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alessandro milesi
(9 results)?
Comparison of Protein- or Amino Acid-Based Supplements in the Rehabilitation of Men with Severe Obesity: A Randomized Controlled Pilot Study.
J Clin Med. 2023 Jun 25;12(13):4257. doi: 10.3390/jcm12134257.
J Clin Med. 2023.
PMID: 37445292
Free PMC article.
Recurrent transient global amnesia as presenting symptoms of CADASIL.
Pradotto L, Orsi L, Mencarelli M, Caglio M, Lauro D, Milesi A, Di Blasio A, Mauro A.
Pradotto L, et al. Among authors: milesi a.
Clin Case Rep. 2016 Sep 28;4(11):1045-1048. doi: 10.1002/ccr3.666. eCollection 2016 Nov.
Clin Case Rep. 2016.
PMID: 27830070
Free PMC article.
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Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy.
Magliano L, Obici L, Sforzini C, Mazzeo A, Russo M, Cappelli F, Fenu S, Luigetti M, Tagliapietra M, Gemelli C, Leonardi L, Tozza S, Pradotto LG, Citarelli G, Mauro A, Manganelli F, Antonini G, Grandis M, Fabrizi GM, Sabatelli M, Pareyson D, Perfetto F, Merlini G, Vita G; ATTRv Collaborators.
Magliano L, et al.
Orphanet J Rare Dis. 2021 Apr 7;16(1):163. doi: 10.1186/s13023-021-01812-6.
Orphanet J Rare Dis. 2021.
PMID: 33827635
Free PMC article.
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Fibroblasts and Endothelial Cells in Three-Dimensional Models: A New Tool for Addressing the Pathogenesis of Systemic Sclerosis as a Prototype of Fibrotic Vasculopathies.
Bodio C, Milesi A, Lonati PA, Chighizola CB, Mauro A, Pradotto LG, Meroni PL, Borghi MO, Raschi E.
Bodio C, et al. Among authors: milesi a.
Int J Mol Sci. 2024 Feb 28;25(5):2780. doi: 10.3390/ijms25052780.
Int J Mol Sci. 2024.
PMID: 38474040
Free PMC article.
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Amyloid polyneuropathy following domino liver transplantation.
Pradotto L, Franchello A, Milesi A, Romagnoli R, Bigoni M, Vigna L, Di Sapio A, Salizzoni M, Mauro A.
Pradotto L, et al. Among authors: milesi a.
Muscle Nerve. 2012 Jun;45(6):918-9. doi: 10.1002/mus.23265.
Muscle Nerve. 2012.
PMID: 22581551
No abstract available.
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A new NOTCH3 mutation presenting as primary intracerebral haemorrhage.
Pradotto L, Orsi L, Daniele D, Caroppo P, Lauro D, Milesi A, Sellitti L, Mauro A.
Pradotto L, et al. Among authors: milesi a.
J Neurol Sci. 2012 Apr 15;315(1-2):143-5. doi: 10.1016/j.jns.2011.12.003. Epub 2011 Dec 27.
J Neurol Sci. 2012.
PMID: 22206696
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Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation.
Pradotto L, Mencarelli M, Bigoni M, Milesi A, Di Blasio A, Mauro A.
Pradotto L, et al. Among authors: milesi a.
J Neurol Sci. 2016 Dec 15;371:81-84. doi: 10.1016/j.jns.2016.10.029. Epub 2016 Oct 19.
J Neurol Sci. 2016.
PMID: 27871455
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