Genetic Infiltrative Cardiomyopathies. - Wikidata - wikimedia - TriplyDB

Genetic Infiltrative Cardiomyopathies.

Genetic Infiltrative Cardiomyopathies.

http://www.wikidata.org/entity/Q54986978

about

Genetic Infiltrative Cardiomyopathies.

http://www.wikidata.org/entity/Q54986978

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh

2018年學術文章

@zh-hant

name

Genetic Infiltrative Cardiomyopathies.

@en

Genetic Infiltrative Cardiomyopathies.

@nl

type

label

Genetic Infiltrative Cardiomyopathies.

@en

Genetic Infiltrative Cardiomyopathies.

@nl

prefLabel

Genetic Infiltrative Cardiomyopathies.

@en

Genetic Infiltrative Cardiomyopathies.

@nl

P1433

Q54986978-2972200A-2583-4CB5-837C-296E879C2AAF

P1476

Q54986978-67BEAB8C-1FA4-4801-BAFE-E2DF5131F2C6

P2093

Q54986978-661AC61B-643D-48B6-AFE5-FDD36174C740

Q54986978-7FBD93AC-917A-4C02-BAA0-394143BBB368

Q54986978-93E4EC18-85CC-44A8-A2BB-555D71B86BCA

P2860

Q54986978-02345174-C55D-4EB1-973D-A5DC14559270

Q54986978-02507157-5B85-430F-8223-8C2C71F87828

Q54986978-0317FBF2-089A-4560-8FA9-A717FE21DCC4

Q54986978-03E255EC-41D8-4AD3-BA10-C1D4B9052AD0

Q54986978-08777CEC-D4CD-4AA1-80D1-F7F815D9FFB4

Q54986978-0953CF11-1EBE-48E3-9867-979D1C195799

Q54986978-0AB6D871-8556-43D4-A729-01B0CC5EC5E6

Q54986978-0C88F854-9A61-4887-B0DD-261BEA27263B

Q54986978-0E09EB1E-0B3D-44C8-93CC-4847FB21163A

Q54986978-0EAD2D4D-2228-4903-81FD-1803E86851BF

P304

Q54986978-95DE25D4-4605-447A-9E52-07413A4F5431

P31

Q54986978-2AC8882F-95B2-42AB-B772-C59F0D2D6150

P356

Q54986978-2509EFA9-0EB9-42B8-B71E-AA9269DBBBDF

P433

Q54986978-B5009070-7197-4793-8C7E-4D0179380632

P478

Q54986978-10B593AA-F5B3-4C22-9651-3977DF3A978B

P577

Q54986978-BBE2A058-82CF-466D-81DD-DE9644EC27E5

P698

Q54986978-644D2038-1324-4253-A3BF-D79C9122033A

P932

Q54986978-E4FB30AC-BB60-4534-AEA1-A3DF16E1BBD9

P356

J.HFC.2017.12.003

P1433

Heart failure clinics

P1476

Genetic Infiltrative Cardiomyopathies.

@en

P2093

Luisa Mestroni

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

Mary E Sweet

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

Matthew R G Taylor

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

P2860

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

Ca2+ channel blockers reverse iron overload by a new mechanism via divalent metal transporter-1

Fatal congenital heart glycogenosis caused by a recurrent activating R531Q mutation in the gamma 2-subunit of AMP-activated protein kinase (PRKAG2), not by phosphorylase kinase deficiency.

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

Danon disease: clinical features, evaluation, and management

Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs

Primary hyperoxalurias: disorders of glyoxylate detoxification

Danon disease - dysregulation of autophagy in a multisystem disorder with cardiomyopathy

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype

P304

215-224

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

P31

scholarly article

P356

10.1016/J.HFC.2017.12.003

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

P433

2

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

P478

14

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

P577

2018-04-01T00:00:00Z

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

P698

29525649

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

P932

5894511

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