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Expanding the phenotype of children presenting with hypoventilation with biallelic TBCK pathogenic variants and literature review.
Sabanathan S, Gulhane D, Mankad K, Davison J, Ong MT, Phadke R, Robinson R, Spiller M, Wakeling E, Ramdas S, Brady AF, Balasubramanian M, Munot P. Sabanathan S, et al. Among authors: munot p. Neuromuscul Disord. 2023 Jan;33(1):50-57. doi: 10.1016/j.nmd.2022.10.004. Epub 2022 Oct 25. Neuromuscul Disord. 2023. PMID: 36522252 Review.
The neuropathological consequences of CDKL5 mutation.
Paine SM, Munot P, Carmichael J, Das K, Weber MA, Prabhakar P, Jacques TS. Paine SM, et al. Among authors: munot p. Neuropathol Appl Neurobiol. 2012 Dec;38(7):744-7. doi: 10.1111/j.1365-2990.2012.01292.x. Neuropathol Appl Neurobiol. 2012. PMID: 22812903 No abstract available.
Childhood optic neuritis clinical features and outcome.
Absoud M, Cummins C, Desai N, Gika A, McSweeney N, Munot P, Hemingway C, Lim M, Nischal KK, Wassmer E. Absoud M, et al. Among authors: munot p. Arch Dis Child. 2011 Sep;96(9):860-2. doi: 10.1136/adc.2009.175422. Epub 2010 Jun 16. Arch Dis Child. 2011. PMID: 20554767
The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
Rodríguez Cruz PM, Cossins J, Estephan EP, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Chow G, Carr A, Manzur A, Robb S, Munot P, Wei Liu W, Banka S, Fraser H, De Goede C, Zanoteli E, Conti Reed U, Sage A, Gratacos M, Macaya A, Dusl M, Senderek J, Töpf A, Hofer M, Knight R, Ramdas S, Jayawant S, Lochmüller H, Palace J, Beeson D. Rodríguez Cruz PM, et al. Among authors: munot p. Brain. 2019 Jun 1;142(6):1547-1560. doi: 10.1093/brain/awz107. Brain. 2019. PMID: 31081514 Free PMC article.
Paediatric myasthenia gravis: Prognostic factors for drug free remission.
Vecchio D, Ramdas S, Munot P, Pitt M, Beeson D, Knight R, Rodríguez Cruz P, Vincent A, Jayawant S, DeVile C, Buckley C, Hilton-Jones D, Robb S, Palace J. Vecchio D, et al. Among authors: munot p. Neuromuscul Disord. 2020 Feb;30(2):120-127. doi: 10.1016/j.nmd.2019.11.008. Epub 2019 Nov 21. Neuromuscul Disord. 2020. PMID: 32001147
63 results