Publicaciones (47) Publicaciones de Gustavo Lorenzo Sanz

2018

  1. RNA-Seq blood transcriptome profiling in familial attention deficit and hyperactivity disorder (ADHD)

    Psychiatry Research, Vol. 270, pp. 544-546

  2. Reduced cerebrospinal fluid monoamines in Alexander's disease: a clue to a symptomatic therapy

    European Journal of Neurology

2017

  1. Clinical rating scale for pantothenate kinase-associated neurodegeneration: A pilot study

    Movement Disorders, Vol. 32, Núm. 11, pp. 1620-1630

  2. Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes

    PLoS ONE, Vol. 12, Núm. 11

2016

  1. Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis

    Cellular and Molecular Life Sciences, Vol. 73, Núm. 13, pp. 2583-2599

  2. Unidad de Neurología Pediátrica del Hospital Universitario Ramón y Cajal

    Revista española de pediatría: clínica e investigación, Vol. 72, Núm. 2, pp. 105-107

  3. Unidad de neurología pediátrica del Hospital Universitario Ramón y Cajal

    Revista Espanola de Pediatria, Vol. 72, Núm. 2, pp. 105-107

2015

  1. Sturge-weber syndrome without nevus facial: Leptomeningeal angiomatosis front with favorable evolution

    Revista de Neurologia

2014

  1. Distrofias musculares

    Tratado de pediatría (Editorial Médica Panamericana), pp. 2282-2293

  2. Refractory status epilepticus presenting as shaken baby syndrome

    Revista de Neurologia, Vol. 58, Núm. 12, pp. 548-552

2013

  1. Response to methylphenidate by adult and pediatric patients with attention-deficit/hyperactivity disorder: The spanish multicenter dihana study

    Neuropsychiatric Disease and Treatment, Vol. 9, pp. 211-218

2011

  1. [Involvement of vesicular monoamine transporter in attention deficit hyperactivity disorder].

    Revista de neurologia, Vol. 52 Suppl 1

2007

  1. Aspectos clínicos

    Anales de Pediatria Continuada, Vol. 5, Núm. 5, pp. 245-252

2004

  1. Hypothalamic adipic hypernatraemia syndrome with normal osmoregulation of vasopressin

    European Journal of Pediatrics, Vol. 163, Núm. 10, pp. 580-583

2003

  1. Electroencephalographic alterations in children with attention deficit hyperactivity disorder

    Revista de Neurologia, Vol. 37, Núm. 10, pp. 904-908

2001

  1. Estudio abierto con tiagabina en epilepsia parcial

    Revista de Neurologia, Vol. 32, Núm. 11, pp. 1041-1046

2000

  1. A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

    Neuromuscular Disorders, Vol. 10, Núm. 7, pp. 493-496

  2. Prevesical abscess secondary to pubis symphysis septic arthritis

    Pediatric Infectious Disease Journal, Vol. 19, Núm. 9, pp. 896-898

1998

  1. Enfermedad de Menkes con citocromo oxidasa normal en fibroblastos: Presentacion de un caso y puesta al dia

    Anales Espanoles de Pediatria, Vol. 49, Núm. 1, pp. 85-88

  2. Focal myositis: A paediatric case and review of the literature

    Revista de Neurologia, Vol. 27, Núm. 157, pp. 505-508