Koenig MK - Search Results

1

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: koenig mk. 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.

2

Presentation and diagnosis of mitochondrial disorders in children.

Koenig MK. Koenig MK. Pediatr Neurol. 2008 May;38(5):305-13. doi: 10.1016/j.pediatrneurol.2007.12.001. Pediatr Neurol. 2008. PMID: 18410845 Free PMC article. Review.

3

Regression of subependymal giant cell astrocytoma with rapamycin in tuberous sclerosis complex.

Koenig MK, Butler IJ, Northrup H. Koenig MK, et al. J Child Neurol. 2008 Oct;23(10):1238-9. doi: 10.1177/0883073808321764. J Child Neurol. 2008. PMID: 18952591 Free PMC article.

4

Friedreich-like ataxia as an initial manifestation of mitochondrial DNA 8344A>G mutation.

Chevallier JA, Koenig MK. Chevallier JA, et al. Among authors: koenig mk. J Child Neurol. 2012 Aug;27(8):1056-8. doi: 10.1177/0883073811431012. Epub 2012 Jan 12. J Child Neurol. 2012. PMID: 22241709

5

Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 Iinternational Tuberous Sclerosis Complex Consensus Conference.

Northrup H, Krueger DA; International Tuberous Sclerosis Complex Consensus Group. Northrup H, et al. Pediatr Neurol. 2013 Oct;49(4):243-54. doi: 10.1016/j.pediatrneurol.2013.08.001. Pediatr Neurol. 2013. PMID: 24053982 Free PMC article.

6

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: koenig mk. Pulm Med. 2014;2014:467576. doi: 10.1155/2014/467576. Epub 2014 Dec 23. Pulm Med. 2014. PMID: 25587443 Free PMC article.

7

Identification of HIBCH gene mutations causing autosomal recessive Leigh syndrome: a gene involved in valine metabolism.

Soler-Alfonso C, Enns GM, Koenig MK, Saavedra H, Bonfante-Mejia E, Northrup H. Soler-Alfonso C, et al. Among authors: koenig mk. Pediatr Neurol. 2015 Mar;52(3):361-5. doi: 10.1016/j.pediatrneurol.2014.10.023. Epub 2014 Nov 7. Pediatr Neurol. 2015. PMID: 25591832

8

The neuroimaging of Leigh syndrome: case series and review of the literature.

Bonfante E, Koenig MK, Adejumo RB, Perinjelil V, Riascos RF. Bonfante E, et al. Among authors: koenig mk. 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.

9

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: koenig mk. 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.

10

Expanding the Phenotypic Spectrum of CACNA1H Mutations.

Chourasia N, Ossó-Rivera H, Ghosh A, Von Allmen G, Koenig MK. Chourasia N, et al. Among authors: koenig mk. Pediatr Neurol. 2019 Apr;93:50-55. doi: 10.1016/j.pediatrneurol.2018.11.017. Epub 2018 Dec 19. Pediatr Neurol. 2019. PMID: 30686625

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