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Neutral lipid-storage disease with myopathy and extended phenotype with novel PNPLA2 mutation.
Muscle Nerve. 2016 Apr;53(4):644-8. doi: 10.1002/mus.24983. Epub 2016 Feb 22.
Muscle Nerve. 2016.
PMID: 26600210
Review.
Analysis of Children and Adolescents with Familial Hypercholesterolemia.
Minicocci I, Pozzessere S, Prisco C, Montali A, di Costanzo A, Martino E, Martino F, Arca M.
Minicocci I, et al. Among authors: pozzessere s.
J Pediatr. 2017 Apr;183:100-107.e3. doi: 10.1016/j.jpeds.2016.12.075. Epub 2017 Feb 1.
J Pediatr. 2017.
PMID: 28161202
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Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency.
Leuzzi V, Carducci CA, Carducci CL, Pozzessere S, Burlina A, Cerone R, Concolino D, Donati MA, Fiori L, Meli C, Ponzone A, Porta F, Strisciuglio P, Antonozzi I, Blau N.
Leuzzi V, et al. Among authors: pozzessere s.
Clin Genet. 2010 Mar;77(3):249-57. doi: 10.1111/j.1399-0004.2009.01306.x. Epub 2009 Jan 3.
Clin Genet. 2010.
PMID: 20059486
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Exon deletions of the phenylalanine hydroxylase gene in Italian hyperphenylalaninemics.
Cali F, Ruggeri G, Vinci M, Meli C, Carducci C, Leuzzi V, Pozzessere S, Schinocca P, Ragalmuto A, Chiavetta V, Micciche S, Romano V.
Cali F, et al. Among authors: pozzessere s.
Exp Mol Med. 2010 Feb 28;42(2):81-6. doi: 10.3858/emm.2010.42.2.009.
Exp Mol Med. 2010.
PMID: 19946181
Free PMC article.
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Tyrosine hydroxylase deficiency presenting with a biphasic clinical course.
Giovanniello T, Leuzzi V, Carducci C, Carducci C, Sabato ML, Artiola C, Santagata S, Pozzessere S, Antonozzi I.
Giovanniello T, et al. Among authors: pozzessere s.
Neuropediatrics. 2007 Aug;38(4):213-5. doi: 10.1055/s-2007-991151.
Neuropediatrics. 2007.
PMID: 18058633
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Erythrocyte phenotype in a pregnant woman of Sri Lanka. Description of the case and complications related to communication problems.
Ringressi A, Cunsolo V, Malentacchi F, Pozzessere S.
Ringressi A, et al. Among authors: pozzessere s.
Ann Ist Super Sanita. 2018 Jan-Mar;54(1):35-39. doi: 10.4415/ANN_18_01_08.
Ann Ist Super Sanita. 2018.
PMID: 29616672
Free article.
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HLA class I expression on human platelets is highly variable and correlates with distinct allele group frequencies.
Cantisani R, Del Re V, Toraldo F, Cantara S, Pozzessere S, Marotta G, Spreafico A.
Cantisani R, et al. Among authors: pozzessere s.
Blood Transfus. 2024 Jan 11. doi: 10.2450/BloodTransfus.571. Online ahead of print.
Blood Transfus. 2024.
PMID: 38315535
Free article.
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