Suppression of Frequent Ventricular Ectopy in a Patient with Hypertrophic Heart Disease with Ranolazine: A Case Report

ανά Murdock, David K, Kaliebe, Jeffrey W
Έκδοση 2011

The Triglyceride to HDL Ratio and Its Relationship to Insulin Resistance in Pre- and Postpubertal Children: Observation from the Wausau SCHOOL Project

ανά Olson, Karen, Hendricks, Bryan, Murdock, David K.
Έκδοση 2012

The Use Of Oral Ranolazine To Convert New Or Paroxysmal Atrial Fibrillation: A Review Of Experience With Implications For Possible "Pill In The Pocket" Approach To Atrial Fibrillat...

ανά Murdock, David K, Kersten, Mary, Kaliebe, Jeff, Larrain, German
Έκδοση 2009

Electrophysiological Changes of the Atrium in Patients with Lone Paroxysmal Atrial Fibrillation

ανά Murdock, David K, Reiffel, James, Kaliebe, Jeff, Larrain, German
Τόπος έκδοσης J Atr Fibrillation (2010)

The effect of ranolazine on maintaining sinus rhythm in patients with resistant atrial fibrillation

ανά Murdock, David K, Overton, Naomi, Kersten, Mary, Kaliebe, Jeff, Devecchi, Fausto
Έκδοση 2008

Combining optical tweezers and patch clamp for studies of cell membrane electromechanics

ανά Qian, Feng, Ermilov, Sergey, Murdock, David, Brownell, William E., Anvari, Bahman
Έκδοση 2004

Effects of Chlorpromazine on Mechanical Properties of the Outer Hair Cell Plasma Membrane

ανά Murdock, David R., Ermilov, Sergey A., Spector, Alexander A., Popel, Aleksander S., Brownell, William E., Anvari, Bahman
Έκδοση 2005

Whole-Exome Sequencing for Diagnosis of Turner Syndrome: Toward Next-Generation Sequencing and Newborn Screening

ανά Murdock, David R., Donovan, Frank X., Chandrasekharappa, Settara C., Banks, Nicole, Bondy, Carolyn, Muenke, Maximilian, Kruszka, Paul
Τόπος έκδοσης J Clin Endocrinol Metab (2017)

A dose‐ranging study of a new, once‐daily, dual‐component drug product containing niacin extended‐release and lovastatin

ανά Hunninghake, Donald B., McGovern, Mark E., Koren, Michael, Brazg, Ronald, Murdock, David, Weiss, Stuart, Pearson, Thomas
Τόπος έκδοσης Clin Cardiol (2006)

Community‐based recruitment and exome sequencing indicates high diagnostic yield in adults with intellectual disability

ανά Sabo, Aniko, Murdock, David, Dugan, Shannon, Meng, Qingchang, Gingras, Marie‐Claude, Hu, Jianhong, Muzny, Donna, Gibbs, Richard
Τόπος έκδοσης Mol Genet Genomic Med (2020)

Genotype–Phenotype Correlation of Congenital Anomalies in Multiple Congenital Anomalies Hypotonia Seizures Syndrome (MCAHS1)/ PIGN-Related Epilepsy

ανά Fleming, Leah, Lemmon, Monica, Beck, Natalie, Johnson, Maria, Mu, Weiyi, Murdock, David, Bodurtha, Joann, Hoover-Fong, Julie, Cohn, Ronald, Bosemani, Thangamadhan, Barañano, Kristin, Hamosh, Ada
Τόπος έκδοσης Am J Med Genet A (2015)

Whole-Exome Sequencing Identifies Compound Heterozygous Mutations in WDR62 in Siblings With Recurrent Polymicrogyria

ανά Murdock, David R., Clark, Gary D., Bainbridge, Matthew N., Newsham, Irene, Wu, Yuan-Qing, Muzny, Donna M., Cheung, Sau Wai, Gibbs, Richard A., Ramocki, Melissa B.
Έκδοση 2011

Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition

ανά Murdock, David R., Jiang, Yunyun, Wangler, Michael, Khayat, Michael M., Sabo, Aniko, Juusola, Jane, McWalter, Kirsty, Schatz, Krista Sondergaard, Gunay-Aygun, Meral, Gibbs, Richard A.
Τόπος έκδοσης Cold Spring Harb Mol Case Stud (2019)

Whole-Exome Sequencing as a diagnostic tool in a child with Atypical Episodic Muscle Weakness

ανά Hanchard, Neil A., Murdock, David R., Magoulas, Pilar L., Bainbridge, Matthew, Muzny, Donna, Wu, YuanQing, Wang, Min, Lupski, James R., Gibbs, Richard A., Brown, Chester W.
Έκδοση 2012

SIX3 Deletions and Incomplete Penetrance in Families Affected by Holoprosencephaly

ανά Stokes, Bethany, Berger, Seth I., Hall, Beth A., Weiss, Karin, Hadley, Donald W., Murdock, David R., Ramanathan, Subhadra, Clark, Robin D., Roessler, Erich, Kruszka, Paul, Muenke, Maximilian
Τόπος έκδοσης Congenit Anom (Kyoto) (2017)

Structural variation and missense mutation in SBDS associated with Shwachman-Diamond syndrome

ανά Carvalho, Claudia M B, Zuccherato, Luciana W, Williams, Christopher L, Neill, Nicholas J, Murdock, David R, Bainbridge, Matthew, Jhangiani, Shalini N, Muzny, Donna M, Gibbs, Richard A, Ip, Wan, Guillerman, Robert Paul, Lupski, James R, Bertuch, Alison A
Έκδοση 2014

The phenotypic spectrum of Xia-Gibbs syndrome

ανά Jiang, Yunyun, Wangler, Michael F., McGuire, Amy L., Lupski, James R., Posey, Jennifer E., Khayat, Michael M., Murdock, David R., Sanchez-Pulido, Luis, Ponting, Chris P., Xia, Fan, Hunter, Jill V., Meng, Qingchang, Murugan, Mullai, Gibbs, Richard A.
Τόπος έκδοσης Am J Med Genet A (2018)

Whole-Genome Sequencing for Optimized Patient Management

ανά Bainbridge, Matthew N., Wiszniewski, Wojciech, Murdock, David R., Friedman, Jennifer, Gonzaga-Jauregui, Claudia, Newsham, Irene, Reid, Jeffrey G., Fink, John K., Morgan, Margaret B., Gingras, Marie-Claude, Muzny, Donna M., Hoang, Linh D., Yousaf, Shahed, Lupski, James R., Gibbs, Richard A.
Έκδοση 2011

Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia–Gibbs syndrome

ανά Khayat, Michael M., Li, He, Chander, Varuna, Hu, Jianhong, Hansen, Adam W., Li, Shoudong, Traynelis, Josh, Shen, Hua, Weissenberger, George, Stossi, Fabio, Johnson, Hannah L., Lupski, James R., Posey, Jennifer E., Sabo, Aniko, Meng, Qingchang, Murdock, David R., Wangler, Michael, Gibbs, Richard A.
Τόπος έκδοσης Hum Mutat (2021)

De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy

ανά Chung, Hyung-lok, Mao, Xiao, Wang, Hua, Park, Ye-Jin, Marcogliese, Paul C., Rosenfeld, Jill A., Burrage, Lindsay C., Liu, Pengfei, Murdock, David R., Yamamoto, Shinya, Wangler, Michael F., Chao, Hsiao-Tuan, Long, Hongyu, Feng, Li, Bacino, Carlos A., Bellen, Hugo J., Xiao, Bo
Τόπος έκδοσης Am J Hum Genet (2020)