Showing
1 - 5
results of
5
Skip to content
VuFind
Log in
Library Catalogue Plus
Library
Subject guides
Databases
Referencing
Catalogue
Articles Plus
Keyword
Title
Author
Subject
Find
Advanced Search
Search Results - Jornholt, J.
Search Results - Jornholt, J.
Showing
1 - 5
results of
5
Refine Results
Sort
Relevance
Date Descending
Author
Title
1
Loading…
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood
by
Muravyev, A
,
Vershinina, T
,
Tesner, P
,
Sjoberg, G
,
Fomicheva, Yu
,
Äajbiková, N. Novák
,
Kozyreva, A
,
Zhuk, S
,
Mamaeva, E
,
Tarnovskaya, S
,
Jornholt, J
,
Sokolnikova, P
,
Pervunina, T
,
Vasichkina, E
,
Sejersen, T
,
Kostareva, A
Published in
Orphanet journal of rare diseases
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
2
Loading…
P5404Hotspot mutation in FLNC gene as a cause of restrictive cardiomyopathy associated with congenital myopathy development
by
Kiselev, A.
,
Knyazeva, A.
,
Sergushichev, A.
,
Hudiakov, A.
,
Pervunina, T.
,
Vershinina, T.
,
Nikitina, I.
,
Rudenko, D.
,
Vasichkina, E.
,
Jornholt, J.
,
Sjoberg, G.
,
Sejersen, T.
,
Kostareva, A.
Published in
European heart journal
Get full text
Article
Save to List
Saved in:
3
Loading…
P1606Mutation in MYOF gene is associated with ventricular arrhythmias and limb girdle muscle phenotype
by
Kiselev, A.
,
Dmitrieva, R.
,
Smolina, N.
,
Khudiakov, A.
,
Sergushichev, A.
,
Mikhailov, E.
,
Mitrophanova, L.
,
Rudenko, D.
,
Jornholt, J.
,
Sjoberg, G.
,
Sejersen, T.
,
Kostareva, A.
Published in
European heart journal
Get full text
Article
Save to List
Saved in:
4
Loading…
Hotspot mutation in FLNC gene as a cause of restrictive cardiomyopathy associated with congenital myopathy development
by
Kiselev, A
,
Knyazeva, A
,
Sergushichev, A
,
Hudiakov, A
,
Pervunina, T
,
Vershinina, T
,
Nikitina, I
,
Rudenko, D
,
Vasichkina, E
,
Jornholt, J
,
Sjoberg, G
,
Sejersen, T
,
Kostareva, A
Get full text
Conference Proceeding
Save to List
Saved in:
5
Loading…
Mutation in MYOF gene is associated with ventricular arrhythmias and limb girdle muscle phenotype
by
Kiselev, A
,
Dmitrieva, R
,
Smolina, N
,
Khudiakov, A
,
Sergushichev, A
,
Mikhailov, E
,
Mitrophanova, L
,
Rudenko, D
,
Jornholt, J
,
Sjoberg, G
,
Sejersen, T
,
Kostareva, A
Get full text
Conference Proceeding
Save to List
Saved in:
Search Tools:
RSS Feed
Email Search
Save Search
Back
Refine Results
Page will reload when a filter is selected or excluded.
Limit To
Peer Reviewed
5 results
5
Full Text
5 results
5
Format
Articles
3 results
3
Conference Proceedings
2 results
2
Journal Title
European Heart Journal
2 results
2
Orphanet Journal Of Rare Diseases
1 results
1
Subjects
Medicin Och Hälsovetenskap
3 results
3
Age
1 results
1
Amino Acid Substitution
1 results
1
Cardiology
1 results
1
Cardiomyopathy
1 results
1
Childhood
1 results
1
Children
1 results
1
Congenital Diseases
1 results
1
Congenital Myopathy
1 results
1
Congestive Heart Failure
1 results
1
Data Processing
1 results
1
Diagnosis
1 results
1
Electromyography
1 results
1
Ethics
1 results
1
Flnc-Associated Phenotype
1 results
1
Genes
1 results
1
Genetic Analysis
1 results
1
Genetics & Heredity
1 results
1
Genotype & Phenotype
1 results
1
Heart
1 results
1
Year of Publication
From:
To:
Source
Free E-Journal (出版社公開部分のみ)
5 results
5
Oxford University Press:jisc Collections:oxford Journal Archive: Access Period 2024-2025
4 results
4
Auth Library Subscriptions: Oxford University Press
4 results
4
Doaj Directory Of Open Access Journals
1 results
1
Science Citation Index Expanded (Web Of Science)
1 results
1
Ingentaconnect Journals
1 results
1
Road: Directory Of Open Access Scholarly Resources
1 results
1
Proquest - Publicly Available Content Database
1 results
1
Pubmed Central
1 results
1
Springerlink Contemporary
1 results
1