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pro vyhledávání: '"Parjeet Kaur Gharial"'
Autor:
Parjeet Kaur Gharial
Publikováno v:
InnovAiT: Education and inspiration for general practice. 15:294-300
Haemoglobinopathies are inherited disorders of the globin component of haemoglobin. Genetic mutations lead to an altered structure of haemoglobin, as in sickle cell disease, or reduced quantity of haemoglobin, as in thalassaemia. Significant haemoglo
Autor:
William S, Bolton, Parjeet Kaur, Gharial, Christopher, Akhunbay-Fudge, Paul, Chumas, Ryan K, Mathew, Ian A, Anderson
Publikováno v:
Neurosurgical Focus. 52:E4
OBJECTIVE Recent evidence has suggested that an admission neutrophil-to-lymphocyte ratio (NLR) of ≥ 5.9 predicts delayed cerebral ischemia (DCI) in aneurysmal subarachnoid hemorrhage (aSAH). The primary aims of this study were to assess reproducibi