Research Terms
Endocrine Diseases Hereditary Diseases
Seigel J, Weinstein DA, Hillman R, Colbert B, Matthews B, Bachrach B. Glycogen Storage Disease Type III Presenting as Non-Ketotic Hypoglycemia: Use of Mutation Analysis to Non-Invasively Confirm the Diagnosis. Journal of Pediatric Endocrinology and Metabolism, 2008; 21: 587-90.
DHJ Martens DHJ, Rake JP, Schwarz M, Ullrich K, Weinstein DA, Merkel M, Sauer PHH, Smit GPA. Pregnancies in glycogen storage disease Ia. American Journal of Obstetrics and Gynecology; 2008; 198: 646e1-7.
Storch E, Keeley M,
Kim SY, Weinstein DA, Starost MF,
Bernier AV, Sentner CP, Correia CE, Theriaque DW, Shuster JJ, Smit GP, and Weinstein DA. Hyperlipidemia in Glycogen Storage Disease Type III: Impact of Age and Metabolic Control. Journal of Inherited Metabolic Disease, 2008; 31: 729-32.
Correia CE, Bhattacharya K, Lee P, Shuster JJ, Theriaque DW, Shankar M, Smit GPA, and Weinstein DA. Use of Modified Therapy to Extend Fasting in Glycogen Storage Disease Types Ia and Ib. American Journal of Clinical Nutrition, 2008; 88: 1272-6.
Bernier AV, Correia CE, Haller MJ, Theriaque DW, Shuster JJ, and Weinstein DA. Vascular dysfunction in glycogen storage disease type
Dagli AI, Zori RT, Mccune H, Ivsic T, Maisenbacher MK, and Weinstein DA. Reversal of glycogen storage disease type IIIa related hypertrophic cardiomyopathy with modification of diet. Journal of Inherited Metabolic Disease, 2008. [Epub ahead of print March 30, 2009; PMID 19322675]