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  1. 21

    THE Effects of Motivational Interviewing on Motion Sickness by Unal DEMIRTAS, Mehmet Ergin DIPCIN, Mehmet CETIN

    Published 2015-12-01
    “…We want to share our experiences about motion sickness and the effects of motivational interviewing on motion sickness. …”
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    Pediatric Sickle Cell Disease in Sudan: Complications and Management by Meysaa Talha, Bashier Osman, Safa Abdalla, Hind Mirghani, Iman Abdoon

    Published 2022-01-01
    “…Background. Sickle cell disease (SCD) is a life-threatening genetic disorder due to the formation of sickle hemoglobin molecule (HbS) that polymerizes in hypoxic conditions leading to SCD-related complications. …”
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    Cardiovascular Characterization of Children and Adolescents with Sickle Cell Anemia by Nancy González Vales, Ximena Laura Graña, Lucía Díaz Morejón, Tamara Sánchez Estrada, Belkis Rodríguez Jorge, Ifraín Machín Caride

    Published 2020-02-01
    “…<strong>Foundation:</strong> sickle cell anemia is a severe chronic hemolytic anemia with a high morbidity and mortality rate. …”
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  8. 28

    Sickle Cell Trait Causing Splanchnic Venous Thrombosis by Priyanka Saxena, Pratibha Dhiman, Chhagan Bihari, Archana Rastogi

    Published 2015-01-01
    “…Sickle cell trait is considered as a benign condition as these individuals carry only one defective gene and typically have their life span similar to the normal population without any health problems related to sickle cell. …”
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  9. 29

    The modern use of hydroxyurea for children with sickle cell anemia by Charles T. Quinn, Russell E. Ware

    Published 2025-01-01
    “…Elevated fetal hemoglobin (HbF) serves as the most important treatment response, as HbF delays sickle hemoglobin polymerization and reduces erythrocyte sickling. …”
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    From sick old man to mythical hero by Sandra Pitcher, Tammy Frankland, Nicola Jones

    Published 2022-10-01
    “…The paper concludes, however, by documenting the immense power of Mandela’s legacy as played out in the press, and how, after death, his carefully constructed legacy rose above the damage of his prolonged illness, elevating him from a sick old man and reinforcing him as a mythical revolutionary. …”
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  15. 35

    Serum Sickness following Tetanus Toxoid Injection by Saja alhawal, Manar Aldarwish, Zainab Almoosa

    Published 2021-01-01
    “…Serum sickness is an allergic reaction that frequently occurs in patients after the injection of foreign protein or serum. …”
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  16. 36

    'Micro-Tina' and 'Micro-Gemma' Miniature Dwarf Tomatoes by John W. Scott, Brent K. Harbaugh, E. A. Baldwin

    Published 2005-04-01
    “… 'Micro-Tina' is a red-fruited, miniature dwarf tomato (Lycopersicon esculentum Mill.) cultivar of a type similar to 'Micro-Tom' (Scott and Harbaugh, 1989) but with sweeter flavor. …”
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  17. 37

    'Micro-Tina' and 'Micro-Gemma' Miniature Dwarf Tomatoes by John W. Scott, Brent K. Harbaugh, E. A. Baldwin

    Published 2005-04-01
    “… 'Micro-Tina' is a red-fruited, miniature dwarf tomato (Lycopersicon esculentum Mill.) cultivar of a type similar to 'Micro-Tom' (Scott and Harbaugh, 1989) but with sweeter flavor. …”
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    Article
  18. 38

    Safety of Pegfilgrastim (Neulasta) in Patients with Sickle Cell Trait/Anemia by Pashtoon Murtaza Kasi, Mrinal M. Patnaik, Prema P. Peethambaram

    Published 2013-01-01
    “…Prescribing information available on manufacturer’s website for the drug warns us about possible severe sickle cell crises related to the medication but does not report the actual incidence or the use in patients with sickle cell trait. …”
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  19. 39

    Sickle Cell Beta-Plus Thalassemia with Subcapsular Hematoma of the Spleen by Suyash Dahal, Sumit Dahal, Dipesh K. C. Ghimire, Ebad Ur Rahman, Eliza Sharma

    Published 2017-01-01
    “…While splenic complications like hypersplenism, sequestration crisis, and infarction are commonly reported in sickle cell variants like sickle cell beta-plus thalassemia, splenic rupture with hematoma is rare. …”
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  20. 40

    Inflammatory pathways and anti‐inflammatory therapies in sickle cell disease by Karina Tozatto‐Maio, Felipe A. Rós, Ricardo Weinlich, Vanderson Rocha

    Published 2024-12-01
    “…Abstract Sickle cell disease (SCD) is a monogenic disease, resulting from a single‐point mutation, that presents a complex pathophysiology and high clinical heterogeneity. …”
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