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A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood-onset Cognitive Deficit.
Published in:
Epilepsia (Series 4), 2004, v. 45, n. 3, p. 294, doi. 10.1111/j.0013-9580.2004.33203.x
By:
- Annesi, Grazia;
- Sofia, Vito;
- Gambardella, Antonio;
- Candanio, Innocenza C. Ciro;
- Spadafora, Patrizia;
- Annesi, Ferdinanda;
- Cutuli, Nunzio;
- De Marco, Elvira V.;
- Civitelli, Donatella;
- Carrideo, Sara;
- Tarantino, Patrizia;
- Barone, Rita;
- Zappia, Mario;
- Quattrone, Aldo
Publication type:
Article
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
Published in:
Movement Disorders, 2008, v. 23, n. 3, p. 460, doi. 10.1002/mds.21892
By:
- De Marco, Elvira V.;
- Annesi, Grazia;
- Tarantino, Patrizia;
- Rocca, Francesca E.;
- Provenzano, Giovanni;
- Civitelli, Donatella;
- Cirò Candiano, Innocenza C.;
- Annesi, Ferdinanda;
- Carrideo, Sara;
- Condino, Francesca;
- Nicoletti, Giuseppe;
- Messina, Demetrio;
- Novellino, Fabiana;
- Morelli, Maurizio;
- Quattrone, Aldo
Publication type:
Article
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
Published in:
Movement Disorders, 2006, v. 21, n. 2, p. 252, doi. 10.1002/mds.20681
By:
- Valentino, Paola;
- Annesi, Grazia;
- Cirò Candiano, Innocenza C.;
- Annesi, Ferdinanda;
- Civitelli, Donatella;
- Tarantino, Patrizia;
- Naso, Francesco;
- Spadafora, Patrizia;
- Carrideo, Sara;
- De Marco, Elvira V.;
- Consoli, Domenico;
- Zappia, Mario;
- Gambardella, Antonio;
- Quattrone, Aldo
Publication type:
Article
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease.
Published in:
Movement Disorders, 2000, v. 15, n. 1, p. 120, doi. 10.1002/1531-8257(200001)15:1<120::AID-MDS1019>3.0.CO;2-S
By:
- Oliveri, Rosario L.;
- Annesi, Grazia;
- Zappia, Mario;
- Civitelli, Donatella;
- De Marco, Elvira V.;
- Pasqua, Angela A.;
- Annesi, Ferdinanda;
- Spadafora, Patrizia;
- Gambardella, Antonio;
- Nicoletti, Giuseppe;
- Branca, Damiano;
- Caracciolo, Manuela;
- Aguglia, Umberto;
- Quattrone, Aldo
Publication type:
Article

Found: 4

A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood-onset Cognitive Deficit.

Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.

Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.

The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease.