Progression in primary lateral sclerosis: a prospective analysis (Q35013428)

5 August 2017

title

Progression in primary lateral sclerosis: a prospective analysis (English)

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5 August 2017

Mary Kay Floeter

1

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5 August 2017

Reversa Mills

series ordinal

2

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5 August 2017

publication date

1 October 2009

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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

5 August 2017

published in

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5 August 2017

volume

10

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5 August 2017

issue

5-6

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5 August 2017

page(s)

339-346

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Prognostic factors in ALS: A critical review

5 August 2017

cites work

1 reference

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8 July 2018

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Natural history and clinical features of the flail arm and flail leg ALS variants

8 July 2018

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8 July 2018

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TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis

8 July 2018

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8 July 2018

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8 July 2018

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Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up

8 July 2018

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Onset and progression in inherited ALS determined by motor neurons and microglia

8 July 2018

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8 July 2018

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Primary lateral sclerosis, hereditary spastic paraplegia, and mutations in the alsin gene: historical background for the first International Conference

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Mills' syndrome: ascending (or descending) progressive hemiplegia: a hemiplegic form of primary lateral sclerosis?

8 July 2018

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The tuning fork revisited

8 July 2018

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8 July 2018

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8 July 2018

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Can Selection of Rapidly Progressing Patients Shorten Clinical Trials in Amyotrophic Lateral Sclerosis?

21 January 2018

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Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction

21 January 2018

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21 January 2018

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Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes

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21 January 2018

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Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees

25 October 2018

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Clinical phenotypes and natural progression for motor neuron disease: Analysis from an Australian database

9 December 2018

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12 December 2020

Sporadically occurring neurologic disease: HSP genes and apparently sporadic spastic paraplegia

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12 December 2020

Primary lateral sclerosis: clinical and laboratory features in 25 patients

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12 December 2020

The natural history of primary lateral sclerosis

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12 December 2020

Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene

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12 December 2020

Hereditary spastic paraplegia

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12 December 2020

Predictability of disease progression in amyotrophic lateral sclerosis

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12 December 2020

Primary lateral sclerosis as a phenotypic manifestation of familial ALS

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12 December 2020

Pure primary lateral sclerosis--Case reports

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12 December 2020

A rating scale for amyotrophic lateral sclerosis: description and preliminary experience

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12 December 2020

Interrater reliability of a modified Ashworth scale of muscle spasticity

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12 December 2020

10.3109/17482960903171136

Identifiers

DOI

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5 August 2017

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5 August 2017

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