Search Results - "Yassin, N.A."

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    A challenging case of hereditary type 1 tyrosinaemia associated with persistent diarrhoea : case report and literature review by Mogahed, E.A., Yassin, N.A., El-Karaksy, H.

    “…Hereditary tyrosinaemia type 1 (HT1) is a rare inherited genetic disorder attributed to deficiency of the enzyme fumarylacetoacetate hydrolase (FAH). HT1 may…”
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    Journal Article
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    Activation of migration of endogenous stem cells by erythropoietin as potential rescue for neurodegenerative diseases by Khairallah, M.I, Kassem, L.A, Yassin, N.A, Gamal el Din, M.A, Zekri, M, Attia, M

    Published in Brain research bulletin (01-03-2016)
    “…Highlights • LPS induced neuroinflammation is characterized by cognitive decline. • LPS induces amyloid plaques deposition and astroglial activation. • EPO…”
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    Journal Article
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    A challenging case of hereditary type 1 tyrosinaemia associated with persistent diarrhoea: Case report and literature review by Yassin, N A, Mogahed, E A, El-Karaksy, H

    “…Hereditary tyrosinaemia type 1 (HT1) is a rare inherited genetic disorder attributed to deficiency of the enzyme fumarylacetoacetate hydrolase (FAH). HT1 may…”
    Get full text
    Journal Article
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