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Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report.
J Pediatr Endocrinol Metab. 2022 Nov 10;36(1):91-95. doi: 10.1515/jpem-2022-0365. Print 2023 Jan 27.
J Pediatr Endocrinol Metab. 2022.
PMID: 36351286
Ischemic and bleeding risk by type 2 diabetes clusters in patients with acute coronary syndrome.
Cavallari I, Maddaloni E, Gragnano F, Patti G, Antonucci E, Calabrò P, Cirillo P, Gresele P, Palareti G, Pengo V, Pignatelli P, Marcucci R; START-ANTIPLATELET collaborators.
Cavallari I, et al.
Intern Emerg Med. 2021 Sep;16(6):1583-1591. doi: 10.1007/s11739-021-02640-z. Epub 2021 Feb 22.
Intern Emerg Med. 2021.
PMID: 33616877
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