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Literature DB >> 4426134

Hereditary spastic paraplegia in Western Norway.

H Skre.

Abstract

Entities: Disease

Mesh：

Year: 1974 PMID： 4426134 DOI： 10.1111/j.1399-0004.1974.tb00647.x

Source DB: PubMed Journal: Clin Genet ISSN： 0009-9163 Impact factor: 4.438

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Cited

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11 in total

Review 1. Hereditary spastic paraparesis: a review of new developments.

Authors: C McDermott; K White; K Bushby; P Shaw
Journal: J Neurol Neurosurg Psychiatry Date: 2000-08 Impact factor: 10.154

2. The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland.

Authors: P McMonagle; S Webb; M Hutchinson
Journal: J Neurol Neurosurg Psychiatry Date: 2002-01 Impact factor: 10.154

3. Prevalence of hereditary ataxias and paraplegias in the province of Torino, Italy.

Authors: F Brignolio; M Leone; A Tribolo; M G Rosso; P Meineri; D Schiffer
Journal: Ital J Neurol Sci Date: 1986-08

4. Cerebellar degeneration in dominantly inherited spastic paraplegia.

Authors: C L Scholtz; M Swash
Journal: J Neurol Neurosurg Psychiatry Date: 1985-02 Impact factor: 10.154

5. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.

Authors: P Hedera; S Rainier; D Alvarado; X Zhao; J Williamson; B Otterud; M Leppert; J K Fink
Journal: Am J Hum Genet Date: 1999-02 Impact factor: 11.025

6. Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements.

Authors: Mark Braschinsky; Riin Tamm; Christian Beetz; Elena Sachez-Ferrero; Elve Raukas; Siiri-Merike Lüüs; Katrin Gross-Paju; Catherine Boillot; Federico Canzian; Andres Metspalu; Sulev Haldre
Journal: BMC Neurol Date: 2010-03-09 Impact factor: 2.474

Hereditary spastic paraplegia in Western Norway.

Review 1. Hereditary spastic paraparesis: a review of new developments.

2. The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland.

3. Prevalence of hereditary ataxias and paraplegias in the province of Torino, Italy.

4. Cerebellar degeneration in dominantly inherited spastic paraplegia.

5. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.

6. Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements.

7. Familial cerebral palsy associated with normal intelligence.

8. Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.

9. The coexistence of multiple sclerosis and hereditary spastic paraparesis in a patient.

10. The high prevalence of hereditary spastic paraplegia in Sardinia, insular Italy.