The University of Siena PhD Course in
Genetics, Oncology and Clinical Medicine


PhD Graduate

Dalila RONDINELLA 

PhD Program years: 2007 - 2011







PUBLICATIONS DURING THE PHD PROGRAM
  1. Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
    Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R, Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B, Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F, Renieri A.
    J Med Genet. 2010 Jan;47(1):49-53. Epub 2009 Jul 2

  2. FOXG1 is responsible for the congenital variant of Rett syndrome.
    Ariani F, Hayek G, Rondinella D, Artuso R, Mencarelli MA, Spanhol-Rosseto A, Pollazzon M, Buoni S, Spiga O, Ricciardi S, Meloni I, Longo I, Mari F, Broccoli V, Zappella M, Renieri A.
    Am J Hum Genet. 2008 Jul;83(1):89-93. Epub 2008 Jun 19.
ABSTRACTS OF CONFERENCE DURING THE PHD PROGRAM
  1. Male Rett Syndrome patient with mosaic MECP2 mutation. (World Rett Syndrome congress, Parigi, Francia, 10-13 ottobre 2008)

  2. Congenital Rett Syndrome Variant (World Rett Syndrome congress, Parigi, Francia, 10-13 ottobre 2008)

  3. FOXG1 is responsible for the Congenital Variant of Rett Syndrome (ASHG 2008, Philadelphia, Pennsylvania, USA, 11-15 novembre 2008)

  4. Il gene FOXG1 è responsabile della variante congenita della sindrome di Rett (Congresso nazionale sigu 2008, Genova, Italia, 23-25 novembre 2008)

  5. Congenital variant of Rett syndrome due to the FOXG1 gene (ESHG 2009, Vienna, Austria, 23-26 maggio 2009)

  6. Diagnostic flow-chart for Rett syndrome (1st European Congress on Rett Syndrome, Milano, Italia, 5-7 giugno 2009.

  7. A novel mild phenotype associated with FOXG1 gene (ESHG 2010, Gothenburg, Sweden, 12-15 giugno 2010) 

ACTIVITY DURING THE PHD PROGRAM

TRAINING PERIOD ABROAD
  • Hosting Institution Name
    Location
    Period dates

  • Hosting Institution Name
    Location
    Period dates