Erythropoietic protoporphyria in the U.K.: clinical features and effect on quality of life von Holme, S.A., Anstey, A.V., Finlay, A.Y., Elder, G.H., Badminton, M.N.

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Late presentation of erythropoietic protoporphyria: case report and genetic analysis of family members von Berroeta, L., Man, I., Goudie, D.R., Whatley, S.D., Elder, G.H., Ibbotson, S.H.

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Molecular epidemiology of erythropoietic protoporphyria in the U.K von Whatley, S.D., Mason, N.G., Holme, S.A., Anstey, A.V., Elder, G.H., Badminton, M.N.

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Serum 25-hydroxyvitamin D in erythropoietic protoporphyria von Holme, S.A., Anstey, A.V., Badminton, M.N., Elder, G.H.

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Detection of latent variegate porphyria by fluorescence emission spectroscopy of plasma von LONG, C., SMYTH, S.J., WOOLF, J., MURPHY, G.M., FINLAY, A.Y., NEWCOMBE, R.G., ELDER, G.H.

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Molecular epidemiology of erythropoietic protoporphyria in the U.K: Molecular epidemiology of EPP von Whatley, S.D., Mason, N.G., Holme, S.A., Anstey, A.V., Elder, G.H., Badminton, M.N.

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Acute intermittent porphyria caused by an arginine to histidine substitution (R26H) in the cofactor-binding cleft of porphobilinogen deaminase von Llewellyn, D.H., Whatley, S., Elder, G.H.

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From Childhood to the Later Years: Pathways of Human Development von Crosnoe, Robert, Elder, Glen H.

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family process model of economic hardship and adjustment of early adolescent boys von Conger, R.D, Conger, K.J, Elder, G.H. Jr, Lorenz, F.O, Simons, R.L, Whitbeck, L.B

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Variations in Grandparenting von Mueller, Margaret M., Wilhelm, Brenda, Elder, Glen H.

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Homozygous acute intermittent porphyria : compound heterozygosity for adjacent base transitions in the same codon of the porphobilinogen deaminase gene von LLEWELLYN, D. H, SMYTH, S. J, ELDER, G. H, HUTCHESSON, A. C, RATTENBURY, J. M, SMITH, M. F

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Abstract No. 1Epidemiology of erythropoietic protoporphyria: the U.K. experience von Holme, S.A., Anstey, A.V., Finlay, A.Y., Elder, G.H., Badminton, M.N.

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Abstract No. 1
Epidemiology of erythropoietic protoporphyria: the U.K. experience von Holme, S.A., Anstey, A.V., Finlay, A.Y., Elder, G.H., Badminton, M.N.

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Erythropoietic protoporphyria in the U.K.: clinical features and effect on quality of life: EPP, clinical features and quality of life von Holme, S.A., Anstey, A.V., Finlay, A.Y., Elder, G.H., Badminton, M.N.

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A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma - reply von Holme, S.A., Anstey, A.V., Whatley, S.D., Elder, G.H., Badminton, M.N.

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Linking economic hardship to marital quality and instability von Conger, R.D, Elder, G.H. Jr, Lorenz, F.O, Conger, K.J, Simons, R.L, Whitbeck, L.B, Huck, S, Melby, J.N

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Hepatoerythropoietic porphyria: a missense mutation in the UROD gene is associated with mild disease and an unusual porphyrin excretion pattern von Armstrong, D.K.B., Sharpe, P.C., Chambers, C.R., Whatley, S.D., Roberts, A.G., Elder, G.H.

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S081 Update on enzyme and molecular defects in porphyria von Elder, G.H.

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Military Times and Turning Points in Men's Lives von Elder, Glen H

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Homozygous variegate porphyria: a compound heterozygote with novel mutations in the protoporphyrinogen oxidase gene von Palmer, R.A., Elder, G.H., Barrett, D_f., Keohane, S.G.

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