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Page 1
Guidelines for reporting clinical features in cases with MECP2 mutations.
Kerr AM, Nomura Y, Armstrong D, Anvret M, Belichenko PV, Budden S, Cass H, Christodoulou J, Clarke A, Ellaway C, d'Esposito M, Francke U, Hulten M, Julu P, Leonard H, Naidu S, Schanen C, Webb T, Engerstrom IW, Yamashita Y, Segawa M. Kerr AM, et al. Among authors: julu p. Brain Dev. 2001 Jul;23(4):208-11. doi: 10.1016/s0387-7604(01)00193-0. Brain Dev. 2001. PMID: 11376997
Treating hypoxia in a feeble breather with Rett syndrome.
Julu PO, Witt Engerström I, Hansen S, Apartopoulos F, Engerström B; ESSRA group. Julu PO, et al. Brain Dev. 2013 Mar;35(3):270-3. doi: 10.1016/j.braindev.2012.04.004. Epub 2012 May 20. Brain Dev. 2013. PMID: 22617859
Variant of Rett syndrome and CDKL5 gene: clinical and autonomic description of 10 cases.
Pini G, Bigoni S, Engerström IW, Calabrese O, Felloni B, Scusa MF, Di Marco P, Borelli P, Bonuccelli U, Julu PO, Nielsen JB, Morin B, Hansen S, Gobbi G, Visconti P, Pintaudi M, Edvige V, Romanelli A, Bianchi F, Casarano M, Battini R, Cioni G, Ariani F, Renieri A, Benincasa A, Delamont RS, Zappella M; ESRRA group. Pini G, et al. Among authors: julu po. Neuropediatrics. 2012 Feb;43(1):37-43. doi: 10.1055/s-0032-1308856. Epub 2012 Mar 19. Neuropediatrics. 2012. PMID: 22430159
Normal reactions to orthostatic stress in Rett syndrome.
Larsson G, Julu PO, Witt Engerström I, Sandlund M, Lindström B. Larsson G, et al. Res Dev Disabil. 2013 Jun;34(6):1897-905. doi: 10.1016/j.ridd.2013.02.027. Epub 2013 Apr 11. Res Dev Disabil. 2013. PMID: 23584170
48 results