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

מאת Yang, Yi, Gu, Li-Qiang, Burnette, William B., Li, Jun
הוצא לאור ב J Neurol Sci (2016)

Multidisciplinary Perioperative Care for Children with Neuromuscular Disorders

מאת Kynes, J. Matthew, Blakely, Martin, Furman, Kevin, Burnette, William B., Modes, Katharina B.
הוצא לאור ב Children (Basel) (2018)

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

מאת Soslow Jonathan H, Damon Bruce M, Burnette William B, Parra David, Markham Larry W
יצא לאור 2013-01-01

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

מאת Soslow, Jonathan H, Damon, Bruce M, Burnette, William B, Parra, David, Markham, Larry W
יצא לאור 2013

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

מאת 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.
יצא לאור 2014

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

מאת 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.
הוצא לאור ב Int J Mol Sci (2020)