Search Results - Sharrard, M.J

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  1. 1
    P038 Combined defects of the pyruvate dehydrogenase complex and respiratory chain responsive to ubiquinone and riboflavin

    P038 Combined defects of the pyruvate dehydrogenase complex and respiratory chain responsive to ubiquinone and riboflavin by Ng, J, Sharrard, M.J, Olpin, S.E, Athiraman, N, Mordekar, S.R

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  2. 2
    P17.8 Phosphoserine Aminotransferase Deficiency-The Story so Far

    P17.8 Phosphoserine Aminotransferase Deficiency-The Story so Far by Davies, E., Sharrard, M.J., Baxter, P.

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  3. 3
    P05.6 Corticospinal Tract Calcification in Krabbe's Disease

    P05.6 Corticospinal Tract Calcification in Krabbe's Disease by Davies, E., Sharrard, M.J., Raghavan, A., Mordekar, S.R.

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  4. 4
    P04.11 Unilateral Periventricular Leucomalacia in Association with Pyruvate Dehydrogenase Deficiency

    P04.11 Unilateral Periventricular Leucomalacia in Association with Pyruvate Dehydrogenase Deficiency by Sharma, R., Sharrard, M.J., Connolly, D.J., Mordekar, S.R.

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  5. 5
    Serine and glycine deficiency associated with severe phenotype and no enzyme deficiency

    Serine and glycine deficiency associated with severe phenotype and no enzyme deficiency by Ramsbottom, A.C, Sharrard, M.J, Bonham, J, Rittey, C, Watkinson, J, Allen, J.C

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  6. 6
    Carnitine‐acylcarnitine translocase deficiency ‐ a mild phenotype

    Carnitine‐acylcarnitine translocase deficiency ‐ a mild phenotype by Olpin, S.E., Bonham, J.R., Downing, M., Manning, N.J., Pollitt, R.J., Sharrard, M.J., Tanner, M.S.

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