Antonio G. García

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

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

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.

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.

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.

Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation

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

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.

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.

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

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

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.

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

E. Gallardo, J. Infante, P. Sánchez-Juan, 2014, 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.

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.

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.

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.

CMT1A duplication: refining the minimal adult phenotype

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

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

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

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.

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

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

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.

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

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

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

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

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.

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

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

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.

Malignant Cerebral Edema Secondary to Gliadel Wafers in the Early Postsurgical Period

Antonio G. García, A. B. Fernández, E. Lazo, 2015 .

Acute Flaccid Myelitis With Early, Severe Compound Muscle Action Potential Amplitude Reduction: A 3-Year Follow-up of a Child Patient.

C. Ortez, J. Berciano, Antonio G. García, 2018, Journal of clinical neuromuscular disease.

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.

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

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

Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.

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

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

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

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

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

Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation

O. Combarros, K. Claeys, E. Gallardo, 2008, Journal of Neurology.

Charcot–Marie–Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study

O. Combarros, I. Mateo, E. Gallardo, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

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.

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 .

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.

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.

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.

Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias.

Antonio G. García, S. Álvarez-Paradelo, J. Berciano, 2011 .

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

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

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

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

Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias.

J. Infante, J. Berciano, Antonio G. García, 2011, Neurología.

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.

This item is the archived peer-reviewed author-version of: Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1 Reference:

B. Menten, E. Gallardo, J. Infante, 2017 .

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

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