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Year Number of Results
2015 3
2016 1
2017 1
2018 1
2019 5
2020 8
2021 4
2022 5
2023 4
2024 4
2025 5

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37 results

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Page 1
Targeting Mast Cells: Sodium Cromoglycate as a Possible Treatment of Lipedema.
Bonetti G, Michelini S, Donato K, Dhuli K, Medori MC, Micheletti C, Marceddu G, Herbst KL, Cristoni S, Fulcheri E, Buffelli F, Bertelli M. Bonetti G, et al. Among authors: buffelli f. Clin Ter. 2023 Nov-Dec;174(Suppl 2(6)):256-262. doi: 10.7417/CT.2023.2496. Clin Ter. 2023. PMID: 37994773 Free article.
Novel KIF26A variants associated with pediatric intestinal pseudo-obstruction (PIPO) and brain developmental defects.
Nosrati MSS, Doustmohammadi A, Severino M, Romano F, Zafari M, Nemati AH, Velmans C, Netzer C, Breuer J, Broekaert IJ, Joachim A, Almasri N, Kruer MC, Skidmore P, Bisarad P, Hoque J, Bakhtiari S, Torella A, Nigro V, Buffelli F, Fulcheri E, Müller A, Zara F, Capra V, Scala M. Nosrati MSS, et al. Among authors: buffelli f. Clin Genet. 2025 Jan;107(1):83-90. doi: 10.1111/cge.14621. Epub 2024 Sep 21. Clin Genet. 2025. PMID: 39305096 Free PMC article.
Genetics of lipedema: new perspectives on genetic research and molecular diagnoses.
Paolacci S, Precone V, Acquaviva F, Chiurazzi P, Fulcheri E, Pinelli M, Buffelli F, Michelini S, Herbst KL, Unfer V, Bertelli M; GeneOb Project. Paolacci S, et al. Among authors: buffelli f. Eur Rev Med Pharmacol Sci. 2019 Jul;23(13):5581-5594. doi: 10.26355/eurrev_201907_18292. Eur Rev Med Pharmacol Sci. 2019. PMID: 31298310 Free article. Review.
Steroid-converting enzymes in human adipose tissues and fat deposition with a focus on AKR1C enzymes.
Kiani AK, Mor M, Bernini A, Fulcheri E, Michelini S, Herbst KL, Buffelli F, Belgrado JP, Kaftalli J, Stuppia L, Dautaj A, Dhuli K, Guda T, Manara E, Maltese PE, Michelini S, Chiurazzi P, Paolacci S, Ceccarini MR, Beccari T, Bertelli M. Kiani AK, et al. Among authors: buffelli f. Eur Rev Med Pharmacol Sci. 2021 Dec;25(1 Suppl):23-32. doi: 10.26355/eurrev_202112_27330. Eur Rev Med Pharmacol Sci. 2021. PMID: 34890031 Free article. Review.
Primary Lung Tumors in Children: Insights from a Single-Center Case Series.
Borgia P, Cafferata B, Paratore C, Anfigeno L, Conte A, Florio A, Gallizia A, Del Monte M, Buffelli F, Rizzo F, Damasio MB, Salvati P, Perri K, Garaventa A, Battaglia T, Livellara V, Conte M, Rossi GA, Vellone VG, Torre M, Castellani C, Sacco O. Borgia P, et al. Among authors: buffelli f. J Clin Med. 2025 Mar 22;14(7):2173. doi: 10.3390/jcm14072173. J Clin Med. 2025. PMID: 40217628 Free PMC article.
A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications.
Scala M, Leong NCP, Uyen Le TN, Zhang Y, Wu Y, Severino M, Madia F, Shams Nosrati MS, Dostmohammadi A, Capra V, Paladini D, Buffelli F, Fulcheri E, Cappato S, Menta L, Bocciardi R, Zara F, Nguyen LN. Scala M, et al. Among authors: buffelli f. Eur J Hum Genet. 2025 Mar 25. doi: 10.1038/s41431-025-01836-7. Online ahead of print. Eur J Hum Genet. 2025. PMID: 40133703
37 results