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Results: 1-9 |
Results: 9
VARIABLE HISTOLOGICAL EXPRESSION IN A XP21 MANIFESTING CARRIER
Authors: PALMUCCI L DORIGUZZI C MONGINI T CHIADOPIAT L UGO I SAGGIORATO C
Citation: L. Palmucci et al., VARIABLE HISTOLOGICAL EXPRESSION IN A XP21 MANIFESTING CARRIER, Brain pathology, 7(4), 1997, pp. 1120-1120
SYSTEMATIC USE OF DYSTROPHIN TESTING IN MUSCLE BIOPSIES - RESULTS IN 201 CASES
Authors: DORIGUZZI C PALMUCCI L MONGINI T CHIADOPIAT L MANISCALCO M RESTAGNO G
Citation: C. Doriguzzi et al., SYSTEMATIC USE OF DYSTROPHIN TESTING IN MUSCLE BIOPSIES - RESULTS IN 201 CASES, European journal of clinical investigation, 27(4), 1997, pp. 352-358
BCL-2 DISTRIBUTION IN NEUROEPITHELIAL TUMORS - AN IMMUNOHISTOCHEMICALSTUDY
Authors: SCHIFFER D CAVALLA P MIGHELI A GIORDANA MT CHIADOPIAT L
Citation: D. Schiffer et al., BCL-2 DISTRIBUTION IN NEUROEPITHELIAL TUMORS - AN IMMUNOHISTOCHEMICALSTUDY, Journal of neuro-oncology, 27(2), 1996, pp. 101-109
QUANTITATIVE AND QUALITATIVE ALTERATIONS OF DYSTROPHIN ARE EXPRESSED IN MUSCLE-CELL CULTURES OF XP21 MUSCULAR-DYSTROPHY PATIENTS (DUCHENNE AND BECKER TYPE)
Authors: MONGINI T DORIGUZZI C PALMUCCI L CHIADOPIAT L
Citation: T. Mongini et al., QUANTITATIVE AND QUALITATIVE ALTERATIONS OF DYSTROPHIN ARE EXPRESSED IN MUSCLE-CELL CULTURES OF XP21 MUSCULAR-DYSTROPHY PATIENTS (DUCHENNE AND BECKER TYPE), European journal of clinical investigation, 26(4), 1996, pp. 322-324
METACHROMATIC DYE - CA- A STUDY OF 382 MUSCLE BIOPSIES(+ ATPASE METHOD IN PATHOLOGICAL MUSCLE )
Authors: DORIGUZZI C PALMUCCI L MONGINI T MANISCALCO M CHIADOPIAT L DEANGELIS MS
Citation: C. Doriguzzi et al., METACHROMATIC DYE - CA- A STUDY OF 382 MUSCLE BIOPSIES(+ ATPASE METHOD IN PATHOLOGICAL MUSCLE ), European journal of histochemistry, 38(1), 1994, pp. 23-28
UNUSUAL EXPRESSION AND VERY MILD COURSE OF XP21 MUSCULAR-DYSTROPHY (BECKER TYPE) IN A 60-YEAR-OLD MAN WITH 26-PERCENT DELETION OF THE DYSTROPHIN GENE
Authors: PALMUCCI L DORIGUZZI C MONGINI T RESTAGNO G CHIADOPIAT L MANISCALCO M
Citation: L. Palmucci et al., UNUSUAL EXPRESSION AND VERY MILD COURSE OF XP21 MUSCULAR-DYSTROPHY (BECKER TYPE) IN A 60-YEAR-OLD MAN WITH 26-PERCENT DELETION OF THE DYSTROPHIN GENE, Neurology, 44(3), 1994, pp. 541-543
ADULT-ONSET NEMALINE MYOPATHY - A DISTINCT NOSOLOGIC ENTITY
Authors: PALMUCCI L DORIGUZZI C MONGINI T CHIADOPIAT L
Citation: L. Palmucci et al., ADULT-ONSET NEMALINE MYOPATHY - A DISTINCT NOSOLOGIC ENTITY, Clinical neuropathology, 12(3), 1993, pp. 153-155
EXERCISE INTOLERANCE AND RECURRENT MYOGLOBINURIA AS THE ONLY EXPRESSION OF XP21 BECKER TYPE MUSCULAR-DYSTROPHY
Authors: DORIGUZZI C PALMUCCI L MONGINI T CHIADOPIAT L RESTAGNO G FERRONE M
Citation: C. Doriguzzi et al., EXERCISE INTOLERANCE AND RECURRENT MYOGLOBINURIA AS THE ONLY EXPRESSION OF XP21 BECKER TYPE MUSCULAR-DYSTROPHY, Journal of neurology, 240(5), 1993, pp. 269-271
CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH FAMILIAL JUNCTIONAL EPIDERMOLYSIS-BULLOSA LETALIS
Authors: DORIGUZZI C PALMUCCI L MONGINI T BERTOLOTTO A MANISCALCO M CHIADOPIAT L ZINA AM BUNDINO S
Citation: C. Doriguzzi et al., CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH FAMILIAL JUNCTIONAL EPIDERMOLYSIS-BULLOSA LETALIS, European neurology, 33(6), 1993, pp. 454-460
Risultati: 1-9 |