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Author/Creator Luca, Alessandro De

1. F02 A cluster of HD in italy with several subjects carrying cag expansion homozygousity in different generations and genetic risk over 50%. (September 2018)

Authors:
Squitieri, Ferdinando; Dema, Maria Giovanna; Borrelli, Cristiana; Consoli, Federica; Luca, Alessandro De; Migliore, Simone
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 89(2018)Supplement 1
Page Start:
A41
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. JAG1 Mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot. Issue 12 (16th August 2013)

Authors:
Digilio, Maria Cristina; Luca, Alessandro De; Lepri, Francesca; Guida, Valentina; Ferese, Rosangela; Dentici, Maria Lisa; Angioni, Adriano; Marino, Bruno; Dallapiccola, Bruno
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 12(2013:Dec.)
Page Start:
3133
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. JAG1 Mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot. Issue 12 (16th August 2013)

Authors:
Digilio, Maria Cristina; Luca, Alessandro De; Lepri, Francesca; Guida, Valentina; Ferese, Rosangela; Dentici, Maria Lisa; Angioni, Adriano; Marino, Bruno; Dallapiccola, Bruno
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 12(2013:Dec.)
Page Start:
3133
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗