A rapid method to isolate (GT)n repeats from yeast artificial chromosomes.

Por Pandolfo, M
Publicado em 1992

A Pvu II RFLP in the human ADH3 gene.

Por Pandolfo, M, Smith, M
Publicado em 1988

An anonymous DNA probe (LAMP 92) detects a Pvu II polymorphism on human chromosome 9 [D9S29]

Por Pandolfo, M, Wagner, C, Smith, M
Publicado em 1988

A TaqI RFLP in the locus D9S29 on human chromosome 9.

Por Weitnauer, L, Antonelli, A, Pandolfo, M
Publicado em 1989

Clinical, molecular, and PET study of a case of aceruloplasminaemia presenting with focal cranial dyskinesia

Por Haemers, I, Kono, S, Goldman, S, Gitlin, J, Pandolfo, M
Publicado em 2004

Single stranded DNA binding proteins derive from hnRNP proteins by proteolysis in mammalian cells.

Por Pandolfo, M, Valentini, O, Biamonti, G, Morandi, C, Riva, S
Publicado em 1985

Mammalian single-stranded DNA binding proteins and heterogeneous nuclear RNA proteins have common antigenic determinants.

Por Valentini, O, Biamonti, G, Pandolfo, M, Morandi, C, Riva, S
Publicado em 1985

Late onset MLD with normal nerve conduction associated with two novel missense mutations in the ASA gene

Por Gallo, S, Randi, D, Bertelli, M, Salviati, A., Pandolfo, M
Publicado em 2004

A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.

Por Lorenzetti, D, Pareyson, D, Sghirlanzoni, A, Roa, B B, Abbas, N E, Pandolfo, M, Di Donato, S, Lupski, J R
Publicado em 1995

Mammalian single-stranded DNA binding protein UP I is derived from the hnRNP core protein A1.

Por Riva, S, Morandi, C, Tsoulfas, P, Pandolfo, M, Biamonti, G, Merrill, B, Williams, K R, Multhaup, G, Beyreuther, K, Werr, H
Publicado em 1986

Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.

Por Elsea, S H, Juyal, R C, Jiralerspong, S, Finucane, B M, Pandolfo, M, Greenberg, F, Baldini, A, Stover, P, Patel, P I
Publicado em 1995

A SYSTEMATIC REVIEW OF THE LITERATURE CONCERNING THE RELATIONSHIP BETWEEN OBESITY AND MORTALITY IN THE ELDERLY

Por DONINI, L. M., SAVINA, C., GENNARO, E., DE FELICE, M. R., ROSANO, A., PANDOLFO, M. M., BALZO, V. DEL, CANNELLA, C., RITZ, P., CHUMLEA, WM. C.
Publicado em 2012

Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

Por Matilla-Dueñas, A., Ashizawa, T., Brice, A., Magri, S., McFarland, K. N., Pandolfo, M., Pulst, S. M., Riess, O., Rubinsztein, D. C., Schmidt, J., Schmidt, T., Scoles, D. R., Stevanin, G., Taroni, F., Underwood, B. R., Sánchez, I.
Publicado em 2014

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: A 2-year follow-up study

Por Jacobi, H., Bauer, P., Giunti, P., Labrum, R., Sweeney, M.G., Charles, P., Dürr, A., Marelli, C., Globas, C., Linnemann, C., Schöls, L., Rakowicz, M., Rola, R., Zdzienicka, E., Schmitz-Hübsch, T., Fancellu, R., Mariotti, C., Tomasello, C., Baliko, L., Melegh, B., Filla, A., Rinaldi, C., van de Warrenburg, B.P., Verstappen, C.C.P., Szymanski, S., Berciano, J., Infante, J., Timmann, D., Boesch, S., Hering, S., Depondt, C., Pandolfo, M., Kang, J.-S., Ratzka, S., Schulz, J., Tezenas du Montcel, S., Klockgether, T.
Publicado em 2011