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1979
2025

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Year Number of Results
1979 1
1980 1
1985 1
1990 1
1991 3
1992 2
1993 2
1994 6
1995 3
1998 1
2004 2
2007 2
2008 2
2011 1
2012 1
2013 1
2014 1
2015 1
2016 2
2017 1
2018 1
2019 5
2020 3
2023 2
2024 1
2025 0

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42 results

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Page 1
Hemolytic anemia.
Dhaliwal G, Cornett PA, Tierney LM Jr. Dhaliwal G, et al. Am Fam Physician. 2004 Jun 1;69(11):2599-606. Am Fam Physician. 2004. PMID: 15202694 Free article. Review.
Hemolysis presents as acute or chronic anemia, reticulocytosis, or jaundice. The diagnosis is established by reticulocytosis, increased unconjugated bilirubin and lactate dehydrogenase, decreased haptoglobin, and peripheral blood smear findings. ...
Hemolysis presents as acute or chronic anemia, reticulocytosis, or jaundice. The diagnosis is established by reticulocytosis, …
Favism: Clinical Features at Different Ages.
Beretta A, Manuelli M, Cena H. Beretta A, et al. Nutrients. 2023 Jan 10;15(2):343. doi: 10.3390/nu15020343. Nutrients. 2023. PMID: 36678214 Free PMC article. Review.
Laboratory findings are characterized by anemia, reticulocytosis, elevated bilirubin level, and sometimes urinary urobilinogen and methemoglobinemia. ...
Laboratory findings are characterized by anemia, reticulocytosis, elevated bilirubin level, and sometimes urinary urobilinogen and me …
Laboratory Approach to Hemolytic Anemia.
Jamwal M, Sharma P, Das R. Jamwal M, et al. Indian J Pediatr. 2020 Jan;87(1):66-74. doi: 10.1007/s12098-019-03119-8. Epub 2019 Dec 10. Indian J Pediatr. 2020. PMID: 31823208 Review.
The pathognomic finding is a reduced red cell life span with severe anemia or, compensated hemolysis accompanied by reticulocytosis. The diagnostic workup or laboratory approach for hemolytic anemias is based on methodical step-wise testing which includes red blood cell mo …
The pathognomic finding is a reduced red cell life span with severe anemia or, compensated hemolysis accompanied by reticulocytosis. …
Congenital Hemolytic Anemia.
Haley K. Haley K. Med Clin North Am. 2017 Mar;101(2):361-374. doi: 10.1016/j.mcna.2016.09.008. Epub 2016 Dec 8. Med Clin North Am. 2017. PMID: 28189176 Review.
The laboratory features include anemia, hyperbilirubinemia, and reticulocytosis. For some congenital hemolytic anemias, splenectomy is curative. However, in other diseases, avoidance of drugs and toxins is the best therapy. ...
The laboratory features include anemia, hyperbilirubinemia, and reticulocytosis. For some congenital hemolytic anemias, splenectomy i …
Clinical Applications of Hemolytic Markers in the Differential Diagnosis and Management of Hemolytic Anemia.
Barcellini W, Fattizzo B. Barcellini W, et al. Dis Markers. 2015;2015:635670. doi: 10.1155/2015/635670. Epub 2015 Dec 27. Dis Markers. 2015. PMID: 26819490 Free PMC article. Review.
Prosthetic valve replacement and stenting are also associated with intravascular and chronic hemolysis. Compensatory reticulocytosis may be inadequate/absent in case of marrow involvement, iron/vitamin deficiency, infections, or autoimmune reaction against bone marrow-prec …
Prosthetic valve replacement and stenting are also associated with intravascular and chronic hemolysis. Compensatory reticulocytosis
Anemia in newborn.
Lokeshwar MR, Dalal R, Manglani M, Shah N. Lokeshwar MR, et al. Indian J Pediatr. 1998 Sep-Oct;65(5):651-61. doi: 10.1007/BF02731037. Indian J Pediatr. 1998. PMID: 10773920 Review.
They further increase in first 2 days of life. Reticulocytosis and presence of nucleated red cells are normally seen in first week of life. ...
They further increase in first 2 days of life. Reticulocytosis and presence of nucleated red cells are normally seen in first week of …
Sickle Cell Disease and Stroke.
Hirtz D, Kirkham FJ. Hirtz D, et al. Pediatr Neurol. 2019 Jun;95:34-41. doi: 10.1016/j.pediatrneurol.2019.02.018. Epub 2019 Feb 27. Pediatr Neurol. 2019. PMID: 30948147 Review.
The risk factors in sickle cell disease for cognitive impairment, overt ischemic stroke, silent cerebral infarction, overt hemorrhagic stroke, and vasculopathy defined by transcranial Doppler or magnetic resonance angiography overlap, with severe acute and chronic anemia, acute c …
The risk factors in sickle cell disease for cognitive impairment, overt ischemic stroke, silent cerebral infarction, overt hemorrhagic strok …
Investigation of macrocytic anemia.
Ward PC. Ward PC. Postgrad Med. 1979 Feb;65(2):203-7, 209, 212-3. doi: 10.1080/00325481.1979.11715063. Postgrad Med. 1979. PMID: 368738 Review.
The three most common causes of macrocytosis--vitamin B12 or folate deficiency, liver disease, and reticulocytosis--usually can be differentiated on the basis of red cell indexes and morphologic findings. Bone marrow studies are not indicated. In reticulocytosis, th …
The three most common causes of macrocytosis--vitamin B12 or folate deficiency, liver disease, and reticulocytosis--usually can be di …
Vitamin B12 deficiency and metabolism-mediated thrombotic microangiopathy (MM-TMA).
Sabry W, Elemary M, Burnouf T, Seghatchian J, Goubran H. Sabry W, et al. Transfus Apher Sci. 2020 Feb;59(1):102717. doi: 10.1016/j.transci.2019.102717. Epub 2019 Dec 31. Transfus Apher Sci. 2020. PMID: 31902683 Review.
Perhaps some minor modification of this scoring system by changing the parameters of hemolysis to include reticulocytosis and rather than and/or other hemolytic parameters could even help refine this identification....
Perhaps some minor modification of this scoring system by changing the parameters of hemolysis to include reticulocytosis and rather …
Management of Red Cell Alloimmunization in Pregnancy.
Moise KJ Jr, Abels EA. Moise KJ Jr, et al. Obstet Gynecol. 2024 Oct 1;144(4):465-480. doi: 10.1097/AOG.0000000000005709. Epub 2024 Aug 15. Obstet Gynecol. 2024. PMID: 39146538 Review.
Neonatal phototherapy and "top-up" transfusions attributable to suppressed reticulocytosis often are still required for therapy after delivery....
Neonatal phototherapy and "top-up" transfusions attributable to suppressed reticulocytosis often are still required for therapy after …
42 results