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Clinical correlations in 16 patients with total or partial laminin alpha2 deficiency characterized using antibodies against 2 fragments of the protein.

• Lucia Ovidia Morandi, Claudia Di Blasi, +9 authors Marina Mora
• Archives of neurology
• 1999

BACKGROUND Many patients with classic congenital muscular dystrophy have been found to have partial or total deficiency of the alpha2 chain of laminin 2 (merosin). This deficiency has mostly been… (More)

Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression

• Massimo Lanfossi, Francesca Cozzi, +7 authors Marina Mora
• Acta Neuropathologica
• 1999

Canine X-linked muscular dystrophy (CXMD) is genetically homologous to Duchenne muscular dystrophy and shares the severe myopathy and lethal clinical development of the human disease. We used… (More)

Concomitant deficiency of β- and γ-sarcoglycans in 20 α-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects

• Rita Barresi, Valeria Confalonieri, +11 authors Lucia Morandi
• Acta Neuropathologica
• 1997

We have investigated the expression, using immunohistochemistry, of β- and γ-sarcoglycans in the muscles of 20 patients in whom previous screening had revealed a deficiency of α-sarcoglycan. α-, β-… (More)

Concomitant deficiency of beta- and gamma-sarcoglycans in 20 alpha-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects.

• Rita Barresi, Valeria Confalonieri, +11 authors Lucia Morandi
• Acta neuropathologica
• 1997

We have investigated the expression, using immunohistochemistry, of beta- and gamma-sarcoglycans in the muscles of 20 patients in whom previous screening had revealed a deficiency of… (More)

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