N98S mutation in NEFL gene is dominantly inherited with a phenotype of polyneuropathy and cerebellar atrophy

von Yang, Yi, Gu, Li-Qiang, Burnette, William B., Li, Jun
Veröffentlicht in J Neurol Sci (2016)

Multidisciplinary Perioperative Care for Children with Neuromuscular Disorders

von Kynes, J. Matthew, Blakely, Martin, Furman, Kevin, Burnette, William B., Modes, Katharina B.
Veröffentlicht in Children (Basel) (2018)

T1 mapping is abnormal before decline in EF in patients with Becker and Duchenne muscular dystrophy

von Soslow Jonathan H, Damon Bruce M, Burnette William B, Parra David, Markham Larry W
Veröffentlicht 2013-01-01

T1 mapping is abnormal before decline in EF in patients with Becker and Duchenne muscular dystrophy

von Soslow, Jonathan H, Damon, Bruce M, Burnette, William B, Parra, David, Markham, Larry W
Veröffentlicht 2013

Mechanism, Prevalence, and More Severe Neuropathy Phenotype of the Charcot-Marie-Tooth Type 1A Triplication

von Liu, Pengfei, Gelowani, Violet, Zhang, Feng, Drory, Vivian E., Ben-Shachar, Shay, Roney, Erin, Medeiros, Adam C., Moore, Rebecca J., DiVincenzo, Christina, Burnette, William B., Higgins, Joseph J., Li, Jun, Orr-Urtreger, Avi, Lupski, James R.
Veröffentlicht 2014

The BDNF rs6265 Polymorphism is a Modifier of Cardiomyocyte Contractility and Dilated Cardiomyopathy

von Raucci, Frank J., Singh, Anand Prakash, Soslow, Jonathan, Markham, Larry W., Zhong, Lin, Aljafar, Wejdan, Lessiohadi, Natasja, Awgulewitsch, Cassandra P., Umbarkar, Prachi, Zhang, Qinkun, Cannon, Presley L., Buchowski, Maciej, Roland, Joseph T., Carrier, Erica J., Burnette, William B., Hatzopoulos, Antonis K., Lal, Hind, Galindo, Cristi L.
Veröffentlicht in Int J Mol Sci (2020)