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Year Number of Results
2001 2
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Page 1
Red Blood Cell Transfusion in the Intensive Care Unit.
Raasveld SJ, de Bruin S, Reuland MC, van den Oord C, Schenk J, Aubron C, Bakker J, Cecconi M, Feldheiser A, Meier J, Müller MCA, Scheeren TWL, McQuilten Z, Flint A, Hamid T, Piagnerelli M, Tomic Mahecic T, Benes J, Russell L, Aguirre-Bermeo H, Triantafyllopoulou K, Chantziara V, Gurjar M, Myatra SN, Pota V, Elhadi M, Gawda R, Mourisco M, Lance M, Neskovic V, Podbregar M, Llau JV, Quintana-Diaz M, Cronhjort M, Pfortmueller CA, Yapici N, Nielsen ND, Shah A, de Grooth HJ, Vlaar APJ; InPUT Study Group. Raasveld SJ, et al. JAMA. 2023 Nov 21;330(19):1852-1861. doi: 10.1001/jama.2023.20737. JAMA. 2023. PMID: 37824112 Free PMC article.
N-Substituted l-Iminosugars for the Treatment of Sanfilippo Type B Syndrome.
De Pasquale V, Esposito A, Scerra G, Scarcella M, Ciampa M, Luongo A, D'Alonzo D, Guaragna A, D'Agostino M, Pavone LM. De Pasquale V, et al. J Med Chem. 2023 Feb 9;66(3):1790-1808. doi: 10.1021/acs.jmedchem.2c01617. Epub 2023 Jan 25. J Med Chem. 2023. PMID: 36696678 Free PMC article.
Sanfilippo syndrome comprises a group of four genetic diseases due to the lack or decreased activity of enzymes involved in heparan sulfate (HS) catabolism. HS accumulation in lysosomes and other cellular compartments results in tissue and organ dysfunctions, leading to a …
Sanfilippo syndrome comprises a group of four genetic diseases due to the lack or decreased activity of enzymes involved in heparan s …
Late-onset mucopolysaccharidosis type IIIA mimicking Usher syndrome.
De Falco A, Karali M, Criscuolo C, Testa F, Barillari MR, Scarpato M, Gaudieri V, Cuocolo A, Russo A, Nigro V, Simonelli F, Banfi S, Brunetti-Pierri N. De Falco A, et al. Am J Med Genet A. 2024 May;194(5):e63517. doi: 10.1002/ajmg.a.63517. Epub 2023 Dec 27. Am J Med Genet A. 2024. PMID: 38149346
Mucopolysaccharidosis type IIIA (MPS IIIA or Sanfilippo syndrome type A) is an autosomal recessive lysosomal storage disorder caused by pathogenic variants in the SGSH gene encoding N-sulfoglucosamine sulfohydrolase, an enzyme involved in the degradation of heparan sulfate …
Mucopolysaccharidosis type IIIA (MPS IIIA or Sanfilippo syndrome type A) is an autosomal recessive lysosomal storage disorder caused …
Invasive cryptococcal disease in COVID-19: systematic review of the literature and analysis.
Pipitone G, Spicola D, Abbott M, Sanfilippo A, Onorato F, Di Lorenzo F, Ficalora A, Buscemi C, Alongi I, Imburgia C, Ciusa G, Agrenzano S, Gizzi A, Guida Marascia F, Granata G, CimÒ F, Verde MS, Di Bernardo F, Scafidi A, Mazzarese V, Sagnelli C, Petrosillo N, Cascio A, Iaria C. Pipitone G, et al. Infez Med. 2023 Mar 1;31(1):6-12. doi: 10.53854/liim-3101-2. eCollection 2022. Infez Med. 2023. PMID: 36908394 Free PMC article. Review.
Effectiveness of Rehabilitative Intervention on Pain, Postural Balance, and Quality of Life in Women with Multiple Vertebral Fragility Fractures: A Prospective Cohort Study.
Scaturro D, Rizzo S, Sanfilippo V, Giustino V, Messina G, Martines F, Falco V, Cuntrera D, Moretti A, Iolascon G, Letizia Mauro G. Scaturro D, et al. J Funct Morphol Kinesiol. 2021 Mar 3;6(1):24. doi: 10.3390/jfmk6010024. J Funct Morphol Kinesiol. 2021. PMID: 33802536 Free PMC article.
The impact of COVID-19 epidemic on eating disorders: A longitudinal observation of pre versus post psychopathological features in a sample of patients with eating disorders and a group of healthy controls.
Castellini G, Cassioli E, Rossi E, Innocenti M, Gironi V, Sanfilippo G, Felciai F, Monteleone AM, Ricca V. Castellini G, et al. Int J Eat Disord. 2020 Nov;53(11):1855-1862. doi: 10.1002/eat.23368. Epub 2020 Aug 28. Int J Eat Disord. 2020. PMID: 32856333 Free PMC article.
11 results