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The Journal of Nutrition|May 22, 2007
Response of phenylketonuria to tetrahydrobiopterinKimberlee Michals-Matalon, Gita Bhatia, Flemming Guttler, et al.
Journal of Child Neurology|October 24, 2003
Metabolic changes in the knockout mouse for Canavan's disease: implications for patients with Canavan's diseaseSankar Surendran, Kimberlee M Matalon, Sylvia Szucs, et al.
European Journal of Medical Genetics|May 31, 2016
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorderGifty Bhat, Danielle LaGrave, Alison Millson, et al.
Clinical Dysmorphology|June 24, 2010
Pericentric inversion, inv(14)(p11.2q22.3), in a 9-month old with features of Goldenhar syndromeJill K Northup, Dena Matalon, Judy C Hawkins, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|June 16, 2009
Association between cytokine gene polymorphisms and risk for upper respiratory tract infection and acute otitis mediaKrystal Revai, Janak A Patel, James J Grady, et al.
Molecular Genetics and Metabolism|September 7, 2005
Response of patients with phenylketonuria in the US to tetrahydrobiopterinReuben Matalon, Kimberlee Michals-Matalon, Richard Koch, et al.
Plos One|April 11, 2014
Polymorphisms of immunity genes and susceptibility to otitis media in childrenJohanna Nokso-Koivisto, Tasnee Chonmaitree, Kristofer Jennings, et al.
Biochemical and Biophysical Research Communications|April 6, 2004
High level of orexin A observed in the phenylketonuria mouse brain is due to the abnormal expression of prepro-orexinSankar Surendran, Peter L Rady, Sylvia Szucs, et al.
Neuroscience Letters|June 1, 2005
Altered expression of myocilin in the brain of a mouse model for phenylketonuria (PKU)Sankar Surendran, Dena Matalon, Stephen K Tyring, et al.
Journal of Child Neurology|December 31, 2003
Mild elevation of N-acetylaspartic acid and macrocephaly: diagnostic problemSankar Surendran, Fiona J Bamforth, Alicia Chan, et al.
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