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Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry.
BMJ Open. 2016 Jan 5;6(1):e007798. doi: 10.1136/bmjopen-2015-007798.
BMJ Open. 2016.
PMID: 26733561
Free PMC article.
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes.
Ricci G, Ruggiero L, Vercelli L, Sera F, Nikolic A, Govi M, Mele F, Daolio J, Angelini C, Antonini G, Berardinelli A, Bucci E, Cao M, D'Amico MC, D'Angelo G, Di Muzio A, Filosto M, Maggi L, Moggio M, Mongini T, Morandi L, Pegoraro E, Rodolico C, Santoro L, Siciliano G, Tomelleri G, Villa L, Tupler R.
Ricci G, et al. Among authors: d amico mc.
J Neurol. 2016 Jun;263(6):1204-14. doi: 10.1007/s00415-016-8123-2. Epub 2016 Apr 28.
J Neurol. 2016.
PMID: 27126453
Free PMC article.
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A Case of Normal Pressure Hydrocephalus in Adult-Onset Pompe Disease.
D'Amico MC, Di Tommaso V, Di Giacomo R, Di Muzio A, Onofrj M.
D'Amico MC, et al.
J Neuromuscul Dis. 2015;2(s1):S14.
J Neuromuscul Dis. 2015.
PMID: 27858612
No abstract available.
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Holmes-Like Tremor in Ataxia With Oculomotor Apraxia Type 2.
D'Amico MC, Borrelli I, Zhuzhuni H, D'Amico A, Di Giacomo R, Mancinelli L, di Tommaso V, Di Muzio A, Onofrj M.
D'Amico MC, et al.
Mov Disord Clin Pract. 2014 Jul 28;1(3):261-262. doi: 10.1002/mdc3.12070. eCollection 2014 Sep.
Mov Disord Clin Pract. 2014.
PMID: 30713863
Free PMC article.
No abstract available.
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Ascertainment bias in dementias: a secondary to tertiary centre analysis in Central Italy and conceptual review.
Bonanni L, Bontempo G, Borrelli I, Bifolchetti S, Buongarzone MP, Carlesi N, Carolei A, Ciccocioppo F, Colangelo U, Colonna G, Desiderio M, Ferretti S, Fiorelli L, D'Alessio O, D'Amico A, D'Amico MC, De Lucia R, Del Re L, Di Blasio F, Di Giacomo R, Di Iorio A, Di Santo E, Di Giuseppe M, Felice N, Litterio P, Gabriele A, Mancino E, Manzoli L, Maruotti V, Mearelli S, Molino G, Monaco D, Nuccetelli F, Onofrj M, Perfetti B, Sacchet C, Sensi F, Sensi S, Sucapane P, Taylor JP, Thomas A, Viola P, Viola S, Zito M, Zhuzhuni H.
Bonanni L, et al. Among authors: d amico mc.
Aging Clin Exp Res. 2013 Jun;25(3):265-74. doi: 10.1007/s40520-013-0039-4. Epub 2013 Jun 20.
Aging Clin Exp Res. 2013.
PMID: 23784725
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Updates on Somatoform Disorders (SFMD) in Parkinson's Disease and Dementia with Lewy Bodies and discussion of phenomenology.
Onofrj M, Thomas A, Tiraboschi P, Wenning G, Gambi F, Sepede G, Di Giannantonio M, Di Carmine C, Monaco D, Maruotti V, Ciccocioppo F, D'Amico MC, Bonanni L.
Onofrj M, et al. Among authors: d amico mc.
J Neurol Sci. 2011 Nov 15;310(1-2):166-71. doi: 10.1016/j.jns.2011.07.010. Epub 2011 Aug 2.
J Neurol Sci. 2011.
PMID: 21813140
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Protracted benefit from paradoxical kinesia in typical and atypical parkinsonisms.
Bonanni L, Thomas A, Anzellotti F, Monaco D, Ciccocioppo F, Varanese S, Bifolchetti S, D'Amico MC, Di Iorio A, Onofrj M.
Bonanni L, et al. Among authors: d amico mc.
Neurol Sci. 2010 Dec;31(6):751-6. doi: 10.1007/s10072-010-0403-5. Epub 2010 Sep 22.
Neurol Sci. 2010.
PMID: 20859648
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ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.
Nanetti L, Sarto E, Castaldo A, Magri S, Mongelli A, Rossi Sebastiano D, Canafoglia L, Grisoli M, Malaguti C, Rivieri F, D'Amico MC, Di Bella D, Franceschetti S, Mariotti C, Taroni F.
Nanetti L, et al. Among authors: d amico mc.
J Neurol. 2019 Feb;266(2):378-385. doi: 10.1007/s00415-018-9141-z. Epub 2018 Dec 4.
J Neurol. 2019.
PMID: 30515630
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