Elena Cellini; Silvia Piacentini; Benedetta Nacmias; Paolo Forleo; Andrea Tedde; Silvia Bagnoli; Monica Ciantelli; Sandro Sorbi (2002). A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.. ARCHIVES OF NEUROLOGY, vol. 59, pp. 1952-1953, ISSN:0003-9942

  B. Nacmias;A. Tedde;P. Forleo;S. Piacentini;S. Latorraca;B.M. Guarnieri;L. Ortenzi;A. Bartoli;C. Petruzzi;A. Serio;S. Sorbi (2001). Psychosis, serotonin receptor polymorphism and Alzheimer's disease. ARCHIVES OF GERONTOLOGY AND GERIATRICS, vol. 33, pp. 279-283, ISSN:0167-4943 DOI  

  Sandro Sorbi; Benedetta Nacmias; Stefania Latorraca; Paolo Forleo; Silvia Piacentini (2001). La malattia di Alzheimer. LE SCIENZE - QUADERNI, vol. 119, pp. 22-29, ISSN:1124-9285

  Nacmias B.; Tedde A.; Cellini E.; Forleo P.; Orlacchio A.; Guarnieri B.M.; Petruzzi C.; D’Andrea F.; Serio S.; Sorbi S. (2001). A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease. NEUROSCIENCE LETTERS, vol. 299, pp. 9-12, ISSN:0304-3940

  S. Sorbi; P. Forleo; C. Fani; S. Piacentini (2000). Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia.. CLINICAL NEUROPHARMACOLOGY, vol. 23, pp. 114-118, ISSN:0362-5664

  S. Sorbi; P. Forleo; E. Cellini; B. Nacmias; A. Tedde; S. Piacentini (2000). Genetic Analysis of familial and sporadic cases of spinocerebellar ataxias in Italian patients. In: 5th Congress of the european Society for clinical Farmacology, Opatja (Croatia), May 17-21, pp. 109-114.

  S. Sorbi; P. Forleo; E. Cellini; S. Piacentini; A. Serio; B. Guarnieri; C. Petruzzi (2000). Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat.. ARCHIVES OF NEUROLOGY, vol. 57, pp. 1380-1382, ISSN:0003-9942

  B. Nacmias; G. Marcon; A. Tedde; P. Forleo; S. Latorraca; S. Piacentini; L. Amaducci; S. Sorbi (1998). Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease.. NEUROSCIENCE LETTERS, vol. 244, pp. 85-88, ISSN:0304-3940

  S. Sorbi; B. Nacmias; P. Forleo (1998). Molecular genetics of Alzheimer's disease.. AGING, vol. 10, pp. 157-..., ISSN:0394-9532

  S. Sorbi; B. Nacmias; A. Tedde; S. Latorraca; P. Forleo; B. M. Guarnieri; C. Petruzzi; E. Daneluzzo; L. Ortenzi; S. Piacentini; L. Amaducci (1998). No implication of apolipoprotein E polymorphism in Italian schizophrenic patients.. NEUROSCIENCE LETTERS, vol. 244, pp. 118-120, ISSN:0304-3940

  S. Sorbi; B. Nacmias; A. Tedde; P. Forleo; S. Piacentini; S. Latorraca; L. Amaducci (1997). Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease.. NEUROSCIENCE LETTERS, vol. 222, pp. 132-134, ISSN:0304-3940

  S. Sorbi; P. Forleo; B. Nacmias (1997). Alzheimer's disease: phenotypes and genotypes.. FUNCTIONAL NEUROLOGY, vol. 12, pp. 147-151, ISSN:0393-5264

  M. Marinoni; A. Ginanneschi; P. Forleo; L. Amaducci (1997). Technical limits in transcranial Doppler recording: inadequate acoustic windows.. ULTRASOUND IN MEDICINE AND BIOLOGY, vol. 23, pp. 1275-1277, ISSN:0301-5629

  Sorbi S.; Nacmias B.; Repice A.; Forleo P.; Latorraca S.; Tedde A.; Larosa M (1996). Genetica della malattia di Alzheimer. GIORNALE DI GERONTOLOGIA, vol. 44, pp. 683-686, ISSN:0017-0305

  Sandro Sorbi;Benedetta Nacmias;Paolo Forleo;Silvia Piacentini;Luigi Amaducci;Leandro Provinciali (1993). APP717 and Alzheimer's disease in Italy. NATURE GENETICS, vol. 4, pp. 10-10, ISSN:1061-4036 DOI  

  Sorbi S.; Tesco G.; Nacmias B.; Mortilla M.; Forleo P.; Latorraca S.; Piersanti P.; Piacentini S.; Amaducci L. (1992). Absence of APP717 mutation in Italian FAD families. INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY, vol. 7, pp. 304-304, ISSN:0885-6230

  S. Sorbi;B. Nacmias;M. Mortilla;S. Piacentini;G. Marcon;P. Piersanti;C. Ballerini;P. Forleo;S. Latorraca;G. Tesco;L. Amaducci (1991). Linkage Analysis in Italian Pedigrees with Autosomal Dominant Familial Alzheimer’s DiseaseCerebral Ischemia and Dementia. In: Hartmann A., Kuschnisky W., Hoyer S. Cerebral Ischemia and Dementia, pp. 185-186, Heidelberg: Springer, ISBN:9783642762086. DOI