(Q48505824)

English

Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopy

scientific article published on 6 April 2006

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopy (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

prion protein family

0 references

inherited prion disease

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

Alison K. Godbolt

object named as

A Godbolt

4

0 references

author name string

R J Cordery

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

D G MacManus

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

J Collinge

5

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

M N Rossor

6

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

publication date

6 April 2006

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

48

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

6

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

428-433

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

https://scigraph.springernature.com/pub.10.1007/s00234-006-0068-1

0 references

Cerebral and cerebellar atrophy on serial magnetic resonance imaging in an initially symptom free subject at risk of familial prion disease

1 reference

https://api.crossref.org/works/10.1007%2FS00234-006-0068-1

21 January 2018

Magnetic resonance spectroscopy in AD.

1 reference

https://api.crossref.org/works/10.1007%2FS00234-006-0068-1

21 January 2018

Regional metabolic patterns in mild cognitive impairment and Alzheimer's disease: A 1H MRS study

1 reference

https://api.crossref.org/works/10.1007%2FS00234-006-0068-1

21 January 2018

Prion diseases of humans and animals: their causes and molecular basis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proton magnetic resonance spectroscopy in Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Florid plaques and new variant Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Magnetic resonance spectroscopic abnormalities in sporadic and variant Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diffusion-weighted MRI in two cases of familial Creutzfeldt--Jakob disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MRI of Creutzfeldt-Jakob disease: imaging features and recommended MRI protocol

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proton magnetic resonance spectroscopy of a patient with Gerstmann-Straussler-Scheinker disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multinuclear NMR studies on the energy metabolism of glial and neuronal cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Panencephalitic Creutzfeldt-Jakob disease. Unusual presentation of magnetic resonance imaging and proton magnetic resonance spectroscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In-vivo monitoring of neuronal loss in Creutzfeldt-Jakob disease by proton magnetic resonance spectroscopy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Gerstmann-Sträussler-Scheinker syndrome with a Pro102Leu mutation in the prion protein gene and atypical MRI findings, hyperthermia, tachycardia, and hyperhidrosis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantification of neurons in Alzheimer and control brains with ex vivo high resolution magic angle spinning proton magnetic resonance spectroscopy and stereology

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changes in N-acetylaspartate and myo-inositol detected in the cerebral cortex of hamsters with Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MR spectroscopic pulvinar sign in a case of variant Creutzfeldt-Jakob disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of metabolite concentrations from localized in vivo proton NMR spectra

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High brain myo-inositol levels in the predementia phase of Alzheimer's disease in adults with Down's syndrome: a 1H MRS study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osmoregulatory changes in myo-inositol content and Na+/myo-inositol cotransport in rat cortical astrocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16598479

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00234-006-0068-1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16598479

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=Q48505824&oldid=2200626701"