Arterial spin labeling perfusion in acute Wernicke encephalopathy: a case series discussion

por Ann, Phoebe, Chen, Mark, Naidich, Thomas, Belani, Puneet, Nael, Kambiz
Publicado 2023

Diagnosis and Supportive Management of Fucosidosis: A Case Report

por Kaur, Arpanjeet, Dhaliwal, Arshdeep S, Raynes, Hillary, Naidich, Thomas P, Kaufman, David M
Publicado 2019

Fatal cerebral infarct in a child with COVID-19

por Kihira, Shingo, Morgenstern, Peter F., Raynes, Hillary, Naidich, Thomas P., Belani, Puneet
Publicado 2020

Mirror Movements Identified in Patients with Moebius Syndrome

por Webb, Bryn D., Frempong, Tamiesha, Naidich, Thomas P., Gaspar, Harald, Jabs, Ethylin Wang, Rucker, Janet C.
Publicado 2014

Giant chondrosarcoma of the falx in an adolescent: A case report

por Kessler, Remi A., Saade, Mia, Chapman, Emily K., Feng, Rui, Naidich, Thomas P., Fowkes, Mary E., Bederson, Joshua B., Morgenstern, Peter F.
Publicado 2021

Case report: A novel biallelic FTO variant causing multisystem anomalies with severe epilepsy, widening the spectrum of FTO syndrome

por Mayman, Naomi, Wei, Jiangbo, Cai, Shangjun, Soman, Rohan, Raynes, Hillary, La Vega-Talbott, Maite, He, Chuan, Naidich, Thomas, Raju, G. Praveen, Kathiresu Nageshwaran, Sathiji
Publicado 2023

Sub-millimeter variation in human locus coeruleus is associated with dimensional measures of psychopathology: An in vivo ultra-high field 7-Tesla MRI study

por Morris, Laurel S., Tan, Aaron, Smith, Derek A., Grehl, Mora, Han-Huang, Kuang, Naidich, Thomas P., Charney, Dennis S., Balchandani, Priti, Murrough, James W., Kundu, Prantik
Publicado 2020

BK virus encephalopathy and sclerosing vasculopathy in a patient with hypohidrotic ectodermal dysplasia and immunodeficiency

por Darbinyan, Armine, Major, Eugene O., Morgello, Susan, Holland, Steven, Ryschkewitsch, Caroline, Monaco, Maria Chiara, Naidich, Thomas P., Bederson, Joshua, Malaczynska, Joanna, Ye, Fei, Gordon, Ronald, Cunningham-Rundles, Charlotte, Fowkes, Mary, Tsankova, Nadejda M.
Publicado 2016

Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency

por Webb, Bryn D, Nowinski, Sara M, Solmonson, Ashley, Ganesh, Jaya, Rodenburg, Richard J, Leandro, Joao, Evans, Anthony, Vu, Hieu S, Naidich, Thomas P, Gelb, Bruce D, DeBerardinis, Ralph J, Rutter, Jared, Houten, Sander M
Publicado 2023