Papers 1985 – 1995

1995 (3)

Curcio F, Mercuri E, De Sensi AM, Bruni AC: La Startle Disease (Iperekplexia): descrizione di un caso clinico. Convivia Medica 1995; 4: 1-5
Foncin JF, Bruni AC, Montesi MP: Detection of Homozygosity by Descent. Eur J Hum Genet 1995; 3: 203-204
Sherrington R, Rogaev E, Liang Y, Rogaeva E, Levesque G, Ikada M, et al.: Cloning of a gene bearing missense mutation in early-onset familial Alzheimer’s disease. Nature 1995; 375: 754-760

1994 (3)

Curcio F, Mercuri E, Falvo V, Bruni AC: Nevo flammeo e convulsioni. Convivia Medica 1994; (6): 1-4
Rainero I, Bergamini L, Bruni AC, Ferini-Strambi L, Foncin JF, Gei G, et al.: A new Italian pedigree with early-onset Alzheimer’s Disease. J Geriatr Psychiatr Neurol 1994; (7): 28-32
Mortilla M, Amaducci L, Bruni AC, Montesi MP, Trubnikov A, DeCataldo S, et al.: Absence of APP713 mutation in Italian and Russian families with schizophrenia. Neurosc Letters 1994; 165:45-47

1993 (2)

Bruni AC, Montesi MP, Rainero I, Ferini-Strambi L, Macciardi F, Pinessi L, et al.: The power of systematic genealogical studies: link between two families with Alzheimer’s Disease. J. Neurol. Sci 1993; 14: 239-244

Rogaev E, Lukiw WJ, Vilarino D, Haines JL, Rogaeva E, Tsuda T, et al. : Analysis of the c-FOS gene on chromosome 14 and the amyloid precursor protein gene in familial Alzheimer’s disease. Neurology 1993; 43: 2275-2279

1992 (5)

Bruni AC: Ricerca storica e genetica molecolare. Il Corriere Calabrese 1992; 1: 91-94

St George-Hyslop PH, Haines JL, Rogaev E, Mortilla M, Vaula G, Pericak-Vance MA, et al.: Genetic evidence for a novel Familial Alzheimer’s Disease locus on chromosome 14. Nature Genetics 1992; (2): 330-334

Vaula G, Mortilla M, Tupler R, Lukiw WJ, Tanzi RE, Nee L, et al.: A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene. Neurosci Lett 1992; 144: 46-48

St George-Hyslop PH, Crapper-McClachlan D, Haines JL, Bruni AC, Foncin JF, Lukiw WJ, et al.: Molecular genetic evidence for etiologic heterogeneity of Alzheimer’s Disease. Heterogeneity of Alzheimer’s Disease. In F.Boller, F.Forette, Z. Khachaturian, (eds). 1992; 88-95

Bruni AC, Montesi MP, Salmon D, Perre J, EI Hachimi KH, Foncin JF: Alzheimer’s disease: a model from the quantitative study of a large kindred. J Geriatr Psychiatry Neurol 1992; 3(5): 126-131

1991 (3)

Bruni AC, Montesi MP, Gei G, Rainero I, Ermio C, Foncin JF: The common origin of Familial Alzheimer’s Disease in Calabria. Alzheimer’s Disease: Basic Mechanisms, Diagnosis and Therapeutic Strategies. Iqbal, McLachlan,Winblad,Wisniewski….. (eds). 1991; 58: 451-455

Bergamini L, Pinessi L, Rainero I, Brunetti E, Cerrato P, Cosentino L, et al.: Familial Alzheimer’s Disease: evidences for clinical and genetic heterogeneity. Acta Neurologica 1991; 13: 534-537

Bruni AC, Montesi MP: Phenotypic heterogeneity in Alzheimer’s Disease. Acta Neurologica 1991; 13: 527-533

1990 (2)

Bruni AC, Montesi MP: Genetic Engineering. Alzheimer’s Disease:Treatment and Lon-Term Management. L.Cummings, B.Miller-Marcel Dekker (eds). 1990; (21): 303-321

St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, et al.: Genetic linkage studies suggest that Alzheimer’s is not a single homogeneous disorder. Nature 1990; 347: 194-197

1989 (3)

St George-Hyslop PH, Polinsky R, Tanzi RE, Haines JL, Nee L, Growdon J et al.: Familial and Sporadic Alzheimer’s Disease: Molecular Genetic Approaches. Familial Alzheimer’s Disease: Molecular Genetics and Clinical Perspectives. Miner,Richter,Blass,Valentine,Winters-Mi (eds). 1989;

Foncin JF, Salmon D, Bruni AC: Notes on the Methods for the Study of Kindreds with Familial Alzheimer’s Disease. Familial Alzheimer’s Disease Molecular Genetics and Clinical Perspectives. G.D. Mininer – Marcel Dekker (eds). 1989; 45-53

Bruni AC, Montesi MP, Manfredi R, Gei G, Ermio C, Caruso G: Un esteso ceppo con probabile Psicosi Maniaco Depressiva. Rivista Italiana di Psichiatria 1989; 4(24): 175-181

1988 (4)

Foncin JF, Salmon D, Bruni AC: Extended Kindreds a a Model for Research on Alzheimer’s Disease. Genetics and Alzheimer’s Disease. Fondation Ipsen (eds). 1988; : 13-30
St George-Hyslop PH, Farrer LA, Haines JL, Myers R, Polinsky R, Nee L et al.: Molecular Genetic Strategies in Familial Alzheimer’s Disease: Theoretical and Practical Considerations. Genetics and Alzheimer’s Disease. Fondation Ipsen (eds). 1988; : 109-115
Gei G, Foncin JF, Bruni AC: La genealogia come metodo di indagine: unificazione di due famiglie affette da Malattia di A Fidia Biomedical Information 1988; 8: 8-11
St George-Hyslop PH, Haines JL, Farrer LA, Tanzi RE, Hobbs WJ, Polinsky R, et al: Molecular genetics of autosomal dominant familial Alzheimer’s Disease. Current Communications in Molecular Biology: Molecular Biology of Alzheimer’s Disease. C.E.Finch, P.Davies (eds). 1988; : 159-168

1987 (3)

St George-Hyslop PH, Polinsky R, Nee L, Tanzi RE, Haines JL, Conneally PM, et al.: Search for Familial Alzheimer’s Disease Gene. Alzheimer’s Disease: Advances in Basic Research and Therapies. Wurtman,Cork, Growdon (eds). 1987; 25-37
St George-Hyslop PH, Tanzi RE, Polinsky R, Haines JL, Never L, Nee L, et al.: The genetic defect causing Familial Alzheimer’s Disease maps on chromosome 21. Science 1987; 235: 885-890
St George-Hyslop PH, Tanzi RE, Polinsky R, Never L, Pollen D, Drachman D et al.: Absence of duplication of Chromosome 21 Genes in Familial and Sporadic Alzheimer’s Disease. Science 1987; 238: 664-666

1986 (1)

Foncin JF, Salmon D, Bruni AC: Genetics of Alzheimer’s disease:a large kindred with apparent Mendelian transmission; possible implication for a linkage study. New Concept in Alzheimer’s Disease. M.Briley, A.Kato, M.Weber MacMillian eds (eds). 1986; 242-256

1985 (1)

Foncin JF, Salmon D, Supino-Viterbo V, Feldman RG, Macchi G, Marotti P, et al.: Demence presenile d’Alzheimer transmise dans une famille etendue. Neurol 1985; (141): 194-202