Rezultati - David A. Weinstein
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Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene od Deeksha Bali, Jennifer Goldstein, Keri Fredrickson, Catherine Rehder, Anne Boney, Stephanie Austin, David A. Weinstein, Richard E. Lutz, Avihu Boneh, Priya S. Kishnani
Izdano 2013Artigo -
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Impaired intestinal iron absorption in Crohnʼs disease correlates with disease activity and markers of inflammation od Gaith Semrin, Douglas S. Fishman, Athos Bousvaros, Anna Zholudev, Andrew C. Saunders, Catherine E. Correia, Elizabeta Nemeth, Richard J. Grand, David A. Weinstein
Izdano 2006Artigo -
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Hepcidin, Interleukin-6 Levels and Iron Metabolism Parameters in Patients with Hepatic Glycogen Storage Diseases: A Cross-Sectional Study od 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
Izdano 2024Artigo -
15
Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease od 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
Izdano 2009Artigo -
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Safety issues associated with dietary management in patients with hepatic glycogen storage disease od 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
Izdano 2018Artigo -
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Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome od 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
Izdano 2016Artigo -
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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) od 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
Izdano 2019Artigo -
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Recommendations from the Pediatric Endocrine Society for Evaluation and Management of Persistent Hypoglycemia in Neonates, Infants, and Children od 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
Izdano 2015Artigo -
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Re-Evaluating “Transitional Neonatal Hypoglycemia”: Mechanism and Implications for Management od 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
Izdano 2015Revisão
Iskalna orodja:
Sorodne teme
Medicine
Internal medicine
Glycogen storage disease
Endocrinology
Disease
Glycogen
Hypoglycemia
Gastroenterology
Pediatrics
Diabetes mellitus
Glycogen storage disease type I
Biology
Intensive care medicine
Pathology
Genetics
Insulin
Gene
Differential diagnosis
Enzyme replacement therapy
Guideline
Inflammation
Insulin resistance
Adenoma
Adverse effect
Biochemistry
Cardiomyopathy
Chemistry
Cholesterol
Cirrhosis
Cohort