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Publikováno v:
Neurological Sciences. Oct2002, Vol. 23 Issue 4, p145. 7p.
Autor:
Vianello, M, Vitaliani, R, Pezzani, R, Nicolao, P, Betterle, C, Keir, G, Thompson, E.J, Tavolato, B, Scaravilli, F, Giometto, B *
Publikováno v:
In Journal of the Neurological Sciences 2004 220(1):29-36
Autor:
Avalos, Bryant1 (AUTHOR) bavalosleyva@health.ucsd.edu, Kulbe, Jacqueline R.1 (AUTHOR) jkulbe@health.ucsd.edu, Ford, Mary K.1 (AUTHOR) mkford@health.ucsd.edu, Laird, Anna Elizabeth1 (AUTHOR) alaird@health.ucsd.edu, Walter, Kyle1 (AUTHOR) kcwalter24@gmail.com, Mante, Michael2 (AUTHOR) mm_281@usc.edu, Florio, Jazmin B.2 (AUTHOR) jf_385@usc.edu, Boustani, Ali1 (AUTHOR) aboustani@health.ucsd.edu, Chaillon, Antoine3 (AUTHOR) achaillon@health.ucsd.edu, Schlachetzki, Johannes C. M.4 (AUTHOR) jschlachetzki@health.ucsd.edu, Sundermann, Erin E.1 (AUTHOR) esundermann@health.ucsd.edu, Volsky, David J.5,6 (AUTHOR) david.volsky@mssm.edu, Rissman, Robert A.2 (AUTHOR) r.rissman@usc.edu, Ellis, Ronald J.1,4 (AUTHOR) roellis@health.ucsd.edu, Letendre, Scott L.1,3 (AUTHOR) sletendre@ucsd.edu, Iudicello, Jennifer1 (AUTHOR) jiudicello@health.ucsd.edu, Fields, Jerel Adam1 (AUTHOR) jafields@health.ucsd.edu
Publikováno v:
Viruses (1999-4915). Oct2024, Vol. 16 Issue 10, p1509. 27p.
Autor:
Zuliani, L, Vitaliani, R, Zoccarato, M, Spinazzi, M, Argentiero, V, Dainese, F, Gigli, Gl, Inzitari, D, Tavolato, B, Vincent, A, Giometto, B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cdd9541ce673f8079ffe9c27ba4c1084
https://hdl.handle.net/11368/3002562
https://hdl.handle.net/11368/3002562
Autor:
Nicolao P 1, 2, Carella M2, 7, Giometto B 1, Tavolato B 1, Cattin R 2, Giovannucci-Uzielli ML 3, Vacca M 4, Della Regione F 4, Piva S 5, Bortoluzzi S 5, Gasparini P 6.
Publikováno v:
Human mutation 18 (2001): 132–140.
info:cnr-pdr/source/autori:Nicolao P 1,2, Carella M2,7, Giometto B 1, Tavolato B 1, Cattin R 2, Giovannucci-Uzielli ML 3, Vacca M 4, Della Regione F 4, Piva S 5, Bortoluzzi S 5, Gasparini P 6./titolo:DHPLC analysis of the MECP2 gene in Italian Rett patients/doi:/rivista:Human mutation/anno:2001/pagina_da:132/pagina_a:140/intervallo_pagine:132–140/volume:18
info:cnr-pdr/source/autori:Nicolao P 1,2, Carella M2,7, Giometto B 1, Tavolato B 1, Cattin R 2, Giovannucci-Uzielli ML 3, Vacca M 4, Della Regione F 4, Piva S 5, Bortoluzzi S 5, Gasparini P 6./titolo:DHPLC analysis of the MECP2 gene in Italian Rett patients/doi:/rivista:Human mutation/anno:2001/pagina_da:132/pagina_a:140/intervallo_pagine:132–140/volume:18
Rett Syndrome (RTT) is an X-linked dominant neurodevelopmental disorder, which almost exclusively affects girls, with an estimated prevalence of one in 10,000-15,000 female births. Mutations in the methyl CpG binding protein 2 gene (MECP2) have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::548f2ca5748fafec94b0ae769f8306fb
https://publications.cnr.it/doc/26644
https://publications.cnr.it/doc/26644