PALMUCCI, Laura Maria
PALMUCCI, Laura Maria
Dip. NEUROSCIENZE (attivo dal 01/01/1900 al 30/04/2013)
A defective L_MAG (large myelin-associated glycoprotein) is responsible for an adult-onset autosomal dominant orthochromatic leukodystrophy
2004-01-01 Giordana MT; Palmucci L; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Multidiscliplinary approach to cause and pathogenesis of an adult onset autosomal dominant orthochromatic leukodystrophy
2005-01-01 MT Giordana; L Palmucci; C D’Agostino; M Piccinini; A Brusco; MT Rinaudo
Muscular involvement in Whipple's disease with gastrointestinal sparing
2010-01-01 Vercelli, L.; Palmucci, L.; Vittonatto, E.; Chiadò-Piat, L.; Fenollar, F.; Mongini, T.
Myelin involvement in Niemann-Pick disease type A
2007-01-01 B Votta; M. Piccinini; S Grifoni; L Palmucci; A Heape; B Buccinnà; MT Rinaudo; MT Giordana
Myelin-associated glycoprotein is altered in a familial orthochromatic leukodystrophy
2004-01-01 Giordana MT; Palmucci L; Leombruni S; Vaula G; D'Agostino C; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Myelin-associated glycoprotein is defective in a familail orthochromatic leukodystrophy
2004-01-01 Giordana MT; Palmucci L; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Myelin-associated glycoprotein is defective in a familial orthochromatic leukodystrophy
2004-01-01 Giordana MT; Palmucci L; Piccinini M; Ramondetti C; Rinaudo MT
X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families.
2003-01-01 Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L.