Results 121 to 130 of about 63,717 (177)
Real-world characteristics of systemic mastocytosis in Romania: insights from a reference-center-based descriptive study. [PDF]
Soare D +8 more
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Patient and Advanced Practitioner Perspectives on Symptom Burden and Symptom Management in Indolent Systemic Mastocytosis. [PDF]
Kurtin S +4 more
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Hematology/Oncology Clinics of North America, 2010
An unusual disease, mastocytosis challenges the pathologist with a variety of morphologic appearances and heterogeneous clinical presentations ranging from skin manifestations (pruritus, urticaria, dermatographism) to systemic signs and symptoms indicative of mast cell mediator release, including flushing, hypotension, headache, and anaphylaxis among ...
Tracy I, George, Hans-Peter, Horny
openaire +5 more sources
An unusual disease, mastocytosis challenges the pathologist with a variety of morphologic appearances and heterogeneous clinical presentations ranging from skin manifestations (pruritus, urticaria, dermatographism) to systemic signs and symptoms indicative of mast cell mediator release, including flushing, hypotension, headache, and anaphylaxis among ...
Tracy I, George, Hans-Peter, Horny
openaire +5 more sources
Avapritinib for Systemic Mastocytosis
Expert Review of Hematology, 2021Systemic mastocytosis (SM) is a rare myeloid neoplasm driven in ≈95% of cases by activating KIT mutations, usually D816V. SM can be indolent (ISM), smoldering (SSM) and advanced (AdvSM), the latter characterized by organ damage resulting from infiltrating neoplastic mast cells.
Prithviraj Bose, Srdan Verstovsek
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Blood, 2013
Clinical History: A 77âyear-old woman was seen by her general practitioner because of a changed defecation pattern. On a CT colonography, which was otherwise normal, bone abnormalities were present. The patient had no previous history of malignancy.
Bouvier, Sylvie, Arnaud, Anne
+6 more sources
Clinical History: A 77âyear-old woman was seen by her general practitioner because of a changed defecation pattern. On a CT colonography, which was otherwise normal, bone abnormalities were present. The patient had no previous history of malignancy.
Bouvier, Sylvie, Arnaud, Anne
+6 more sources
Systemic Mastocytosis and the Mastocytosis Syndrome
Journal of Cutaneous Pathology, 1979A patient with extensive systemic mastocytosis and the mastocytosis syndrome was studied by light and electron microscopy. Mast cell proliferation was found in the bone marrow, the liver, spleen and lymph node. In addition, the patient had telangiectasia macularis eruptiva perstans and elevated histamine levels.
G D, Monheit, T, Murad, M, Conrad
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