerve 2009;40(4):640-2.
 
 
12: Schmitz-Hübsch T, Giunti P, Stephenson DA, Globas C, Baliko L, Saccà F,
Mariotti C, Rakowicz M, Szymanski S, Infante J, van de Warrenburg BP, Timmann D,
Fancellu R, Rola R, Depondt C, Schöls L, Zdzienicka E, Kang JS, Döhlinger S,
Kremer B, Melegh B, Filla A, Klockgether T. SCA Functional Index: a useful
compound performance measure for spinocerebellar ataxia. Neurology 2008;71(7):486-92
 
 
13: Schmitz-Hübsch T, Coudert M, Bauer P, Giunti P, Globas C, Baliko L, Filla A,
Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van de
Warrenburg BP, Dürr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C, Schöls
L, Zdienicka E, Kang JS, Döhlinger S, Kremer B, Stephenson DA, Melegh B, Pandolfo
M, di Donato S, du Montcel ST, Klockgether T. Spinocerebellar ataxia types 1, 2,
3, and 6: disease severity and nonataxia symptoms. Neurology 2008;71(13):982-9
 
14: Schmitz-Hübsch T, du Montcel ST, Baliko L, Berciano J, Boesch S, Depondt C,
Giunti P, Globas C, Infante J, Kang JS, Kremer B, Mariotti C, Melegh B, Pandolfo
M, Rakowicz M, Ribai P, Rola R, Schöls L, Szymanski S, van de Warrenburg BP, Dürr
A, Klockgether T, Fancellu R. Scale for the assessment and rating of ataxia:
development of a new clinical scale. Neurology 2006;66(11):1717-20.
 
15: Berciano J, Infante J, García A, de Pablos C, Amer G, Polo JM, Volpini V,
Combarros O. Stiff man-like syndrome and generalized myokymia in spinocerebellar
ataxia type 3. Mov Disord 2006;21(7):1031-5
 
 16: Berciano J, Infante J, García A, Polo JM, Volpini V, Combarros O. Very
late-onset Friedreich's ataxia with minimal GAA1 expansion mimicking multiple
system atrophy of cerebellar type. Mov Disord 2005;20(12):1643-5
 
17: Criscuolo C, Saccà F, De Michele G, Mancini P, Combarros O, Infante J, Garcia
A, Banfi S, Filla A, Berciano J. Novel mutation of SACS gene in a Spanish family
with autosomal recessive spastic ataxia. Mov Disord 2005;20(10):1358-61
  
18: Infante J, Combarros O, Volpini V, Corral J, Llorca J, Berciano J. Autosomal
dominant cerebellar ataxias in Spain: molecular and clinical correlations,
prevalence estimation and survival analysis. Acta Neurol Scand 2005;111(6):391-9
  
19: Infante J, Berciano J, Volpini V, Corral J, Polo JM, Pascual J, Combarros O.
Spinocerebellar ataxia type 2 with Levodopa-responsive parkinsonism culminating
in motor neuron disease. Mov Disord 2004;19(7):848-52
 
20: Berciano J, Infante J, Mateo I, Combarros O. [Hereditary ataxias and
paraplegias: a clinicogenetic review]. Neurologia 2002;17(1):40-51
 

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