(99m)Tc-DPD uptake reflects amyloid fibril composition in hereditary transthyretin amyloidosis

Aims In transthyretin amyloid (ATTR) amyloidosis various principal phenotypes have been described: cardiac, neuropathic, or a mixed cardiac and neuropathic. In addition, two different types of amyloid fibrils have been identified (type A and type B). Type B fibrils have thus far only been found in p...

Full description

Saved in:
Bibliographic Details
Published inUpsala journal of medical sciences Vol. 121; no. 1; p. 17
Main Authors Pilebro, Björn, Suhr, Ole B, Näslund, Ulf, Westermark, Per, Lindqvist, Per, Sundström, Torbjörn
Format Journal Article
LanguageEnglish
Published England 2016
Subjects
Online AccessGet full text
ISSN2000-1967
2000-1967
DOI10.3109/03009734.2015.1122687

Cover

Abstract Aims In transthyretin amyloid (ATTR) amyloidosis various principal phenotypes have been described: cardiac, neuropathic, or a mixed cardiac and neuropathic. In addition, two different types of amyloid fibrils have been identified (type A and type B). Type B fibrils have thus far only been found in predominantly early-onset V30M and in patients carrying the Y114C mutation, whereas type A is noted in all other mutations currently examined as well as in wild-type ATTR amyloidosis. The fibril type is a determinant of the ATTR V30M disease phenotype. (99m)Tc-DPD scintigraphy is a highly sensitive method for diagnosing heart involvement in ATTR amyloidosis. The objective of this study was to determine the relationship between ATTR fibril composition and (99m)Tc-DPD scintigraphy outcome in patients with biopsy-proven ATTR amyloidosis. Methods Altogether 55 patients with biopsy-proven diagnosis of ATTR amyloidosis and amyloid fibril composition determined were examined by (99m)Tc-DPD scintigraphy. The patients were grouped and compared according to their type of amyloid fibrils. Cardiovascular evaluation included ECG, echocardiography, and cardiac biomarkers. The medical records were scrutinized to identify subjects with hypertension or other diseases that have an impact on cardiac dimensions. Results A total of 97% with type A and none of the patients with type B fibrils displayed (99m)Tc-DPD uptake at scintigraphy (p < 0.001). Findings from analyses of cardiac biomarkers, ECG, and echocardiography, though significantly different, could not differentiate between type A and B fibrils in individual patients. Conclusion In ATTR amyloidosis, the outcome of (99m)Tc-DPD scintigraphy is strongly related to the patients' transthyretin amyloid fibril composition.
AbstractList Aims In transthyretin amyloid (ATTR) amyloidosis various principal phenotypes have been described: cardiac, neuropathic, or a mixed cardiac and neuropathic. In addition, two different types of amyloid fibrils have been identified (type A and type B). Type B fibrils have thus far only been found in predominantly early-onset V30M and in patients carrying the Y114C mutation, whereas type A is noted in all other mutations currently examined as well as in wild-type ATTR amyloidosis. The fibril type is a determinant of the ATTR V30M disease phenotype. (99m)Tc-DPD scintigraphy is a highly sensitive method for diagnosing heart involvement in ATTR amyloidosis. The objective of this study was to determine the relationship between ATTR fibril composition and (99m)Tc-DPD scintigraphy outcome in patients with biopsy-proven ATTR amyloidosis. Methods Altogether 55 patients with biopsy-proven diagnosis of ATTR amyloidosis and amyloid fibril composition determined were examined by (99m)Tc-DPD scintigraphy. The patients were grouped and compared according to their type of amyloid fibrils. Cardiovascular evaluation included ECG, echocardiography, and cardiac biomarkers. The medical records were scrutinized to identify subjects with hypertension or other diseases that have an impact on cardiac dimensions. Results A total of 97% with type A and none of the patients with type B fibrils displayed (99m)Tc-DPD uptake at scintigraphy (p < 0.001). Findings from analyses of cardiac biomarkers, ECG, and echocardiography, though significantly different, could not differentiate between type A and B fibrils in individual patients. Conclusion In ATTR amyloidosis, the outcome of (99m)Tc-DPD scintigraphy is strongly related to the patients' transthyretin amyloid fibril composition.
Aims In transthyretin amyloid (ATTR) amyloidosis various principal phenotypes have been described: cardiac, neuropathic, or a mixed cardiac and neuropathic. In addition, two different types of amyloid fibrils have been identified (type A and type B). Type B fibrils have thus far only been found in predominantly early-onset V30M and in patients carrying the Y114C mutation, whereas type A is noted in all other mutations currently examined as well as in wild-type ATTR amyloidosis. The fibril type is a determinant of the ATTR V30M disease phenotype. (99m)Tc-DPD scintigraphy is a highly sensitive method for diagnosing heart involvement in ATTR amyloidosis. The objective of this study was to determine the relationship between ATTR fibril composition and (99m)Tc-DPD scintigraphy outcome in patients with biopsy-proven ATTR amyloidosis. Methods Altogether 55 patients with biopsy-proven diagnosis of ATTR amyloidosis and amyloid fibril composition determined were examined by (99m)Tc-DPD scintigraphy. The patients were grouped and compared according to their type of amyloid fibrils. Cardiovascular evaluation included ECG, echocardiography, and cardiac biomarkers. The medical records were scrutinized to identify subjects with hypertension or other diseases that have an impact on cardiac dimensions. Results A total of 97% with type A and none of the patients with type B fibrils displayed (99m)Tc-DPD uptake at scintigraphy (p < 0.001). Findings from analyses of cardiac biomarkers, ECG, and echocardiography, though significantly different, could not differentiate between type A and B fibrils in individual patients. Conclusion In ATTR amyloidosis, the outcome of (99m)Tc-DPD scintigraphy is strongly related to the patients' transthyretin amyloid fibril composition.Aims In transthyretin amyloid (ATTR) amyloidosis various principal phenotypes have been described: cardiac, neuropathic, or a mixed cardiac and neuropathic. In addition, two different types of amyloid fibrils have been identified (type A and type B). Type B fibrils have thus far only been found in predominantly early-onset V30M and in patients carrying the Y114C mutation, whereas type A is noted in all other mutations currently examined as well as in wild-type ATTR amyloidosis. The fibril type is a determinant of the ATTR V30M disease phenotype. (99m)Tc-DPD scintigraphy is a highly sensitive method for diagnosing heart involvement in ATTR amyloidosis. The objective of this study was to determine the relationship between ATTR fibril composition and (99m)Tc-DPD scintigraphy outcome in patients with biopsy-proven ATTR amyloidosis. Methods Altogether 55 patients with biopsy-proven diagnosis of ATTR amyloidosis and amyloid fibril composition determined were examined by (99m)Tc-DPD scintigraphy. The patients were grouped and compared according to their type of amyloid fibrils. Cardiovascular evaluation included ECG, echocardiography, and cardiac biomarkers. The medical records were scrutinized to identify subjects with hypertension or other diseases that have an impact on cardiac dimensions. Results A total of 97% with type A and none of the patients with type B fibrils displayed (99m)Tc-DPD uptake at scintigraphy (p < 0.001). Findings from analyses of cardiac biomarkers, ECG, and echocardiography, though significantly different, could not differentiate between type A and B fibrils in individual patients. Conclusion In ATTR amyloidosis, the outcome of (99m)Tc-DPD scintigraphy is strongly related to the patients' transthyretin amyloid fibril composition.
Author Suhr, Ole B
Westermark, Per
Sundström, Torbjörn
Lindqvist, Per
Pilebro, Björn
Näslund, Ulf
Author_xml – sequence: 1
  givenname: Björn
  surname: Pilebro
  fullname: Pilebro, Björn
  organization: a Heart Centre, Cardiology, Department of Public Health and Clinical Medicine , Umeå University , Umeå , Sweden
– sequence: 2
  givenname: Ole B
  surname: Suhr
  fullname: Suhr, Ole B
  organization: b Department of Public Health and Clinical Medicine , Umeå University , Umeå , Sweden
– sequence: 3
  givenname: Ulf
  surname: Näslund
  fullname: Näslund, Ulf
  organization: a Heart Centre, Cardiology, Department of Public Health and Clinical Medicine , Umeå University , Umeå , Sweden
– sequence: 4
  givenname: Per
  surname: Westermark
  fullname: Westermark, Per
  organization: c Department of Immunology, Genetics and Pathology , Uppsala University , Uppsala , Sweden
– sequence: 5
  givenname: Per
  surname: Lindqvist
  fullname: Lindqvist, Per
  organization: d Heart Centre, Department of Surgical and Perioperative Sciences, Clinical Physiology , Umeå University , Umeå , Sweden
– sequence: 6
  givenname: Torbjörn
  surname: Sundström
  fullname: Sundström, Torbjörn
  organization: e Department of Radiation Sciences, Diagnostic Radiology , Umeå University , Umeå , Sweden
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26849806$$D View this record in MEDLINE/PubMed
BookMark eNpNkElPwzAQhS1URBf4CSAfyyFlvDSJj6hlkyrBoVyJHGeiGrJhO4f-eyxRJE7zRu-b0ZuZk0nXd0jINYOVYKDuQACoTMgVB7ZeMcZ5mmdnZMYBIGEqzSb_9JTMvf-MXQqZuCDTyEqVQzojH0ul2tu9SbZvWzoOQX8hdVg3aIKnuj02va1obUtnG2r6dui9DbbvqO3oAR1WNmh3pMHpzofD0WGIxmksov6SnNe68Xh1qgvy_viw3zwnu9enl839LhkYT0OiQVel0VwIwLURZYzHJSIACr0udSkx2kyqShqRslJChlVea8O1zlmdo1iQ5e_ewfXfI_pQtNYbbBrdYT_6gmUZz7kSKo3ozQkdyxarYnC2jTcUfz8RPzcNaCY
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.3109/03009734.2015.1122687
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2000-1967
ExternalDocumentID 26849806
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
.55
.GJ
00X
0YH
123
2WC
3O-
4.4
53G
5RE
7X7
8FI
8FJ
8G5
AAFWJ
AALIY
AAPXX
ABDBF
ABUWG
ACGFS
ACUHS
ADBBV
ADCVX
ADRAZ
AENEX
AFKRA
AFPKN
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BABNJ
BAWUL
BCNDV
BENPR
BLEHA
BPHCQ
CCPQU
CGR
CUY
CVF
DIK
DU5
DWQXO
E3Z
EBS
ECM
EIF
EJD
F5P
FYUFA
GNUQQ
GROUPED_DOAJ
GUQSH
H13
HMCUK
HYE
KQ8
M2O
M44
M48
M4Z
NPM
O5R
O5S
O9-
OK1
P2P
PGMZT
PHGZT
PIMPY
PQQKQ
PROAC
RDKPK
RNS
RPM
TDBHL
TFDNU
TFL
TFW
TR2
UKHRP
X7M
ZGI
ZXP
~1N
7X8
OVT
PHGZM
PUEGO
ID FETCH-LOGICAL-p126t-a0adbca2330e5c3b68424ee00e3a5bab4edbc149d4c361b407ed8fac2aa81f8e3
IEDL.DBID M48
ISSN 2000-1967
IngestDate Fri Sep 05 08:08:38 EDT 2025
Thu Apr 03 07:02:31 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords amyloid cardiomyopathy
Amyloidosis hereditary
scintigraphy
transthyretin
echocardiography
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-p126t-a0adbca2330e5c3b68424ee00e3a5bab4edbc149d4c361b407ed8fac2aa81f8e3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 26849806
PQID 1772829396
PQPubID 23479
ParticipantIDs proquest_miscellaneous_1772829396
pubmed_primary_26849806
PublicationCentury 2000
PublicationDate 2016-00-00
PublicationDateYYYYMMDD 2016-01-01
PublicationDate_xml – year: 2016
  text: 2016-00-00
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Upsala journal of medical sciences
PublicationTitleAlternate Ups J Med Sci
PublicationYear 2016
References 9701270 - Transplantation. 1998 Jul 27;66(2):229-33
15695149 - Am J Cardiol. 2005 Feb 15;95(4):535-7
17554795 - Muscle Nerve. 2007 Oct;36(4):411-23
2936235 - Am J Cardiol. 1986 Feb 15;57(6):450-8
26286619 - EMBO Mol Med. 2015 Oct;7(10):1337-49
24620715 - Ups J Med Sci. 2014 Aug;119(3):223-8
3117463 - Clin Exp Immunol. 1987 Sep;69(3):695-701
8182405 - J Intern Med. 1994 May;235(5):479-85
19270053 - Eur J Echocardiogr. 2009 Mar;10(2):165-93
16714055 - Acta Histochem. 2006;108(3):209-13
24474780 - Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1539-44
6329251 - Br Heart J. 1984 Jun;51(6):658-62
21107516 - J Mol Med (Berl). 2011 Feb;89(2):171-80
16044444 - Am J Hematol. 2005 Aug;79(4):319-28
17916581 - Eur Heart J. 2008 Jan;29(2):270-6
23193944 - Curr Med Res Opin. 2013 Jan;29(1):63-76
25559473 - J Am Soc Echocardiogr. 2015 Jan;28(1):1-39.e14
15810051 - J Pathol. 2005 Jun;206(2):224-32
21069320 - Eur J Nucl Med Mol Imaging. 2011 Mar;38(3):470-8
25044787 - Hum Mutat. 2014 Sep;35(9):E2403-12
26308415 - Transplantation. 2015 Sep;99(9):1847-54
14746554 - J Intern Med. 2004 Feb;255(2):159-78
20109604 - Prog Cardiovasc Dis. 2010 Jan-Feb;52(4):347-61
6225293 - Acta Pathol Microbiol Immunol Scand A. 1983 Sep;91(5):343-9
16755827 - J Cardiovasc Magn Reson. 2006;8(3):417-26
21679902 - JACC Cardiovasc Imaging. 2011 Jun;4(6):659-70
23713495 - Amyloid. 2013 Sep;20(3):142-50
15146166 - Lab Invest. 2004 Aug;84(8):981-8
24455993 - Amyloid. 2014 Mar;21(1):35-44
22745357 - Eur Heart J. 2013 Feb;34(7):520-8
25211144 - Amyloid. 2014 Dec;21(4):246-55
17062381 - Amyloid. 2006 Sep;13(3):154-9
16168294 - J Am Coll Cardiol. 2005 Sep 20;46(6):1076-84
12002714 - Eur J Nucl Med Mol Imaging. 2002 Mar;29(3):376-9
14640040 - Amyloid. 2003 Aug;10 Suppl 1:32-8
118839 - Clin Exp Immunol. 1979 Nov;38(2):284-93
25742226 - Clin Nucl Med. 2015 May;40(5):446-7
18729067 - J Pathol. 2008 Oct;216(2):253-61
22395298 - Transplantation. 2012 May 27;93(10):1017-23
References_xml – reference: 118839 - Clin Exp Immunol. 1979 Nov;38(2):284-93
– reference: 23193944 - Curr Med Res Opin. 2013 Jan;29(1):63-76
– reference: 25559473 - J Am Soc Echocardiogr. 2015 Jan;28(1):1-39.e14
– reference: 6225293 - Acta Pathol Microbiol Immunol Scand A. 1983 Sep;91(5):343-9
– reference: 16168294 - J Am Coll Cardiol. 2005 Sep 20;46(6):1076-84
– reference: 20109604 - Prog Cardiovasc Dis. 2010 Jan-Feb;52(4):347-61
– reference: 14746554 - J Intern Med. 2004 Feb;255(2):159-78
– reference: 9701270 - Transplantation. 1998 Jul 27;66(2):229-33
– reference: 8182405 - J Intern Med. 1994 May;235(5):479-85
– reference: 24474780 - Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1539-44
– reference: 26308415 - Transplantation. 2015 Sep;99(9):1847-54
– reference: 17554795 - Muscle Nerve. 2007 Oct;36(4):411-23
– reference: 22395298 - Transplantation. 2012 May 27;93(10):1017-23
– reference: 15146166 - Lab Invest. 2004 Aug;84(8):981-8
– reference: 17062381 - Amyloid. 2006 Sep;13(3):154-9
– reference: 26286619 - EMBO Mol Med. 2015 Oct;7(10):1337-49
– reference: 15695149 - Am J Cardiol. 2005 Feb 15;95(4):535-7
– reference: 12002714 - Eur J Nucl Med Mol Imaging. 2002 Mar;29(3):376-9
– reference: 21679902 - JACC Cardiovasc Imaging. 2011 Jun;4(6):659-70
– reference: 15810051 - J Pathol. 2005 Jun;206(2):224-32
– reference: 19270053 - Eur J Echocardiogr. 2009 Mar;10(2):165-93
– reference: 16755827 - J Cardiovasc Magn Reson. 2006;8(3):417-26
– reference: 14640040 - Amyloid. 2003 Aug;10 Suppl 1:32-8
– reference: 25044787 - Hum Mutat. 2014 Sep;35(9):E2403-12
– reference: 22745357 - Eur Heart J. 2013 Feb;34(7):520-8
– reference: 24455993 - Amyloid. 2014 Mar;21(1):35-44
– reference: 16044444 - Am J Hematol. 2005 Aug;79(4):319-28
– reference: 21069320 - Eur J Nucl Med Mol Imaging. 2011 Mar;38(3):470-8
– reference: 3117463 - Clin Exp Immunol. 1987 Sep;69(3):695-701
– reference: 25211144 - Amyloid. 2014 Dec;21(4):246-55
– reference: 21107516 - J Mol Med (Berl). 2011 Feb;89(2):171-80
– reference: 24620715 - Ups J Med Sci. 2014 Aug;119(3):223-8
– reference: 23713495 - Amyloid. 2013 Sep;20(3):142-50
– reference: 16714055 - Acta Histochem. 2006;108(3):209-13
– reference: 2936235 - Am J Cardiol. 1986 Feb 15;57(6):450-8
– reference: 17916581 - Eur Heart J. 2008 Jan;29(2):270-6
– reference: 18729067 - J Pathol. 2008 Oct;216(2):253-61
– reference: 6329251 - Br Heart J. 1984 Jun;51(6):658-62
– reference: 25742226 - Clin Nucl Med. 2015 May;40(5):446-7
SSID ssj0006073
Score 2.363441
Snippet Aims In transthyretin amyloid (ATTR) amyloidosis various principal phenotypes have been described: cardiac, neuropathic, or a mixed cardiac and neuropathic. In...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 17
SubjectTerms Adult
Aged
Aged, 80 and over
Amyloid - analysis
Amyloid Neuropathies, Familial - diagnostic imaging
Amyloid Neuropathies, Familial - metabolism
Diphosphonates - pharmacokinetics
Female
Humans
Male
Middle Aged
Organotechnetium Compounds - pharmacokinetics
Title (99m)Tc-DPD uptake reflects amyloid fibril composition in hereditary transthyretin amyloidosis
URI https://www.ncbi.nlm.nih.gov/pubmed/26849806
https://www.proquest.com/docview/1772829396
Volume 121
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: KQ8
  dateStart: 19720601
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: KQ8
  dateStart: 20090101
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVAON
  databaseName: DOAJ Directory of Open Access Journals
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: DOA
  dateStart: 20080101
  isFulltext: true
  titleUrlDefault: https://www.doaj.org/
  providerName: Directory of Open Access Journals
– providerCode: PRVEBS
  databaseName: EBSCOhost Academic Search Ultimate
  customDbUrl: https://search.ebscohost.com/login.aspx?authtype=ip,shib&custid=s3936755&profile=ehost&defaultdb=asn
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: ABDBF
  dateStart: 20000401
  isFulltext: true
  titleUrlDefault: https://search.ebscohost.com/direct.asp?db=asn
  providerName: EBSCOhost
– providerCode: PRVBFR
  databaseName: Free Medical Journals
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: DIK
  dateStart: 19730101
  isFulltext: true
  titleUrlDefault: http://www.freemedicaljournals.com
  providerName: Flying Publisher
– providerCode: PRVAQN
  databaseName: PubMed Central
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: RPM
  dateStart: 20090101
  isFulltext: true
  titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/
  providerName: National Library of Medicine
– providerCode: PRVPQU
  databaseName: Health Medical collection
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: 7X7
  dateStart: 20110301
  isFulltext: true
  titleUrlDefault: https://search.proquest.com/healthcomplete
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: ProQuest Central
  customDbUrl: http://www.proquest.com/pqcentral?accountid=15518
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: BENPR
  dateStart: 20110301
  isFulltext: true
  titleUrlDefault: https://www.proquest.com/central
  providerName: ProQuest
– providerCode: PRVAUI
  databaseName: Routledge Open
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: RDKPK
  dateStart: 19720101
  isFulltext: true
  titleUrlDefault: http://www.tandfonline.com/page/openaccess/openjournals
  providerName: Routledge
– providerCode: PRVFZP
  databaseName: Scholars Portal Open Access Journals
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 20250131
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: M48
  dateStart: 19720601
  isFulltext: true
  titleUrlDefault: http://journals.scholarsportal.info
  providerName: Scholars Portal
– providerCode: PRVAWR
  databaseName: Taylor & Francis Open Access
  customDbUrl:
  eissn: 2000-1967
  dateEnd: 20201031
  omitProxy: true
  ssIdentifier: ssj0006073
  issn: 2000-1967
  databaseCode: 0YH
  dateStart: 20100201
  isFulltext: true
  titleUrlDefault: https://www.tandfonline.com
  providerName: Taylor & Francis
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LS8NAEF5qC-JFfL_LCh70EN1kN5vkIKK2pQgtRSz0ZNlXsajpKwX7751JU7woeM5uDjOzM_PNk5ALG5jIhYMQtF-iPSFj5ymbGMQ8EWPGD5TGBudWWza74qkX9kpkVTZWEHD2K7TDfVLd6cf112RxBw_-NkecLLkBOcWhMxgh8UPsiQkkKPHxxMPdUpiDLRZtrJEK2CsfJ-y3xM9MccnyPHTeYw3yGC37fP7-89--aG6TGltks3Am6f2S-9uk5NIdst4q0uW75PUyST6vXoxX69TofJypd0fBImKkfkbVJ2D1oaUDLPr_oFhbXhRw0WFK33CH5zBT0wXN0JwBP7HfMV1dg6OzPdJt1F8em16xUMEb-4HMPMWU1UYFnDMXGq4xByecY8xxFWqlhYPPAJmsMFz6GrCes_FAmUCp2B_Eju-TcjpK3SGhiQOcZqTFaUCCg9rj3AplY62EBSLKI3K-IlIfBBazECp1o_ms74M_H4OTkcCZgyX1-uPlZI0-jp5JYiaP_3H7hGwAV4pwyCkpZ9O5OwMHIdNVshb1oiqpPNTbnedqDrOrOc-_AU-RvDg
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=%2899m%29Tc-DPD+uptake+reflects+amyloid+fibril+composition+in+hereditary+transthyretin+amyloidosis&rft.jtitle=Upsala+journal+of+medical+sciences&rft.au=Pilebro%2C+Bj%C3%B6rn&rft.au=Suhr%2C+Ole+B&rft.au=N%C3%A4slund%2C+Ulf&rft.au=Westermark%2C+Per&rft.date=2016&rft.issn=2000-1967&rft.eissn=2000-1967&rft.volume=121&rft.issue=1&rft.spage=17&rft_id=info:doi/10.3109%2F03009734.2015.1122687&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2000-1967&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2000-1967&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2000-1967&client=summon