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Page 1
Seizure semiology and EEG findings in mitochondrial diseases.
Chevallier JA, Von Allmen GK, Koenig MK. Chevallier JA, et al. Among authors: koenig mk. Epilepsia. 2014 May;55(5):707-712. doi: 10.1111/epi.12570. Epub 2014 Mar 7. Epilepsia. 2014. PMID: 24605851 Free article.
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.
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
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.
Guerrini R, Mei D, Kerti-Szigeti K, Pepe S, Koenig MK, Von Allmen G, Cho MT, McDonald K, Baker J, Bhambhani V, Powis Z, Rodan L, Nabbout R, Barcia G, Rosenfeld JA, Bacino CA, Mignot C, Power LH, Harris CJ, Marjanovic D, Møller RS, Hammer TB; DDD Study; Keski Filppula R, Vieira P, Hildebrandt C, Sacharow S; Undiagnosed Diseases Network; Maragliano L, Benfenati F, Lachlan K, Benneche A, Petit F, de Sainte Agathe JM, Hallinan B, Si Y, Wentzensen IM, Zou F, Narayanan V, Matsumoto N, Boncristiano A, la Marca G, Kato M, Anderson K, Barba C, Sturiale L, Garozzo D, Bei R; ATP6V1A collaborators; Masuelli L, Conti V, Novarino G, Fassio A. Guerrini R, et al. Among authors: koenig mk. Brain. 2022 Aug 27;145(8):2687-2703. doi: 10.1093/brain/awac145. Brain. 2022. PMID: 35675510 Free PMC article.
105 results