(Q47820843)

5 February 2018

review article

1 reference

title

Molecular pathology of fatal familial insomnia (English)

1 reference

5 February 2018

0 references

0 references

9

Elio Lugaresi

Lugaresi E

1 reference

5 February 2018

Lucila Autilio-Gambetti

4

object named as

L. Autilio-Gambetti

Autilio-Gambetti L

1 reference

5 February 2018

Pierluigi Gambetti

10

object named as

Pierluigi Gambetti

1 reference

5 February 2018

Piero Parchi

1

object named as

P. Parchi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

31 December 2024

5

S. Capellari

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

31 December 2024

author name string

Piero Parchi

1

1 reference

5 February 2018

Robert B. Petersen

2

1 reference

5 February 2018

Shu G. Chen

3

1 reference

5 February 2018

Sabina Capellari

5

1 reference

5 February 2018

Lucia Monari

6

1 reference

5 February 2018

Pietro Cortelli

7

1 reference

5 February 2018

Pasquale Montagna

8

1 reference

5 February 2018

R. B. Petersen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

31 December 2024

S. G. Chen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

31 December 2024

L. Monari

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

31 December 2024

P. Cortelli

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

31 December 2024

P. Montagna

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

31 December 2024

language of work or name

English

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9669705

31 December 2024

publication date

1 July 1998

1 reference

5 February 2018

5 April 2006

0 references

July 1998

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9669705

full work available at URL

31 December 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098344

file format

HyperText Markup Language

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

https://europepmc.org/articles/PMC8098344

31 December 2024

file format

HyperText Markup Language

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

https://europepmc.org/articles/PMC8098344?pdf=render

31 December 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

https://doi.org/10.1111/j.1750-3639.1998.tb00176.x

31 December 2024

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9669705

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1750-3639.1998.tb00176.x

31 December 2024

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1750-3639.1998.tb00176.x

31 December 2024

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

31 December 2024

1 reference

5 February 2018

volume

8

1 reference

5 February 2018

issue

3

1 reference

5 February 2018

page(s)

539-548

1 reference

5 February 2018

Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

cites work

1

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent

31 December 2024

2

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy

31 December 2024

3

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Truncated forms of the human prion protein in normal brain and in prion diseases

31 December 2024

6

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Allelic origin of the abnormal prion protein isoform in familial prion diseases

31 December 2024

7

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Cerebral metabolism in fatal familial insomnia: Relation to duration, neuropathology, and distribution of protease-resistent prion protein

31 December 2024

8

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

31 December 2024

9

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease

31 December 2024

10

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

31 December 2024

12

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

31 December 2024

13

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

31 December 2024

15

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Fatal familial insomnia: clinical and pathologic study of five new cases

31 December 2024

16

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

31 December 2024

17

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

31 December 2024

18

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families

31 December 2024

19

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

31 December 2024

20

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Deletions in the prion protein gene are not associated with CJD.

31 December 2024

21

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Regional distribution of protease-resistant prion protein in fatal familial insomnia

31 December 2024

22

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

31 December 2024

23

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

31 December 2024

Typing prion isoforms.

25

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein

31 December 2024

27

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Scrapie prions aggregate to form amyloid-like birefringent rods

31 December 2024

28

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Identification of the prion protein allotypes which accumulate in the brain of sporadic and familial Creutzfeldt-Jakob disease patients

31 December 2024

30

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

31 December 2024

31

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform

31 December 2024

32

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

31 December 2024

33

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129

31 December 2024

34

1 reference

https://api.crossref.org/works/10.1111/J.1750-3639.1998.TB00176.X

31 December 2024

Identifiers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9669705

31 December 2024

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9669705

31 December 2024

1 reference

5 February 2018