婴儿肌张力不全的评估

Jan MM. Misdiagnosis in children with dopa-responsive dystonia. Pediatr Neurol. 2004;31:298-303.

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Fernández-Alvarez E. Prevalence of paediatric movement disorders. In: Fernández-Alvarez E, Arzimanoglou A, Tolosa E, eds. Paediatric movement disorders. Montrouge, France: John Libbey Eurotext; 2005:1-18.

Jankovich J, Penn AS. Severe dystonia and myoglobinuria. Neurology. 1982;32:1195-1197.

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Pierro MM, Bollea L, Di Rosa G, et al. Anoxic brain injury following near-drowning in children. Rehabilitation outcome: three case reports. Brain Inj. 2005;19:1147-1155.

• 摘要

Sanger TD. Toward a definition of childhood dystonia. Curr Opin Pediatr. 2004;16:623-627.

• 摘要

Fernández-Alvarez E. Dystonia. The paediatric perspective. Eur J Neurol. 2010;17(suppl 1):46-51.

• 摘要

Sanger TD, Chen D, Fehlings DL, et al. Definition and classification of hyperkinetic movements in childhood. Mov Disord. 2010;25;1538-1549.

• 摘要

Albanese A, Barnes MP, Bhatia KP, et al. A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force. Eur J Neurol. 2006;13:433-444.

• 摘要

Assmann B, Surtees R, Hoffmann GF. Approach to the diagnosis of neurotransmitter diseases exemplified by the differential diagnosis of childhood-onset dystonia. Ann Neurol. 2003;54(Suppl 6):S18-S24.

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Demirkiran M, Jankovic J. Paroxysmal dyskinesias: clinical features and classification. Ann Neurol. 1995;38:571-579.

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Silver K, Andermannn F. Alternating hemiplegia of childhood: a study of 10 patients and results of flunarizine treatment. Neurology. 1993;43:36-41.

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Shapiro SM, Bhutani VK, Johnson L. Hyperbilirubinemia and kernicterus. Clin Perinatol. 2006;33:387-410.

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Jinnah HA, Visser JE, Harris JC, et al. Delineation of the motor disorder of Lesch-Nyhan disease. Brain. 2006;129:1201-1217.

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Jinnah HA, Harris JC, Nyhan WL. The spectrum of mutations causing HPRT deficiency: an update. Nucleosides Nucleotides Nucleic Acids. 2004;23:1153-1160.

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Carrozzo R, Piemonte F, Tessa A, et al. Infantile mitochondrial disorders. Biosci Rep. 2007;27:105-112.

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Gordon N. Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome). Eur J Paediatr Neurol. 2002;6:243-247.

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Goutieres F. Aicardi-Goutieres syndrome. Brain Dev. 2005;27:201-206.

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Fenichel GM. Paroxysmal disorders. In: Fenichel GM, ed. Clinical pediatric neurology - a signs and symptoms approach. Philadelphia, PA: Elsevier Saunders; 2005:1-45.

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