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Results: 1-7 |
Results: 7
SLEEP-APNEA IN A PATIENT WITH BECKER MUSCULAR-DYSTROPHY
Authors: FERRI R AZAN G CIBELLA F MARRONE O SAMMARCO P DELGRACCO S ELIA M MUSUMECI SA STEFANINI MC
Citation: R. Ferri et al., SLEEP-APNEA IN A PATIENT WITH BECKER MUSCULAR-DYSTROPHY, Italian journal of neurological sciences, 18(1), 1997, pp. 59-60
A NEW FAMILY WITH PERIVENTRICULAR NODULAR HETEROTOPIA AND PECULIAR DYSMORPHIC FEATURES - A PROBABLE X-LINKED DOMINANT TRAIT
Authors: MUSUMECI SA FERRI R ELIA M SCUDERI C DELGRACCO S AZAN G STEFANINI MC
Citation: Sa. Musumeci et al., A NEW FAMILY WITH PERIVENTRICULAR NODULAR HETEROTOPIA AND PECULIAR DYSMORPHIC FEATURES - A PROBABLE X-LINKED DOMINANT TRAIT, Archives of neurology, 54(1), 1997, pp. 61-64
LEIGH-SYNDROME AND PARTIAL DEFICIT OF CYTOCHROME-C-OXIDASE ASSOCIATEDWITH EPILEPSIA PARTIALIS CONTINUA
Authors: ELIA M MUSUMECI SA FERRI R COLAMARIA V AZAN G GRECO D STEFANINI MC
Citation: M. Elia et al., LEIGH-SYNDROME AND PARTIAL DEFICIT OF CYTOCHROME-C-OXIDASE ASSOCIATEDWITH EPILEPSIA PARTIALIS CONTINUA, Brain & development, 18(3), 1996, pp. 207-211
CONGENITAL CEREBELLAR-ATAXIA, MENTAL-RETARDATION, AND ATROPHIC RETINAL LESIONS IN 2 BROTHERS
Authors: FERRI R AZAN G DELGRACCO S ELIA M MUSUMECI SA STEFANINI MC TOSCANO G SETTA F
Citation: R. Ferri et al., CONGENITAL CEREBELLAR-ATAXIA, MENTAL-RETARDATION, AND ATROPHIC RETINAL LESIONS IN 2 BROTHERS, Journal of Neurology, Neurosurgery and Psychiatry, 61(4), 1996, pp. 424-425
UNUSUAL EEG FEATURES IN A CHILD WITH CEREBROCEREBELLAR LISSENCEPHALY
Authors: ELIA M MUSUMECI SA FERRI R CASTANO A AZAN G STEFANINI MC
Citation: M. Elia et al., UNUSUAL EEG FEATURES IN A CHILD WITH CEREBROCEREBELLAR LISSENCEPHALY, Epilepsia, 36, 1995, pp. 78-78
DILATED CARDIOMYOPATHY REQUIRING CARDIAC TRANSPLANTATION AS INITIAL MANIFESTATION OF XP21 BECKER TYPE MUSCULAR-DYSTROPHY
Authors: PICCOLO G AZAN G TONIN P ARBUSTINI E GAVAZZI A BANFI P MORA M MORANDI L TEDESCHI S
Citation: G. Piccolo et al., DILATED CARDIOMYOPATHY REQUIRING CARDIAC TRANSPLANTATION AS INITIAL MANIFESTATION OF XP21 BECKER TYPE MUSCULAR-DYSTROPHY, Neuromuscular disorders, 4(2), 1994, pp. 143-146
IDENTIFICATION OF 3 NOVEL MUTATIONS IN NON-ASHKENAZI ITALIAN PATIENTSWITH MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCY
Authors: TSUJINO S SERVIDEI S TONIN P SHANSKE S AZAN G DIMAURO S
Citation: S. Tsujino et al., IDENTIFICATION OF 3 NOVEL MUTATIONS IN NON-ASHKENAZI ITALIAN PATIENTSWITH MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCY, American journal of human genetics, 54(5), 1994, pp. 812-819
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