Ngā hua rapu - David A. Weinstein

Whakamahine hua
  1. 1
    Glycogen storage diseases: Diagnosis, treatment and outcome

    Glycogen storage diseases: Diagnosis, treatment and outcome mā Margaret A. Chen, David A. Weinstein

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    Regression of Hepatocellular Adenomas with Strict Dietary Therapy in Patients with Glycogen Storage Disease Type I

    Regression of Hepatocellular Adenomas with Strict Dietary Therapy in Patients with Glycogen Storage Disease Type I mā Richard D. Beegle, Laurie M. Brown, David A. Weinstein

    I whakaputaina 2014
    Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Prevention of complications in glycogen storage disease type Ia with optimization of metabolic control

    Prevention of complications in glycogen storage disease type Ia with optimization of metabolic control mā Monika Dambska, EB Labrador, C-L Kuo, David A. Weinstein

    I whakaputaina 2017
    Whiwhi kuputuhi katoa
    Revisão
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  4. 4
    Natural History of Hepatocellular Adenoma Formation in Glycogen Storage Disease Type I

    Natural History of Hepatocellular Adenoma Formation in Glycogen Storage Disease Type I mā David Q. Wang, Laurie M. Fiske, Caroline T. Carreras, David A. Weinstein

    I whakaputaina 2011
    Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    Hepatic glycogen synthase deficiency: An infrequently recognized cause of ketotic hypoglycemia

    Hepatic glycogen synthase deficiency: An infrequently recognized cause of ketotic hypoglycemia mā David A. Weinstein, Catherine E. Correia, Andrew C. Saunders, Joseph I. Wolfsdorf

    I whakaputaina 2005
    Whiwhi kuputuhi katoa
    Revisão
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  6. 6
    Inborn Errors of Metabolism with Hypoglycemia

    Inborn Errors of Metabolism with Hypoglycemia mā David A. Weinstein, Ulrike Steuerwald, Carolina Fischinger Moura de Souza, Terry G. J. Derks

    I whakaputaina 2018
    Whiwhi kuputuhi katoa
    Revisão
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  7. 7
    Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib

    Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib mā Hyun Sik Jun, David A. Weinstein, Young‐Mock Lee, Brian C. Mansfield, Janice Y. Chou

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    Dietary Management of the Glycogen Storage Diseases: Evolution of Treatment and Ongoing Controversies

    Dietary Management of the Glycogen Storage Diseases: Evolution of Treatment and Ongoing Controversies mā Katalin M. Ross, Iris A. Ferrecchia, Kathryn Dahlberg, Monika Dambska, Patrick T. Ryan, David A. Weinstein

    I whakaputaina 2019
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  9. 9
    Reversal of glycogen storage disease type IIIa‐related cardiomyopathy with modification of diet

    Reversal of glycogen storage disease type IIIa‐related cardiomyopathy with modification of diet mā Aditi I Dagli, Roberto T. Zori, Harriet Kling McCune, Tomislav Ivsic, Melissa K. Maisenbacher, David A. Weinstein

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Artigo
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  10. 10
    Aggressive therapy improves cirrhosis in glycogen storage disease type IX

    Aggressive therapy improves cirrhosis in glycogen storage disease type IX mā Laurie A. Tsilianidis, Laurie M. Fiske, Sara D. Siegel, Chris Lumpkin, Kate Hoyt, Melissa Wasserstein, David A. Weinstein

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib

    Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib mā Catherine E. Correia, Kaustuv Bhattacharya, Philip Lee, Jonathan J. Shuster, Douglas W. Theriaque, Meena N. Shankar, Gerrit Smit, David A. Weinstein

    I whakaputaina 2008
    Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene

    Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene mā Deeksha Bali, Jennifer Goldstein, Keri Fredrickson, Catherine Rehder, Anne Boney, Stephanie Austin, David A. Weinstein, Richard E. Lutz, Avihu Boneh, Priya S. Kishnani

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    Impaired intestinal iron absorption in Crohnʼs disease correlates with disease activity and markers of inflammation

    Impaired intestinal iron absorption in Crohnʼs disease correlates with disease activity and markers of inflammation mā Gaith Semrin, Douglas S. Fishman, Athos Bousvaros, Anna Zholudev, Andrew C. Saunders, Catherine E. Correia, Elizabeta Nemeth, Richard J. Grand, David A. Weinstein

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    Hepcidin, Interleukin-6 Levels and Iron Metabolism Parameters in Patients with Hepatic Glycogen Storage Diseases: A Cross-Sectional Study

    Hepcidin, Interleukin-6 Levels and Iron Metabolism Parameters in Patients with Hepatic Glycogen Storage Diseases: A Cross-Sectional Study mā Tatiéle Nalin, Fernanda Sperb‐Ludwig, Marina Siebert, Gustavo Mottin Rizowy, David A. Weinstein, Terry G. J. Derks, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz

    I whakaputaina 2024
    Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease

    Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease mā Priya S. Kishnani, Tzu‐Po Chuang, Deeksha Bali, Dwight D. Koeberl, Stephanie Austin, David A. Weinstein, Elaine Murphy, Ying‐Ting Chen, Keri Boyette, Chu‐Hao Liu, Yuan-Tsong Chen, Ling‐Hui Li

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Artigo
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  16. 16
    Safety issues associated with dietary management in patients with hepatic glycogen storage disease

    Safety issues associated with dietary management in patients with hepatic glycogen storage disease mā Thomas A.H. Steunenberg, Fabian Peeks, Irene J. Hoogeveen, John J. Mitchell, Helen Mundy, Foekje de Boer, Charlotte M. A. Lubout, Carolina F. de Souza, David A. Weinstein, Terry G. J. Derks

    I whakaputaina 2018
    Whiwhi kuputuhi katoa
    Artigo
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  17. 17
    Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome

    Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome mā Christiaan P. Sentner, Irene J. Hoogeveen, David A. Weinstein, René Santer, Elaine Murphy, Patrick McKiernan, Ulrike Steuerwald, Nicholas Beauchamp, Joanna Taybert, Pascal Laforêt, François Petit, Aurélie Hubert, Philippe Labrune, Gerrit Smit, Terry G. J. Derks

    I whakaputaina 2016
    Whiwhi kuputuhi katoa
    Artigo
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  18. 18
    Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

    Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) mā Priya S. Kishnani, Jennifer Goldstein, Stephanie Austin, Pamela Arn, Bert Bachrach, Deeksha Bali, Wendy K. Chung, Areeg El‐Gharbawy, Laurie M. Brown, Stephen G. Kahler, Surekha Pendyal, Katalin M. Ross, Laurie A. Tsilianidis, David A. Weinstein, Michael S. Watson

    I whakaputaina 2019
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  19. 19
    Recommendations from the Pediatric Endocrine Society for Evaluation and Management of Persistent Hypoglycemia in Neonates, Infants, and Children

    Recommendations from the Pediatric Endocrine Society for Evaluation and Management of Persistent Hypoglycemia in Neonates, Infants, and Children mā Paul Thornton, Charles A. Stanley, Diva D. De León, Deborah L. Harris, Morey W. Haymond, Khalid Hussain, Lynne L. Levitsky, M. Hassan Murad, Paul J. Rozance, Rebecca A. Simmons, Mark A. Sperling, David A. Weinstein, Neil H. White, Joseph I. Wolfsdorf

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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  20. 20
    Re-Evaluating “Transitional Neonatal Hypoglycemia”: Mechanism and Implications for Management

    Re-Evaluating “Transitional Neonatal Hypoglycemia”: Mechanism and Implications for Management mā Charles A. Stanley, Paul J. Rozance, Paul Thornton, Diva D. De León, Deborah L. Harris, Morey W. Haymond, Khalid Hussain, Lynne L. Levitsky, M. Hassan Murad, Rebecca A. Simmons, Mark A. Sperling, David A. Weinstein, Neil H. White, Joseph I. Wolfsdorf

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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