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C Angelini

Showing results (191-200 of 531) with videos related to

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Journal of Medical Genetics|November 1, 1994
Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patientsF Schiavon, M L Mostacciuolo, F Saad, et al.
Clinical Genetics|May 22, 2001
Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosisG Siciliano, M Manca, M Gennarelli, et al.
Minerva Chirurgica|July 19, 2001
[Stomach lymphoma]C M Franciosi, C Angelini, C Mussi, et al.
Rivista Di Neurologia|May 1, 1989
Sensory-motor conduction time in amyotrophic lateral sclerosisE Facco, G Micaglio, M C Liviero, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patientsM Gennarelli, M Pavoni, P Amicucci, et al.
Human Molecular Genetics|April 1, 1995
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutationJ Wang, E Pegoraro, E Menegazzo, et al.
Minerva Chirurgica|November 7, 2003
Gastrointestinal carcinoids. Prognosis and survivalR Caprotti, C Angelini, C Mussi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 30, 2005
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1S Salvatori, M Fanin, C P Trevisan, et al.
Advances in Neurology|January 1, 1988
Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage studyG Micaglio, P Fardin, M Battilana, et al.
Neurological Research|January 23, 2010
Quality of life and motor impairment in ALS: Italian validation of ALSAQA Palmieri, G Sorarù, L Lombardi, et al.
Pageof 54

Showing results (191-200 of 531) with videos related to

Sort By:
Pageof 54
Journal of Medical Genetics|November 1, 1994
Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patientsF Schiavon, M L Mostacciuolo, F Saad, et al.
Clinical Genetics|May 22, 2001
Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosisG Siciliano, M Manca, M Gennarelli, et al.
Minerva Chirurgica|July 19, 2001
[Stomach lymphoma]C M Franciosi, C Angelini, C Mussi, et al.
Rivista Di Neurologia|May 1, 1989
Sensory-motor conduction time in amyotrophic lateral sclerosisE Facco, G Micaglio, M C Liviero, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patientsM Gennarelli, M Pavoni, P Amicucci, et al.
Human Molecular Genetics|April 1, 1995
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutationJ Wang, E Pegoraro, E Menegazzo, et al.
Minerva Chirurgica|November 7, 2003
Gastrointestinal carcinoids. Prognosis and survivalR Caprotti, C Angelini, C Mussi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 30, 2005
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1S Salvatori, M Fanin, C P Trevisan, et al.
Advances in Neurology|January 1, 1988
Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage studyG Micaglio, P Fardin, M Battilana, et al.
Neurological Research|January 23, 2010
Quality of life and motor impairment in ALS: Italian validation of ALSAQA Palmieri, G Sorarù, L Lombardi, et al.
Pageof 54