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Results: 1-10 |
Results: 10

Authors: PRELLE A COMI GP TANCREDI L RIGOLETTO C CISCATO P FORTUNATO F NESTI S SCIACCO M ROBOTTI M BAZZI P FELISARI G MOGGIO M SCARLATO G
Citation: A. Prelle et al., SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS, Acta Neuropathologica, 96(5), 1998, pp. 509-514

Authors: PRELLE A COMI GP RIGOLETTO C TURCONI A FELISARI G CISCATO P FORTUNATO F MESSINA S BRESOLIN N MORA M MOGGIO M SCARLATO G
Citation: A. Prelle et al., AN ATYPICAL CASE OF PARTIAL MEROSIN DEFICIENCY CONGENITAL MUSCULAR-DYSTROPHY, Journal of neurology, 244(6), 1997, pp. 391-395

Authors: MARINO C LORUSSO ML MOLTENI M RIGOLETTO C SMERALDI E
Citation: C. Marino et al., ASSOCIATION STUDY USING THE HAPLOTYPE RELATIVE RISK METHOD BETWEEN THE DYSLEXIC COMPLEX PHENOTYPES AND POLYMORPHISMS AT THE DRD4 LOCUS, American journal of medical genetics, 74(6), 1997, pp. 626-627

Authors: RIGOLETTO C MARINO C LORUSSO ML RADAELLI L MOLTENI M
Citation: C. Rigoletto et al., AN ASSOCIATION STUDY BETWEEN BORDERLINE INTELLECTUAL-FUNCTIONING MENTAL DEFICIENCY DURING DEVELOPMENTAL PERIOD AND THE DOPAMINE-RECEPTOR GENE DRD4 USING HAPLOTYPE RELATIVE RISK, American journal of medical genetics, 74(6), 1997, pp. 628-628

Authors: PRELLE A TANCREDI L COMI GP RIGOLETTO C CISCATO P FORTUNATO F FELISARI G MOGGIO M SCARLATO G
Citation: A. Prelle et al., FREQUENCY OF ALPHA-SARCOGLYCAN AND GAMMA-SARCOGLYCAN DEFICIENCY IN A LARGE POPULATION OF MYOPATHIC PATIENTS, Neurology, 48(3), 1997, pp. 3131-3131

Authors: COMI GP CIAFALONI E DESILVA HAR PRELLE A BARDONI A RIGOLETTO C ROBOTTI M BRESOLIN N MOGGIO M FORTUNATO F CISCATO P TURCONI A ROSES AD SCARLATO G
Citation: Gp. Comi et al., A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT (VOL 4, PG 2171, 1995)(1)), Human molecular genetics, 5(4), 1996, pp. 562-562

Authors: PRELLE A RIGOLETTO C MOGGIO M SCIACCO M COMI GP CISCATO P FAGIOLARI G RAPUZZI S BIGNOTTI V SCARLATO G
Citation: A. Prelle et al., ASYMPTOMATIC FAMILIAL HYPERCKEMIA ASSOCIATED WITH DESMIN ACCUMULATIONIN SKELETAL-MUSCLE, Journal of the neurological sciences, 140(1-2), 1996, pp. 132-136

Authors: COMI GP CIAFALONI E DESILVA HAR PRELLE A BARDONI A RIGOLETTO C ROBOTTI M BRESOLIN N MOGGIO M FORTUNATO F CISCATO P TURCONI A ROSE AD SCARLATO G
Citation: Gp. Comi et al., A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT(1)), Human molecular genetics, 4(11), 1995, pp. 2171-2174

Authors: RIGOLETTO C PRELLE A CISCATO P MOGGIO M COMI G FORTUNATO F SCARLATO G
Citation: C. Rigoletto et al., UTROPHIN EXPRESSION DURING HUMAN FETAL DEVELOPMENT, International journal of developmental neuroscience, 13(6), 1995, pp. 585-593

Authors: RAPUZZI S PRELLE A MOGGIO M RIGOLETTO C CISCATO P COMI G FRANCESCA F SCARLATO G
Citation: S. Rapuzzi et al., HIGH SERUM CREATINE-KINASE LEVELS ASSOCIATED WITH CYLINDRICAL SPIRALSAT MUSCLE BIOPSY, Acta Neuropathologica, 90(6), 1995, pp. 660-664
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