arginine has been researched along with Lipodystrophy in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (30.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Al-Haggar, M; Barakat, T; Madej-Pilarczyk, A; Puzianowska-Kuznicka, M; Shams, A | 1 |
| Carani, C; Carli, F; Cocchi, S; Diazzi, C; Guaraldi, G; Madeo, B; Orlando, G; Rochira, V; Zirilli, L | 1 |
| Brown, CA; Lupski, JR; Potocki, L; Shen, JJ | 1 |
| Anderson, CM; Cao, H; Hegele, RA; Jones, DC; Wang, J | 1 |
| Auclair, M; Buendia, B; Capeau, J; Courvalin, JC; Dubosclard, E; Pouchelet, M; Vigouroux, C | 1 |
| Kasuga, M; Kodama, S; Matsuo, M; Matsuo, T; Morishita, Y; Ninomiya, M; Sakurai, T; Seki, A | 1 |
| Blizzard, RM; Huseman, C; Johanson, A; Varma, M | 1 |
| Corbin, A; Hollingsworth, DR; Mabry, CC; Upton, GV | 1 |
| George, J; Herrold, J; Tzagournis, M | 1 |
| Oseid, S | 1 |
10 other study(ies) available for arginine and Lipodystrophy
| Article | Year |
|---|---|
Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu LMNA mutation and in their asymptomatic heterozygotic mothers.
Topics: Acro-Osteolysis; Adult; Amino Acid Substitution; Arginine; Biopsy; Case-Control Studies; Child; Child, Preschool; Egypt; Female; Heterozygote; Homozygote; Humans; Lamin Type A; Leucine; Lipodystrophy; Male; Mandible; Microscopy, Electron, Transmission; Mothers; Mutation, Missense; Pedigree; Progeria; Skin | 2013 |
GH response to GHRH plus arginine is impaired in lipoatrophic women with human immunodeficiency virus compared with controls.
Topics: Adolescent; Adult; Arginine; Case-Control Studies; Cross-Sectional Studies; Female; Growth Hormone-Releasing Hormone; HIV Infections; HIV-1; Human Growth Hormone; Humans; Lipodystrophy; Middle Aged; Prospective Studies; Young Adult | 2012 |
Mandibuloacral dysplasia caused by homozygosity for the R527H mutation in lamin A/C.
Topics: Abnormalities, Multiple; Adolescent; Amino Acid Substitution; Arginine; Craniofacial Abnormalities; Genes, Recessive; Genotype; Histidine; Homozygote; Humans; Lamin Type A; Lipodystrophy; Male; Musculoskeletal Abnormalities; Mutation; Phenotype | 2003 |
Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes.
Topics: Adolescent; Adult; Arginine; Diabetes Mellitus; Female; Genetic Variation; Genotype; Glutamine; Humans; Hyperinsulinism; Hyperlipidemias; Hypertension; Lamin Type A; Lamins; Lipodystrophy; Male; Middle Aged; Nuclear Proteins; Pedigree; Point Mutation | 2000 |
Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene.
Topics: Adult; Arginine; Cell Cycle; Cell Nucleus; Cells, Cultured; DNA-Binding Proteins; Female; Fibroblasts; Genetic Carrier Screening; Genetic Variation; Glutamine; Hot Temperature; Humans; Immunoblotting; Lamin Type A; Lamins; Lipodystrophy; Membrane Proteins; Middle Aged; Mutation, Missense; Nuclear Envelope; Nuclear Pore Complex Proteins; Nuclear Proteins; Solubility; Tryptophan | 2001 |
Congenital generalized lipodystrophy with insulin-resistant diabetes.
Topics: Acanthosis Nigricans; Arginine; Child; Diabetes Mellitus, Type 1; Fatty Acids, Nonesterified; Glucagon; Humans; Insulin Resistance; Leukocytes; Lipodystrophy; Lipoproteins, LDL; Male; Receptor, Insulin; Sulfonylurea Compounds; Triglycerides | 1978 |
Congenital lipodystrophy: An endocrine study in three siblings. I. Disorders of carbohydrate metabolism.
Topics: Adolescent; Adrenocorticotropic Hormone; Antigens; Arginine; Blood Glucose; Child; Child, Preschool; Female; Glucagon; Glucose Tolerance Test; Growth Hormone; Hormones; Humans; Infant; Insulin; Insulin Resistance; Insulin Secretion; Lipid Metabolism; Lipodystrophy; Male; Tolbutamide | 1978 |
Pituitary-hypothalamic dysfunction in generalized lipodystrophy.
Topics: 17-Ketosteroids; Adrenal Cortex Hormones; Adult; Arginine; Child; Corticotropin-Releasing Hormone; Female; Follicle Stimulating Hormone; Growth Hormone; Humans; Hypothalamo-Hypophyseal System; Lipodystrophy; Melanocyte-Stimulating Hormones; Metyrapone; Middle Aged; Pituitary Hormone-Releasing Hormones; Stimulation, Chemical; Thyroid Function Tests; Thyrotropin; Thyroxine | 1973 |
Increased growth hormone in partial and total lipoatrophy.
Topics: Adult; Antigens; Arginine; Child; Chlorpromazine; Chromatography, Gel; Female; Glucose Tolerance Test; Growth Hormone; Humans; Infant; Iodine Isotopes; Lipodystrophy; Male; Middle Aged; Phentolamine; Radioimmunoassay | 1973 |
Studies in congenital generalized lipodystrophy. 3. Growth hormone levels.
Topics: Adolescent; Arginine; Blood Glucose; Child; Child, Preschool; Female; Growth Hormone; Humans; Infant; Insulin; Lipodystrophy; Male; Radioimmunoassay; Vasopressins | 1973 |