Seminars


- 23/5/2002 X-linked Mental Retardation Genes: Why Is The Easy Part  So Hard? (C Schwartz from Greenwood Genetic Center - JC Self Research Institute, South Carolina, USA)

 

- 19/05/2006 Rett syndrome and related disorders (T. Ozçelik, from Bilkent University, Ankara, Turkey)

 

- 21/12/2007 Tight regulation of the alternative splicing of myelin proteolipid protein is necessary for brain development and function: evidence from human disease and a novel mouse model (F. Cambi from University of Kentucky, Lexington, USA)

 

-  07/01/2008 Syndrome families: genotypes and phenotypes (H. Brunner from University, Nijmegen, The Netherlands)


-  08/01/2008 Making a clinical diagnosis (H. Brunner)


14/07/2008 Il network ESDN (European Skeletal Dysplasia Network) come esempio di biobanca virtuale e il suo ruolo nella ricerca sulle displasie scheletriche (A. Superti-Furga from Universität Freiburg, Freiburg, Germany)


- 14/07/2008 Skeletal disorders: classification (A. Superti-Furga,)


- 15/07/2008 Letal Skeletal Dysplasia (A. Superti-Furga,)


- 16/07/2008 Skeletal disorders: differential diagnosis by X-Ray (A. Superti-Furga,)


- 17/07/2008 Osteochondrodyplasias (A. Superti-Furga)


- 18/07/2008 Osteochondrodyplasias (A. Superti-Furga)


- 12/03/2008 Aspetti legislativi e di etica nelle biobanche (A. Superti-Furga)


- 11/03/2008 Cosa sono le biobanche - organizzazione delle biobanche e ruolo del laboratorio (A. Superti-Furga)


- 09/03/2008 Aspetti della ricerca biomedica e clinica legati a materiali biologici (A. Superti-Furga)


- 12/03/2008 Organizzazione delle biobanche e ruolo del laboratorio (A. Superti-Furga)


- 14/07/2008 A virtual image biobank and its diagnostic use for genetic skeletal disorders (A. Superti-Furga)


- 15/07/2008 Differential diagnosis of skeletal dysplasias in the fetus and newborn (A. Superti-Furga)


- 16/07/2008 Molecular nosology and gene families in genetic disorders of the skeleton (A. Superti-Furga,)


- 16/07/2008 ESDN network (S. Unger from Universität Freiburg, Freiburg, Germany)


- 29/12/2008 Le atassie cerebellari cerebellari: dalla clinica alla genetica (F. Cambi from University of Kentucky, Lexington, USA)


- 30/09/2009 Origins of mental retardation across species: clinical, molecular and functional characterizazion of Euchromatin Histone Methyltransferase 1 mutations (H. Van Bokhoven Radboud University, Nijmegen, The Netherlands)


- 22/07/2009 Clinical Features and Molecular Genetics of Hereditary Spinocerebellar Ataxia (F. Cambi, from University of Kentucky, Lexington, USA)