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A focus on the percutaneous therapy of mitral and tricuspid regurgitation.
Frazzetto M, Sanfilippo C, Ferrarotto L, Tamburino C. Frazzetto M, et al. Among authors: sanfilippo c. Eur Heart J Suppl. 2023 Apr 21;25(Suppl B):B155-B160. doi: 10.1093/eurheartjsupp/suad095. eCollection 2023 Apr. Eur Heart J Suppl. 2023. PMID: 37091654 Free PMC article.
Safety and Effectiveness of Concomitant Mitral Transcatheter Edge-to-Edge Repair and Left Atrial Appendage Closure.
Frazzetto M, Sanfilippo C, Costa G, Scandura S, Castania G, De Santis J, Sanfilippo M, Di Salvo ME, Uccello S, Rugiano G, Rizzo S, Barbera C, Tamburino C, Barbanti M, Grasso C. Frazzetto M, et al. Among authors: sanfilippo m, sanfilippo c. J Clin Med. 2023 Jul 18;12(14):4742. doi: 10.3390/jcm12144742. J Clin Med. 2023. PMID: 37510857 Free PMC article.
Safety and Efficacy of Percutaneous Left Atrial Appendage Closure Without Preprocedural Imaging.
Sanfilippo C, Frazzetto M, Costa G, Contrafatto C, Giacalone C, Tricomi G, Barbera C, Rizzo S, De Santis J, Sanfilippo M, Castania G, Di Salvo ME, Scandura S, Tamburino C, Barbanti M, Grasso C. Sanfilippo C, et al. Among authors: sanfilippo m. Circ Cardiovasc Interv. 2024 Jul;17(7):e014183. doi: 10.1161/CIRCINTERVENTIONS.124.014183. Epub 2024 Jun 17. Circ Cardiovasc Interv. 2024. PMID: 38881462 No abstract available.
Abdominal wall complications after kidney transplantation: A clinical review.
Gioco R, Sanfilippo C, Veroux P, Corona D, Privitera F, Brolese A, Ciarleglio F, Volpicelli A, Veroux M. Gioco R, et al. Among authors: sanfilippo c. Clin Transplant. 2021 Dec;35(12):e14506. doi: 10.1111/ctr.14506. Epub 2021 Oct 28. Clin Transplant. 2021. PMID: 34634148 Free PMC article. Review.
Pediatric Interventions in a Sanfilippo Syndrome Patient Under General Anesthesia: A Case Report.
Al Malak A, Issawi H, Hassoun M, Al Halabi M. Al Malak A, et al. Case Rep Dent. 2025 Jan 6;2025:7892363. doi: 10.1155/crid/7892363. eCollection 2025. Case Rep Dent. 2025. PMID: 39811794 Free PMC article.
Background: Mucopolysaccharidosis (MPS) Type III (MPS III) or Sanfilippo syndrome is a rare autosomal recessive inherited metabolic disorder. ...
Background: Mucopolysaccharidosis (MPS) Type III (MPS III) or Sanfilippo syndrome is a rare autosomal recessive inherit …
Multi-omics analyses of early-onset familial Alzheimer's disease and Sanfilippo syndrome zebrafish models reveal commonalities in disease mechanisms.
Barthelson K, Protzman RA, Snel MF, Hemsley K, Lardelli M. Barthelson K, et al. Biochim Biophys Acta Mol Basis Dis. 2025 Jan 9;1871(3):167651. doi: 10.1016/j.bbadis.2024.167651. Online ahead of print. Biochim Biophys Acta Mol Basis Dis. 2025. PMID: 39798820
Sanfilippo syndrome (mucopolysaccharidosis type III, MPSIII) causes childhood dementia, while Alzheimer's disease is the most common type of adult-onset dementia. ...We identified substantially more differentially expressed genes and pathways in MPS III zebra …
Sanfilippo syndrome (mucopolysaccharidosis type III, MPSIII) causes childhood dementia, while Alzheimer's disease is the most …
The Role of Gene Expression Dysregulation in the Pathogenesis of Mucopolysaccharidosis: A Comparative Analysis of Shared and Specific Molecular Markers in Neuronopathic and Non-Neuronopathic Types of the Disease.
Wiśniewska K, Żabińska M, Szulc A, Gaffke L, Węgrzyn G, Pierzynowska K. Wiśniewska K, et al. Int J Mol Sci. 2024 Dec 15;25(24):13447. doi: 10.3390/ijms252413447. Int J Mol Sci. 2024. PMID: 39769211 Free PMC article.
Mucopolysaccharidosis (MPS) comprises a group of inherited metabolic diseases. Each MPS type is caused by a deficiency in the activity of one kind of enzymes involved in glycosaminoglycan (GAG) degradation, resulting from the presence of pathogenic variant(s) of the corres …
Mucopolysaccharidosis (MPS) comprises a group of inherited metabolic diseases. Each MPS type is caused by a deficiency in the activit …
Early investigation of sensorineural hearing loss enables diagnosis of rare metabolic diseases, such as mucopolysaccharidosis type III.
Shrivastava R, Sherwin L, Davison J, Walter S. Shrivastava R, et al. BMJ Case Rep. 2025 Jan 4;18(1):e261859. doi: 10.1136/bcr-2024-261859. BMJ Case Rep. 2025. PMID: 39755556
Early investigation led to a relatively early diagnosis of mucopolysaccharidosis (MPS) type IIIA: Sanfilippo disease which enabled the family to access a novel treatment option which otherwise would not have been possible.Infants with early signs and symptoms of MPS may pr …
Early investigation led to a relatively early diagnosis of mucopolysaccharidosis (MPS) type IIIA: Sanfilippo disease which enabled th …
1,270 results