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Xenia Parisi, M.D.


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Ramia de Cap M, Parisi X, Tahan SR. Exogenous ochronosis associated with dimethoxytolyl propylresorcinol (UP302). J Dermatol. 2021 Jul; 48(7):e312-e313. PMID: 34031918.
    Citations:    Fields:    Translation:Humans
  2. O'Brien KJ, Parisi X, Shelman NR, Merideth MA, Introne WJ, Heller T, Gahl WA, Malicdan MCV, Gochuico BR. Inflammatory bowel disease in Hermansky-Pudlak syndrome: a retrospective single-centre cohort study. J Intern Med. 2021 07; 290(1):129-140. PMID: 33423334.
    Citations:    Fields:    Translation:Humans
  3. Parisi X, Bergerson J, Urban A, Darnell D, Stratton P, Freeman AF. Obstetric and Gynecological Care in Patients with STAT3-Deficient Hyper IgE Syndrome. J Clin Immunol. 2020 10; 40(7):1048-1050. PMID: 32696285.
    Citations: 1     Fields:    Translation:Humans
  4. Espinoza AF, Belfort MA, Shamshirsaz AA, Hudson KM, Parisi X, Nassr AA, Sanz Cortes M, Erfani H, Espinoza J. Association between impedance to blood flow in umbilical arteries and infant survival in twin-to-twin transfusion syndrome. Ultrasound Obstet Gynecol. 2020 04; 55(4):489-495. PMID: 31006926.
    Citations:    Fields:    
  5. Sharma P, Reichert M, Lu Y, Markello TC, Adams DR, Steinbach PJ, Fuqua BK, Parisi X, Kaler SG, Vulpe CD, Anderson GJ, Gahl WA, Malicdan MCV. Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype. PLoS Genet. 2019 05; 15(5):e1008143. PMID: 31125343.
    Citations: 4     Fields:    Translation:HumansAnimalsCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.