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

Por Yang, Yi, Gu, Li-Qiang, Burnette, William B., Li, Jun
Publicado no J Neurol Sci (2016)

Multidisciplinary Perioperative Care for Children with Neuromuscular Disorders

Por Kynes, J. Matthew, Blakely, Martin, Furman, Kevin, Burnette, William B., Modes, Katharina B.
Publicado no Children (Basel) (2018)

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

Por Soslow Jonathan H, Damon Bruce M, Burnette William B, Parra David, Markham Larry W
Publicado em 2013-01-01

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

Por Soslow, Jonathan H, Damon, Bruce M, Burnette, William B, Parra, David, Markham, Larry W
Publicado em 2013

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

Por 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.
Publicado em 2014

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

Por 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.
Publicado no Int J Mol Sci (2020)