Thalamic Massa Intermedia Duplication in a Dysmorphic 14 month-old Toddler

Por Whitehead, Matthew T
Publicado no J Radiol Case Rep (2015)

Tuber Cinereum Diverticula in a 28-Month-Old with Xq21 Deletion Syndrome

Por Whitehead, Matthew T., Vezina, Gilbert
Publicado em 2014

Neuroimaging Features of San Luis Valley Syndrome

Por Whitehead, Matthew T., Lee, Bonmyong
Publicado no Case Rep Radiol (2015)

Interhypothalamic Adhesion in a 9-Month-Old Male with Cleft Palate

Por Whitehead, Matthew T., Angel, Jacqueline D. S.
Publicado em 2013

The association among prematurity, cochlear hyperintensity, and hearing loss

Por Wien, Michael A, Whitehead, Matthew T
Publicado no Neuroradiol J (2017)

Magnetic resonance imaging findings in Axenfeld–Rieger syndrome

Por Whitehead, Matthew T, Choudhri, Asim F, Salim, Sarwat
Publicado em 2013

MR Imaging Findings in Xp21.2 Duplication Syndrome

Por Whitehead, Matthew T, Helman, Guy, Gropman, Andrea L
Publicado no J Radiol Case Rep (2016)

Reduced subarachnoid fluid diffusion in enlarged subarachnoid spaces of infancy

Por Whitehead, Matthew T, Lee, Bonmyong, McCarron, Audrey, Fricke, Stanley T, Vezina, Gilbert
Publicado no Neuroradiol J (2017)

Diffusion characteristics of pediatric pineal tumors

Por Choudhri, Asim F, Whitehead, Matthew T, Siddiqui, Adeel, Klimo, Paul, Boop, Frederick A
Publicado no Neuroradiol J (2015)

Diffusion tensor imaging to guide surgical planning in intramedullary spinal cord tumors in children

Por Choudhri, Asim F., Whitehead, Matthew T., Klimo, Paul, Montgomery, Blake K., Boop, Frederick A.
Publicado no Neuroradiology (2014)

Same Day Tri-Modality Functional Brain Mapping Prior to Resection of a Lesion Involving Eloquent Cortex: Technical Feasibility

Por Choudhri, Asim F., Narayana, Shalini, Rezaie, Roozbeh, Whitehead, Matthew T., McAfee, Samuel S., Wheless, Samuel S., Boop, Frederick A., Papanicolaou, Andrew C.
Publicado em 2013

Loss-of-Function Alanyl-tRNA Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination Defect

Por Simons, Cas, Griffin, Laurie B., Helman, Guy, Golas, Gretchen, Pizzino, Amy, Bloom, Miriam, Murphy, Jennifer L.P., Crawford, Joanna, Evans, Sarah H., Topper, Scott, Whitehead, Matthew T., Schreiber, John M., Chapman, Kimberly A., Tifft, Cyndi, Lu, Katrina B., Gamper, Howard, Shigematsu, Megumi, Taft, Ryan J., Antonellis, Anthony, Hou, Ya-Ming, Vanderver, Adeline
Publicado no Am J Hum Genet (2015)