J. Martı́nez-Matos

发表

Insulin regulation of leptin synthesis and secretion in humans: the model of myotonic dystrophy

R. Casamitjana, J. Gómez, J. Soler, 1999, Clinical endocrinology.

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient

I. Ferrer, L. Goldfarb, M. Olivé, 2008, Neuromuscular Disorders.

Public health surveillance and incidence of adulthood Guillain-Barré syndrome in Spain, 1998–1999: the view from a sentinel network of neurologists

J. Duarte, F. T. I. Group, A. Tobías, 2004, Neurological Sciences.

I. Ferrer, E. Farrero, N. Sambuughin, 2004, Journal of the Neurological Sciences.

Leptin after IGF-I Generation Test in a Patient with Hypopituitarism and Myotonic Dystrophy Disease

J. Gómez, J. Martı́nez-Matos, 2004, Pituitary.

Diagnosis of Charcot-Marie-Tooth Disease

V. Volpini, M. Povedano, C. Casasnovas, 2009, Journal of biomedicine & biotechnology.

Apoptosis is not the mechanism of cell death of muscle fibers in human muscular dystrophies and inflammatory myopathies

I. Ferrer, M. Olivé, J. Montero, 1997, Muscle & nerve.

The absence of survival motor neuron 2 gene may play a role in multifocal motor neuropathy

M. Barceló, M. Baiget, E. Tizzano, 2002, Neurology.

Survival in amyotrophic lateral sclerosis with home mechanical ventilation: the impact of systematic respiratory assessment and bulbar involvement.

J. Escarrabill, E. Farrero, E. Prats, 2005, Chest.

Phenotypic spectrum of MFN2 mutations in the Spanish population

D. Bonneau, V. Volpini, A. Chevrollier, 2009, Journal of Medical Genetics.

Spatial Assessment of the Association between Long-Term Exposure to Environmental Factors and the Occurrence of Amyotrophic Lateral Sclerosis in Catalonia, Spain: A Population-Based Nested Case-Control Study

M. Sáez, M. Barceló, M. Povedano, 2018, Neuroepidemiology.

Multifocal acquired demyelinating sensory and motor neuropathy presenting as idiopathic hypertrophic brachial neuropathy

M. Simó, C. Casasnovas, S. Martínez-Yélamos, 2009, Journal of Neurology, Neurosurgery, and Psychiatry.

Charcot–marie–tooth disease with intermediate conduction velocities caused by a novel mutation in the MPZ gene

V. Volpini, C. Casasnovas, J. Montero, 2010, Muscle & nerve.

Two Spanish families with Charcot–Marie–Tooth type 2A: Clinical, electrophysiological and molecular findings

V. Volpini, C. Casasnovas, J. Montero, 2008, Neuromuscular Disorders.

18F-FDG PET/CT in the evaluation of POEMS syndrome.

S. Martínez-Yélamos, C. Gamez, L. Cano, 2010, European journal of radiology.

[Centronuclear myopathy].

S. Jaumà, M. Olivé, J. Montero, 1993, Neurologia.

Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment.

X. Estivill, N. López-Bigas, P. Gasparini, 2001, Human molecular genetics.

Guillain-Barré Syndrome in Spain, 1985–1997: Epidemiological and Public Health Views

J. Duarte, J. De Pedro-Cuesta, A. Tobías, 2001, European Neurology.

A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia

I. Ferrer, M. Baiget, M. Olivé, 2004, Neuromuscular Disorders.

Antibodies against disialosyl and terminal NeuNAc(α2-3)Gal ganglioside epitopes in acute relapsing sensory ataxic neuropathy

R. Rojas-García, I. Illa, E. Gallardo, 2008, Journal of Neurology.

Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders

I. Ferrer, M. Olivé, M. Povedano, 1997, Neuropathology and applied neurobiology.

Very early electrodiagnostic findings in Guillain‐Barré syndrome

A. Alentorn, M. Povedano, C. Casasnovas, 2011, Journal of the peripheral nervous system : JPNS.

Musk-antibody positive myasthenia gravis presenting with isolated neck extensor weakness

S. Jaumà, M. Povedano, C. Casasnovas, 2007, Neuromuscular Disorders.

GH secretion status in myotonic dystrophy

J. Fernández-Real, M. Navarro, J. Soler, 1993, Psychoneuroendocrinology.

[Dysphagia as the only manifestation of inclusion body myositis].

I. Ferrer, M. Olivé, J. Montero, 1994, Neurología.

Survival in amyotrophic lateral sclerosis with home mechanical ventilation: the impact of systematic respiratory assessment and bulbar involvement.

J. Escarrabill, E. Farrero, E. Prats, 2005, Chest.

Peripheral neuropathy associated with angioimmunoblastic lymphadenopathy

A. F. Sevilla, J. Montero, J. Martı́nez-Matos, 1988, Clinical Neurology and Neurosurgery.

Syringomyelia extending to the corona radiata

C. Majós, S. Martínez-Yélamos, L. Romero-Pinel, 2006, Journal of Neurology.

Development of non-pyramidal neurons in the rat sensorymotor cortex during the fetal and early postnatal periods.

I. Ferrer, J. Martı́nez-Matos, 1981, Journal fur Hirnforschung.