(Q44447343)

English

Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations.

scientific article published on 3 July 2014

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

1 reference

based on heuristic

inferred from title

spastic paraparesis

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

Maria Teresa Bassi

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

Maria Pia Giannoccaro

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

Andrea Citterio

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

author name string

Alessia Arnoldi

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

publication date

3 July 2014

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

261

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

1789-1793

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

describes a project that uses

NMR spectroscopy

1 reference

based on heuristic

inferred from title

https://scigraph.springernature.com/pub.10.1007/s00415-014-7418-4

0 references

Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Classification of the hereditary ataxias and paraplegias

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

A systematic review and quantitative appraisal of fMRI studies of verbal fluency: role of the left inferior frontal gyrus.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Frontopolar cortex mediates abstract integration in analogy

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Cognitive performance in pure and complicated hereditary spastic paraparesis: a neuropsychological and neuroimaging study.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Roles of SAM and DDHD domains in mammalian intracellular phospholipase A1 KIAA0725p.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Generation of lysophosphatidylinositol by DDHD domain containing 1 (DDHD1): Possible involvement of phospholipase D/phosphatidic acid in the activation of DDHD1.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

The actions and metabolism of lysophosphatidylinositol, an endogenous agonist for GPR55.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Making heads or tails of phospholipids in mitochondria

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Disruption of the phosphatidylserine decarboxylase gene in mice causes embryonic lethality and mitochondrial defects

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Subjective cognitive complaints, neuropsychological performance, affective and behavioural symptoms in non-demented patients.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7418-4

21 January 2018

Identifiers

10.1007/S00415-014-7418-4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24989667%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q44447343&oldid=1878910263"