Foti FM - Search Results

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Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene.

Bonanno C, Rodolico C, Töpf A, Foti FM, Liu WW, Beeson D, Toscano A, Lochmüller H. Bonanno C, et al. Among authors: foti fm. Neuromuscul Disord. 2020 Apr;30(4):336-339. doi: 10.1016/j.nmd.2020.02.012. Epub 2020 Feb 24. Neuromuscul Disord. 2020. PMID: 32360402

Is exchange transfusion a possible treatment for neonatal hemochromatosis?

Timpani G, Foti F, Nicolò A, Nicotina PA, Nicastro E, Iorio R. Timpani G, et al. J Hepatol. 2007 Nov;47(5):732-5. doi: 10.1016/j.jhep.2007.07.018. Epub 2007 Aug 30. J Hepatol. 2007. PMID: 17869371

Spontaneous hypercalcemia in patients undergoing dialysis. Etiologic and therapeutic considerations.

Piraino BM, Rault R, Greenberg A, Dominguez JH, Wallia R, Houck P, Segre GV, Chen T, Foti FM, Puschett JB. Piraino BM, et al. Among authors: foti fm. Am J Med. 1986 Apr;80(4):607-15. doi: 10.1016/0002-9343(86)90815-6. Am J Med. 1986. PMID: 3963041

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