C. Iturriaga

Electrophysiological approach to the study of essential tremor in children and adolescents.

J. Valls-Solé, E. Fernández-Álvarez, C. Fusco, 2003, Developmental medicine and child neurology.

Niemann–Pick C disease in Spain: Clinical spectrum and development of a disability scale

M. Pineda, C. Iturriaga, M. Vanier, 2006, Journal of the Neurological Sciences.

Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies

C. Paradas, R. Rojas-García, I. Illa, 2010, Neurology.

Clinicopathological features of genetically confirmed Danon disease

S. Dimauro, I. Nonaka, I. Nishino, 2002, Neurology.

Identification of 25 new mutations in 40 unrelated Spanish Niemann‐Pick type C patients: genotype‐phenotype correlations

C. Iturriaga, M. Pineda, M. Vanier, 2005, Clinical genetics.

Hereditary Motor and Sensory Neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies

L. Kalaydjieva, R. King, P. Thomas, 2000, Neuromuscular Disorders.

Autosomal dominant Emery–Dreifuss muscular dystrophy: a new family with late diagnosis

S. Manilal, K. Schwartz, E. Fernández-Álvarez, 2002, Neuromuscular Disorders.

Mechanical ventilation for ischemic stroke and intracerebral hemorrhage.

C. Iturriaga, J. Ara, Antonio Tejada, 1999, Neurology.

[Aspects of neuropathy in mitochondrial diseases].

R. Artuch, M. Pineda, J. Montoya, 2000, Revista de neurologia.

1α,25(OH)(2)-Vitamin D3 increases dysferlin expression in vitro and in a human clinical trial.

C. Paradas, I. Gich, R. Rojas-García, 2012, Molecular therapy : the journal of the American Society of Gene Therapy.