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Michele E. Paessler, D.O.

Michele E. Paessler, D.O.

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Assistant Professor of Clinical Pathology and Laboratory Medicine
Department: Pathology and Laboratory Medicine

Contact information
Abramson Research Building
Suite 716F
3615 Civic Center Blvd
Philadelphia, PA 19104
Office: 267-426-7309
Fax: 215-590-2130
Muhlenberg College (with honors), Allentown, PA, 1993.
Philadelphia College of Osteopathic Medicine, Philadelphia, PA, 1997.
Permanent link
Perelman School of Medicine > Faculty > Search

Selected Publications

Michele Paessler and Helge Hartung: Dehydrated hereditary stomatocytosis masquerading as MDS. Blood 125(11): 1841, Mar 2015.

Daria V. Babushok, Nieves Perdigones, Juan C. Perin, Timothy S. Olson, Wenda Ye, Jacquelyn J. Roth, Curt Lind, Carine Cattier, Yimei Li8, Helge Hartung, Michele E. Paessler, Dale M. Frank, Hongbo M. Xie, Shanna Cross, Joshua D. Cockroft, Gregory M. Podsakoff, Dimitrios Monos, Jaclyn A. Biegel, Philip J. Mason, Monica Bessler: Emergence of Clonal Hematopoiesis in the Majority of Patients with Acquired Aplastic Anemia. Cancer Cytogenetics 4: 115-28, Feb 2015.

Tamhankar MA, Paessler ME, Kharlip JN, Shekdar KV, Burnham JM, Cole KA: A 16-year-old boy with a suprasellar mass. J Neuroophthalmol. 34(3): 295-300, Sept 2014.

Canna SW, Costa-Reis P, Bernal WE, Chu N, Sullivan KE, Paessler ME, Behrens EM: Brief report: alternative activation of laser-captured murine hemophagocytes. Arthritis Rheumatol 66(6): 1666-71, Jun 2014.

Olson TS1, Chan ES, Paessler ME, Sullivan KE, Frantz CN, Russo P, Bessler M: Liver failure due to hepatic angiosarcoma in an adolescent with dyskeratosis congenita. J Pediatr Hematol Oncol 36(4), May 2014.

Paessler M and Choi J: Relapsed nodular sclerosis Hodgkin lymphoma and therapy-related myeloid sarcoma in a mediastinal mass. Blood (eds.). 123(9): 1291, February 2014.

Paessler M: Case study interpretation Fort Lauderdale: Case 2. Cytometry B Clin Cytom Jan 2014.

Babushok DV1, Xie HM, Roth JJ, Perdigones N, Olson TS, Cockroft JD, Gai X, Perin JC, Li Y, Paessler ME, Hakonarson H, Podsakoff GM, Mason PJ, Biegel JA, Bessler M: Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes. Br J Haematol 2014 (164(1)): 73-82, Jan 2014.

Canna SW1, Wrobel J, Chu N, Kreiger PA, Paessler M, Behrens EM.: Interferon-γ mediates anemia but is dispensable for fulminant toll-like receptor 9-induced macrophage activation syndrome and hemophagocytosis in mice. Arthritis Rheum 7(65): 1764-75, Jul 2013.

Keller MD, Ganesh J, Heltzer M, Paessler M, Bergqvist AG, Baluarte HJ, Watkins D, Rosenblatt DS, Orange JS: Severe combined immunodeficiency resulting from mutations in MTHFD1. Pediatrics 131(2): e629-34, February 2013.

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Last updated: 10/01/2015
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