Pubblicazioni scientifiche indicizzate in PubMed: dalla 101 alla 107

 

101. Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome.

 

Marschik PB, Kaufmann WE, Einspieler C, Bartl-Pokorny KD, Wolin T, Pini G, Budimirovic DB,Zappella M, Sigafoos J.

Res Dev Disabil. 2012 Jun 12;33(6):1749-1756. [Epub ahead of print]

PMID:
 
22699249
 
[PubMed - as supplied by publisher]

Artuso R, Papa FT, Grillo E, Mucciolo M, Yasui DH, Dunaway KW, Disciglio V, Mencarelli MA, Pollazzon M, Zappella M, Hayek G, Mari F, Renieri A, Lasalle JM, Ariani F.

J Hum Genet. 2012 May;57(5):342-4. doi: 10.1038/jhg.2012.30. No abstract available.

PMID:
 
22627645
 
[PubMed - in process]
103.

Reversible autism and intellectual disability in children.

Zappella M.

Am J Med Genet C Semin Med Genet. 2012 May 15;160C(2):111-7. doi: 10.1002/ajmg.c.31328. Epub 2012 Apr 12.

PMID:
 
22499541
 
[PubMed - in process]
104.

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, ZappellaM; ESRRA group.

Neuropediatrics. 2012 Feb;43(1):37-43. Epub 2012 Mar 19.

PMID:
 
22430159
 
[PubMed - in process]
105.

Rett networked database: An integrated clinical and genetic network of rett syndrome databases.

Grillo E, Villard L, Clarke A, Ben Zeev B, Pineda M, Bahi-Buisson N, Hryniewiecka-Jaworska A, Bienvenu T, Armstrong J, Martinez AR, Mari F, Veneselli E, Russo S, Vignoli A, Pini G, Djuric M, Bisgaard AM, Mejaški Bošnjak V, Polgár N, Cogliati F, Ravn K, Pintaudi M, Melegh B, Craiu D, Djukic A, Renieri A.

Hum Mutat. 2012 Jul;33(7):1031-6. doi: 10.1002/humu.22072. Epub 2012 Apr 13.

PMID:
 
22415763
 
[PubMed - in process]
106.

Early speech-language development in females with Rett syndrome: focusing on the preserved speech variant.

Marschik PB, Pini G, Bartl-Pokorny KD, Duckworth M, Gugatschka M, Vollmann R, Zappella M, Einspieler C.

Dev Med Child Neurol. 2012 May;54(5):451-6. doi: 10.1111/j.1469-8749.2012.04123.x. Epub 2012 Feb 21.

PMID:
 
22348320
 
[PubMed - indexed for MEDLINE]
107.

Investigation of modifier genes within copy number variations in Rett syndrome.

Artuso R, Papa FT, Grillo E, Mucciolo M, Yasui DH, Dunaway KW, Disciglio V, Mencarelli MA, Pollazzon M, Zappella M, Hayek G, Mari F, Renieri A, Lasalle JM, Ariani F.

J Hum Genet. 2011 Jul;56(7):508-15. doi: 10.1038/jhg.2011.50. Epub 2011 May 19.

PMID:
 
21593744
 
[PubMed - indexed for MEDLINE] 
Free PMC Article