Corrado Angelini, MD,FAAN - Istituto Di Cura S Camillo - Consultant

Corrado Angelini

MD,FAAN

Istituto Di Cura S Camillo

Consultant

Venezia, Veneto | Italy

Main Specialties: Neurology, Neuromuscular Medicine

Additional Specialties: Neurology

ORCID logohttps://orcid.org/0000-0002-9554-8794


Top Author

Corrado Angelini, MD,FAAN - Istituto Di Cura S Camillo - Consultant

Corrado Angelini

MD,FAAN

Introduction

MD in Padova , Neurology residence University of Padova
Neurological research assistant and associate at Mayo Clinic ,Rochester Minnesota USA
Neurology residence at Neurology Department Mayo Clinic
Visiting Professor UCLA MDA Senior Fellowship,1978
Visiting Professor University of Colorado Denver 1984
Associate and full Professor of Neurology University of Padova 1985,2011
consultant Director Neuromuscular Center and BBMRNR,IRCCS S.Camillo,2011-present

Primary Affiliation: Istituto Di Cura S Camillo - Venezia, Veneto , Italy

Specialties:

Additional Specialties:

Research Interests:


View Corrado Angelini’s Resume / CV

Education

Sep 1970 - Sep 1973
Mayo Clinic Minnesota
Resident/Research Associate
Neurology

Experience

Jan 2010 - Apr 2020
Istituto Di Cura S Camillo
Director
Neuromuscular Center
Feb 1969 - Sep 2011
University of Padova
Professor
Neurology

Publications

85Publications

640Reads

135Profile Views

MicroRNAs and HDAC4 protein expression in the skeletal muscle of ALS patients.

Clin Neuropathol 2020 May/Jun;39(3):105-114

View Article

Download full-text PDF

Source
http://dx.doi.org/10.5414/NP301233DOI Listing
April 2020
1.311 Impact Factor

European Federation of the Neurological Societies guidelines on the diagnostic approach to paucisymptomatic or asymptomatic hyperCKemia.

Muscle Nerve 2020 02 18;61(2):E14-E15. Epub 2019 Dec 18.

Clinical Neurosciences, John Radcliffe Hospital, Oxford, United Kingdom.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mus.26777DOI Listing
February 2020
2.283 Impact Factor

MiRNAs as biomarkers of phenotype in neutral lipid storage disease with myopathy.

Muscle Nerve 2020 02 29;61(2):253-257. Epub 2019 Nov 29.

IRCCS San Camillo Hospital, Venice, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mus.26761DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004093PMC
February 2020
2.283 Impact Factor

Can miR-34a be suitable for monitoring sensorineural hearing loss in patients with mitochondrial disease? A case series.

Int J Neurosci 2020 Feb 20:1-6. Epub 2020 Feb 20.

Otolaryngology Department, University of Perugia, Perugia, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/00207454.2020.1731505DOI Listing
February 2020
1.528 Impact Factor

Authors' reply.

Ther Adv Neurol Disord 2019 23;12:1756286419878316. Epub 2019 Sep 23.

Fondazione Ospedale San Camillo, IRCCS, Venezia, Italia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1756286419878316DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759696PMC
September 2019

A new family with transportinopathy: increased clinical heterogeneity.

Ther Adv Neurol Disord 2019 9;12:1756286419850433. Epub 2019 Jun 9.

TIGEM (Telethon Institute of Genetics and Medicine), University at Campania, Naples, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1756286419850433DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558532PMC
June 2019
16 Reads

Microglia polarization by mitochondrial metabolism modulation: A therapeutic opportunity in neurodegenerative diseases.

Mitochondrion 2019 05 19;46:334-336. Epub 2018 Sep 19.

Fondazione IRCCS San Camillo Hospital, Venice, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.mito.2018.09.003DOI Listing
May 2019
1 Read
3.249 Impact Factor

Advances in imaging of brain abnormalities in neuromuscular disease.

Ther Adv Neurol Disord 2019 6;12:1756286419845567. Epub 2019 May 6.

Fondazione Ospedale San Camillo IRCCS, Venezia, Italia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1756286419845567DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503605PMC
May 2019
16 Reads

Metabolic lipid muscle disorders: biomarkers and treatment.

Ther Adv Neurol Disord 2019 22;12:1756286419843359. Epub 2019 Apr 22.

Laboratory of Cellular Biochemistry and Molecular Biology, CRIBENS, Catholic University of the Sacred Heart, Milan, Italy Psychology Department, Catholic University of the Sacred Heart, Milan, Italy.

Lipid storage myopathies (LSMs) are metabolic disorders of the utilization of fat in muscles due to several different defects. In this review, a molecular update of LSMs is presented and recent attempts of finding treatment options are discussed. The main topics discussed are: primary carnitine deficiency, riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency, neutral lipid storage disorders and carnitine palmitoyl transferase deficiency. The most frequent presentations and genetic abnormalities are summarized. We present their diagnosis utilizing biomedical and morphological biomarkers and possible therapeutic interventions. The treatment of these metabolic disorders is a subject of active translational research but appears, in some cases, still elusive.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1756286419843359DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477769PMC
April 2019
10 Reads
4.200 Impact Factor

Clinical and genetic characterization of an Italian family with slow-channel syndrome.

Neurol Sci 2019 Mar 12;40(3):503-507. Epub 2018 Dec 12.

Department of Biology, University of Padova, Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10072-018-3645-2DOI Listing
March 2019
2 Reads
1.495 Impact Factor

MyomiRNAs Dysregulation in ALS Rehabilitation.

Brain Sci 2019 Jan 10;9(1). Epub 2019 Jan 10.

Fondazione Ospedale San Camillo IRCCS, via Alberoni 70, 30126 Venezia, Italy.

View Article

Download full-text PDF

Source
http://www.mdpi.com/2076-3425/9/1/8
Publisher Site
http://dx.doi.org/10.3390/brainsci9010008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356197PMC
January 2019
15 Reads

Regulation of ER-mitochondria contacts by Parkin via Mfn2.

Pharmacol Res 2018 12 13;138:43-56. Epub 2018 Sep 13.

Department of Biology, University of Padova, Padova, Italy; Fondazione Ospedale San Camillo, IRCCS, Lido di Venezia, Venezia, Italy. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S10436618183032
Publisher Site
http://dx.doi.org/10.1016/j.phrs.2018.09.006DOI Listing
December 2018
17 Reads
4.408 Impact Factor

Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.

Lipids Health Dis 2018 Nov 13;17(1):254. Epub 2018 Nov 13.

Fondazione Ospedale San Camillo IRCCS, via Alberoni 70, 30126, Venice, Italy.

Background: Deficiency of electron transfer flavoprotein dehydrogenase (ETFDH) is associated with multiple acyl-CoA dehydrogenase deficiency (MADD). This disorder is an autosomal recessive lipid storage myopathy (LSM) that exhibits a wide range of clinical features, including myopathy, weakness and multisystem dysfunctions. Many patients with late onset of MADD improve when treated with riboflavin and are also referred to as RR-MADD (riboflavin-responsive multiple Acyl-CoA dehydrogenase disorder).

Methods: In this study, we report the clinical and genetic characterization of a novel RR-MADD patient. Biochemical data were obtained from analysis of muscle and plasma samples. DNA and RNA were extracted from peripheral blood, and sequence analysis and expression study of ETFDH gene were performed. Finally, the impact of mutations on ETFDH folding was evaluated using bioinformatic tools.

Results: Patient initially presented with vomiting, muscle weakness, and acidosis. Muscle biopsy revealed typical myopathological patterns of lipid storage myopathy and blood acylcarnitine profiles showed a combined elevation of long and medium chain acylcarnitines, supporting the diagnosis of RR-MADD. Molecular analysis of ETFDH gene revealed two heterozygous mutations, a novel splice variation in intron 10, c.1285?+?1G?>?A, and the previously reported c.560C?>?T missense mutation. RT-PCR analysis showed an alteration of ETFDH RNA splicing which in turn should lead to the production of a truncated protein. The in silico prediction analysis of ETFDH tridimensional structure demonstrated that the missense mutation resulted in instability and loss of protein activation, while the splice site variation induced a dramatic conformational change of the truncated protein. After MCT diet supplemented with carnitine and riboflavin, the patient showed significant biochemical and clinical improvement, in spite of severe molecular defect.

Conclusion: This case report extends the spectrum of ETFDH mutations in MADD, providing further evidence that patients presenting at least one missense mutation in the FAD-binding domain may respond to either carnitine or riboflavin treatment, due to the recovery of some enzymatic activity.

View Article

Download full-text PDF

Source
https://lipidworld.biomedcentral.com/articles/10.1186/s12944
Publisher Site
http://dx.doi.org/10.1186/s12944-018-0903-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234560PMC
November 2018
43 Reads
2.219 Impact Factor

ERRATUM: Effects of combined endurance and resistance training in Amyotrophic Lateral Sclerosis: A pilot, randomized, controlled study.

Eur J Transl Myol 2018 07 20;28(3):7842. Epub 2018 Sep 20.

Neurorehabilitation Department, San Camillo Hospital Foundation, Institute of Care and Research, Venice. Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4081/ejtm.2018.7842DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176392PMC
July 2018
3 Reads

Effects of Functional Electrical Stimulation Lower Extremity Training in Myotonic Dystrophy Type I: A Pilot Controlled Study.

Am J Phys Med Rehabil 2016 11;95(11):809-817

From the IRCCS San Camillo Hospital Foundation, Venice, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/PHM.0000000000000497DOI Listing
November 2016
29 Reads
2.012 Impact Factor

New Pathogenetic Mechanisms that Link Autophagy to Pompe Disease.

J Neuromuscul Dis 2015;2(s1):S9

Dulbecco Telethon Institute at Venetian Institute of Molecular Medicine, Padova, Italy.

View Article

Download full-text PDF

Source
January 2015
2 Reads

A pilot trial with clenbuterol in amyotrophic lateral sclerosis.

Amyotroph Lateral Scler 2006 Dec;7(4):246-8

Department of Neurosciences, Neurology Unit, Piove di Sacco Hospital, Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/14660820600600558DOI Listing
December 2006
33 Reads

Limb-girdle muscular dystrophies: heterogeneity of clinical phenotypes and pathogenetic mechanisms.

Authors:
C Angelini

Acta Myol 2004 Dec;23(3):130-6

Department of Neurosciences, University of Padua, Italy.

View Article

Download full-text PDF

Source
December 2004
5 Reads

Myopathy with tubular aggregates and hypertrophic cardiomyopathy in a patient with type IIA von Willebrand disease.

Haematologia (Budap) 1996 ;27(4):201-8

Institute of Medical Semeiotics, Padua, Italy.

View Article

Download full-text PDF

Source
January 2004
1 Read

Morphological changes in late onset acid Maltase deficient patients with splicing gene mutation.

Acta Myol 2003 Dec;22(3):90-6

Department of Neurosciences, University of Padova, Venetian Institute of Molecular Medicine, Padova, Italy.

View Article

Download full-text PDF

Source
December 2003
1 Read

Role of gabapentin in spinal muscular atrophy: results of a multicenter, randomized Italian study.

J Child Neurol 2003 Aug;18(8):537-41

Neuromuscular Unit, Istituto Ortopedico Rizzoli, Bologna, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/08830738030180080501DOI Listing
August 2003
12 Reads
1.666 Impact Factor

Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facioscapulo human muscular dystrophy. A potential target for pharmacological treatment?

J Neuropathol Exp Neurol 2001 Mar;60(3):302-12

Department of Biomedical Sciences, Institute of Experimental and Laboratory Medicine, University of Padua, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/jnen/60.3.302DOI Listing
March 2001
2 Reads
3.797 Impact Factor

Unilateral calf hypertrophy due to S1-radiculopathy.

Neuromuscul Disord 2000 Oct;10(7):514

Department of Neurological and Psychiatric Sciences, Neuromuscular Center, University of Padua, Italy.

View Article

Download full-text PDF

Source
October 2000
1 Read
2.638 Impact Factor

Multiple symmetric lipomatosis: evidence for mitochondrial dysfunction.

J Clin Neuromuscul Dis 2000 Mar;1(3):124-30

From the Depatmetns of * Internal Medicince and daggerNeurology, University of Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/00131402-200003000-00002DOI Listing
March 2000
1 Read

Acute quadriplegic myopathy in a 17-month-old boy.

J Child Neurol 2000 Jan;15(1):63-6

Department of Pediatrics, University of Padua, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/088307380001500115DOI Listing
January 2000
2 Reads
1.666 Impact Factor

Motor neuron disease in the Padua district of Italy: an epidemiological study.

Neuroepidemiology 1996 ;15(4):173-9

Department of Neurology, University of Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000109905DOI Listing
November 1996
1 Read
2.558 Impact Factor

[Imaging of the thymus gland in myasthenia gravis (computerized tomography and magnetic resonance)].

Radiol Med 1995 Oct;90(4):404-9

Istituto di Radiologia, Università di Padova.

View Article

Download full-text PDF

Source
October 1995
1 Read
1.368 Impact Factor

Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up.

Eur Neurol 1995 ;35(4):230-5

Istituto di Clinica delle Malattie Nervose e Mentali, Università degli Studi di Padova, Italia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000117134DOI Listing
October 1995
1 Read
1.362 Impact Factor

Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1.

Neuroepidemiology 1995 ;14(2):49-53

Department of Biology, University of Padua, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000109778DOI Listing
April 1995
1 Read
2.558 Impact Factor

[Description of two cases of retrobrachiocephalic thymus gland].

Minerva Chir 1994 Oct;49(10):1013-8

Istituto di Chirurgia Generale I, Università degli Studi di Padova.

View Article

Download full-text PDF

Source
October 1994
3 Reads
0.707 Impact Factor

Single muscle fibre analyses in 2 brothers with succinate dehydrogenase deficiency.

Eur Neurol 1994 ;34(2):95-8

Department of Neurology, University of Würzburg, FRG.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000117016DOI Listing
June 1994
1 Read
1.362 Impact Factor

Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis.

Neuroepidemiology 1993 ;12(6):326-30

Department of Biology, University of Padua, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000110334DOI Listing
March 1994
1 Read
2.558 Impact Factor

Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidation.

Crit Rev Clin Lab Sci 1992 ;29(3-4):217-42

Regional Neuromuscular Center, University of Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/10408369209114601DOI Listing
February 1993
2 Reads
3.692 Impact Factor

Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect.

Jpn Heart J 1993 Jan;34(1):63-77

Neuromuscular Center, University of Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1536/ihj.34.63DOI Listing
January 1993
1 Read

Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia).

Hum Genet 1992 Nov;90(3):231-4

Dipartimento di Biologia, Università di Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/BF00220067DOI Listing
November 1992
1 Read
4.824 Impact Factor

Epidemiology of spinal muscular atrophies in a sample of the Italian population.

Neuroepidemiology 1992 ;11(1):34-8

Department of Biology, University of Padua, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000110905DOI Listing
July 1992
1 Read
2.558 Impact Factor

Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies.

Rev Neurol (Paris) 1991 ;147(6-7):542-8

Institute of Clinical Neurology, University of Milan, Italy.

View Article

Download full-text PDF

Source
January 1992
1 Read
0.601 Impact Factor

Echocardiographic and pulsed Doppler features in glycogen storage disease type II of the heart (Pompe's disease).

Acta Cardiol 1991 ;46(1):107-14

Division of Cardiology, Hospital of Vicenza, Italy.

View Article

Download full-text PDF

Source
June 1991
1 Read
0.561 Impact Factor

Serum lipids, lipoprotein analysis and apoprotein A-I, A-II and B levels in Friedreich's ataxia.

Eur Neurol 1990 ;30(3):132-7

Institute of Internal Medicine, Medical Pathology, University of Padua, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000117329DOI Listing
August 1990
3 Reads
1.362 Impact Factor

Evolution of cardiac involvement in progressive ophthalmoplegia with deleted mitochondrial DNA.

Jpn Heart J 1990 Jan;31(1):115-20

Department of Cardiology, University of Padua Medical School, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1536/ihj.31.115DOI Listing
January 1990
2 Reads

Sensory-motor conduction time in amyotrophic lateral sclerosis.

Riv Neurol 1989 May-Jun;59(3):108-12

Istituto di Anestesiologia e Rianimazione, Università di Padova.

View Article

Download full-text PDF

Source
January 1990
1 Read

Intellectual impairment and cognitive evoked potentials in myotonic dystrophy.

J Nerv Ment Dis 1989 Dec;177(12):750-4

Department of Psychiatry, School of Medicine, University of Padua, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/00005053-198912000-00007DOI Listing
December 1989
1 Read
1.812 Impact Factor

[Myopathies caused by defects of lipid and carbohydrate metabolism].

Riv Neurol 1988 Jan-Feb;58(1):15-25

Centro Regionale Malattie Neuromuscolari, Università, Padova.

View Article

Download full-text PDF

Source
October 1988
1 Read

Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage study.

Adv Neurol 1988 ;48:209-19

Department of Neurology, University of Padua, Italy.

View Article

Download full-text PDF

Source
January 1988
1 Read

Quantitative histopathology in congenital myopathies.

Riv Neurol 1987 Jul-Aug;57(4):261-8

Clinica Neurologica, Università, Padova.

View Article

Download full-text PDF

Source
December 1987
1 Read

[Psychological aspects of neuromuscular diseases].

Minerva Pediatr 1986 Aug;38(15-16):683-4

View Article

Download full-text PDF

Source
August 1986
1 Read
0.723 Impact Factor

Sensory, motor, and autonomic neuropathy in patients with multiple symmetric lipomatosis.

Medicine (Baltimore) 1985 Nov;64(6):388-93

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/00005792-198511000-00003DOI Listing
November 1985
1 Read
5.723 Impact Factor

A childhood case of hypokalemic periodic paralysis.

Acta Neurol (Napoli) 1984 Apr;6(2):147-51

View Article

Download full-text PDF

Source
April 1984
172 Reads

[Preliminary study on the use of acetylcarnitine in patients with mental deterioration].

Riv Neurol 1982 May-Jun;52(3):185-97

View Article

Download full-text PDF

Source
December 1982
1 Read

[Report of two patients with fibromuscular dysplasia of the internal carotid artery (author's transl)].

Riv Patol Nerv Ment 1981 May-Jun;101(3):139-50

View Article

Download full-text PDF

Source
September 1981
4 Reads

Myopathological findings in progressive myoclonus epilepsy.

Acta Neuropathol Suppl 1981 ;7:334-7

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-3-642-81553-9_96DOI Listing
June 1981
1 Read

[Lafora disease complicating myoclonus epilepsy. Report of 3 cases].

Riv Neurol 1980 Sep-Oct;50(5):338-49

View Article

Download full-text PDF

Source
April 1981
5 Reads

[Systemic carnitine deficiency: its place in Reye's syndrome (author's transl)].

Nouv Presse Med 1981 Feb;10(7):499-502

View Article

Download full-text PDF

Source
February 1981
1 Read

Guanidine hydrochloride in infantile and juvenile spinal muscular atrophy. A double blind controlled study.

Acta Neurol (Napoli) 1980 Dec;2(6):460-5

View Article

Download full-text PDF

Source
December 1980
1 Read

[Aminoacid levels in Werding-Hoffmann and Kugelberg-Welander diseases (author's transl)].

Riv Patol Nerv Ment 1978 Nov-Dec;99(6):317-26

View Article

Download full-text PDF

Source
January 1980
1 Read

[Thymus gland scan in myasthenia gravis: experience in 52 patients].

Riv Patol Nerv Ment 1978 Jul-Aug;99(4):244-54

View Article

Download full-text PDF

Source
August 1979
1 Read

Oculo cranio-somatic syndrome: mitochondrial alterations and lactic acidemia.

Acta Neurol (Napoli) 1979 Feb;1(1):59-63

View Article

Download full-text PDF

Source
February 1979
1 Read

[Polyneuropathies due to adhesives. Histopathological and ultrastructural studies].

Acta Neurol (Napoli) 1976 Jan-Feb;31(1):105

View Article

Download full-text PDF

Source
December 1976
1 Read

Progressive supranuclear palsy: report of two cases (author's transl).

Riv Patol Nerv Ment 1975 May-Jun;96(3):159-65

View Article

Download full-text PDF

Source
September 1976
1 Read

[Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract].

Minerva Med 1976 Jul;67(33):2104-12

View Article

Download full-text PDF

Source
July 1976
1 Read
1.202 Impact Factor

[Hypertrophic ischemic neuropathies].

Authors:
C Angelini L Rubini

Acta Neurol (Napoli) 1974 Jul-Aug;29(4):347-56

View Article

Download full-text PDF

Source
May 1975
1 Read

Fingerprint body myopathy, a newly recognized congenital muscle disease.

Mayo Clin Proc 1972 Jun;47(6):377-88

View Article

Download full-text PDF

Source
June 1972
1 Read
6.262 Impact Factor

[Behavior of serum isoenzymes of lactic dehydrogenase in various muscular diseases].

Acta Neurol (Napoli) 1970 Nov-Dec;25(6):633-54

View Article

Download full-text PDF

Source
June 1971
4 Reads

[Therapy of Parkinson's disease with L-dopa. Preliminary considerations on 40 cases].

Riv Sper Freniatr Med Leg Alien Ment 1970 Dec;94(6):1516-26

View Article

Download full-text PDF

Source
December 1970
1 Read

[Thyrotoxic and hypothyroid myopathy. Biochemical and histopathological study].

Authors:
C Angelini

Riv Patol Nerv Ment 1970 Jun;91(3):123-38

View Article

Download full-text PDF

Source
June 1970
1 Read

Top co-authors

M Fanin
M Fanin

University of Padova

3
Tiziana Mongini
Tiziana Mongini

Neurological Clinic

3
Eugenio Mercuri
Eugenio Mercuri

Catholic University

3
G Testa
G Testa

Dipartimento di Medicina Clinica e Scienze Cardiovascolari ed Immunologiche

3
Vincenzo Nigro
Vincenzo Nigro

Seconda Università degli Studi di Napoli

3
Enrico Bertini
Enrico Bertini

Laboratory of Molecular Medicine

3
Luisa Politano
Luisa Politano

Second University of Naples

3
Annalaura Torella
Annalaura Torella

Seconda Università degli Studi di Napoli

3