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Robert P. Hasserjian
Researcher at Harvard University
Publications - 343
Citations - 21234
Robert P. Hasserjian is an academic researcher from Harvard University. The author has contributed to research in topics: Medicine & Myeloid leukemia. The author has an hindex of 53, co-authored 284 publications receiving 16118 citations. Previous affiliations of Robert P. Hasserjian include Hammersmith Hospital & Partners HealthCare.
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Case records of the Massachusetts General Hospital. Case 11-2007. A 59-year-old man with neck pain, weakness in the arms, and cranial-nerve palsies.
TL;DR: A 59-year-old man was admitted to this hospital with fever and the subacute onset of progressive neurologic symptoms that included multiple cranial-nerve palsies, and analysis of the cerebrospinal fluid disclosed a lymphocytic pleocytosis and elevated protein and glucose levels.
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The current approach to the diagnosis of myelodysplastic syndromes
TL;DR: The principles of bone marrow interpretation with respect to the diagnosis and classification of MDS in the current era will be discussed, including accurate morphologic interpretation, use of flow cytometry and immunohistochemistry, appropriate use of cytogenetics, and the emerging role of molecular genetics.
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Reactive versus neoplastic bone marrow: problems and pitfalls.
TL;DR: A combination of excellent diagnostic samples, appropriate ancillary tests, and knowledge of the clinical context provides the best background to distinguish between the common reactive and neoplastic processes that involve the bone marrow and to avoid diagnostic pitfalls in making these distinctions.
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Case records of the Massachusetts General Hospital. Case 9-2011. A 37-year-old man with flushing and hypotension.
Mandakolathur R. Murali,Mariana Castells,James Y Song,David M. Dudzinski,Robert P. Hasserjian +4 more
TL;DR: A 37-year-old man was admitted to the hospital because of flushing and hypotension with near-syncope with similar episodes with increasing frequency during the past 12 years.
Journal ArticleDOI
Contribution of clonal hematopoiesis to adult-onset hemophagocytic lymphohistiocytosis.
Peter Miller,Peter Miller,Adam S. Sperling,Christopher J. Gibson,Kaushik Viswanathan,Cecilia A. Castellano,Marie McConkey,John J Ceremsak,Martin S. Taylor,Sebastian Birndt,Florian Perner,Jon E. Arnason,Mridul Agrawal,Mridul Agrawal,Alison M. Schram,Sarah Nikiforow,German Pihan,Robert P. Hasserjian,Jon C. Aster,Paul La Rosée,Elizabeth A. Morgan,Nancy Berliner,Benjamin L. Ebert,Benjamin L. Ebert +23 more
TL;DR: The data suggests that clonal hematopoiesis (CH) is more common in individuals with adult-onset HLH and can contribute to the pathophysiology of this disease.