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Growth hormone treatment in children with familial dysautonomia.
Kamboj MK, Axelrod FB, David R, Geffner ME, Novogroder M, Oberfield SE, Turco JH, Maayan C, Kohn B. Kamboj MK, et al. Among authors: maayan c. J Pediatr. 2004 Jan;144(1):63-7. doi: 10.1016/j.jpeds.2003.10.065. J Pediatr. 2004. PMID: 14722520
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
Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation.
Lefler S, Cohen MA, Kantor G, Cheishvili D, Even A, Birger A, Turetsky T, Gil Y, Even-Ram S, Aizenman E, Bashir N, Maayan C, Razin A, Reubinoff BE, Weil M. Lefler S, et al. Among authors: maayan c. PLoS One. 2015 Oct 5;10(10):e0138807. doi: 10.1371/journal.pone.0138807. eCollection 2015. PLoS One. 2015. PMID: 26437462 Free PMC article.
Lack of migraine in headaches of familial dysautonomia patients.
Shihman B, Steiner I, Yovchev I, Maayan C. Shihman B, et al. Among authors: maayan c. J Neural Transm (Vienna). 2013 Mar;120(3):399-402. doi: 10.1007/s00702-012-0903-y. Epub 2012 Oct 9. J Neural Transm (Vienna). 2013. PMID: 23053351
94 results