Toward an Understanding of the Cause of Mitral Valve Prolapse

av Towbin, Jeffrey A.
Publicerad 1999

INHERITED CARDIOMYOPATHIES

av Towbin, Jeffrey A.
I publikationen Circ J (2014)

Ion Channel Dysfunction Associated With Arrhythmia, Ventricular Noncompaction, and Mitral Valve Prolapse: A New Overlapping Phenotype

av Towbin, Jeffrey A.
I publikationen J Am Coll Cardiol (2014)

Arrhythmogenic Right Ventricular Cardiomyopathy: A Paradigm of Overlapping Disorders

av Towbin, Jeffrey A.
I publikationen Ann Noninvasive Electrocardiol (2008)

Pediatric Primary Dilated Cardiomyopathy Gene Testing and Variant Reclassification: Does It Matter?

av Towbin, Jeffrey A.
I publikationen J Am Heart Assoc (2020)

Sarcoglycan, the heart, and skeletal muscles: new treatment, old drug?

av Towbin , Jeffrey A., Bowles, Neil E.
Publicerad 2001

Left Ventricular Noncompaction in a Family with Lamin A/C Gene Mutation

av Parent, John J., Towbin, Jeffrey A., Jefferies, John L.
I publikationen Tex Heart Inst J (2015)

A Woman with Incidental Findings of Ventricular Aneurysms and a Desmosomal Cardiomyopathy

av Ly, Suntharo, Marcus, Frank I., Xu, Tianhong, Towbin, Jeffrey A.
Publicerad 2008

Idiopathic and Primary Cardiomyopathies in Children

av Lipshultz, Steven E., Colan, Steven D., Towbin, Jeffrey A., Wilkinson, James D.
Publicerad 2008

Prolonged QT in a 13‐Year‐Old Patient with Down Syndrome and Complete Atrioventricular Canal Defect

av Tisma‐Dupanovic, Svjetlana, Gowdamarajan, Rengasamy, Goldenberg, Ilan, Huang, David T., Knilans, Timothy, Towbin, Jeffrey A.
I publikationen Ann Noninvasive Electrocardiol (2011)

Transcription factor neuromancer/TBX20 is required for cardiac function in Drosophila with implications for human heart disease

av Qian, Li, Mohapatra, Bhagyalaxmi, Akasaka, Takeshi, Liu, Jiandong, Ocorr, Karen, Towbin, Jeffrey A., Bodmer, Rolf
Publicerad 2008

Left ventricular noncompaction cardiomyopathy in Duchenne muscular dystrophy carriers

av Parent, John J., Moore, Ryan A., Taylor, Michael D., Towbin, Jeffrey A., Jefferies, John L.
I publikationen J Cardiol Cases (2014)

Molecular Screening by Polymerase Chain Reaction Detects Panleukopenia Virus DNA in Formalin-Fixed Hearts from Cats with Idiopathic Cardiomyopathy and Myocarditis

av Meurs, Kathryn M, Fox, Philip R, Magnon, Alexander L, Liu, Si-Kwang, Towbin, Jeffrey A
I publikationen Cardiovasc Pathol (2000)

Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism

av Scaglia, Fernando, Scheuerle, Angela E, Towbin, Jeffrey A, Armstrong, Dawna L, Sweetman, Lawrence, Wong, Lee-Jun C
Publicerad 2002

GSK3- and PRMT-1–dependent modifications of desmoplakin control desmoplakin–cytoskeleton dynamics

av Albrecht, Lauren V., Zhang, Lichao, Shabanowitz, Jeffrey, Purevjav, Enkhsaikhan, Towbin, Jeffrey A., Hunt, Donald F., Green, Kathleen J.
I publikationen J Cell Biol (2015)

Dissection of Z-disc myopalladin gene network involved in the development of restrictive cardiomyopathy using system genetics approach

av Gu, Qingqing, Mendsaikhan, Uzmee, Khuchua, Zaza, Jones, Byron C, Lu, Lu, Towbin, Jeffrey A, Xu, Biao, Purevjav, Enkhsaikhan
I publikationen World J Cardiol (2017)

Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

av Tsubata, Shinichi, Bowles, Karla R., Vatta, Matteo, Zintz, Carmelann, Titus, Jack, Muhonen, Linda, Bowles, Neil E., Towbin, Jeffrey A.
Publicerad 2000

A nonsense SCN5A mutation associated with Brugada type ECG and intraventricular conduction defects

av Samani, Kaveh, Ai, Tomohiko, Towbin, Jeffrey A., Brugada, Ramon, Shuraih, Mossaab, Xi, Yutao, Wu, Geru, Cheng, Jie, Vatta, Matteo
Publicerad 2009

Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemia

av Niss, Omar, Fleck, Robert, Makue, Fowe, Alsaied, Tarek, Desai, Payal, Towbin, Jeffrey A., Malik, Punam, Taylor, Michael D., Quinn, Charles T.
I publikationen Blood (2017)

Clinical, Genetic, and Electrophysiologic Characteristics of a New Pas‐Domain HERG Mutation (M124R) Causing Long QT Syndrome

av Shushi, Liat, Kerem, Batsheva, Goldmit, Maya, Peretz, Asher, Attali, Bernard, Medina, Aron, Towbin, Jeffrey A., Kurokawa, Junko, Kass, Robert S., Benhorin, Jesaia
I publikationen Ann Noninvasive Electrocardiol (2005)