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Items: 1 to 20 of 305

1.

ERRATA.

[No authors listed]

Acta Myol. 2017 Sep 1;36(3):183. eCollection 2017 Sep.

2.

ERRATA.

[No authors listed]

Acta Myol. 2017 Sep 1;36(3):182. eCollection 2017 Sep.

3.

Bethlem myopathy in a Portuguese patient - case report.

Martins AI, Maarque C, Pinto-Basto J, Negrão L.

Acta Myol. 2017 Sep 1;36(3):178-181. eCollection 2017 Sep.

4.

Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects.

Bianco A, Bisceglia L, Trerotoli P, Russo L, D'Agruma L, Guerriero S, Petruzzella V.

Acta Myol. 2017 Sep 1;36(3):163-177. eCollection 2017 Sep.

5.

Multi-slice MRI reveals heterogeneity in disease distribution along the length of muscle in Duchenne muscular dystrophy.

Chrzanowski SM, Baligand C, Willcocks RJ, Deol J, Schmalfuss I, Lott DJ, Daniels MJ, Senesac C, Walter GA, Vandenborne K.

Acta Myol. 2017 Sep 1;36(3):151-162. eCollection 2017 Sep.

6.

Arrhythmogenic right ventricular cardiomyopathy in Boxer dogs: the diagnosis as a link to the human disease.

Vischer AS, Connolly DJ, Coats CJ, Fuentes VL, McKenna WJ, Castelletti S, Pantazis AA.

Acta Myol. 2017 Sep 1;36(3):135-150. eCollection 2017 Sep.

7.

Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of life.

Lehmann-Horn F, D'Amico A, Bertini E, Lomonaco M, Merlini L, Nelson KR, Philippi H, Siciliano G, Spaans F, Jurkat-Rott K.

Acta Myol. 2017 Sep 1;36(3):125-134. eCollection 2017 Sep.

8.

Complete resolution of left atrial appendage thrombosis with oral dabigatran etexilate in a patient with Myotonic Dystrophy type 1 and atrial fibrillation.

Rago A, Papa AA, Arena G, Mosella M, Cassese A, Palladino A, Golino P.

Acta Myol. 2017 Dec 1;36(4):218-222. eCollection 2017 Dec.

9.

Is the epicardial left ventricular lead implantation an alternative approach to percutaneous attempt in patients with Steinert disease? A case report.

Papa AA, Rago A, Petillo R, D'Ambrosio P, Scutifero M, Feo M, Maiello C, Palladino A.

Acta Myol. 2017 Dec 1;36(4):213-217. eCollection 2017 Dec.

10.

Three new cases of dilated cardiomyopathy caused by mutations in LMNA gene.

Sivitskaya LN, Danilenko NG, Vaikhanskaya TG, Kurushka TV, Davydenko OG.

Acta Myol. 2017 Dec 1;36(4):207-212. eCollection 2017 Dec.

11.

The multifaceted clinical presentation of VCP-proteinopathy in a Greek family.

Papadimas GK, Paraskevas GP, Zambelis T, Karagiaouris C, Bourbouli M, Bougea A, Walter MC, Schumacher NU, Krause S, Kapaki E.

Acta Myol. 2017 Dec 1;36(4):203-206. eCollection 2017 Dec.

12.

Study of anti-Müllerian hormone levels in patients with Myotonic Dystrophy Type 1. Preliminary results.

Ergoli M, Venditti M, Dotolo R, Picillo E, Minucci S, Politano L.

Acta Myol. 2017 Dec 1;36(4):199-202. eCollection 2017 Dec.

13.

Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry.

Vittonatto E, Boschi S, CHIADò-Piat L, Ponzalino V, Bortolani S, Brusa C, Rainero I, Ricci F, Vercelli L, Mongini T.

Acta Myol. 2017 Dec 1;36(4):191-198. eCollection 2017 Dec.

14.
15.

Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costs.

Magliano L, Scutifero M, Patalano M, Sagliocchi A, Zaccaro A, Civati F, Brighina E, Vita G, Messina S, Sframeli M, Lombardo ME, Scalise R, Colia G, Catteruccia M, Berardinelli A, Motta MC, Gaiani A, Semplicini C, Bello L, Astrea G, Ricci G, D'Angelo MG, Vita G, Pane M, D'Amico A, Balottin U, Angelini C, Battini R, Politano L.

Acta Myol. 2017 Jun;36(2):41-45. Review. Erratum in: Acta Myol. 2017 Sep 01;36(3):183.

16.

Effect on lung function of mounthpiece ventilation in Steinert disease. A case report.

Annunziata A, Fiorentino G, Esquinas A.

Acta Myol. 2017 Mar;36(1):33-35.

17.

Congenital myasthenic syndrome: phenotypic variability in patients harbouring p.T159P mutation in CHRNE gene.

Ardissone A, Moroni I, Bernasconi P, Brugnoni R.

Acta Myol. 2017 Mar;36(1):28-32.

18.

Mitochondrial ANT-1 related adPEO leading to cognitive impairment: is there a link?

Simoncini C, Siciliano G, Tognoni G, Mancuso M.

Acta Myol. 2017 Mar;36(1):25-27.

19.

Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventions.

Politano L, Scutifero M, Patalano M, Sagliocchi A, Zaccaro A, Civati F, Brighina E, Vita G, Messina S, Sframeli M, Lombardo ME, Scalise R, Colia G, Catteruccia M, Berardinelli A, Motta MC, Gaiani A, Semplicini C, Bello L, Astrea G, Ricci G, D'Angelo MG, Vita G, Pane M, D'Amico A, Balottin U, Angelini C, Battini R, Magliano L.

Acta Myol. 2017 Mar;36(1):19-24. Erratum in: Acta Myol. 2017 Sep 01;36(3):182.

20.

Personality traits in patients with myotonic dystrophy type 2.

Paunic T, Peric S, Parojcic A, Savic-Pavicevic D, Vujnic M, Pesovic J, Basta I, Lavrnic D, Rakocevic-Stojanovic V.

Acta Myol. 2017 Mar;36(1):14-18.

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