MOSTACCIUOLO, MARIA LUISA

MOSTACCIUOLO, MARIA LUISA  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Duchenne muscular dystrophy. A population study. 1977 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + HUMAN GENETICS - -
Duchenne muscular dystrophy: data from family studies. 1980 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + HUMAN GENETICS - -
[Steinert's dystrophia myotonica . Epidemiological and clinical aspects]. 1986 MOSTACCIUOLO, MARIA LUISAARMANI, MARIO MINERVA PEDIATRICA - -
[Genetic counseling in hereditary neuromuscular diseases]. 1986 MOSTACCIUOLO, MARIA LUISA + MINERVA PEDIATRICA - -
Sporadic cases in Duchenne Muscular Dystrophy. A reappraisal through segregation analysis on 988 sibships 1987 RUSSO, ANTONELLAMOSTACCIUOLO, MARIA LUISA + HUMAN GENETICS - -
Genetic epidemiology of myotonic dystrophy. 1987 MOSTACCIUOLO, MARIA LUISAARMANI, MARIOANGELINI, CORRADO + GENETIC EPIDEMIOLOGY - -
Familial ALS: clinical, genetic and morphological features. 1987 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY - -
Population data on benign and severe forms of X-linked muscular dystrophy. 1987 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + HUMAN GENETICS - -
Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage study. 1988 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + ADVANCES IN NEUROLOGY - -
Problems in genetic counseling in a family with an "atypical" centronuclear myopathy. 1989 MOSTACCIUOLO, MARIA LUISA + AMERICAN JOURNAL OF MEDICAL GENETICS - -
Genetic epidemiology of hereditary motor sensory neuropathies (type I). 1991 MOSTACCIUOLO, MARIA LUISA + AMERICAN JOURNAL OF MEDICAL GENETICS - -
X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region. 1991 MOSTACCIUOLO, MARIA LUISA + HUMAN GENETICS - -
A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions. 1992 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISA + HUMAN MOLECULAR GENETICS - -
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene. 1992 MOSTACCIUOLO, MARIA LUISA + NEUROMUSCULAR DISORDERS - -
Correlation between clinical and molecular features in two MELAS families. 1992 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia). 1992 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + HUMAN GENETICS - -
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients. 1992 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + JOURNAL OF MEDICAL GENETICS - -
Epidemiology of spinal muscular atrophies in a sample of the Italian population. 1992 MOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + NEUROEPIDEMIOLOGY - -
Cardiac involvement in Becker muscular dystrophy 1993 MELACINI, PAOLAFANIN, MARINADANIELI, GIAN ANTONIOFASOLI, GIUSEPPEANGELINI, CORRADOVITIELLO, LIBEROBUJA, GIANFRANCOMOSTACCIUOLO, MARIA LUISAPEGORARO, ELENADALLA VOLTA, SERGIO + JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY - -
Patterns of deletions of the dystrophin gene in different European populations. 1993 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISA + HUMAN GENETICS - -