Gustavo
Lorenzo Sanz
Profesor/a Asociado/a en CC. de la Salud
Argitalpenak (47) Gustavo Lorenzo Sanz argitalpenak
2018
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RNA-Seq blood transcriptome profiling in familial attention deficit and hyperactivity disorder (ADHD)
Psychiatry Research, Vol. 270, pp. 544-546
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Reduced cerebrospinal fluid monoamines in Alexander's disease: a clue to a symptomatic therapy
European Journal of Neurology
2017
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Clinical rating scale for pantothenate kinase-associated neurodegeneration: A pilot study
Movement Disorders, Vol. 32, Núm. 11, pp. 1620-1630
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Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes
PLoS ONE, Vol. 12, Núm. 11
2016
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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
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Unidad de Neurología Pediátrica del Hospital Universitario Ramón y Cajal
Revista española de pediatría: clínica e investigación, Vol. 72, Núm. 2, pp. 105-107
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Unidad de neurología pediátrica del Hospital Universitario Ramón y Cajal
Revista Espanola de Pediatria, Vol. 72, Núm. 2, pp. 105-107
2015
2014
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Distrofias musculares
Tratado de pediatría (Editorial Médica Panamericana), pp. 2282-2293
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Refractory status epilepticus presenting as shaken baby syndrome
Revista de Neurologia, Vol. 58, Núm. 12, pp. 548-552
2013
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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
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[Involvement of vesicular monoamine transporter in attention deficit hyperactivity disorder].
Revista de neurologia, Vol. 52 Suppl 1
2007
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Aspectos clínicos
Anales de Pediatria Continuada, Vol. 5, Núm. 5, pp. 245-252
2004
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Hypothalamic adipic hypernatraemia syndrome with normal osmoregulation of vasopressin
European Journal of Pediatrics, Vol. 163, Núm. 10, pp. 580-583
2003
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Electroencephalographic alterations in children with attention deficit hyperactivity disorder
Revista de Neurologia, Vol. 37, Núm. 10, pp. 904-908
2001
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Estudio abierto con tiagabina en epilepsia parcial
Revista de Neurologia, Vol. 32, Núm. 11, pp. 1041-1046
2000
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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
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Prevesical abscess secondary to pubis symphysis septic arthritis
Pediatric Infectious Disease Journal, Vol. 19, Núm. 9, pp. 896-898
1998
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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
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Focal myositis: A paediatric case and review of the literature
Revista de Neurologia, Vol. 27, Núm. 157, pp. 505-508