(Q36203594)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

review article

1 reference

title

Primary lateral sclerosis, hereditary spastic paraplegia and amyotrophic lateral sclerosis: discrete entities or spectrum? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

31 December 2019

main subject

0 references

hereditary spastic paraplegia

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Paul H. Gordon

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

Michael J Strong

series ordinal

1

1 reference

12 August 2017

Paul H Gordon

series ordinal

2

1 reference

12 August 2017

1 March 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases

31 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

page(s)

8-16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

What is primary lateral sclerosis?

31 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Microtubule-associated tau protein positive neuronal and glial inclusions in ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Cognition, language, and speech in amyotrophic lateral sclerosis: a review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Primary lateral sclerosis: a neuropsychological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Atypical motor neuron disease and related motor syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Upper motor neuron predominant degeneration with frontal and temporal lobe atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Sporadic amyotrophic lateral sclerosis resembling primary lateral sclerosis: report of an autopsy case and a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Advances in the hereditary spastic paraplegias

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

The basic aspects of therapeutics in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Survival prediction in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

The epidemiology of motor neuron diseases: a review of recent studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Prevalence and correlates of neuropsychological deficits in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Clinical and radiographic features of dural arteriovenous fistula, a treatable cause of myelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Copper deficiency myelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Analysis of motor pathway involvement in konzo using transcranial electrical and magnetic stimulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

New aspects in pathogenesis of konzo: neural cell damage directly caused by linamarin contained in cassava (Manihot esculenta Crantz).

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

The hereditary spastic paraplegias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820410021267

10.1080/14660820410021267

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16036421%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference