Harvard Catalyst Profiles

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Miki Nishitani, 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. Nishitani M, Moerdler S, Kesselheim J. Perceptions of the stressful job search for pediatric hematology/oncology fellows. Pediatr Blood Cancer. 2023 04; 70(4):e30226. PMID: 36715452.
    Citations:    Fields:    Translation:Humans
  2. Mangada KL, Moffet J, Nishitani M, Albuquerque S, Duncan CN. Interprofessional Team-based Care of the Hematopoietic Cell Transplantation Patient With Hepatic Veno-occlusive Disease/Sinusoidal Obstruction Syndrome. J Pediatr Hematol Oncol. 2023 01 01; 45(1):12-17. PMID: 36598959; PMCID: PMC9809996.
    Citations:    Fields:    Translation:Humans
  3. Nishitani M, Alali M, Hageman JR, Nubani R, Chong G, Tran L, Husain AN, Rosebush J. Hyperferritinemia: A Diagnostic Marker for Disseminated Neonatal Herpes Simplex Virus Infection? Pediatr Ann. 2021 Jun; 50(6):e264-e267. PMID: 34115559.
    Citations:    Fields:    Translation:Humans
  4. Merke DP, Chen W, Morissette R, Xu Z, Van Ryzin C, Sachdev V, Hannoush H, Shanbhag SM, Acevedo AT, Nishitani M, Arai AE, McDonnell NB. Tenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2013 Feb; 98(2):E379-87. PMID: 23284009; PMCID: PMC3565116.
    Citations: 31     Fields:    Translation:Humans
  5. Finkielstain GP, Kim MS, Sinaii N, Nishitani M, Van Ryzin C, Hill SC, Reynolds JC, Hanna RM, Merke DP. Clinical characteristics of a cohort of 244 patients with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2012 Dec; 97(12):4429-38. PMID: 22990093; PMCID: PMC3513542.
    Citations: 92     Fields:    Translation:Humans
  6. Chen W, Xu Z, Nishitani M, Van Ryzin C, McDonnell NB, Merke DP. Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Genet. 2012 Dec; 131(12):1889-94. PMID: 22886582; PMCID: PMC3493742.
    Citations: 7     Fields:    Translation:Humans
  7. Yamamichi S, Fujiwara Y, Kikuchi T, Nishitani M, Matsushita Y, Hasumi K. Extracellular histone induces plasma hyaluronan-binding protein (factor VII activating protease) activation in vivo. Biochem Biophys Res Commun. 2011 Jun 10; 409(3):483-8. PMID: 21600885.
    Citations: 18     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.