| Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease DA Weinstein, CN Roy, MD Fleming, MF Loda, JI Wolfsdorf, NC Andrews Blood, The Journal of the American Society of Hematology 100 (10), 3776-3781, 2002 | 955 | 2002 |
| Recommendations from the pediatric endocrine society for evaluation and management of persistent hypoglycemia in neonates, infants, and children PS Thornton, CA Stanley, DD De Leon, D Harris, MW Haymond, ... The Journal of pediatrics 167 (2), 238-245, 2015 | 668 | 2015 |
| Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics PS Kishnani, SL Austin, JE Abdenur, P Arn, DS Bali, A Boney, WK Chung, ... Genetics in Medicine 16 (11), e1-e1, 2014 | 455 | 2014 |
| Glycogen storage disease type III diagnosis and management guidelines PS Kishnani, SL Austin, P Arn, DS Bali, A Boney, LE Case, WK Chung, ... Genetics in Medicine 12 (7), 446-463, 2010 | 326 | 2010 |
| Re-evaluating “transitional neonatal hypoglycemia”: mechanism and implications for management CA Stanley, PJ Rozance, PS Thornton, DD De Leon, D Harris, ... The Journal of pediatrics 166 (6), 1520-1525. e1, 2015 | 287 | 2015 |
| Impaired intestinal iron absorption in Crohn's disease correlates with disease activity and markers of inflammation G Semrin, DS Fishman, A Bousvaros, A Zholudev, AC Saunders, ... Inflammatory bowel diseases 12 (12), 1101-1106, 2006 | 257 | 2006 |
| Glycogen storage diseases. JI Wolfsdorf, DA Weinstein Metabolic Aspects of Chronic Liver Disease, 269, 2003 | 253 | 2003 |
| Hepatocellular carcinoma in glycogen storage disease type Ia: a case series LM Franco, V Krishnamurthy, D Bali, DA Weinstein, P Arn, B Clary, ... Journal of inherited metabolic disease 28, 153-162, 2005 | 251 | 2005 |
| Renal disease in type I glycogen storage disease JY Chou, BC Mansfield, DA Weinstein Genetic Diseases of the Kidney, 693-708, 2009 | 245 | 2009 |
| Urinary hepcidin in congenital chronic anemias SL Kearney, E Nemeth, EJ Neufeld, D Thapa, T Ganz, DA Weinstein, ... Pediatric blood & cancer 48 (1), 57-63, 2007 | 234 | 2007 |
| Loss of high‐affinity agonist binding to M1 muscarinic receptors in Alzheimer's disease: implications for the failure of cholinergic replacement therapies DD Flynn, DA Weinstein, DC Mash Annals of Neurology: Official Journal of the American Neurological …, 1991 | 179 | 1991 |
| Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome CP Sentner, IJ Hoogeveen, DA Weinstein, R Santer, E Murphy, ... Journal of inherited metabolic disease 39, 697-704, 2016 | 178 | 2016 |
| Pediatric Endocrine Society. Recommendations from the Pediatric Endocrine Society for evaluation and management of persistent hypoglycemia in neonates, infants, and children PS Thornton, CA Stanley, DD De Leon, D Harris, MW Haymond, ... J Pediatr 167 (2), 238-45, 2015 | 153 | 2015 |
| Hepatic glycogen synthase deficiency: an infrequently recognized cause of ketotic hypoglycemia DA Weinstein, CE Correia, AC Saunders, JI Wolfsdorf Molecular genetics and metabolism 87 (4), 284-288, 2006 | 150 | 2006 |
| Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib HS Jun, DA Weinstein, YM Lee, BC Mansfield, JY Chou Blood, the Journal of the American Society of Hematology 123 (18), 2843-2853, 2014 | 141 | 2014 |
| 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) PS Kishnani, J Goldstein, SL Austin, P Arn, B Bachrach, DS Bali, ... Genetics in Medicine 21 (4), 772-789, 2019 | 139 | 2019 |
| Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease DA Weinstein, JI Wolfsdord European journal of pediatrics 161, S35-S39, 2002 | 137 | 2002 |
| Natural history of hepatocellular adenoma formation in glycogen storage disease type I DQ Wang, LM Fiske, CT Carreras, DA Weinstein The Journal of pediatrics 159 (3), 442-446, 2011 | 132 | 2011 |
| Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib CE Correia, K Bhattacharya, PJ Lee, JJ Shuster, DW Theriaque, ... The American journal of clinical nutrition 88 (5), 1272-1276, 2008 | 125 | 2008 |
| Glycogen storage diseases: phenotypic, genetic, and biochemical characteristics, and therapy JI Wolfsdorf, IA Holm, DA Weinstein Endocrinology and metabolism clinics of North America 28 (4), 801-823, 1999 | 119 | 1999 |
