Shelley D Miyamoto
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Explore the profile of Shelley D Miyamoto including associated specialties, affiliations and a list of published articles.
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84
Citations
850
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Recent Articles
11.
Sucharov C, Neltner B, Pietra A, Karimpour-Fard A, Patel J, Ho C, et al.
Circ Heart Fail
. 2023 Mar;
16(6):e010291.
PMID: 36880380
Background: Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiomyopathy. Pathogenic germline variation in genes encoding the sarcomere is the predominant cause of disease. However diagnostic features, including unexplained left...
12.
Almond C, Sleeper L, Rossano J, Bock M, Pahl E, Auerbach S, et al.
Am Heart J
. 2023 Feb;
260:100-112.
PMID: 36828201
Background: Currently there are no immunosuppression regimens FDA-approved to prevent rejection in pediatric heart transplantation (HT). In recent years, everolimus (EVL) has emerged as a potential alternative to standard tacrolimus...
13.
Opotowsky A, Allen K, Bucholz E, Burns K, Del Nido P, Fenton K, et al.
J Am Coll Cardiol
. 2022 Dec;
80(23):2239-2250.
PMID: 36456054
The National Heart, Lung, and Blood Institute convened a workshop in August 2021 to identify opportunities in pediatric and congenital cardiovascular research that would improve outcomes for individuals with congenital...
14.
Stone M, Albertz M, Galambos C, Twite M, Campbell D, Maria M, et al.
Semin Cardiothorac Vasc Anesth
. 2022 Aug;
26(4):315-322.
PMID: 36006828
Cardiac tumors remain rare in children with benign pathologies predominating. Indications for surgical management often result from compromised ventricular chamber size, biventricular outflow tract obstruction, impaired ventricular function, or the...
15.
Baybayon-Grandgeorge A, Pietra A, Miyamoto S, Garcia A
J Cardiovasc Dev Dis
. 2022 May;
9(5).
PMID: 35621863
Significant surgical and medical advances over the past several decades have resulted in a growing number of infants and children surviving with hypoplastic left heart syndrome (HLHS) and other congenital...
16.
Jone P, John A, Oster M, Allen K, Tremoulet A, Saarel E, et al.
Circulation
. 2022 Apr;
145(19):e1037-e1052.
PMID: 35400169
Coronavirus disease 2019 (COVID-19) resulted in a global pandemic and has overwhelmed health care systems worldwide. In this scientific statement, we describe the epidemiology, pathophysiology, clinical presentations, treatment, and outcomes...
17.
Schuchardt E, Miyamoto S, Crombleholme T, Karimpour-Fard A, Korst A, Neltner B, et al.
J Cardiovasc Dev Dis
. 2022 Feb;
9(2).
PMID: 35200691
Twin-twin transfusion syndrome (TTTS) is a rare but serious cause of fetal cardiomyopathy with poorly understood pathophysiology and challenging prognostication. This study sought a nonbiased, comprehensive assessment of amniotic fluid...
18.
Chatfield K, Sparagna G, Specht K, Whitcomb L, Omar A, Miyamoto S, et al.
J Inherit Metab Dis
. 2021 Nov;
45(1):111-124.
PMID: 34821394
Barth syndrome (BTHS) is an X-linked disorder that results from mutations in the TAFAZZIN gene, which encodes a phospholipid transacylase responsible for generating the mature form of cardiolipin in inner...
19.
Fraley C, Milgrom S, Kondapalli L, Taylor M, Mestroni L, Miyamoto S
Children (Basel)
. 2021 Sep;
8(9).
PMID: 34572260
Cardiotoxicity is a well-recognized late effect among childhood cancer survivors. With various pediatric cancers becoming increasingly curable, it is imperative to understand the disease burdens that survivors may face in...
20.
Jeffrey D, Pires Da Silva J, Garcia A, Jiang X, Karimpour-Fard A, Toni L, et al.
JCI Insight
. 2021 Aug;
6(19).
PMID: 34383712
Dilated cardiomyopathy (DCM) is the most common form of cardiomyopathy and main indication for heart transplantation in children. Therapies specific to pediatric DCM remain limited due to lack of a...