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Page 1
The neuroimaging of Leigh syndrome: case series and review of the literature.
Pediatr Radiol. 2016 Apr;46(4):443-51. doi: 10.1007/s00247-015-3523-5. Epub 2016 Jan 6.
Pediatr Radiol. 2016.
PMID: 26739140
Review.
Involvement of Cerebellum in Leigh Syndrome: Case Report and Review of the Literature.
Chourasia N, Adejumo RB, Patel RP, Koenig MK.
Chourasia N, et al. Among authors: adejumo rb.
Pediatr Neurol. 2017 Sep;74:97-99. doi: 10.1016/j.pediatrneurol.2017.05.008. Epub 2017 May 19.
Pediatr Neurol. 2017.
PMID: 28739363
Review.
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Sleep disordered breathing in children with mitochondrial disease.
Mosquera RA, Koenig MK, Adejumo RB, Chevallier J, Hashmi SS, Mitchell SE, Pacheco SE, Jon C.
Mosquera RA, et al. Among authors: adejumo rb.
Pulm Med. 2014;2014:467576. doi: 10.1155/2014/467576. Epub 2014 Dec 23.
Pulm Med. 2014.
PMID: 25587443
Free PMC article.
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Reply to the Letter to the Editor by Josef Finsterer and Sinda Zarrouk-Mahjoub.
Chourasia N, Adejumo R, Patel R, Koenig MK.
Chourasia N, et al. Among authors: adejumo r.
Pediatr Neurol. 2018 Jan;78:e11. doi: 10.1016/j.pediatrneurol.2017.09.011. Epub 2017 Sep 21.
Pediatr Neurol. 2018.
PMID: 29169869
No abstract available.
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Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy.
Nmezi B, Giorgio E, Raininko R, Lehman A, Spielmann M, Koenig MK, Adejumo R, Knight M, Gavrilova R, Alturkustani M, Sharma M, Hammond R, Gahl WA, Toro C, Brusco A, Padiath QS.
Nmezi B, et al. Among authors: adejumo r.
Neurol Genet. 2019 Jan 24;5(1):e305. doi: 10.1212/NXG.0000000000000305. eCollection 2019 Feb.
Neurol Genet. 2019.
PMID: 30842973
Free PMC article.
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A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.
Mucha BE, Banka S, Ajeawung NF, Molidperee S, Chen GG, Koenig MK, Adejumo RB, Till M, Harbord M, Perrier R, Lemyre E, Boucher RM, Skotko BG, Waxler JL, Thomas MA, Hodge JC, Gecz J, Nicholl J, McGregor L, Linden T, Sisodiya SM, Sanlaville D, Cheung SW, Ernst C, Campeau PM.
Mucha BE, et al. Among authors: adejumo rb.
Genet Med. 2019 May;21(5):1058-1064. doi: 10.1038/s41436-018-0290-3. Epub 2018 Sep 24.
Genet Med. 2019.
PMID: 30245510
Free article.
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Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.
Mucha BE, Banka S, Ajeawung NF, Molidperee S, Chen GG, Koenig MK, Adejumo RB, Till M, Harbord M, Perrier R, Lemyre E, Boucher RM, Skotko BG, Waxler JL, Thomas MA, Hodge JC, Gecz J, Nicholl J, McGregor L, Linden T, Sisodiya SM, Sanlaville D, Cheung SW, Ernst C, Campeau PM.
Mucha BE, et al. Among authors: adejumo rb.
Genet Med. 2019 Sep;21(9):2159-2160. doi: 10.1038/s41436-018-0413-x.
Genet Med. 2019.
PMID: 30643220
Free article.
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