PALMUCCI, Laura Maria

PALMUCCI, Laura Maria  

Dip. NEUROSCIENZE (attivo dal 01/01/1900 al 30/04/2013)  

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Risultati 1 - 8 di 8 (tempo di esecuzione: 0.036 secondi).
Titolo Data di pubblicazione Autore(i) File
A defective L_MAG (large myelin-associated glycoprotein) is responsible for an adult-onset autosomal dominant orthochromatic leukodystrophy 2004 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 MT Giordana; L Palmucci; C D’Agostino; M Piccinini; A Brusco; MT Rinaudo
Muscular involvement in Whipple's disease with gastrointestinal sparing 2010 Vercelli, L.; Palmucci, L.; Vittonatto, E.; Chiadò-Piat, L.; Fenollar, F.; Mongini, T.
Myelin involvement in Niemann-Pick disease type A 2007 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 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 Giordana MT; Palmucci L; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Myelin-associated glycoprotein is defective in a familial orthochromatic leukodystrophy 2004 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 Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L.