SPECTRUM OF Xp21 MUSCULAR DYSTROPHY RESULTING FROM THE SYSTEMIC INVESTIGATION OF MUSCLE DISEASES BY ANTIDYSTROPHIN ANTIBODIES: IDENTIFICATION OF UNUSUAL PHENOTYPES
- 2 Anni 1993/1995
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Systematic use of dystrophin testing in muscle biopsies: Results in 201 cases
- JOURNAL OF NEUROLOGY
EXERCISE INTOLERANCE AND RECURRENT MYOGLOBINURIA AS THE ONLY EXPRESSION OF XP21 BECKER TYPE MUSCULAR-DYSTROPHY
- NEUROGENETICS
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease
- NEUROLOGY
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
