FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

E Menegazzo

Research Profile

Disorders

Chemicals & Drugs

Physiology

Concepts & Ideas

Anatomy

Geographic Areas

Italy

Genes & Molecular Sequences

Alleles

Procedures

Co-author Network

Publications

TOP 3
Giuliana Perini; E Menegazzo; Mario Ermani; M Zara; A Gemma; E Ferruzza; Massimo Gennarelli; Corrado Angelini
Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients.
Massimo Gennarelli; M Pavoni; Paola Amicucci; Corrado Angelini; E Menegazzo; G Zelano; Giuseppe Novelli; Bruno Dallapiccola
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients.
Corrado Angelini; Marina Fanin; E Menegazzo; MP Freda; DJ Duggan; Eric Hoffman
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of E Menegazzo (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

1999: Giuliana Perini; E Menegazzo; Mario Ermani; M Zara; A Gemma; E Ferruzza; Massimo Gennarelli; Corrado Angelini
Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients.
Biological psychiatry 1999;46(3):425-31.
1999: Massimo Gennarelli; M Pavoni; Paola Amicucci; Corrado Angelini; E Menegazzo; G Zelano; Giuseppe Novelli; Bruno Dallapiccola
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients.
Neuromuscular disorders : NMD 1999;9(4):215-9.
1998: Corrado Angelini; Marina Fanin; E Menegazzo; MP Freda; DJ Duggan; Eric Hoffman
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient.
Muscle & nerve 1998;21(6):769-75.
1998: Maria Lisa Marcon; Chiara Briani; Mario Ermani; E Menegazzo; Vincenzo Iurilli; Giuseppe Feltrin; Giuseppe Novelli; Massimo Gennarelli; Corrado Angelini
Positive correlation of CTG expansion and pharyngoesophageal alterations in myotonic dystrophy patients.
Italian journal of neurological sciences 1998;19(2):75-80.
1996: Massimo Gennarelli; Giuseppe Novelli; F Andreasi Bassi; Lluis Martorell; M Cornet; E Menegazzo; Maria Luisa Mostacciuolo; J M Martinez; Corrado Angelini; Antonio Pizzuti; Montserrat Baiget; Bruno Dallapiccola
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.
American journal of medical genetics 1996;65(4):342-7.
1996: I Mastrogiacomo; G Bonanni; E Menegazzo; C Santarossa; E Pagani; Massimo Gennarelli; Corrado Angelini
Clinical and hormonal aspects of male hypogonadism in myotonic dystrophy.
Italian journal of neurological sciences 1996;17(1):59-65.
1995: A Massari; Massimo Gennarelli; E Menegazzo; Antonio Pizzuti; Vincenzo Silani; I Mastrogiacomo; E Pagani; Corrado Angelini; G Scarlato; Giuseppe Novelli
Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm.
Journal of neurology 1995;242(6):379-83.
1995: J Wang; Elena Pegoraro; E Menegazzo; Massimo Gennarelli; R C Hoop; Corrado Angelini; Eric Hoffman
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation.
Human molecular genetics 1995;4(4):599-606.
1995: Giuseppe Novelli; Massimo Gennarelli; E Menegazzo; Corrado Angelini; Bruno Dallapiccola
Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeats.
Neuromuscular disorders : NMD 1995;5(2):157-9.
1995: Paola Melacini; C Villanova; E Menegazzo; Giuseppe Novelli; G Danieli; Giulio Rizzoli; Giuseppe Fasoli; Corrado Angelini; Gianfranco Buja; M Miorelli
Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy.
Journal of the American College of Cardiology 1995;25(1):239-45.
1994: I Mastrogiacomo; E Pagani; Giuseppe Novelli; Corrado Angelini; Massimo Gennarelli; E Menegazzo; G Bonanni; Bruno Dallapiccola
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutation.
Journal of endocrinological investigation 1994;17(5):381-3.
1993: Giuseppe Novelli; Massimo Gennarelli; E Menegazzo; Maria Luisa Mostacciuolo; Antonio Pizzuti; C Fattorini; D Tessarolo; G Tomelleri; M Giacanelli; Gian Antonio Danieli
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients.
Biochemical medicine and metabolic biology 1993;50(1):85-92.
1993: Corrado Angelini; E Menegazzo; Marina Fanin
Multifactorial study of inflammatory myopathies. Report of 29 cases.
Italian journal of neurological sciences 1993;14(1):69-76.
1991: L Pasqui; L Pistollato; M Castagna; M A Tumini; Carlo Pietro Trevisan; E Menegazzo; O Garbin
[Epidemiologic study of epilepsy in the population of Este-Montagnana (U.L.S.S. 22-Veneto Region)].
Rivista di neurologia 1991;61(1):20-2.