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Literature DB >> 19466386

Movement disorders in children: recent advances in management.

Abstract

In recent years there has been a growing interest towards pediatric movement disorders (PMD). The data derived from the synthesis of clinical observation, neuroimaging, biochemical and, molecular genetics studies have allowed for the identification of a significant number of pediatric diseases featuring movement disorders. The purpose of this review is to outline an approach to the advances in management of dystonia, neurotransmitter disorders, tics, and paroxysmal dyskinetic syndromes starting in children younger than 18 yr of age.

Entities: Disease Species

Mesh：

Substances：

Year: 2009 PMID： 19466386 DOI： 10.1007/s12098-009-0138-6

Source DB: PubMed Journal: Indian J Pediatr ISSN： 0019-5456 Impact factor: 1.967

18 in total

1. Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiency.

Authors: N Nardocci; G Zorzi; N Blau; E Fernandez Alvarez; M Sesta; L Angelini; M Pannacci; F Invernizzi; B Garavaglia
Journal: Neurology Date: 2003-01-28 Impact factor: 9.910

Review 2. Toward a definition of childhood dystonia.

Authors: Terence D Sanger
Journal: Curr Opin Pediatr Date: 2004-12 Impact factor: 2.856

3. A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa.

Authors: F Asmus; V Horber; J Pohlenz; D Schwabe; A Zimprich; M Munz; M Schöning; T Gasser
Journal: Neurology Date: 2005-06-14 Impact factor: 9.910

4. Tyrosine hydroxylase deficiency: clinical manifestations of catecholamine insufficiency in infancy.

Authors: Padraic J Grattan-Smith; Ron A Wevers; Gerry C Steenbergen-Spanjers; Victor S C Fung; John Earl; Bridget Wilcken
Journal: Mov Disord Date: 2002-03 Impact factor: 10.338

5. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197.

Authors: G Auburger; T Ratzlaff; A Lunkes; H W Nelles; B Leube; F Binkofski; H Kugel; W Heindel; R Seitz; R Benecke; O W Witte; T Voit
Journal: Genomics Date: 1996-01-01 Impact factor: 5.736

6. Mutations in TITF-1 are associated with benign hereditary chorea.

Authors: Guido J Breedveld; Jeroen W F van Dongen; Cesare Danesino; Andrea Guala; Alan K Percy; Leon S Dure; Peter Harper; Lazarus P Lazarou; Herma van der Linde; Marijke Joosse; Annette Grüters; Marcy E MacDonald; Bert B A de Vries; Willem Frans M Arts; Ben A Oostra; Heiko Krude; Peter Heutink
Journal: Hum Mol Genet Date: 2002-04-15 Impact factor: 6.150

7. Onset of Gilles de la Tourette's syndrome before 1 year of age.

Authors: L Burd; J Kerbeshian
Journal: Am J Psychiatry Date: 1987-08 Impact factor: 18.112

8. Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families.

Authors: Nardo Nardocci; Giovanna Zorzi; Chiara Barzaghi; Federica Zibordi; Claudia Ciano; Daniele Ghezzi; Barbara Garavaglia
Journal: Mov Disord Date: 2008-01 Impact factor: 10.338

9. Fever-induced dystonia.

Authors: Joseph M Dooley; Scott Furey; Kevin E Gordon; Ellen P Wood
Journal: Pediatr Neurol Date: 2003-02 Impact factor: 3.372

10. Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

Authors: Arvid Suls; Peter Dedeken; Karolien Goffin; Hilde Van Esch; Patrick Dupont; David Cassiman; Judith Kempfle; Thomas V Wuttke; Yvonne Weber; Holger Lerche; Zaid Afawi; Wim Vandenberghe; Amos D Korczyn; Samuel F Berkovic; Dana Ekstein; Sara Kivity; Philippe Ryvlin; Lieve R F Claes; Liesbet Deprez; Snezana Maljevic; Alberto Vargas; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; Koen Van Laere; Peter De Jonghe; Wim Van Paesschen
Journal: Brain Date: 2008-06-24 Impact factor: 13.501

5 in total

Movement disorders in children: recent advances in management.

1. Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiency.

Review 2. Toward a definition of childhood dystonia.

3. A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa.

4. Tyrosine hydroxylase deficiency: clinical manifestations of catecholamine insufficiency in infancy.

5. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197.

6. Mutations in TITF-1 are associated with benign hereditary chorea.

7. Onset of Gilles de la Tourette's syndrome before 1 year of age.

8. Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families.

9. Fever-induced dystonia.

10. Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

Review 1. Monoamine neurotransmitter disorders--clinical advances and future perspectives.

2. A childhood case of symptomatic essential and psychogenic palatal tremor.

3. Movement Disorders in Inherited Metabolic Diseases in Children.

Review 4. What is new for monoamine neurotransmitter disorders?

Review 5. Clinical features and pharmacotherapy of childhood monoamine neurotransmitter disorders.