Compounds > arginine

arginine and Deficiency, Glucosephosphatase

arginine has been researched along with Deficiency, Glucosephosphatase in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (14.29)	18.7374
1990's	2 (28.57)	18.2507
2000's	2 (28.57)	29.6817
2010's	1 (14.29)	24.3611
2020's	1 (14.29)	2.80

Authors

Authors	Studies
Abuduxikuer, K; Fang, LJ; Huang, KY; Yan, XM; Zhu, H	1
Biberoglu, G; Hasanoğlu, A; Kasapkara, A; Kasapkara, ÇS; Tümer, L	1
Chen, L; Du, C; Duan, S; Geng, Q; Guo, Y; He, Y; Jiang, C; Jiang, W; Li, H; Lin, Q; Liu, C; Liu, P; Qi, Y; Ren, X; Si, E; Tian, Q; Wen, J; Ye, W; Yu, G; Zhang, Q; Zheng, Y	1
Baynes, JW; den Hollander, NC; Graaff, R; Mulder, DJ; Smit, AJ; Smit, GP; Thorpe, SR	1
Bashan, N; Carmi, R; Hershkovitz, E; Moses, S; Parvari, R	1
Hackel, C; Norato, DY; Reis, FC; Sartorato, EL	1
Edgar, PJ; Fujimoto, WY; Greene, ML; Howell, RR; Lockwood, DH; Merimee, TJ; Seegmiller, JE	1

Other Studies

7 other study(ies) available for arginine and Deficiency, Glucosephosphatase

Article	Year
An infant presenting with extreme hypertriglyceridemia diagnosed as glycogen storage disease type Ia. Journal of pediatric endocrinology & metabolism : JPEM, 2020, May-21, Volume: 33, Issue:6 Topics: Amino Acid Substitution; Arginine; Diagnosis, Differential; Female; Genetic Testing; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Histidine; Homozygote; Humans; Hypertriglyceridemia; Infant; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Severity of Illness Index; Triglycerides	2020
Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I. Journal of pediatric endocrinology & metabolism : JPEM, 2013, Volume: 26, Issue:5-6 Topics: Adolescent; Arginine; Child; Child, Preschool; Fatty Acids; Female; Glycogen Storage Disease Type I; Humans; Hyperlipidemias; Hypolipidemic Agents; Lipid Peroxidation; Male	2013
Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese population. Human genetics, 2006, Volume: 119, Issue:5 Topics: Amino Acid Substitution; Arginine; China; Female; Genetic Testing; Genetic Variation; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glycogen Storage Disease Type I; Humans; Male; NADP; Protein Structure, Secondary; Structure-Activity Relationship	2006
Advanced glycation end products and the absence of premature atherosclerosis in glycogen storage disease Ia. Journal of inherited metabolic disease, 2007, Volume: 30, Issue:6 Topics: Adolescent; Adult; Arginine; Atherosclerosis; Carotid Arteries; Collagen; Female; Glycation End Products, Advanced; Glycogen Storage Disease Type I; Humans; Lysine; Male; Oxidative Stress; Risk; Skin; Tunica Intima; Tunica Media	2007
Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim Arab. Journal of inherited metabolic disease, 1995, Volume: 18, Issue:1 Topics: Arab World; Arginine; Base Sequence; Cysteine; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Humans; Jews; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational	1995
A novel mutation in a Brazilian patient with glycogen storage disease type 1a. Journal of inherited metabolic disease, 1998, Volume: 21, Issue:4 Topics: Arginine; Brazil; Glucose-6-Phosphatase; Glycine; Glycogen Storage Disease Type I; Humans; Mutation; Polymorphism, Single-Stranded Conformational	1998
Insulin secretion in type I glycogen storage disease. Diabetes, 1969, Volume: 18, Issue:11 Topics: Adolescent; Adult; Arginine; Blood Glucose; Glucose Tolerance Test; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Hypoglycemia; Insulin; Insulin Secretion; Middle Aged	1969