标题
Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs
作者
关键词
-
出版物
Nutrients
Volume 13, Issue 11, Pages 3828
出版商
MDPI AG
发表日期
2021-10-28
DOI
10.3390/nu13113828
参考文献
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注意：仅列出部分参考文献，下载原文获取全部文献信息。- Enteral tube feeding in patients receiving dietary treatment for metabolic diseases: A retrospective analysis in a large French cohort
- (2021) Claire-Marine Bérat et al. Molecular Genetics and Metabolism Reports
- Impaired Very‐Low‐Density Lipoprotein catabolism links hypoglycemia to hypertriglyceridemia in Glycogen Storage Disease type Ia
- (2021) Joanne A. Hoogerland et al. JOURNAL OF INHERITED METABOLIC DISEASE
- A retrospective in‐depth analysis of continuous glucose monitoring datasets for patients with hepatic glycogen storage disease: Recommended outcome parameters for glucose management
- (2021) Fabian Peeks et al. JOURNAL OF INHERITED METABOLIC DISEASE
- A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single‐center study and the generation of www.emergencyprotocol.net
- (2021) Alessandro Rossi et al. JOURNAL OF INHERITED METABOLIC DISEASE
- A triple-blinded crossover study to evaluate the short-term safety of sweet manioc starch for the treatment of glycogen storage disease type Ia
- (2021) Vaneisse C. L. Monteiro et al. Orphanet Journal of Rare Diseases
- Impact of glycogen storage disease type I on adult daily life: a survey
- (2021) Sven F. Garbade et al. Orphanet Journal of Rare Diseases
- Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases
- (2021) Jésica Tamara Jacoby et al. Nutrients
- A standard set of person‐centred outcomes for diabetes mellitus: results of an international and unified approach
- (2020) J. Nano et al. DIABETIC MEDICINE
- Imbalanced cortisol concentrations in glycogen storage disease type I: evidence for a possible link between endocrine regulation and metabolic derangement
- (2020) Alessandro Rossi et al. Orphanet Journal of Rare Diseases
- A case report of acute pancreatitis with glycogen storage disease type IA in an adult patient and review of the literature
- (2020) Jiaoyu Ai et al. MEDICINE
- GLIM criteria for the diagnosis of malnutrition – A consensus report from the global clinical nutrition community
- (2019) T. Cederholm et al. Journal of Cachexia Sarcopenia and Muscle
- Glycemic control and complications in glycogen storage disease type I: Results from the Swiss registry
- (2019) Nathalie Kaiser et al. MOLECULAR GENETICS AND METABOLISM
- Gene therapy for glycogen storage diseases
- (2019) Priya S Kishnani et al. HUMAN MOLECULAR GENETICS
- Hepatic glycogen storage diseases are associated to microbial dysbiosis
- (2019) Karina Colonetti et al. PLoS One
- Cornstarch requirements of the adult glycogen storage disease Ia population: A retrospective review
- (2019) Kathryn R. Dahlberg et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Dietary Management of the Glycogen Storage Diseases: Evolution of Treatment and Ongoing Controversies
- (2019) Katalin M Ross et al. Advances in Nutrition
- 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
- Glycogen storage disease type Ia: Adult presentation with microcytic anemia and liver adenomas
- (2018) Wouter Moest et al. HEPATOLOGY
- Role of continuous glucose monitoring in the management of glycogen storage disorders
- (2018) Mrudu Herbert et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Inborn Errors of Metabolism with Hypoglycemia
- (2018) David A. Weinstein et al. PEDIATRIC CLINICS OF NORTH AMERICA
- Clinical and biochemical heterogeneity between patients with glycogen storage disease type IA: the added value of CUSUM for metabolic control
- (2017) Fabian Peeks et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Inflammatory Bowel Disease in Glycogen Storage Disease Type Ia
- (2017) Nicole T. Lawrence et al. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
- The Care Continuum: An Evolving Model for Care and Research in Rare Diseases
- (2017) Erika F. Augustine et al. PEDIATRICS
- Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management
- (2016) Kimihiko Oishi et al. PEDIATRIC TRANSPLANTATION
- Glycogen storage disease type Ia (GSDIa) but not Glycogen storage disease type Ib (GSDIb) is associated to an increased risk of metabolic syndrome: possible role of microsomal glucose 6-phosphate accumulation
- (2015) Daniela Melis 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
- Type I glycogen storage diseases: disorders of the glucose-6-phosphatase/glucose-6-phosphate transporter complexes
- (2014) Janice Y. Chou et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Pregnancy in Women With Glycogen Storage Disease Ia and Ib
- (2014) Iris A. Ferrecchia et al. JOURNAL OF PERINATAL & NEONATAL NURSING
- Liver transplantation in glycogen storage disease type I
- (2014) Susanna JB Boers et al. Orphanet Journal of Rare Diseases
- Continuous glucose monitoring in children with glycogen storage disease type I
- (2013) Ç S Kasapkara et al. EUROPEAN JOURNAL OF CLINICAL NUTRITION
- Dietary treatment of glycogen storage disease type Ia: Uncooked cornstarch and/or continuous nocturnal gastric drip-feeding?
- (2013) Terry G.J. Derks et al. MOLECULAR GENETICS AND METABOLISM
- Characterization and pathogenesis of anemia in glycogen storage disease type Ia and Ib
- (2012) David Q. Wang et al. GENETICS IN MEDICINE
- Bone mineral density in glycogen storage disease type Ia and Ib
- (2012) Laurie A. Minarich et al. GENETICS IN MEDICINE
- Fertility and pregnancy in women affected by glycogen storage disease type I, results of a multicenter Italian study
- (2012) Annalisa Sechi et al. JOURNAL OF INHERITED METABOLIC DISEASE
- The use of continuous glucose monitoring in the practical management of glycogen storage disorders
- (2011) Fiona J. White et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Natural History of Hepatocellular Adenoma Formation in Glycogen Storage Disease Type I
- (2011) David Q. Wang et al. JOURNAL OF PEDIATRICS
- Glucose-6-phosphatase deficiency
- (2011) Roseline Froissart et al. Orphanet Journal of Rare Diseases
- Neuroendocrine responses to hypoglycemia
- (2010) Nolawit Tesfaye et al. Annals of the New York Academy of Sciences
- Glycogen Storage Disease Type III diagnosis and management guidelines
- (2010) Priya S Kishnani et al. GENETICS IN MEDICINE
- Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases
- (2010) Stuart A. Scott et al. HUMAN MUTATION
- An adult male patient with multiple adenomas and a hepatocellular carcinoma: Mild Glycogen Storage Disease type Ia
- (2010) David Cassiman et al. JOURNAL OF HEPATOLOGY
- Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy
- (2010) Janice Y. Chou et al. Nature Reviews Endocrinology
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