Agnosia visual aperceptiva en paciente con Síndrome de Krabbe[poster ganador]

  1. F. Robles
  2. C. Fournier
  3. J. Melero
  4. L. López
  5. C. Rodríguez
  6. M. García
  7. L. González
Aldizkaria:
Sanidad militar: revista de sanidad de las Fuerzas Armadas de España

ISSN: 1887-8571

Argitalpen urtea: 2014

Alea: 70

Zenbakia: 1

Orrialdeak: 20-21

Mota: Artikulua

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Beste argitalpen batzuk: Sanidad militar: revista de sanidad de las Fuerzas Armadas de España

Erreferentzia bibliografikoak

  • Krabbe, KH. (1916). A new familial infantile form of diffuse brain sclerosis. Brain (Oxford). 39. 74-115
  • González Gutiérrez-Solana, L, López-Marín, L. (2009). Enfermedades Raras relacionadas con Organelas: Lisosomas, Peroxisomas y Sistemas Golgi y Pre-Golgi. Curso de formación en enfermedades raras metabólicas.
  • Duffner, PK, Jalal, K, Carter, RL. (2009). The Hunter's Hope Krabbe family database. Pediatr Neurol.. 40. 13
  • Shapiro, EG, Klein, KA. (1994). Advances in Child neuropsychology. Springer-Verlag. New York.
  • Duffner, PK, Barczykowski, A, Jalal, K, Yan, L, Kay, DM, Carter, RL. (2011). Early Infantile Krabbe Disease: Results of the World-Wide Krabbe Registry. Pediatr Neurol.. 45. 141
  • Duffner, PK, Barczykowski, A, Kay, DM, Jalal, K, Yan, L, Abdelhalim, A. (2012). Later Onset Phenotypes of Krabbe Disease: Result´s of the World-Wide Krabbe Registry. Pediatr Neurol.. 46. 298-306
  • Vanier, MT, Caillaud, C. (2012). Inborn metabolic diseases: Diagnosis and treatment. 5. Springer-Verlag. Berlin.
  • Lyon, G, Kolodny, EH, Pastores, GM. (2006). Neurology of hereditary metabolic diseases of children. 3. Mc Graw Hill. New York.
  • Gelinas, J, Liao, P, Lehman, A. (2012). Child Neurology: Krabbe disease: a potentially treatable white matter disorder. Neurology. 79. 170
  • Abdelhalim, A, Alberico, RA, Barczykowski, A, Duffner, PK. (2014). Patterns of Magnetic Resonance imaging Abnormalities in Symptomatic Patients With Krabbe Disease Correspond to Phenotype. Pediatr Neurol.. 50. 127
  • Lantos, JD. (2011). Dangerous and expensive screening and treatment for rare childhood diseases: the case of krabbe desease. Dev Disabil Res Rev.. 17. 15
  • Kim, SU. (2014). Lysosomal storage diseases: Stem cell-based cell- and gene-therapy. Cell trasplant.
  • Farah, MJ. (2004). Visual Agnosia. 2. MIT press/Bradford Books. Cambridge.
  • De Renzi, E. (1999). Handbook of Clinical and Experimental Neuropsychology. Psychology Press.
  • García-García, R, Cacho-Gutiérrez, LJ. (2004). Prosopagnosia ¿entidad única o múltiple?. Rev Neurol.. 38. 682
  • Klein, KA, Shapiro, EG. (1992). Visual agnosia in children: A new and different look. J Clin Exp Neuropsychol.. 14.
  • Fournier, MC. (2002). Neuropsicología Infantil. Editorial Mapfre. Madrid.
  • Schoenberg, MR, Scott, JG. (2011). The Little Black Book of Neuropsychology. Springer. New York.
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