Keywords
> MYOBASE > HEALTH > medicine > medical specialty > cardiology-angiology > cardiovascular diseases > cardiac diseases > cardiomyopathy > dilated cardiomyopathy
dilated cardiomyopathySynonymscardiomyopathie congestive ;cardiomyopathie non obstructive ;CMDP ;CMNO ;myocardiopathie dilatée ;myocardiopathie non obstructive ;DCM dilated cardiomyopathy |
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Skriver SV ; Krett B ; Poulsen NS ; Krag T ; Walas HR ; Christensen AH ; Bundgaard H ; Vissing J ; Vissing CR | 08/11/2023Guide
Collectif | 10/2022Ce protocole national de diagnostic et de soins (PNDS) explicite aux professionnels concernés la prise en charge diagnostique et thérapeutique optimale et le parcours de soins d’un malade atteint de laminopathie avec atteinte cardiaque. Il a été[...]Article
Hershberger RE ; Jordan E | 07/04/2022Initial Posting: July 27, 2007; Last Update: April 7, 2022. The purpose of this overview is to increase clinician awareness of the genetic basis of dilated cardiomyopathy (DCM) and the benefits of early diagnosis and management to individuals[...]Article
Nicolas HA ; Bertrand AT ; Labib S ; Mohamed-Uvaize M ; Bolongo PM ; Wu WY ; Bilinska ZT ; Bonne G ; Akimenko MA ; Tesson F | Switzerland | 31/10/2020Article
Gigli M ; Merlo M ; Graw SL ; Barbati G ; Rowland TJ ; Slavov DB ; Stolfo D ; Haywood ME ; Dal Ferro M ; Altinier A ; Ramani F ; Brun F ; Cocciolo A ; Puggia I ; Morea G ; McKenna WJ ; La Rosa FG ; Taylor MRG ; Sinagra G ; Mestroni L | United States | 09/2019Article
Hackman P ; Savarese M ; Carmignac V ; Udd B ; Salih MA | 11/04/2019Initial Posting: January 12, 2012; Last Update: April 11, 2019. Clinical characteristics. Salih myopathy is characterized by muscle weakness (manifest during the neonatal period or in early infancy) and delayed motor development; children ac[...]Article
Veerapandiyan A ; Statland JM ; Tawil R | 07/06/2018Initial Posting: November 22, 2004; Last Update: June 7, 2018. Clinical characteristics. Andersen-Tawil syndrome (ATS) is characterized by a triad of: episodic flaccid muscle weakness (i.e., periodic paralysis); ventricular arrhythmias and p[...]Article
Purkey NJ, Author ; Lin A ; Murray JM ; Gowen M ; Shuttleworth P ; Maeda K ; Almond CS ; Rosenthal DN ; Chen S | 2018Article
Captur G, Author ; Arbustini E ; Bonne G ; Syrris P ; Mills K ; Wahbi K ; Mohiddin SA ; McKenna WJ ; Pettit S ; Ho CY ; Muchir A ; Gissen P ; Elliott PM ; Moon JC | 2018Article
Adachi K, Author ; Hashiguchi S ; Saito M ; Kashiwagi S ; Miyazaki T ; Kawai H ; Yamada H ; Iwase T ; Akaike M ; Takao S ; Kobayashi M ; Ishizaki M ; Matsumura T ; Mori Yoshimura M ; Kimura E | 2018Comment in: Muscle, cardiac, and cerebral manifestations in female carriers of dystrophin variants. [J Neurol Sci. 2018]Article
Finsterer J, Author ; Stollberger C | 2018Comment on: Detection and management of cardiomyopathy in female dystrophinopathy carriers. [J Neurol Sci. 2018]Article
Russo V, Author ; Papa AA ; Williams EA ; Rago A ; Palladino A ; Politano L ; Nigro G | 21/12/2017Comment in: Editorial commentary: Preserving myocardium in muscular dystrophy patients using ACE inhibition. [Trends Cardiovasc Med. 2018]Article
Janin A, Author ; N'guyen K ; Habib G ; Dauphin C ; Chanavat V ; Bouvagnet P ; Eschalier R ; Streichenberger N ; Chevalier P ; Millat G | 2017Article
Vest KE, Author ; Phillips BL ; Banerjee A ; Apponi LH ; Dammer EB ; Xu W ; Zheng D ; Yu J ; Tian B ; Pavlath GK ; Corbett AH | 2017Article
Mori M, Author ; Bailey LA ; Estrada J ; Rehder CW ; Li JS ; Rogers JG ; Bali DS ; Buckley AF ; Kishnani PS | 2017Article