A triple-blinded crossover study to evaluate the short-term safety of sweet manioc starch for the treatment of glycogen storage disease type Ia

Research priorities for liver glycogen storage disease: An international priority setting partnership with the James Lind Alliance

(2019) Fabian Peeks et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Sleep and quality of life of patients with glycogen storage disease on standard and modified uncooked cornstarch

(2018) Isabelle Rousseau-Nepton et al.   MOLECULAR GENETICS AND METABOLISM

The industrial applications of cassava: current status, opportunities and prospects

(2017) Shubo Li et al.   JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE

Determination of amylose/amylopectin ratio of starches

(2015) Tatiéle Nalin et al.   JOURNAL OF INHERITED METABOLIC DISEASE

A pilot longitudinal study of the use of waxy maize heat modified starch in the treatment of adults with glycogen storage disease type I: a randomized double-blind cross-over study

(2015) Kaustuv Bhattacharya et al.   Orphanet Journal of Rare Diseases

Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics

(2014) Priya S. Kishnani et al.   GENETICS IN MEDICINE

In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseases

(2014) Tatiéle Nalin et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Glucose-6-phosphatase deficiency

(2011) Roseline Froissart et al.   Orphanet Journal of Rare Diseases

Relation between estimates of cornstarch digestibility by the Englyst in vitro method and glycemic response, subjective appetite, and short-term food intake in young men

(2010) G Harvey Anderson et al.   AMERICAN JOURNAL OF CLINICAL NUTRITION

Neonatal Gene Therapy of Glycogen Storage Disease Type Ia Using a Feline Immunodeficiency Virus–based Vector

(2010) Albert Grinshpun et al.   MOLECULAR THERAPY