Familial Amyotrophic Lateral Sclerosis with a Novel G85S Mutation of Superoxide Dismutase 1 Gene: Clinical Features of Lower Motor Neuron Disease

Internal Medicine ◽

10.2169/internalmedicine.49.2720 ◽

2010 ◽

Vol 49 (2) ◽

pp. 183-186 ◽

Author(s):

Takanori Takazawa ◽

Ken Ikeda ◽

Takehisa Hirayama ◽

Kiyokazu Kawabe ◽

Yoshikazu Nakamura ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Motor Neuron ◽

Motor Neuron Disease ◽

Clinical Features ◽

Lower Motor Neuron ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Lower Motor Neuron Disease ◽

Lateral Sclerosis

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Spontaneous activity in electromyography may differentiate certain benign lower motor neuron disease forms from amyotrophic lateral sclerosis

Journal of the Neurological Sciences ◽

10.1016/j.jns.2015.06.002 ◽

2015 ◽

Vol 355 (1-2) ◽

pp. 143-146 ◽

Author(s):

Manu E. Jokela ◽

Satu K. Jääskeläinen ◽

Satu Sandell ◽

Johanna Palmio ◽

Sini Penttilä ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Motor Neuron ◽

Motor Neuron Disease ◽

Spontaneous Activity ◽

Lower Motor Neuron ◽

Lower Motor Neuron Disease ◽

Lateral Sclerosis

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Issues & Opinions: Amyotrophic lateral sclerosis: Lower motor neuron disease spreading to upper motor neurons

Muscle & Nerve ◽

10.1002/mus.880160810 ◽

1993 ◽

Vol 16 (8) ◽

pp. 864-869 ◽

Author(s):

Samuel M. Chou ◽

Forbes H. Norris

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Motor Neuron ◽

Motor Neuron Disease ◽

Motor Neurons ◽

Lower Motor Neuron ◽

Lower Motor Neuron Disease ◽

Disease Spreading ◽

Upper Motor Neurons ◽

Lateral Sclerosis

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Nerve ultrasound in the differentiation of multifocal motor neuropathy (MMN) and amyotrophic lateral sclerosis with predominant lower motor neuron disease (ALS/LMND)

Journal of Neurology ◽

10.1007/s00415-015-7927-9 ◽

2015 ◽

Vol 263 (1) ◽

pp. 35-44 ◽

Author(s):

Kai F. Loewenbrück ◽

Julia Liesenberg ◽

Markus Dittrich ◽

Jochen Schäfer ◽

Beate Patzner ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Motor Neuron ◽

Motor Neuron Disease ◽

Multifocal Motor Neuropathy ◽

Lower Motor Neuron ◽

Motor Neuropathy ◽

Nerve Ultrasound ◽

Lower Motor Neuron Disease ◽

Lateral Sclerosis

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Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis

Journal of Neurochemistry ◽

10.1046/j.1471-4159.2002.01211.x ◽

2002 ◽

Vol 83 (5) ◽

pp. 1030-1042 ◽

Author(s):

Makoto Urushitani ◽

Junko Kurisu ◽

Kayoko Tsukita ◽

Ryosuke Takahashi

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Motor Neuron ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Neuron Death ◽

Proteasomal Inhibition ◽

Motor Neuron Death ◽

Lateral Sclerosis

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Transgenic mouse model for familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation

Neuropathology ◽

10.1046/j.1440-1789.2001.00361.x ◽

2001 ◽

Vol 21 (1) ◽

pp. 82-92 ◽

Author(s):

Noriyuki Shibata

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Mouse Model ◽

Transgenic Mouse ◽

Transgenic Mouse Model ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Lateral Sclerosis

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New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: Inclusions containing SOD1 in neurons and astrocytes

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders ◽

10.1080/14660820050515160 ◽

2000 ◽

Vol 1 (3) ◽

pp. 163-184 ◽

Author(s):

Shinsuke Kato ◽

Miki Takikawa ◽

Kenji Nakashima ◽

Asao Hirano ◽

Don W Cleveland ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutations ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Sod1 Gene ◽

Lateral Sclerosis

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Neuropathology of familial amyotrophic lateral sclerosis patients with superoxide dismutase 1 gene mutation

Neuropathology ◽

10.1111/j.1440-1789.1998.tb00132.x ◽

1998 ◽

Vol 18 (4) ◽

pp. 363-369 ◽

Author(s):

Asao Hirano

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutation ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Lateral Sclerosis

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MRI detects early hindlimb muscle atrophy in Gly93Ala superoxide dismutase-1 (G93A SOD1) transgenic mice, an animal model of familial amyotrophic lateral sclerosis

NMR in Biomedicine ◽

10.1002/nbm.861 ◽

2004 ◽

Vol 17 (1) ◽

pp. 28-32 ◽

Author(s):

Keith J. Brooks ◽

Mark D. W. Hill ◽

Paul D. Hockings ◽

David G. Reid

Keyword(s):

Animal Model ◽

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Transgenic Mice ◽

Muscle Atrophy ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Hindlimb Muscle ◽

G93a Sod1 ◽

Lateral Sclerosis

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Treatment for familial amyotrophic lateral sclerosis/motor neuron disease

10.1002/14651858.cd006153 ◽

2006 ◽

Author(s):

Michael Benatar ◽

Jerome Kurent ◽

Dan Moore

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Motor Neuron ◽

Motor Neuron Disease ◽

Familial Amyotrophic Lateral Sclerosis ◽

Lateral Sclerosis

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Stability of Mutant Superoxide Dismutase-1 Associated with Familial Amyotrophic Lateral Sclerosis Determines the Manner of Copper Release and Induction of Thioredoxin in Erythrocytes

Biochemical and Biophysical Research Communications ◽

10.1006/bbrc.1998.8265 ◽

1998 ◽

Vol 244 (2) ◽

pp. 605

Author(s):

Yasuko Ogawa ◽

Hiroaki Kosaka ◽

Toyohumi Nakanishi ◽

Akira Shimizu ◽

Nagato Ohoi ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Copper Release ◽

Lateral Sclerosis

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