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