response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study
Burton, B. K, Grange, D. K, Milanowski, A, Vockley, G, Feillet, F, Crombez, E. A, Abadie, V, Harding, C. O, Cederbaum, S, Dobbelaere, D, Smith, A, Dorenbaum, A
Published in Journal of inherited metabolic disease (01.10.2007)
Published in Journal of inherited metabolic disease (01.10.2007)
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Journal Article
Home visits in the Danish High Risk and Resilience Study – VIA 7: assessment of the home environment of 508 7‐year‐old children born to parents diagnosed with schizophrenia or bipolar disorder
Gantriis, D. L., Thorup, A. A. E., Harder, S., Greve, A. N., Henriksen, M. T., Zahle, K. K., Stadsgaard, H., Ellersgaard, D., Burton, B. K., Christiani, C. J., Spang, K., Hemager, N., Uddin, Md. J., Jepsen, J. R. M., Plessen, K. J., Nordentoft, M., Mors, O., Bliksted, V.
Published in Acta psychiatrica Scandinavica (01.08.2019)
Published in Acta psychiatrica Scandinavica (01.08.2019)
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Journal Article
Alexander disease with serial MRS and a new mutation in the glial fibrillary acidic protein gene
Bassuk, A G, Joshi, A, Burton, B K, Larsen, M B, Burrowes, D M, Stack, C
Published in Neurology (14.10.2003)
Published in Neurology (14.10.2003)
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Journal Article
Aging and neural spatial contrast sensitivity: Photopic vision
Burton, Kerri B., Owsley, Cynthia, Sloane, Michael E.
Published in Vision research (Oxford) (01.05.1993)
Published in Vision research (Oxford) (01.05.1993)
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Journal Article
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
Robin, Nathaniel H, Feldman, George J, Aronson, Adam L, Mitchell, Heather F, Weksberg, Rosanna, Leonard, Claire O, Burton, Barbara K, Josephson, Kevin D, Laxová, Renata, Aleck, Kyrieckos A, Allanson, Judith E, Guion-Almeida, Maria Leine, Martin, Rick A, Leichtman, Lawrence G, Price, R. Arlen, Opitz, John M, Muenke, Maximilian
Published in Nature genetics (01.12.1995)
Published in Nature genetics (01.12.1995)
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Journal Article
Limb anomalies associated with chorionic villus sampling
Burton, B K, Schulz, C J, Burd, L I
Published in Obstetrics and gynecology (New York. 1953) (01.05.1992)
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Published in Obstetrics and gynecology (New York. 1953) (01.05.1992)
Journal Article
Importance of surgical history in diagnosing mucopolysaccharidosis type II (Hunter syndrome): Data from the Hunter Outcome Survey
Mendelsohn, Nancy J., Harmatz, Paul, Bodamer, Olaf, Burton, Barbara K., Giugliani, Roberto, Jones, Simon A., Lampe, Christina, Malm, Gunilla, Steiner, Robert D., Parini, Rossella
Published in Genetics in medicine (01.12.2010)
Published in Genetics in medicine (01.12.2010)
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Journal Article
Correction of ureagenesis after gene transfer in an animal model and after liver transplantation in humans with ornithine transcarbamylase deficiency
BATSHAW, M. L, ROBINSON, M. B, XUEHAI YE, PABIN, C, DAIKHIN, Y, BURTON, B. K, WILSON, J. M, YUDKOFF, M
Published in Pediatric research (01.11.1999)
Published in Pediatric research (01.11.1999)
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Journal Article
Congenital nephrosis as a cause of elevated alpha-fetoprotein
Albright, S G, Warner, A A, Seeds, J W, Burton, B K
Published in Obstetrics and gynecology (New York. 1953) (01.11.1990)
Published in Obstetrics and gynecology (New York. 1953) (01.11.1990)
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Journal Article
Pregnancy outcome in women with low midtrimester maternal serum unconjugated estriol
Santolaya-Forgas, J, Jessup, J, Burd, L I, Prins, G S, Burton, B K
Published in Journal of reproductive medicine (01.02.1996)
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Published in Journal of reproductive medicine (01.02.1996)
Journal Article
Oromandibular-limb hypogenesis syndrome following chorionic villus sampling
Gruber, Benjamin, Burton, Barbara K.
Published in International journal of pediatric otorhinolaryngology (01.03.1994)
Published in International journal of pediatric otorhinolaryngology (01.03.1994)
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Journal Article