Search Results - "Abba, Aisha"

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  1. 1

    Determinants of splenic preservation among patients with sickle cell disease in North‐Eastern Nigeria by Ladu, Adama I., Jeffery, Caroline, Farate, Abubakar, Farouk, Abubakar G., Abba, Aisha M., Adekile, Adekunle, Bates, Imelda

    Published in Tropical medicine & international health (01-08-2023)
    “…Objective In patients with sickle cell disease (SCD), the spleen commonly enlarges during early childhood, but undergoes reduction in size and fibrosis from…”
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    Journal Article
  2. 2

    Clinical and laboratory factors associated with splenic dysfunction among patients with sickle cell disease in a malaria endemic region by Ladu, Adama I, Satumari, Ngamarju A, Abba, Aisha M, Abulfathi, Fatima A, Jeffery, Caroline, Adekile, Adekunle, Bates, Imelda

    “…ABSTRACT Background Although loss of splenic function is the expected natural course for individuals with sickle cell disease (SCD), factors such as high HbF…”
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    Journal Article
  3. 3

    Evaluation of two red cell inclusion staining methods for assessing spleen function among sickle cell disease patients in North-East Nigeria by Ladu, Adama I, Satumari, Ngamarju A, Abba, Aisha M, Abulfathi, Fatima A, Jeffery, Caroline, Adekile, Adekunle, Bates, Imelda

    Published in PLOS global public health (2023)
    “…The loss of splenic function is associated with an increased risk of infection in sickle cell disease (SCD); however, spleen function is rarely documented…”
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    Journal Article
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    Pattern of anaemic crises in Paediatric Sickle Cell Anaemic Patients seen at the University of Maiduguri Teaching Hospital, North-eastern Nigeria by Machoko Y, Yenti, G. Farouk, Abubakar, M Yusuf, Hauwa, I. Ladu, Adama, M Abba, Aisha, P. Ambe, Jose

    Published in Kanem journal of medical sciences (25-06-2023)
    “…Background: Sickle cell anaemia (SCA) is the commonest haemoglobinopathy worldwide. The main presentation is chronic anaemia often exacerbated during periods…”
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    Journal Article
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    Proteinuric and nonproteinuric chronic kidney disease among patients with sickle cell anaemia (HbSS) attending a tertiary hospital in north-eastern Nigeria by Sulaiman, Mohammed Maina, Ladu, Adama Isah, Abba, Aisha Mohammed, Bukar, Audu Abdullahi

    Published in Hematology/oncology and stem cell therapy (01-09-2021)
    “…Individuals with sickle cell anaemia (SCA) may manifest various forms of renal abnormalities. Proteinuria is an early marker of renal dysfunction and a strong…”
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    Journal Article
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