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1966
2025

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Year Number of Results
1966 1
1967 2
1974 1
1977 1
1980 1
1985 1
1989 3
1993 2
1995 1
2009 1
2010 1
2011 1
2014 1
2025 0

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16 results

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Page 1
Anemia in cancer.
Zucker S. Zucker S. Cancer Invest. 1985;3(3):249-60. doi: 10.3109/07357908509039786. Cancer Invest. 1985. PMID: 3891030 Review.
Immunoglobulin inhibitors of erythropoiesis occur in the rare entity, pure red cell aplasia, which is sometimes associated with thymomas. Autoimmune hemolytic anemia and microangiopathic hemolytic anemia can also occur in patients with solid cancers, pointing out th …
Immunoglobulin inhibitors of erythropoiesis occur in the rare entity, pure red cell aplasia, which is sometimes associated with thymomas. Au …
Anemia and cancer.
Steinberg D. Steinberg D. CA Cancer J Clin. 1989 Sep-Oct;39(5):296-304. doi: 10.3322/canjclin.39.5.296. CA Cancer J Clin. 1989. PMID: 2513101 Free article. Review. No abstract available.
Differential diagnosis of anemia and cancer.
Leite C, Hoogstraten B. Leite C, et al. CA Cancer J Clin. 1977 Mar-Apr;27(2):88-99. doi: 10.3322/canjclin.27.2.88. CA Cancer J Clin. 1977. PMID: 402990 Free article. Review. No abstract available.
Osteopetrosis: a rare cause of anemia--review of literature.
Saluja S, Bhandari S, Aggarwal S, Kapoor S. Saluja S, et al. Indian J Pathol Microbiol. 2009 Jul-Sep;52(3):363-7. doi: 10.4103/0377-4929.54995. Indian J Pathol Microbiol. 2009. PMID: 19679962 Review.
The leading clinical features are pallor, growth failure, hepatosplenomegaly.On hematological examination, anemia, thrombocytopenia, leucocytosis and myelophthisic anemia are commonly observed in this disease. We are highlighting osteopetrosis as a rare cause …
The leading clinical features are pallor, growth failure, hepatosplenomegaly.On hematological examination, anemia, thrombocytopenia, …
Microangiopathic hemolytic anemia and leukoerythroblastic blood film heralding bone marrow metastatic gastroesophageal adenocarcinoma.
Rauh MJ, Al Habeeb A, Chang H. Rauh MJ, et al. Pathol Res Pract. 2011 Feb 15;207(2):121-3. doi: 10.1016/j.prp.2010.07.003. Epub 2010 Aug 5. Pathol Res Pract. 2011. PMID: 20691546 Review.
Herein, we report the case of a patient with a history of gastric cancer, who presented seven years following apparently successful surgery and adjuvant chemo-radio-therapy, with blood film findings of microangiopathic hemolytic anemia (MAHA), thrombocytopenia, and leukoer …
Herein, we report the case of a patient with a history of gastric cancer, who presented seven years following apparently successful surgery …
Osteopetrosis. Current clinical considerations.
Shapiro F. Shapiro F. Clin Orthop Relat Res. 1993 Sep;(294):34-44. Clin Orthop Relat Res. 1993. PMID: 8358940 Review.
There are three clinical groups: infantile-malignant autosomal recessive, fatal within the first few years of life (in the absence of effective therapy); intermediate autosomal recessive, appears during the first decade of life but does not follow a malignant course; and autosoma …
There are three clinical groups: infantile-malignant autosomal recessive, fatal within the first few years of life (in the absence of effect …
Microangiopathic hemolytic anemia as an initial presentation of metastatic cancer of unknown primary origin.
Lin YC, Chang HK, Sun CF, Shih LY. Lin YC, et al. South Med J. 1995 Jun;88(6):683-7. doi: 10.1097/00007611-199506000-00021. South Med J. 1995. PMID: 7777893 Review.
Microangiopathic hemolytic anemia (MAHA) is a well-documented but rare complication of disseminated cancer; it usually occurs in the late or terminal stage of cancer. ...After careful workup, we failed to find the primary site of cancer. The anemia and thrombocytope …
Microangiopathic hemolytic anemia (MAHA) is a well-documented but rare complication of disseminated cancer; it usually occurs in the …
16 results