Search Results - Grange, Dorothy K.

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  1. 1
    K(ATP) channels and cardiovascular disease: Suddenly a syndrome

    K(ATP) channels and cardiovascular disease: Suddenly a syndrome by Nichols, Colin G., Singh, Gautam K., Grange, Dorothy K.

    Published 2013
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  2. 2
    Case Report: Congenital Knee Dislocation in a Patient with Larsen Syndrome and a Novel Filamin B Mutation

    Case Report: Congenital Knee Dislocation in a Patient with Larsen Syndrome and a Novel Filamin B Mutation by Dobbs, Matthew B., Boehm, Stephanie, Grange, Dorothy K., Gurnett, Christina A.

    Published 2008
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  3. 3
    Executive Strategic Processing during Verbal Fluency Performance in Children with Phenylketonuria

    Executive Strategic Processing during Verbal Fluency Performance in Children with Phenylketonuria by Banerjee, Pia, Grange, Dorothy K., Steiner, Robert D., White, Desiree A.

    Published 2010
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  4. 4
    Processing Speed and Executive Abilities in Children with Phenylketonuria

    Processing Speed and Executive Abilities in Children with Phenylketonuria by Janos, Alicia L., Grange, Dorothy K., Steiner, Robert D., White, Desirée A.

    Published 2012
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  5. 5
    Relationship between age and white matter integrity in children with phenylketonuria

    Relationship between age and white matter integrity in children with phenylketonuria by Wesonga, Erika, Shimony, Joshua S., Rutlin, Jerrel, Grange, Dorothy K., White, Desiree A.

    Published 2016
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  6. 6
    Brain White Matter Integrity Mediates the Relationship Between Phenylalanine Control and Executive Abilities in Children with Phenylketonuria

    Brain White Matter Integrity Mediates the Relationship Between Phenylalanine Control and Executive Abilities in Children with Phenylketonuria by Hood, Anna, Rutlin, Jerrel, Shimony, Joshua S., Grange, Dorothy K., White, Desiree A.

    Published 2016
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  7. 7
    Variability in Phenylalanine Control Predicts IQ and Executive Abilities in Children with Phenylketonuria

    Variability in Phenylalanine Control Predicts IQ and Executive Abilities in Children with Phenylketonuria by Hood, Anna, Grange, Dorothy K., Christ, Shawn E., Steiner, Robert, White, Desirée A.

    Published 2014
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  8. 8
    Developmental Trajectories of Executive and Verbal Processes in Children with Phenylketonuria

    Developmental Trajectories of Executive and Verbal Processes in Children with Phenylketonuria by Hawks, Zoë W., Strube, Michael, Johnson, Neco, Grange, Dorothy K., White, Desirée A.

    Published 2018
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  9. 9
    Continuous Renal Replacement Therapy for Two Neonates With Hyperammonemia

    Continuous Renal Replacement Therapy for Two Neonates With Hyperammonemia by Markham, Christopher, Williams, Caroline, Miller, Cory, Grange, Dorothy K., Davis, T. Keefe, Remy, Kenneth E.

    Published 2021
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  10. 10
    Pretreatment cognitive and neural differences between sapropterin dihydrochloride responders and non-responders with phenylketonuria

    Pretreatment cognitive and neural differences between sapropterin dihydrochloride responders and non-responders with phenylketonuria by Hawks, Zoë, Shimony, Joshua, Rutlin, Jerrel, Grange, Dorothy K., Christ, Shawn E., White, Desirée A.

    Published 2017
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  11. 11
    Dichotomous roles of TBX3 in the establishment of atrioventricular conduction pathways in the human heart

    Dichotomous roles of TBX3 in the establishment of atrioventricular conduction pathways in the human heart by Nguyen, Hoang H., Grange, Dorothy K., Johnson, Mark C., Van Hare, George F., Jay, Patrick Y.

    Published 2018
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  12. 12
    Fatal COVID‐19 infection in a patient with long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: A case report

    Fatal COVID‐19 infection in a patient with long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: A case report by Wongkittichote, Parith, Watson, James R., Leonard, Jennifer M., Toolan, Elizabeth R., Dickson, Patricia I., Grange, Dorothy K.

    Published 2020
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  13. 13
    Overnight Pulse Oximetry for Evaluation of Sleep Apnea among Children with Trisomy 21

    Overnight Pulse Oximetry for Evaluation of Sleep Apnea among Children with Trisomy 21 by Coverstone, Andrea M., Bird, Merielle, Sicard, Melissa, Tao, Yu, Grange, Dorothy K., Cleveland, Claudia, Molter, David, Kemp, James S.

    Published 2014
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  14. 14
    Addition of H19 ‘Loss of Methylation Testing’ for Beckwith-Wiedemann Syndrome (BWS) Increases the Diagnostic Yield

    Addition of H19 ‘Loss of Methylation Testing’ for Beckwith-Wiedemann Syndrome (BWS) Increases the Diagnostic Yield by Lennerz, Jochen K., Timmerman, Robert J., Grange, Dorothy K., DeBaun, Michael R., Feinberg, Andrew P., Zehnbauer, Barbara A.

    Published 2010
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  15. 15
    Response Monitoring in Children With Phenylketonuria

    Response Monitoring in Children With Phenylketonuria by Araujo, Gabriel C., Christ, Shawn E., Steiner, Robert D., Grange, Dorothy K., Nardos, Binyam, McKinstry, Robert C., White, Desirée A.

    Published 2009
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  16. 16
    Neurologic and neuroimaging manifestations of Cantú syndrome: A case series

    Neurologic and neuroimaging manifestations of Cantú syndrome: A case series by Leon Guerrero, Christopher R., Pathak, Sheel, Grange, Dorothy K., Singh, Gautam K., Nichols, Colin G., Lee, Jin-Moo, Vo, Katie D.

    Published 2016
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  17. 17
    White and gray matter brain development in children and young adults with phenylketonuria

    White and gray matter brain development in children and young adults with phenylketonuria by Hawks, Zoë, Hood, Anna M., Lerman-Sinkoff, Dov B., Shimony, Joshua S., Rutlin, Jerrel, Lagoni, Daniel, Grange, Dorothy K., White, Desirée A.

    Published 2019
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  18. 18
    Cantu syndrome–associated SUR2 (ABCC9) mutations in distinct structural domains result in K(ATP) channel gain-of-function by differential mechanisms

    Cantu syndrome–associated SUR2 (ABCC9) mutations in distinct structural domains result in K(ATP) channel gain-of-function by differential mechanisms by McClenaghan, Conor, Hanson, Alex, Sala-Rabanal, Monica, Roessler, Helen I., Josifova, Dragana, Grange, Dorothy K., van Haaften, Gijs, Nichols, Colin G.

    Published 2018
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  19. 19
    Three‐dimensional facial morphology in Cantú syndrome

    Three‐dimensional facial morphology in Cantú syndrome by Roessler, Helen I., Shields, Kathleen, Grange, Dorothy K., Knoers, Nine V.A.M., van Haaften, Gijs, Hammond, Peter, van Haelst, Mieke M.

    Published 2020
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  20. 20
    Clinical utility gene card for: Cantú syndrome

    Clinical utility gene card for: Cantú syndrome by Kirk, Edwin P, Scurr, Ingrid, van Haaften, Gijs, van Haelst, Mieke M, Nichols, Colin G, Williams, Maggie, Smithson, Sarah F, Grange, Dorothy K

    Published 2017
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