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Year Number of Results
1970 1
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1976 1
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1979 4
1981 2
1984 1
1991 1
1994 3
1995 1
1996 1
1998 3
1999 1
2000 1
2001 1
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2011 1
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2014 3
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2020 2
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51 results

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Page 1
The new INCLEN diagnostic tool - a comment.
Poulton A, Sudarsanam A. Poulton A, et al. Among authors: sudarsanam a. Indian Pediatr. 2014 Jun;51(6):448-9. Indian Pediatr. 2014. PMID: 24986278 Free article. No abstract available.
Expanding the phenotypic spectrum of CLCN2-related leucoencephalopathy and ataxia.
Nóbrega PR, R B de Paiva A, Souza KS, de Souza JLB, G S B Lima PL, da Silva DJ, Pitombeira MS, Borges VK, Dias DA, Bispo LM, Santos CF, Freua F, Silva PDS, Alves IS, Portella LB, Cunha PR, Salomao RPA, Pedroso JL, Miyajima VP, Miyajima F, Cali E, Wade C, Sudarsanam A, O'Driscoll M, Hayton T, Barsottini OGP, Klebe S, Kok F, Lucato LT, Houlden H, Depienne C, Lynch DS, Braga-Neto P. Nóbrega PR, et al. Among authors: sudarsanam a. Brain Commun. 2023 Oct 17;6(1):fcad273. doi: 10.1093/braincomms/fcad273. eCollection 2024. Brain Commun. 2023. PMID: 38173802 Free PMC article.
Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement.
Kaiyrzhanov R, Mohammed SEM, Maroofian R, Husain RA, Catania A, Torraco A, Alahmad A, Dutra-Clarke M, Grønborg S, Sudarsanam A, Vogt J, Arrigoni F, Baptista J, Haider S, Feichtinger RG, Bernardi P, Zulian A, Gusic M, Efthymiou S, Bai R, Bibi F, Horga A, Martinez-Agosto JA, Lam A, Manole A, Rodriguez DP, Durigon R, Pyle A, Albash B, Dionisi-Vici C, Murphy D, Martinelli D, Bugiardini E, Allis K, Lamperti C, Reipert S, Risom L, Laugwitz L, Di Nottia M, McFarland R, Vilarinho L, Hanna M, Prokisch H, Mayr JA, Bertini ES, Ghezzi D, Østergaard E, Wortmann SB, Carrozzo R, Haack TB, Taylor RW, Spinazzola A, Nowikovsky K, Houlden H. Kaiyrzhanov R, et al. Among authors: sudarsanam a. Am J Hum Genet. 2022 Sep 1;109(9):1692-1712. doi: 10.1016/j.ajhg.2022.07.007. Am J Hum Genet. 2022. PMID: 36055214 Free PMC article.
Case Report: ISG15 deficiency caused by novel variants in two families and effective treatment with Janus kinase inhibition.
Burleigh A, Moraitis E, Al Masroori E, Al-Abadi E, Hong Y, Omoyinmi E, Titheradge H, Stals K, Jones WD, Gait A, Jayarajan V, Di WL, Sebire N, Solman L, Ogboli M, Welch SB, Sudarsanam A, Wacogne I, Price-Kuehne F, Jensen B, Brogan PA, Eleftheriou D. Burleigh A, et al. Among authors: sudarsanam a. Front Immunol. 2023 Dec 5;14:1287258. doi: 10.3389/fimmu.2023.1287258. eCollection 2023. Front Immunol. 2023. PMID: 38115997 Free PMC article.
Sturge-Weber syndrome: from the past to the present.
Sudarsanam A, Ardern-Holmes SL. Sudarsanam A, et al. Eur J Paediatr Neurol. 2014 May;18(3):257-66. doi: 10.1016/j.ejpn.2013.10.003. Epub 2013 Nov 7. Eur J Paediatr Neurol. 2014. PMID: 24275166 Review.
COVID-19 and vascular surgery at a central London teaching hospital.
Rolls A, Sudarsanam A, Luo X, Aylwin C, Bicknell CD, Davies AH, Gibbs RGJ, Jaffer U, Jenkins MP, Nott D, Riga CV, Shalhoub J, Sritharan G, Standfield NJ. Rolls A, et al. Among authors: sudarsanam a. Br J Surg. 2020 Aug;107(9):e311-e312. doi: 10.1002/bjs.11765. Epub 2020 Jun 22. Br J Surg. 2020. PMID: 32567675 Free PMC article. No abstract available.
51 results