Antonio Garcı́a

发表

Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion

O. Combarros, J. Infante, J. Berciano, 2001, Muscle & nerve.

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

O. Combarros, E. Gallardo, J. Infante, 2011, Journal of Neurology.

Charcot-Marie-Tooth disease: a review with emphasis on the pathophysiology of pes cavus

O. Combarros, E. Gallardo, J. Infante, 2011 .

Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles.

O. Combarros, E. Gallardo, J. Berciano, 2006, Brain : a journal of neurology.

Initial semeiology in children with Charcot–Marie–Tooth disease 1A duplication

O. Combarros, J. Berciano, Antonio G. García, 2003, Muscle & nerve.

Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot–Marie–Tooth disease 1A duplication

O. Combarros, J. Berciano, Antonio G. García, 2000, Neuromuscular Disorders.

A longitudinal clinical and electrophysiologic study

O. Combarros, J. Berciano, J. Calleja, 2012 .

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

O. Combarros, E. Gallardo, J. Infante, 2009, Journal of Neurology.

CMT1A duplication: refining the minimal adult phenotype

O. Combarros, I. Mateo, E. Gallardo, 2008, Journal of the peripheral nervous system : JPNS.

Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood

O. Combarros, J. Berciano, Antonio G. García, 1998, Neurology.

Electromyographic tendon reflex recording: An accurate and comfortable method for diagnosis of charcot‐marie‐tooth disease type 1a

J. Berciano, A. Pelayo-Negro, Antonio G. García, 2015, Muscle & nerve.

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

E. Gallardo, J. Infante, A. Jordanova, 2017, Journal of Neurology.

Proximal nerve lesions in early Guillain–Barré syndrome: implications for pathogenesis and disease classification

E. Gallardo, M. Berciano, J. Berciano, 2017, Journal of Neurology.

Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.

J. Infante, J. Berciano, Antonio G. García, 2013, Handbook of clinical neurology.

Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies.

K. Fischbeck, C. Shaw, C. Ludlow, 2010, Brain : a journal of neurology.

Fulminant Guillain–Barré Syndrome with universal inexcitability of peripheral nerves: A clinicopathological study

M. Berciano, I. Illa, J. Berciano, 1997, Muscle & nerve.

Spinal nerve involvement in early Guillain–Barré syndrome: A clinico-electrophysiological, ultrasonographic and pathological study

E. Gallardo, M. Berciano, P. Sánchez-Juan, 2015, Clinical Neurophysiology.

Acute motor conduction block neuropathy: Another Guillain-Barré syndrome variant

J. Berciano, Antonio G. García, Antonio Garcı́a, 2004, Neurology.

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

B. Menten, E. Gallardo, V. Timmerman, 2016, Annals of neurology.

Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation

O. Combarros, E. Gallardo, V. Timmerman, 2011, Journal of Neurology.

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

T. López-Alburquerque, E. Gallardo, J. Infante, 2016, Journal of Neurology.

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

E. Gallardo, J. Infante, A. Jordanova, 2015, Journal of Neurology.

Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.

S. Züchner, E. Storey, K. Claeys, 2009, Brain : a journal of neurology.

Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix‐Saguenay

G. De Michele, J. Berciano, C. Criscuolo, 2008, Muscle & nerve.

Early axonal Guillain-Barré syndrome with normal peripheral conduction: imaging evidence for changes in proximal nerve segments

E. Gallardo, J. Berciano, A. Pelayo-Negro, 2015, Journal of Neurology, Neurosurgery & Psychiatry.

Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6

S. Tezenas du Montcel, L. Schöls, T. Schmitz-Hübsch, 2016, The Cerebellum.

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

J. Infante, J. Berciano, J. Gazulla, 2018, Journal of Neurology.

Very late‐onset Friedreich's ataxia with minimal GAA1 expansion mimicking multiple system atrophy of cerebellar type

O. Combarros, V. Volpini, J. Infante, 2005, Movement disorders : official journal of the Movement Disorder Society.

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

E. Gallardo, J. Infante, P. Sánchez-Juan, 2019, Acta neurologica Scandinavica.

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

O. Combarros, E. Gallardo, J. Infante, 2013, Journal of Neurology.

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

O. Combarros, E. Gallardo, J. Infante, 2010, Journal of Neurology.

Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia

O. Combarros, G. De Michele, A. Filla, 2005, Movement disorders : official journal of the Movement Disorder Society.

Stiff man–like syndrome and generalized myokymia in spinocerebellar ataxia type 3

O. Combarros, V. Volpini, J. Infante, 2006, Movement disorders : official journal of the Movement Disorder Society.

Ia afferent fibers in peripheral nerve disorders: Evidence for divergent vulnerability

J. Infante, J. Berciano, Antonio Garcı́a, 2021, Clinical Neurophysiology Practice.

Reversible conduction failure on the deep tendon reflex response recording in early Guillain-Barré syndrome

J. Berciano, M. J. Sedano, Antonio G. García, 2018, Clinical neurophysiology practice.

J. Infante, J. Berciano, E. M. de Lucas, 2019, Journal of Neurology.

Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6

S. Tezenas du Montcel, L. Schöls, T. Schmitz-Hübsch, 2015, The Cerebellum.

Phenotype and clinical evolution of Charcot-Marie-Tooth disease type 1A duplication.

O. Combarros, E. Gallardo, J. Berciano, 2009, Advances in experimental medicine and biology.

Paroxysmal cervicobrachial cough-induced pain in a patient with syringomyelia extending into spinal cord posterior gray horns

M. Poca, J. Sahuquillo, J. Berciano, 2007, Journal of Neurology.

Cryptogenic gelastic epilepsy of frontal lobe origin: A paediatric case report

J. Herranz, Antonio G. García, M. A. Gutierrez, 2000, Seizure.

Comment on paraparetic Guillain–Barré syndrome: Non‐demyelinating reversible conduction failure restricted to the lower limbs

E. Gallardo, J. Berciano, A. Pelayo-Negro, 2017, Muscle & nerve.

Epilepsia partialis continua in progressive multifocal leukoencephalopathy: A motor cortex isolation syndrome

A. Ariza, M. Berciano, J. Berciano, 2003, Movement disorders : official journal of the Movement Disorder Society.

Nerve ultrasonography in early Guillain‐Barré syndrome: a need for large prospective studies

E. Gallardo, M. Berciano, P. Sánchez-Juan, 2014, Journal of the peripheral nervous system : JPNS.

Severe Guillain‐Barré syndrome: sorting out the pathological hallmark in an electrophysiological axonal case

M. Berciano, I. Illa, J. Berciano, 2009, Journal of the peripheral nervous system : JPNS.

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

J. Infante, J. Berciano, Antonio G. García, 2009, Muscle & nerve.