Last Updated: 09/26/2026
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Found 8 publications
Cardiology clinic patient attitudes toward and potential personal utility of genetic testing: Findings from a unique multiracial clinical sample.
Journal: Journal of genetic counseling
Published: December 23, 2021
Utility of Neonatal Findings in Early Diagnosis of a Case of Haberland Syndrome.
Journal: Journal of pediatric genetics
Published: January 20, 2021
Complicated ventricular arrhythmia and hematologic myeloproliferative disorder in RIT1-associated Noonan syndrome: Expanding the phenotype and review of the literature.
Journal: Molecular genetics & genomic medicine
Published: November 07, 2019
McArdle disease: a "pediatric" disorder presenting in an adult with acute kidney injury.
Journal: CEN case reports
Published: April 20, 2017
Clinical diagnostic exome evaluation for an infant with a lethal disorder: genetic diagnosis of TARP syndrome and expansion of the phenotype in a patient with a newly reported RBM10 alteration.
Journal: BMC medical genetics
Published: June 24, 2016
Trial ultrasound-guided continuous left stellate ganglion blockade before surgical gangliolysis in a patient with a left ventricular assist device and intractable ventricular tachycardia: a pain control application to a complex hemodynamic condition.
Journal: ASAIO journal (American Society for Artificial Internal Organs : 1992)
Published: October 12, 2014
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Last Updated: 09/26/2026