XeniaParisiMD

PubMed

• Myeloid neoplasm with <10% blasts and t(3;5)(q25.1;q34)/NPM::MLF1: A classification dilemma.
  Fnu Sameeta, Hong Fang, Wei Wang, Zhenya Tang, Sa A Wang, Gokce A Toruner, Xenia Parisi, Joseph D Khoury, Ghayas Issa, Guillermo Garcia-Manero, L Jeffrey Medeiros, Gui...> ;American Journal of Hematology. 2024 Mar 5
• Papillary Cystadenofibroma of the Epididymis: A Case Report.
  Xenia Parisi, Alexander Feinstein, Yekaterina Merkulova, Marc Rodriguez, Yue Sun> ;International Journal of Surgical Pathology. 2023 Sep 16
• Primary Adrenal Epithelioid Angiosarcoma: A Case Report.
  Xenia Parisi, Masa Peric, Andrew E Bennett, Alyaa Al-Ibraheemi, Yue Sun> ;International Journal of Surgical Pathology. 2023 Jul 17
• Purpura fulminans due to Capnocytophaga canimorsus.
  Xenia Parisi, Germán Pihán> ;British Journal of Haematology. 2023 Aug 1
• 1 citations
  Dogliotti and Phillips classifications are unsuitable for grading the histopathological findings of exogenous ochronosis.
  Maximiliano Ramia de Cap, Xenia Parisi, Steven R Tahan> ;Journal of Cutaneous Pathology. 2022 May 1
• 2 citations
  Exogenous ochronosis associated with dimethoxytolyl propylresorcinol (UP302).
  Maximiliano Ramia de Cap, Xenia Parisi, Steven R. Tahan> ;The Journal of Dermatology. 2021 May 25
• 3 citations
  Obstetric and Gynecological Care in Patients with STAT3-Deficient Hyper IgE Syndrome.
  Xenia Parisi, Jenna R.E. Bergerson, Amanda Urban, Dirk Darnell, Pamela Stratton, Alexandra F. Freeman> ;Journal of Clinical Immunology. 2020 Jul 21
• 18 citations
  Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
  Prashant Sharma, Marie C. Reichert, Yan Lu, Thomas C. Markello, David R. Adams, Peter J. Steinbach, Brie K. Fuqua, Xenia Parisi, Stephen G. Kaler, Chris D. Vulpe, Greg...> ;Plos Genetics. 2019 May 24
• Novel mutations in CLN6 cause late-infantile neuronal ceroid lipofuscinosis without visual impairment in two unrelated patients.
  Chin, J. J.,Behnam, B.,Davids, M.,Sharma, P.,Zein, W. M.,Wang, C.,Chepa-Lotrea, X.,Gallantine, W. B.,Toro, C.,Adams, D. R.,Tifft, C. J.,Gahl, W. A.,Malicdan, MCV.> ;Mol. Genet. Metab.. 2018 Dec 12
• Early infantile-onset epileptic encephalopathy 28 due to a homozygous microdeletion involving the WWOX gene in a region of uniparental disomy.
  Davids M, Markello T, Wolfe LA, Chepa-Lotrea X, Tifft CJ, Gahl WA, Malicdan MCV> ;Human mutation. 2018-11-18
• Bi-allelic CCDC47 Variants Cause a Disorder Characterized by Woolly Hair, Liver Dysfunction, Dysmorphic Features, and Global Developmental Delay.
  Morimoto M, Waller-Evans H, Ammous Z, Song X, Strauss KA, Pehlivan D, Gonzaga-Jauregui C, Puffenberger EG, Holst CR, Karaca E, Brigatti KW, Maguire E, Coban-Akdemir ZH...> ;American journal of human genetics. 2018-10-25
• Compound heterozygosity for loss-of-function GARS variants results in a multisystem developmental syndrome that includes severe growth retardation.
  Oprescu SN, Chepa-Lotrea X, Takase R, Golas G, Markello TC, Adams DR, Toro C, Gropman AL, Hou YM, Malicdan MCV, Gahl WA, Tifft CJ, Antonellis A> ;Human mutation. 2017-07-14
• Successful Interferon-Free Therapy of Chronic Hepatitis C Virus Infection Normalizes Natural Killer Cell Function.
  Serti E, Chepa-Lotrea X, Kim YJ, Keane M, Fryzek N, Liang TJ, Ghany M, Rehermann B> ;Gastroenterology. 2015-03-06
• Ribavirin improves the IFN-γ response of natural killer cells to IFN-based therapy of hepatitis C virus infection.
  Werner JM, Serti E, Chepa-Lotrea X, Stoltzfus J, Ahlenstiel G, Noureddin M, Feld JJ, Liang TJ, Rotman Y, Rehermann B> ;Hepatology (Baltimore, Md.). 2014-08-13
• Endobiont viruses sensed by the human host - beyond conventional antiparasitic therapy.
  Fichorova RN, Lee Y, Yamamoto HS, Takagi Y, Hayes GR, Goodman RP, Chepa-Lotrea X, Buck OR, Murray R, Kula T, Beach DH, Singh BN, Nibert ML> ;PloS one. 2012-11-07
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