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Literature DB >> 16567917

Juvenile amyotrophic lateral sclerosis.

Abstract

Juvenile amytrophic lateral sclerosis (JALS) is a type of motor neuron disease presenting before 25 years of age. It is characterized by a combination of upper and lower motor signs. It may be familial or sporadic. We are reporting a sporadic case of JALS with onset of symptoms at 4 years of age. Diagnostic criteria and a brief review of literature are presented.

Entities: Disease

Mesh：

Year: 2006 PMID： 16567917 DOI： 10.1007/bf02825486

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

11 in total

1. Plasmapheresis in amyotrophic lateral sclerosis.

Authors: M R Olarte; R S Schoenfeldt; G McKiernan; L P Rowland
Journal: Ann Neurol Date: 1980-12 Impact factor: 10.422

2. Autosomal dominant juvenile amyotrophic lateral sclerosis.

Authors: B A Rabin; J W Griffin; B J Crain; M Scavina; P F Chance; D R Cornblath
Journal: Brain Date: 1999-08 Impact factor: 13.501

3. Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?

Authors: P De Jonghe; M Auer-Grumbach; J Irobi; K Wagner; B Plecko; M Kennerson; D Zhu; E De Vriendt; V Van Gerwen; G Nicholson; H-P Hartung; V Timmerman
Journal: Brain Date: 2002-06 Impact factor: 13.501

4. Juvenile amyotrophic lateral sclerosis with unusual presentation: a case report.

Authors: A Panagariya; A Garg; B Sharma
Journal: Neurol India Date: 2003-09 Impact factor: 2.117

5. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Authors: A Hentati; K Bejaoui; M A Pericak-Vance; F Hentati; M C Speer; W Y Hung; D A Figlewicz; J Haines; J Rimmler; C Ben Hamida
Journal: Nat Genet Date: 1994-07 Impact factor: 38.330

6. Effect on weakness and spasticity in amyotrophic lateral sclerosis of thyrotropin-releasing hormone.

Authors: W K Engel; T Siddique; J T Nicoloff
Journal: Lancet Date: 1983-07-09 Impact factor: 79.321

7. Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy.

Authors: M Ben Hamida; F Hentati; C Ben Hamida
Journal: Brain Date: 1990-04 Impact factor: 13.501

Juvenile amyotrophic lateral sclerosis.

1. Plasmapheresis in amyotrophic lateral sclerosis.

2. Autosomal dominant juvenile amyotrophic lateral sclerosis.

3. Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?

4. Juvenile amyotrophic lateral sclerosis with unusual presentation: a case report.

5. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

6. Effect on weakness and spasticity in amyotrophic lateral sclerosis of thyrotropin-releasing hormone.

7. Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy.

8. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

9. A new hypothesis of the etiology of amyotrophic lateral sclerosis. The DNA hypothesis.

10. Wasted leg syndrome: a clinical, electrophysiological and histopathological study.

Review 1. Juvenile Amyotrophic Lateral Sclerosis: A Review.

2. Sex-dependent effects of amyloid precursor-like protein 2 in the SOD1-G37R transgenic mouse model of MND.