Enza Maria Valente And NotItalie

List of bibliographic references

Number of relevant bibliographic references: 4.

Ident.	Authors (with country if any)	Title
000568	Katja Lohmann [Allemagne] ; Alexander Schmidt ; Arne Schillert ; Susen Winkler ; Alberto Albanese ; Frank Baas ; Anna Rita Bentivoglio ; Friederike Borngr Ber ; Norbert Brüggemann ; Giovanni Defazio ; Francesca Del Sorbo ; Günther Deuschl ; Mark J. Edwards ; Thomas Gasser ; Pilar G Mez-Garre ; Julia Graf ; Justus L. Groen ; Anne Grünewald ; Johann Hagenah ; Claudia Hemmelmann ; Hans-Christian Jabusch ; Ryuji Kaji ; Meike Kasten ; Hideshi Kawakami ; Vladimir S. Kostic ; Maria Liguori ; Pablo Mir ; Alexander Münchau ; Felicia Ricchiuti ; Stefan Schreiber ; Katharina Siegesmund ; Marina Svetel ; Marina A J. Tijssen ; Enza Maria Valente ; Ana Westenberger ; Kirsten E. Zeuner ; Simone Zittel ; Eckart Altenmüller ; Andreas Ziegler ; Christine Klein	Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?
000727	Maja Kojovic [Royaume-Uni] ; Isabel Pareés ; Tania Lampreia ; Karolina Pienczk-Reclawowicz ; Georgia Xiromerisiou ; Ignacio Rubio-Agusti ; Milica Kramberger ; Miryam Carecchio ; Anas M. Alazami ; Francesco Brancati ; Jaroslaw Slawek ; Zvezdan Pirtosek ; Enza Maria Valente ; Fowzan S. Alkuraya ; Mark J. Edwards ; Kailash P. Bhatia	The syndrome of deafness-dystonia: clinical and genetic heterogeneity.
000A34	Miryam Carecchio [Royaume-Uni] ; Monia Magliozzi ; Massimiliano Copetti ; Alessandro Ferraris ; Laura Bernardini ; Monica Bonetti ; Giovanni Defazio ; Mark J. Edwards ; Isabella Torrente ; Fabio Pellegrini ; Cristoforo Comi ; Kailash P. Bhatia ; Enza Maria Valente	Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria.
000D30	Vinko Palada ; Sandra Stiern ; Nicola Glöckle ; Pilar G Mez-Garre ; Fatima Carrillo ; Pablo Mir ; Krzysztof Szczaluba ; Michele Tinazzi ; Domenico Ajena ; Marta Romani ; Enza Maria Valente ; Ulrich Müller ; Peter Bauer ; Olaf Riess ; Thomas Ott ; Kathrin Grundmann	Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.

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