Advances in psychiatry and nuerology


ISSN 1230-2813
ISSN online 2720-5371 

JCR Impact Factor: 1.5
CiteScore 2025: 2.0
MNiSW: 70
Index Copernicus 2023: 153.00

Indexed in PubMed.

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  • Involvement of the supraoxide dysmutase in the pathogenesis of the atrophic lateral sclerosis ( ALS)

Archive 1992–2014

1997, tom 6, zeszyt 1
Varia

Involvement of the supraoxide dysmutase in the pathogenesis of the atrophic lateral sclerosis ( ALS)

Tadeusz Pietras1, PIOTR MAZERANT2
1. Kliniki Pneumonologii i Alergologii AM w Łodzi
2. AM w Łodzi (student)
Postępy Psychiatrii i Neurologii, 1997, 6, 67-71
Keywords: reactive oxygen forms, superoxide dismutase, ALS
Summary

Atrophic lateral sclerosis (ALS) is a disease resulting from degeneration of motor neurons in the CNS and spinal cord. In 5 to 20% of cases it is an autosomal dominating hereditary disease. About 20% of patients suffering from the familial atrophic lateral sclerosis (FALS) have a point mutation in the gene coding copper-zinc superoxide dismutase (CuZnSOD). The authors suggest that the major role both in the etiology and progression of the ALS falls to reactive forms of oxygen, while the CuZnSOD dysfunction is a factor predestinating to this disease development.

Correspondence address
Dr Tadeusz Pietras,
Klinika Pneumonologii i Alergologii AM,
ul. Kopcińskiego 22,
90-153 Łódź
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