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1988 1
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2009 2
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67 results

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Page 1
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort.
de Bruyn A, Montagnese F, Holm-Yildiz S, Scharff Poulsen N, Stojkovic T, Behin A, Palmio J, Jokela M, De Bleecker JL, de Visser M, van der Kooi AJ, Ten Dam L, Domínguez González C, Maggi L, Gallone A, Kostera-Pruszczyk A, Macias A, Łusakowska A, Nedkova V, Olive M, Álvarez-Velasco R, Wanschitz J, Paradas C, Mavillard F, Querin G, Fernández-Eulate G, Quinlivan R, Walter MC, Depuydt CE, Udd B, Vissing J, Schoser B, Claeys KG. de Bruyn A, et al. Among authors: gallone a. Brain. 2023 Sep 1;146(9):3800-3815. doi: 10.1093/brain/awad088. Brain. 2023. PMID: 36913258
A New Vision of IgA Nephropathy: The Missing Link.
Sallustio F, Curci C, Di Leo V, Gallone A, Pesce F, Gesualdo L. Sallustio F, et al. Among authors: gallone a. Int J Mol Sci. 2019 Dec 26;21(1):189. doi: 10.3390/ijms21010189. Int J Mol Sci. 2019. PMID: 31888082 Free PMC article. Review.
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity.
Gorgoglione D, Sabbatini D, Riguzzi P, Capece G, Pane M, Servidei S, Briganti M, Sancricca C, Bruschi F, Ardissone A, Masson R, Gallone A, Maggi L, Picillo E, Politano L, Petrosino A, Vianello S, Penzo M, Villa M, Sframeli M, Allegra C, Barp A, Di Bari A, Salmin F, Albamonte E, Colacicco G, Panicucci C, Traverso M, Palermo C, Lerario A, Velardo D, D'Angelo MG, Berardinelli A, Gardani A, Nicotra R, Parravicini S, Siciliano G, Ricci G, Torri F, Gadaleta G, Urbano G, Rolle E, Ricci F, D'Amico A, Catteruccia M, Pini A, Giannotta M, Battini R, Marinella G, Previtali SC, Zambon AA, Ferlini A, Fortunato F, Magri F, Mongini TE, Sansone VA, Bruno C, Messina S, Nigro V, Moroni I, Mercuri E, Bello L, Pegoraro E. Gorgoglione D, et al. Among authors: gallone a. Brain. 2025 May 13;148(5):1695-1706. doi: 10.1093/brain/awae358. Brain. 2025. PMID: 39499670
Medical treatment for adenomyosis: long term use of progestins.
Vannuccini S, La Torre F, Toscano F, Speciale AR, Giani M, Tureli D, Manzi V, Gallone A, Petraglia F. Vannuccini S, et al. Among authors: gallone a. Gynecol Endocrinol. 2025 Dec;41(1):2511329. doi: 10.1080/09513590.2025.2511329. Epub 2025 May 27. Gynecol Endocrinol. 2025. PMID: 40424290 Free article.
A transcriptomics study of hereditary angioedema attacks.
Castellano G, Divella C, Sallustio F, Montinaro V, Curci C, Zanichelli A, Bonanni E, Suffritti C, Caccia S, Bossi F, Gallone A, Schena FP, Gesualdo L, Cicardi M. Castellano G, et al. Among authors: gallone a. J Allergy Clin Immunol. 2018 Sep;142(3):883-891. doi: 10.1016/j.jaci.2018.03.016. Epub 2018 May 4. J Allergy Clin Immunol. 2018. PMID: 29729940 Free article.
A renal biopsy-anchored multi-marker signature involving AOPEP SNP-driven splicing, miR-27b-3p and glycated albumin for stratifying renal damage in type 2 diabetes.
Conserva F, Pesce F, Cinefra C, Marvulli TM, Bari ID, Stasi A, Faienza MF, Rossini M, Montinaro A, Squiccimarro E, Sclavo G, Schirinzi A, Serio FD, Nair V, Fermin D, Menon R, Otto E, Sallustio F, Gallone A, Stallone G, Zaza G, Laviola L, Fiorentino M, Giorgino F, Gomez MF, Kretzler M, Gesualdo L, Pontrelli P. Conserva F, et al. Among authors: gallone a. Diabetes Res Clin Pract. 2025 Nov;229:112460. doi: 10.1016/j.diabres.2025.112460. Epub 2025 Sep 9. Diabetes Res Clin Pract. 2025. PMID: 40934963 Free article.
Autosomal recessive Bethlem myopathy: a 30-year journey.
Gallone A, Riolo G, Ruggieri A, Iannibelli E, Salerno F, Nicolini De Gaetano L, Carnazzi A, Maggi L, Gibertini S. Gallone A, et al. J Neurol. 2025 Jun 23;272(7):473. doi: 10.1007/s00415-025-13214-w. J Neurol. 2025. PMID: 40550965 Free PMC article. No abstract available.
67 results