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Scholar Results 1 - 10 of about 18 citing Lanzkron: Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease. (0.38 sec) 

Interferon-α therapy in bcr-abl-negative myeloproliferative neoplasms


JJ Kiladjian, C Chomienne, P Fenaux - Leukemia, 2008 - nature.com
Interferon (IFN) was the first cytokine discovered 50 years ago, with a wide
range of biological properties, including immunomodulatory, proapoptotic and
antiangiogenic activities, that rapidly raised interest in its therapeutic ...
Cited by 13 - Related articles - All 4 versions

Hemoglobin research and the origins of molecular medicine

- hematologylibrary.org
AN Schechter - Blood, 2008 - bloodjournal.hematologylibrary.org
Much of our understanding of human physiology, and of many aspects of pathology,
has its antecedents in laboratory and clinical studies of hemoglobin. Over the
last century, knowledge of the genetics, functions, and diseases of the ...
Cited by 9 - Related articles - All 8 versions

Haemoglobin F modulation in childhood sickle cell disease

- critcaremed.com
S Trompeter, I Roberts - British Journal of Haematology - pt.wkhealth.com
Cited by 2 - Related articles - All 6 versions

Pain Management in Sickle Cell Disease: Palliative Care Begins at Birth?

- hematologylibrary.org
L Benjamin - Hematology, 2008 - asheducationbook.hematologylibrary.org
People with sickle cell disease (SCD) are living longer, but their lives are
impacted even more by the unpredictable intermittent or constant pain that is
often poorly managed over a lifetime. To address this problem, an ...
Cited by 1 - Related articles - All 6 versions

[CITATION] Specific therapies for sickle cell disease


DCIOF POLYMERIZATION, ROFIH …
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[PDF] Exposure to Hydroxyurea and Pregnancy Outcomes in Patients With Sickle Cell Anemia


SK Ballas, WFMC PhD, N Guo, L DeCastro, R … - JOURNAL OF THE NATIONAL MEDICAL …, 2009 - nmanet.org
Methods In MSH there were 299 study participants: 153 were female (77, or 50.7%,
in the hydroxyurea group; 76, or 51.7%, in the placebo group) and 146 were male
(75, or 49.3%, in the hydroxyurea group; 71, or 48.3%, in the placebo ...
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[PDF] Medication Adherence and Associated Outcomes in Medicaid Enrollees with Sickle Cell …


SD Candrilli, 2009 - etd.ohiolink.edu
Page 1. MEDICATION ADHERENCE AND ASSOCIATED OUTCOMES IN MEDICAID ENROLLEES
WITH SICKLE CELL DISEASE DISSERTATION Presented in Partial ...
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Role of hydroxycarbamide in prevention of complications in patients with sickle cell disease


NM Wiles, J Howard, 2009 - pubmedcentral.nih.gov
Sickle cell disease (SCD) is a genetically inherited condition caused by a point
mutation in the beta globin gene. This results in the production of the abnormal
hemoglobin, sickle hemoglobin (HbS). Hydroxycarbamide, is an antimetabolite/ ...
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Cyanide, Peroxide and Nitric Oxide Formation in Solutions of Hydroxyurea Causes Cellular …


KJ Kuong, A Kuzminov - Journal of Molecular Biology, 2009 - Elsevier
Hydroxyurea (HU) is a potent remedy against a variety of ailments and an
efficient inhibitor of DNA synthesis, yet its pharmacology is unclear. HU acts
in Escherichia coli by the same mechanism as it does in eukaryotes, via ...
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[PDF] In vitro induction of fetal hemoglobin in erythroid cells derived from CD133+ cells by …


A Atashi, M SOLEYMANI, S Kaviani, A … - IRANIAN JOURNAL OF BIOTECHNOLOGY, 2008 - sid.ir
Abstract Increased fetal hemoglobin (HbF) in β-globin gene dis- orders
ameliorates the clinical symptoms of the under- lying disease. 5-azacytidine,
butyrate and hydroxyurea, have been shown to activate γ-globin gene ...
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