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Pathology of mitochondrial encephalomyopathies.
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Pathology of mitochondrial encephalomyopathies
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
author name string
Harvey B Sarnat
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
José Marín-García
series ordinal
2
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stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
publication date
1 May 2005
1 reference
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Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
published in
Canadian Journal of Neurological Sciences
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
volume
32
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
page(s)
152-166
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
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Cell sorting experiments link persistent mitochondrial DNA damage with loss of mitochondrial membrane potential and apoptotic cell death
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Crossref
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7 January 2021
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1 reference
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reference URL
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7 January 2021
based on heuristic
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7 January 2021
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7 January 2021
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7 January 2021
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Crossref
reference URL
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7 January 2021
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Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.
1 reference
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7 January 2021
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7 January 2021
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Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype
1 reference
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Crossref
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7 January 2021
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Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency
1 reference
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Crossref
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7 January 2021
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Crossref
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7 January 2021
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https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
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https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
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1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
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Severe depletion of mitochondrial DNA in spinal muscular atrophy
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https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
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Late-onset mitochondrial myopathy
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic value of succinate ubiquinone reductase activity in the identification of patients with mitochondrial DNA depletion
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies and the role of the pathologist in the molecular era.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial biogenesis defects and neuromuscular disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Vitamin E regulation of mitochondrial superoxide generation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Peripheral neuropathy associated with mitochondrial myopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathy and mitochondrial myopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Kearns-Sayre syndrome with a novel mitochondrial DNA deletion
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebellar ataxia and coenzyme Q10 deficiency
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Primary and secondary defects of the mitochondrial respiratory chain
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Does the patient have a mitochondrial encephalomyopathy?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Atypical MELAS associated with mitochondrial tRNA(Lys) gene A8296G mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Statin-associated myopathy with normal creatine kinase levels
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy simulating spinal muscular atrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Location and recycling of mitochondrial alpha-tocopherol
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in the muscle of patients with zidovudine myopathy is segmental and affects both mitochondrial DNA- and nuclear DNA-encoded subunits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe mitochondrial cytopathy with complete A-V block, PEO, and mtDNA deletions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial uncoupling protein-2 protects the immature brain from excitotoxic neuronal death.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homoplasmic MELAS A3243G mtDNA mutation in a colon cancer sample
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Skin manifestations of a patient with mitochondrial encephalomyopathy with lactic acidosis and strokelike episodes (MELAS syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Depletion of the other genome-mitochondrial DNA depletion syndromes in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA depletion presenting prenatally with skin edema and multisystem disease immediately after birth
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of mtDNA disrupts mitochondrial function and structure, but not biogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adult glycogenosis II with paracrystalline mitochondrial inclusions and Hirano bodies in skeletal muscle.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Toward cloning of a novel ataxia gene: refined assignment and physical map of the IOSCA locus (SCA8) on 10q24
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Septo-optic dysplasia associated with a new mitochondrial cytochrome b mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interaction between anticonvulsants and human placental carnitine transporter
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Statin cardiomyopathy? A potential role for Co-Enzyme Q10 therapy for statin-induced changes in diastolic LV performance: description of a clinical protocol
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Valproate treatment induces lipid globule accumulation with ultrastructural abnormalities of mitochondria in skeletal muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial dysfunction in adult-onset myopathies with structural abnormalities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial function in muscle from elderly athletes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effectiveness of creatine monohydrate in mitochondrial encephalomyopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of late-onset MELAS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coenzyme Q-responsive Leigh's encephalopathy in two sisters
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rapid visual recovery after coenzyme q10 treatment of leber hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coenzyme Q10 with multiple vitamins is generally ineffective in treatment of mitochondrial disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cellular redox activity of coenzyme Q10: effect of CoQ10 supplementation on human skeletal muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100003929
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S0317167100003929
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
PubMed publication ID
16018150
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16018150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16018150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
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