Limit search to available items
Nearby Subjects are:
Result Page   Prev Next
Add Marked to Bag Add All On Page Add Marked to My Lists
Mark   Year Entries
 

Granulocytic Leukemias -- See Leukemia, Myeloid


Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites
  1
 

Granulocytic Leukemias, Chronic -- See Leukemia, Myelogenous, Chronic, BCR-ABL Positive


Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS
  1
 

Granulocytopenia -- See Agranulocytosis


A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS)
  1
 

Granulocytopenias -- See Agranulocytosis


A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS)
  1
 

Granuloma -- See Also the narrower term Chronic granulomatous disease


  1
Granuloma.   4
 

Granuloma benignum -- See Sarcoidosis


  1
 

Granuloma fungoides -- See Mycosis fungoides


  1
 

Granuloma, Hodgkin -- See Hodgkin Disease


A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen
  1
 

Granuloma, Hodgkin's -- See Hodgkin Disease


A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen
  1
 

Granuloma, Malignant -- See Hodgkin Disease


A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen
  1
Granuloma -- Pathophysiology. : Neoplastic mimics in thoracic and cardiovascular pathology / Mark R. Wick, Henry D. Tazelaar  2013 1
Granuloma, Plasma Cell -- pathology. : Neoplastic mimics in thoracic and cardiovascular pathology / Mark R. Wick, Henry D. Tazelaar  2013 1
 

Granuloma Pyogenicum -- See Granuloma, Pyogenic


A disorder of the skin, the oral mucosa, and the gingiva, that usually presents as a solitary polypoid capillary hemangioma often resulting from trauma. It is manifested as an inflammatory response with similar characteristics to those of a granuloma
  1
 

Granuloma Telangiecticum -- See Granuloma, Pyogenic


A disorder of the skin, the oral mucosa, and the gingiva, that usually presents as a solitary polypoid capillary hemangioma often resulting from trauma. It is manifested as an inflammatory response with similar characteristics to those of a granuloma
  1
Granuloma venereum. : Tik Merauke An Epidemic Like No Other  2022 1
Granuloma venereum -- New Guinea -- History -- 20th century : Tik Merauke An Epidemic Like No Other  2022 1
 

Granulomatoses, Allergic -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
 

Granulomatoses, Langerhans Cell -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Granulomatosis, Allergic -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
 

Granulomatosis, Langerhans Cell -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Granulomatosis, Wegener -- See Granulomatosis with Polyangiitis


A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN
  1
 

Granulomatosis, Wegener's -- See Granulomatosis with Polyangiitis


A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN
  1
 

Granulomatosis with Polyangiitides -- See Granulomatosis with Polyangiitis


A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN
  1
Granulomatosis with Polyangiitis : Vasculitis in clinical practice / Richard A. Watts, David G.I. Scott, editors  2010 1
 

Granulomatous Allergic Angiitides -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
 

Granulomatous Allergic Angiitis -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
 

Granulomatous Angiitides, Allergic -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
 

Granulomatous Angiitis, Allergic -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
  Granulomatous Colitis -- 2 Related Subjects   2
 

Granulomatous disease, Chronic -- See Chronic granulomatous disease


  1
  Granulomatous Enteritis -- 2 Related Subjects   2
 

Granulomatous Rosacea -- See Rosacea


A cutaneous disorder primarily of convexities of the central part of the FACE, such as FOREHEAD; CHEEK; NOSE; and CHIN. It is characterized by FLUSHING; ERYTHEMA; EDEMA; RHINOPHYMA; papules; and ocular symptoms. It may occur at any age but typically after age 30. There are various subtypes of rosacea: erythematotelangiectatic, papulopustular, phymatous, and ocular (National Rosacea Society's Expert Committee on the Classification and Staging of Rosacea, J Am Acad Dermatol 2002; 46:584-7)
  1
 

Granulomatous Slack Skin -- See Lymphoma, T-Cell, Cutaneous


A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders
  1
 

Granulomatous Vasculitides, Eosinophilic -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
 

Granulomatous Vasculitis, Eosinophilic -- See Churg-Strauss Syndrome


Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA
  1
Granulom√©trie. : Particle size measurements : fundamentals, practice, quality / Henk G. Merkus  2009 1
 

Granulosa Cell, Cumulus -- See Cumulus Cells


The granulosa cells of the cumulus oophorus which surround the OVUM in the GRAAFIAN FOLLICLE. At OVULATION they are extruded with OVUM
  1
 

Granulosa Cells, Cumulus -- See Cumulus Cells


The granulosa cells of the cumulus oophorus which surround the OVUM in the GRAAFIAN FOLLICLE. At OVULATION they are extruded with OVUM
  1
 

Granulosus Infection, Echinococcus -- See Echinococcosis


An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation
  1
 

Granulosus Infections, Echinococcus -- See Echinococcosis


An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation
  1
Granville-Barker, Harley, 1877-1946 -- Criticism and interpretation : Reimagining Shakespeare's playhouse : early modern staging conventions in the twentieth century / Joe Falocco  2010 1
 

Granville Co., N.C -- See Granville County (N.C.)


  1
African Americans -- Employment -- North Carolina -- Granville County -- History -- 19th century. : Making freedom pay : North Carolina freedpeople working for themselves, 1865-1900 / Sharon Ann Holt  2000 1
African Americans -- North Carolina -- Granville County -- Economic conditions -- 19th century. : Making freedom pay : North Carolina freedpeople working for themselves, 1865-1900 / Sharon Ann Holt  2000 1
 

Granville County (N.C.) -- See Also Orange County (N.C.)


  1
Granville County (N.C.) -- Economic conditions : Making freedom pay : North Carolina freedpeople working for themselves, 1865-1900 / Sharon Ann Holt  2000 1
Granville, Granville George Leveson-Gower, Earl, 1815-1891 -- Correspondence. : The political correspondence of Mr. Gladstone and Lord Granville 1868-1876 / edited for the Royal Historical Society by Agatha Ramm  1952 1
 

Granville, Granville George Levison-Gower, Earl, 1815-1891 -- See Granville, Granville George Leveson-Gower, Earl, 1815-1891


  1
Granville, Harriet Granville, Countess, 1785-1862. : Lady of the House : Elite 19th Century Women and Their Role in the English Country House  2018 1
Add Marked to Bag Add All On Page Add Marked to My Lists
Result Page   Prev Next