Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes.
Abell, K; Tolusso, L; Smith, N; Hopkin, R; Vawter-Lee, M; Habli, M; Riddle, S; Calvo-Garcia, MA; Guan, Q; Bierbrauer, K; et al.
Birth Defects Research.
2020;
112:1733-1737.
The increasing global burden of childhood disability: A call for action.
Vawter-Lee, M; McGann, PT.
Pediatrics.
2020;
146:e20201119-e20201119.
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms.
Chung, H; Wangler, MF; Marcogliese, PC; Jo, J; Ravenscroft, TA; Zuo, Z; Duraine, L; Sadeghzadeh, S; Li-Kroeger, D; Schmidt, RE; et al.
Neuron.
2020;
106:589-606.e6.
Clinical Letter: A case report of targeted therapy with sirolimus for NPRL3 epilepsy.
Vawter-Lee, M; Franz, DN; Fuller, CE; Greiner, HM.
Seizure-European Journal of Epilepsy.
2019;
73:43-45.
CNTNAP1-Related Congenital Hypomyelinating Neuropathy.
Lesmana, H; Lee, MV; Hosseini, SA; Burrow, TA; Hallinan, B; Bove, K; Schapiro, M; Hopkin, RJ.
Pediatric Neurology.
2019;
93:43-49.
Teaching Video NeuroImages: Ictal vomiting in a child.
Aungaroon, G; Vawter-Lee, M.
Neurology.
2018;
91:e1836-e1837.
Outcome of Isolated Absent Septum Pellucidum Diagnosed by Fetal Magnetic Resonance Imaging (MRI) Scan.
Vawter-Lee, MM; Wasserman, H; Thomas, CW; Nichols, B; Nagaraj, UD; Schapiro, M; Venkatesan, C.
Journal of Child Neurology.
2018;
33:693-699.
Clinical Reasoning: A neonate with micrognathia and hypotonia.
Vawter-Lee, MM; Seals, SS; Thomas, CW; Venkatesan, C.
Neurology.
2016;
86:e80-e84.