Autosomal Dominant Juvenile Amyotrophic LS

J Gordon Millichap

doi:10.15844/pedneurbriefs-13-9-9

Autosomal Dominant Juvenile Amyotrophic LS

Pediatric Neurology Briefs

Volume 13 (1999): Issue 9

By: J Gordon Millichap

Open Access

|Sep 1999

Abstract

The clinical and electrodiagnostic findings in 49 affected family members and neuropathological findings from two autopsies of a Maryland kindred with autosomal dominant juvenile amyotrophic lateral sclerosis (ALS) are reported from Johns Hopkins University and Hospital, Baltimore, MD.

References

Rabin BA Griffin JW Crain BJ Scavina M Chance PF Cornblath DR Autosomal dominant juvenile amyotrophic lateral sclerosis Brain 1999 Aug 122 Pt 8 1539 50 10.1093/brain/122.8.1539 10430837
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-13-9-9 | Journal eISSN: 2166-6482

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Language: English

Page range: 71 - 71

Published on: Sep 1, 1999

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Amyotrophic Lateral Sclerosis,

Sensory Conduction,

Dorsal Root Ganglia

© 1999 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 13 (1999): Issue 9