Localization of a Gene for Familial Hemophagocytic Lymphohistiocytosis at Chromosome 9q21.3-22 by Homozygosity Mapping
Ohadi, Mina, Lalloz, Michel R.A., Sham, Pak, Zhao, Jinghua, Dearlove, Andrew M., Shiach, Caroline, Kinsey, Sally, Rhodes, Michael, Layton, D. Mark
Published in American journal of human genetics (1999)
Published in American journal of human genetics (1999)
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Characterization of erosion and failure processes of spark plugs after field service in natural gas engines
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Conference Proceeding
Rapid Identification of Hemoglobin Variants by Electrospray Ionization Mass Spectrometry
Wild, B.J., Green, B.N., Cooper, E.K., Lalloz, M.R.A., Erten, S., Stephens, A.D., Layton, D.M.
Published in Blood cells, molecules, & diseases (01.05.2001)
Published in Blood cells, molecules, & diseases (01.05.2001)
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P1522: LONG‐TERM EFFICACY AND SAFETY OF THE ORAL PYRUVATE KINASE ACTIVATOR MITAPIVAT IN ADULTS WITH NON–TRANSFUSION‐DEPENDENT ALPHA‐ OR BETA‐THALASSEMIA
Kuo, K. H. M., Layton, D. M., Lal, A., Al‐Samkari, H., Bhatia, J., Kosinski, P. A., Tong, B., Lynch, M., Uhlig, K., Vichinsky, E. P.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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P1562: CHARACTERIZING IRON OVERLOAD BY AGE IN PATIENTS DIAGNOSED WITH PYRUVATE KINASE DEFICIENCY – A DESCRIPTIVE ANALYSIS FROM THE PEAK REGISTRY
Bianchi, P., Grace, R. F., Vives Corrons, J.‐L., Glader, B., Glenthøj, A., Kanno, H., Kuo, K. H., Lander, C., Layton, D. M., Pospíŝilová, D., Viprakasit, V., Williams, J., Yan, Y., McGee, B., Beers, E. J.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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P1544: BONE MINERAL DENSITY REMAINS STABLE IN PYRUVATE KINASE DEFICIENCY PATIENTS RECEIVING LONG‐TERM TREATMENT WITH MITAPIVAT
Al‐Samkari, H., Grace, R. F., Glenthøj, A., Andres, O., Barcellini, W., Galactéros, F., Kuo, K. H. M., Layton, D. M., Morado Arias, M., Viprakasit, V., Dong, Y., Tai, F., Grekas, L., Khoja, K., Gheuens, S., McGee, B., Porter, J. B., Beers, E. J.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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P1545: DURABILITY OF HEMOGLOBIN RESPONSE AND REDUCTION IN TRANSFUSION BURDEN IS MAINTAINED OVER TIME IN PATIENTS WITH PYRUVATE KINASE DEFICIENCY TREATED WITH MITAPIVAT IN A LONG‐TERM EXTENSION STUDY
Grace, R. F., Glenthøj, A., Barcellini, W., Verhovsek, M., Rothman, J. A., Morado Arias, M., Layton, D. M., Andres, O., Galactéros, F., Beers, E. J., Onodera, K., Viprakasit, V., Chonat, S., Porter, J. B., Judge, M. P., Kosinski, P. A., Hawkins, P., Gheuens, S., Xu, R., McGee, B., Beynon, V., Al‐Samkari, H.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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P1548: LONG‐TERM TREATMENT WITH ORAL MITAPIVAT IS ASSOCIATED WITH NORMALIZATION OF HEMOGLOBIN LEVELS IN PATIENTS WITH PYRUVATE KINASE DEFICIENCY
Barcellini, W., Grace, R. F., Al‐Samkari, H., Glenthøj, A., Rothman, J. A., Morado Arias, M., Layton, D. M., Andres, O., DiBacco, M., Hawkins, P., Judge, M. P., Tai, F., Morales‐Arias, J., Beynon, V., Beers, E. J.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis
Datz, Christian, Lalloz, Michel R.A., Vogel, Wolfgang, Graziadei, Ivo, Hackl, Franz, Vautier, Guy, Layton, D.Mark, Maier-Dobersberger, Theresia, Ferenci, Peter, Penner, Edward, Sandhofer, Friedrich, Bomford, Adrian, Paulweber, Bernhard
Published in Journal of hepatology (01.11.1997)
Published in Journal of hepatology (01.11.1997)
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Molecular analysis of the genotype-phenotype relationship in factor X deficiency
MILLAR, D. S, ELLISTON, L, CACHIA, P, PASI, K. J, LAYTON, D. M, COOPER, D. N, DEEX, P, KRAWCZAK, M, WACEY, A. I, REYNAUD, J, NIEUWENHUIS, H. K, BOLTON-MAGGS, P, MANNUCCI, P. M, REVERTER, J. C
Published in Human genetics (01.02.2000)
Published in Human genetics (01.02.2000)
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Diagnosis of pyrimidine 5′‐nucleotidase deficiency suspected from a blood film
Al‐Jafar, Hassan A., Layton, D. M., Robertson, Lynn, Escuredo, Emilia, Bain, Barbara J.
Published in American journal of hematology (01.12.2013)
Published in American journal of hematology (01.12.2013)
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Haemophagocytic lymphohistiocytosis: experience at two U.K. centres
Hirst, W J, Layton, D M, Singh, S, Mieli-Vergani, G, Chessells, J M, Strobel, S, Pritchard, J
Published in British journal of haematology (01.12.1994)
Published in British journal of haematology (01.12.1994)
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Mutation of the human FMS gene (M-CSF receptor) in myelodysplastic syndromes and acute myeloid leukemia
Tobal, K, Pagliuca, A, Bhatt, B, Bailey, N, Layton, D M, Mufti, G J
Published in Leukemia (01.07.1990)
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Published in Leukemia (01.07.1990)
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RESULTS FROM A PHASE 2 STUDY OF MITAPIVAT IN ADULTS WITH NON–TRANSFUSION-DEPENDENT ALPHA- OR BETA-THALASSEMIA
Kuo, KH, Layton, DM, Lal, A, Al-Samkari, H, Bhatia, J, Tong, B, Lynch, M, Uhlig, K, Vichinsky, EP
Published in Hematology, Transfusion and Cell Therapy (01.10.2021)
Published in Hematology, Transfusion and Cell Therapy (01.10.2021)
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