PALMUCCI, Laura Maria
PALMUCCI, Laura Maria
Dip. NEUROSCIENZE (attivo dal 01/01/1900 al 30/04/2013)
[A comparison of histochemical features of some specific phosphatases in progressive muscular dystrophy, in neurogenic myopathies in man and in the denervated rat muscle (author's transl)]
1974-01-01 SCHIFFER D ;GIORDANA MT ;PALMUCCI L ;ROLFO F ;ARDIZZONE G
[Endo- and perimysial connective tissue in primary and secondary myopathies. Histochemical studies]
1976-01-01 GIORDANA MT ;PALMUCCI L ;SCHIFFER D
[Individualization of carriers of Duchenne's muscular dystrophy by quantitative methods]
1986-01-01 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;LEONE M ;GAGNOR E ;POLLO B ;FERRUA R ;SCHIFFER D
[Malignant intracranial and spinal lymphoma and sarcoma: review of our cases from the year 1960 to 1974]
1974-01-01 CROVERI G ;SCHIFFER D ;GIORDANA MT ;PALMUCCI L
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention]
1980-01-01 DORIGUZZI C; BERTOLOTTO A; MONGINI T; MONNIER C; PALMUCCI L; VERZÉ L; SCHIFFER D
[Recent acquisitions and prospects of research on Steinert's myotonic dystrophy. Histochemical and ultrastructural data]
1977-01-01 SCHIFFER D ;GIORDANA MT ;PALMUCCI L ;MONGA G ;MOLLO F
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
A new method for myofibrillar Ca++-ATPase reaction based on the use of metachromatic dyes: its advantages in muscle fibre typing.
1983-01-01 DORIGUZZI C ;MONGINI T ;PALMUCCI L ;SCHIFFER D
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency
2000-01-01 SILVESTRI G; MONGINI T; ODOARDI F; MODONI A; DEROSA G; DORIGUZZI C; L. PALMUCCI; TONALI P; SERVIDEI S
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene
2000-01-01 PIRULLI D; ZEZLINA S; VATTA L; DI STEFANO P; BONIOTTO M; G. TARONE; MONGINI T; UGO I; PALMUCCI L; AMOROSO A; CROVELLA S
Abnormal ubiquitination of axons in normally myelinated white matter in multiple sclerosis brain.
2002-01-01 M. GIORDANA; RICHIARDI P; TREVISAN E; BOGHI A; PALMUCCI L
Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophy.
1992-01-01 MONGINI T ;PALMUCCI L ;DORIGUZZI C ;CHIADOÒ-PIAT L ;RESTAGNO G
Adult onset nemaline myopathy: a distinct nosologic entity?
1993-01-01 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria.
2002-01-01 MONGINI T; DORIGUZZI C; BOSONE I; CHIADÒ-PIAT L; HOFFMAN EP; L. PALMUCCI
Analysis of some factors effecting survival in malignant gliomas.
1979-01-01 SCHIFFER D; CAVICCHIOLI D; GIORDANA MT; PALMUCCI L; PIAZZA A
Atypical histopathological changes in muscle biopsies from two patients with facioscapulohumeral muscular dystrophy
2002-01-01 BOSONE I; MONGINI T; DORIGUZZI C; VERCELLI L; TUPLER R; MORTARA P; L. PALMUCCI
Body building and myoglobinuria: report of three cases.
1988-01-01 DORIGUZZI C; L. PALMUCCI; MONGINI T; ARNAUDO E; BET L; BRESOLIN N
Body building and rhabdomyolysis.
1990-01-01 DORIGUZZI C; L. PALMUCCI; MONGINI T
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected child.
1995-01-01 RESTAGNO G ;FERRONE M ;DORIGUZZI C ;PALMUCCI L ;MONGINI T ;CARBONARA A
Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter.
1978-01-01 PALMUCCI L ;SCHIFFER D ;MONGA G ;MOLLO F ;DE MARCHI M