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Nociception and pain in humans lacking a functional TRPV1 channel.
Katz B, Zaguri R, Edvardson S, Maayan C, Elpeleg O, Lev S, Davidson E, Peters M, Kfir-Erenfeld S, Berger E, Ghazalin S, Binshtok AM, Minke B. Katz B, et al. Among authors: maayan c. J Clin Invest. 2023 Feb 1;133(3):e153558. doi: 10.1172/JCI153558. J Clin Invest. 2023. PMID: 36454632 Free PMC article.
Uncommon side effects of common drugs in patients with familial dysautonomia.
Perl L, Hakimian D, Maayan C, Rekhtman D, Fried E, Salmon-Divon M, Sapozhnikov DM, Cheishvili D. Perl L, et al. Among authors: maayan c. Pharmacoepidemiol Drug Saf. 2022 Feb;31(2):128-140. doi: 10.1002/pds.5326. Epub 2021 Jul 16. Pharmacoepidemiol Drug Saf. 2022. PMID: 34245206
Dry Eye.
Maayan C, Heyman SN. Maayan C, et al. N Engl J Med. 2018 Sep 13;379(11):e19. doi: 10.1056/NEJMc1808906. N Engl J Med. 2018. PMID: 30211496 No abstract available.
Respiratory care in familial dysautonomia: Systematic review and expert consensus recommendations.
Kazachkov M, Palma JA, Norcliffe-Kaufmann L, Bar-Aluma BE, Spalink CL, Barnes EP, Amoroso NE, Balou SM, Bess S, Chopra A, Condos R, Efrati O, Fitzgerald K, Fridman D, Goldenberg RM, Goldhaber A, Kaufman DA, Kothare SV, Levine J, Levy J, Lubinsky AS, Maayan C, Moy LC, Rivera PJ, Rodriguez AJ, Sokol G, Sloane MF, Tan T, Kaufmann H. Kazachkov M, et al. Among authors: maayan c. Respir Med. 2018 Aug;141:37-46. doi: 10.1016/j.rmed.2018.06.017. Epub 2018 Jun 21. Respir Med. 2018. PMID: 30053970 Free PMC article. Review.
Characteristics of ataxic gait in familial dysautonomia patients.
Portnoy S, Maayan C, Tsenter J, Ofran Y, Goldman V, Hiller N, Karniel N, Schwartz I. Portnoy S, et al. Among authors: maayan c. PLoS One. 2018 Apr 26;13(4):e0196599. doi: 10.1371/journal.pone.0196599. eCollection 2018. PLoS One. 2018. PMID: 29698477 Free PMC article.
Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study.
Cheishvili D, Maayan C, Holzer N, Tsenter J, Lax E, Petropoulos S, Razin A. Cheishvili D, et al. Among authors: maayan c. J Mol Neurosci. 2016 Jul;59(3):382-91. doi: 10.1007/s12031-016-0760-5. Epub 2016 Apr 30. J Mol Neurosci. 2016. PMID: 27129499 Clinical Trial.
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability.
Heimer G, Oz-Levi D, Eyal E, Edvardson S, Nissenkorn A, Ruzzo EK, Szeinberg A, Maayan C, Mai-Zahav M, Efrati O, Pras E, Reznik-Wolf H, Lancet D, Goldstein DB, Anikster Y, Shalev SA, Elpeleg O, Ben Zeev B. Heimer G, et al. Among authors: maayan c. Eur J Paediatr Neurol. 2016 Jan;20(1):69-79. doi: 10.1016/j.ejpn.2015.10.003. Epub 2015 Oct 22. Eur J Paediatr Neurol. 2016. PMID: 26542466
97 results