Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I - Wikidata - wikimedia - TriplyDB

Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I

Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I

http://www.wikidata.org/entity/Q35206123

about

Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the Nerves Homologous recombination mediates functional recovery of dysferlin deficiency following AAV5 gene transfer Review of Journal of Cardiovascular Magnetic Resonance 2012.Review of Journal of Cardiovascular Magnetic Resonance 2011.Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma Developed in a Patient with Progressive Muscular Dystrophy: A Case Report and Review of the Literature Prioritizing disease candidate proteins in cardiomyopathy-specific protein-protein interaction networks based on "guilt by association" analysis.Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies.Adeno-associated virus 9 mediated FKRP gene therapy restores functional glycosylation of α-dystroglycan and improves muscle functions Dysferlin mediates the cytoprotective effects of TRAF2 following myocardial ischemia reperfusion injury.Systemic Delivery of Dysferlin Overlap Vectors Provides Long-Term Gene Expression and Functional Improvement for Dysferlinopathy.Progress and challenges in diagnosis of dysferlinopathy.Feature tracking cardiac magnetic resonance imaging: A review of a novel non-invasive cardiac imaging technique.Cardiac complications of congenital disorders of glycosylation (CDG): a systematic review of the literature.Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy.Subepicardial dysfunction leads to global left ventricular systolic impairment in patients with limb girdle muscular dystrophy 2I.Sexually dimorphic skeletal muscle and cardiac dysfunction in a mouse model of limb girdle muscular dystrophy 2i.Respiratory and cardiac function in japanese patients with dysferlinopathy.Skeletal, cardiac, and respiratory muscle function and histopathology in the P448Lneo- mouse model of FKRP-deficient muscular dystrophy.

P2860

Q26750958-E5E23DB7-0B71-46EC-83AA-F6F56B148052 Q27300915-C2F52D79-C41B-45B2-A6ED-A27F29A1A969 Q30446298-38AEAC43-065E-43ED-8C4B-20EC74FB02BA Q30459937-BB26D34F-1D38-46E5-B27B-948262FA1085 Q33786885-B578D946-B02D-4330-BD87-9C68236DB77E Q34937041-372F0EA0-99B1-4D58-87A5-76CE89D3C410 Q36007760-8A021BEB-6099-4683-AFD2-5826300C56D1 Q37254859-3870F1BE-A262-4296-9E70-73F28D1EEEE1 Q37648514-932FF382-17A4-4A8E-88F7-554FB3CA3EB2 Q38679336-D40E121B-4FD3-4EF7-B9C4-B077B2F99925 Q38921880-695D9592-5CBE-405F-8A70-4F65E0CD83A5 Q39313858-9F2E45B8-F076-4871-8838-E117E03D72CC Q39446939-C37990C2-8348-45D5-BE78-AC4CB1E9DF44 Q41899850-1FC0D6B9-9B3A-40F5-9626-C89FEBBA67EF Q45384428-51B66BC0-D12B-409A-ABFE-10C8951931CC Q47714263-0B45E433-E1E7-4CFC-9253-91D5AEEEC52B Q51620573-13DEC397-3DF6-42F5-94A6-1DCD9B7166C6 Q52602020-305C1BF7-0678-4CBA-90CA-971EE8B3EA13

P2860

Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I

http://www.wikidata.org/entity/Q35206123

description

2011 nî lūn-bûn

@nan

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年学术文章

@wuu

2011年学术文章

@zh-cn

2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

name

Cardiovascular magnetic resona ...... e muscular dystrophy 2B and 2I

@ast

Cardiovascular magnetic resona ...... e muscular dystrophy 2B and 2I

@en

type

label

Cardiovascular magnetic resona ...... e muscular dystrophy 2B and 2I

@ast

Cardiovascular magnetic resona ...... e muscular dystrophy 2B and 2I

@en

prefLabel

Cardiovascular magnetic resona ...... e muscular dystrophy 2B and 2I

@ast

Cardiovascular magnetic resona ...... e muscular dystrophy 2B and 2I

@en

P1433

Q35206123-7FE085CF-9776-49BC-A62A-78071BED9C4C

P1476

Q35206123-E34C9C26-6A24-4CC4-89F6-2DE47D18AF06

P2093

Q35206123-2D41E9EF-33E0-46A3-BE06-458516C3D8F8

Q35206123-6B6D7380-FB61-4FB5-8322-C79ACFA0137E

Q35206123-6B7EAEB0-F74D-48AC-8D6C-C0B4E671A14D

Q35206123-772B0BFD-428D-4263-82F5-4CE2F5DEE7BF

Q35206123-7F4EF054-C7BC-4AA6-9631-EB39C6A502B0

Q35206123-84DA80BB-723C-4EEC-A1AE-601B71B3A132

Q35206123-861FE3BE-9ED2-44CA-9766-202DBCC1D6C4

Q35206123-B0A3E2CA-A540-46FD-AD38-23EBC2FF9E36

Q35206123-FB03B9C1-1EB5-43AF-BF01-801E3130DAFE

P2860

Q35206123-0F5DECF6-A547-462B-B798-7F5011C55A47

Q35206123-11B7A876-70DC-4C1C-9B2F-35421528797F

Q35206123-141CB8E3-0F29-4B59-89F1-8BD345A9B041

Q35206123-1835852B-BE1D-4359-A066-8EB2400D6551

Q35206123-20B460F1-A9EE-422D-85C8-BBBE61D977CA

Q35206123-284CDF6D-2D12-46CC-9B4D-1932B9CB95C1

Q35206123-2C22C869-E6EE-4551-808C-6985EB311164

Q35206123-2CEFED69-8C7D-4F24-9BC1-322FB9569489

Q35206123-35F986B4-92B0-4AC8-B98F-A7C72E798E54

Q35206123-3CD507AF-9CE1-452A-85EF-6732FFDFD297

P2888

Q35206123-8ACFD620-72F3-4492-8EE8-D8B80FBE1514

P304

Q35206123-82AE423C-FA0B-4F49-80A6-A531AF458813

P31

Q35206123-32130B62-E4EC-4F93-A82A-15C53A03D771

P356

Q35206123-473692F5-F70A-4E3A-BEA7-68789FAC4C2C

P478

Q35206123-A65CBB43-AE1F-4FFC-A0E4-698B47093F24

P577

Q35206123-EBD6F6DE-DA20-4203-94F5-52A3F056C448

P5875

Q35206123-AFB21D49-1345-4D6F-AEAC-F69F1E78C6C5

P6179

Q35206123-51ACAE48-CA57-44E0-8453-F55250DDC9CB

P698

Q35206123-DE51A19E-103F-48F1-94BB-ABE52A7750AB

P932

Q35206123-95E3B0CE-A2B1-48EE-84B1-AB4D0834F6CF

P356

1532-429X-13-39

P1433

Journal of Cardiovascular Magnetic Resonance

P1476

Cardiovascular magnetic resona ...... e muscular dystrophy 2B and 2I

@en

P2093

Beth McCarthy

http://www.w3.org/2001/XMLSchema#string

Jerry R Mendell

http://www.w3.org/2001/XMLSchema#string

Nicholas Dunn

http://www.w3.org/2001/XMLSchema#string

Orlando P Simonetti

http://www.w3.org/2001/XMLSchema#string

Philip Habib

http://www.w3.org/2001/XMLSchema#string

Sean J Moser

http://www.w3.org/2001/XMLSchema#string

Subha V Raman

http://www.w3.org/2001/XMLSchema#string

Tam Tran

http://www.w3.org/2001/XMLSchema#string

Xiomara Q Rosales

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Cardiac involvement in limb-girdle muscular dystrophy 2I : conventional cardiac diagnostic and cardiovascular magnetic resonance.

Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation.

Circumferential strain analysis identifies strata of cardiomyopathy in Duchenne muscular dystrophy: a cardiac magnetic resonance tagging study.

Cardiac involvement in patients with muscular dystrophies: magnetic resonance imaging phenotype and genotypic considerations.

LGMD2I in a North American population

Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy.

P2888

1532-429x-13-39

P304

39

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1186/1532-429X-13-39

http://www.w3.org/2001/XMLSchema#string

P478

13

http://www.w3.org/2001/XMLSchema#string

P577

2011-08-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

51546647

http://www.w3.org/2001/XMLSchema#string

P6179

1036403324

http://www.w3.org/2001/XMLSchema#string

P698

21816046

http://www.w3.org/2001/XMLSchema#string

P932

3170213

http://www.w3.org/2001/XMLSchema#string