Results 171 to 180 of about 917,566 (209)
Some of the next articles are maybe not open access.
Current Treatment Options in Gastroenterology, 2003
Systemic mastocytosis is a rare clinical disorder characterized by the proliferation of mast cells, which are commonly in the skin but may be found in other body sites as well. Mast cells contain chemically active substances that, on release, produce symptoms associated with the disease.
openaire +2 more sources
Systemic mastocytosis is a rare clinical disorder characterized by the proliferation of mast cells, which are commonly in the skin but may be found in other body sites as well. Mast cells contain chemically active substances that, on release, produce symptoms associated with the disease.
openaire +2 more sources
[Systemic mastocytosis and malignant mastocytosis].
Presse medicale (Paris, France : 1983), 1990Systemic mastocytosis is a rare, often undiagnosed disease characterized by the proliferation of mast cells in several tissues. The clinical symptoms are related to the mast cell infiltrates, but also to the release of numerous mediators. Malignant mastocytosis is a term that refers to two different entities: aggressive mastocytosis, where the outcome ...
O, Lortholary +4 more
openaire +1 more source
DeckerMed Gastroenterology, Hepatology and Endoscopy, 2018
Systemic mastocytosis (SM) is a disease characterized by an abnormal proliferation and accumulation of a clonal population of mast cells in the tissues including the bone marrow, gastrointestinal tract, and skin. In the most common form, indolent mastocytosis, the symptoms are most often due to the consequences of mast cell activation and include ...
openaire +2 more sources
Systemic mastocytosis (SM) is a disease characterized by an abnormal proliferation and accumulation of a clonal population of mast cells in the tissues including the bone marrow, gastrointestinal tract, and skin. In the most common form, indolent mastocytosis, the symptoms are most often due to the consequences of mast cell activation and include ...
openaire +2 more sources
2016
Clinical History Image Findings Discussion Find Diagnosis Differential ...
openaire +1 more source
Clinical History Image Findings Discussion Find Diagnosis Differential ...
openaire +1 more source
Presse medicale (Paris, France : 1983), 2005
Systemic mastocytosis is characterized by abnormal mast cell proliferation in different organs. The 2001 consensus classification distinguishes in separate categories indolent systemic mastocytosis, systemic mastocytosis with concomitant blood disease, aggressive systemic mastocytosis and mast cell leukemia. Clinical manifestations are caused by tissue
O, Fain +6 more
openaire +1 more source
Systemic mastocytosis is characterized by abnormal mast cell proliferation in different organs. The 2001 consensus classification distinguishes in separate categories indolent systemic mastocytosis, systemic mastocytosis with concomitant blood disease, aggressive systemic mastocytosis and mast cell leukemia. Clinical manifestations are caused by tissue
O, Fain +6 more
openaire +1 more source
Orvosi hetilap, 1997
The systemic mastocytosis is a rare disorder, however, the authors recently diagnosed two cases causing diagnostic problems. The diagnosis was proved by bone marrow biopsy in both patients. The authors review the diagnostic pathway considering the pitfalls.
T, Szabó +7 more
openaire +1 more source
The systemic mastocytosis is a rare disorder, however, the authors recently diagnosed two cases causing diagnostic problems. The diagnosis was proved by bone marrow biopsy in both patients. The authors review the diagnostic pathway considering the pitfalls.
T, Szabó +7 more
openaire +1 more source
Systemic mastocytosis and osteoporosis
Osteoporosis International, 1993A, Chines +4 more
openaire +2 more sources