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Genetic and Mitochondrial Metabolic Analyses of an Atypical Form of Leigh Syndrome.
Uittenbogaard M, Sen K, Whitehead M, Brantner CA, Wang Y, Wong LJ, Gropman A, Chiaramello A. Uittenbogaard M, et al. Among authors: whitehead m. Front Cell Dev Biol. 2021 Dec 22;9:767407. doi: 10.3389/fcell.2021.767407. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 35004675 Free PMC article.
Structural brain defects.
Whitehead MT, Fricke ST, Gropman AL. Whitehead MT, et al. Clin Perinatol. 2015 Jun;42(2):337-61, ix. doi: 10.1016/j.clp.2015.02.007. Epub 2015 Apr 4. Clin Perinatol. 2015. PMID: 26042908 Review.
MR Imaging Findings in Xp21.2 Duplication Syndrome.
Whitehead MT, Helman G, Gropman AL. Whitehead MT, et al. J Radiol Case Rep. 2016 May 31;10(5):9-14. doi: 10.3941/jrcr.v10i5.2563. eCollection 2016 May. J Radiol Case Rep. 2016. PMID: 27761175 Free PMC article.
Black Toenail Sign in MELAS Syndrome.
Whitehead MT, Wien M, Lee B, Bass N, Gropman A. Whitehead MT, et al. Pediatr Neurol. 2017 Oct;75:61-65. doi: 10.1016/j.pediatrneurol.2017.06.017. Epub 2017 Jul 12. Pediatr Neurol. 2017. PMID: 28818358
"Cerebral Palsy" in a Patient With Arginase Deficiency.
Jichlinski A, Clarke L, Whitehead MT, Gropman A. Jichlinski A, et al. Semin Pediatr Neurol. 2018 Jul;26:110-114. doi: 10.1016/j.spen.2017.03.016. Epub 2017 Apr 1. Semin Pediatr Neurol. 2018. PMID: 29961498
1,266 results