guanidine has been researched along with Syndrome in 4 studies
Guanidine: A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.
guanidine : An aminocarboxamidine, the parent compound of the guanidines.
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Treatment with guanidine hydrochloride resulted in clinical improvement of the neuromuscular disease, but the patient died of refractory leukemia." | 2.37 | Eaton-Lambert syndrome in a patient with acute T cell lymphocytic leukemia. ( Clinton, ME; Manian, FA; Morrow, JD; Stein, RS, 1988) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| ZACCO, M | 1 |
| PUTIGNANO, T | 1 |
| Shammas, C | 1 |
| Menne, TF | 1 |
| Hilcenko, C | 1 |
| Michell, SR | 1 |
| Goyenechea, B | 1 |
| Boocock, GR | 1 |
| Durie, PR | 1 |
| Rommens, JM | 1 |
| Warren, AJ | 1 |
| Bady, B | 1 |
| Chauplannaz, G | 1 |
| Carrier, H | 1 |
| Morrow, JD | 1 |
| Manian, FA | 1 |
| Clinton, ME | 1 |
| Stein, RS | 1 |
1 review available for guanidine and Syndrome
| Article | Year |
|---|---|
Eaton-Lambert syndrome in a patient with acute T cell lymphocytic leukemia.
Topics: Aged; Electromyography; Female; Guanidine; Guanidines; Humans; Leukemia-Lymphoma, Adult T-Cell; Medi | 1988 |
3 other studies available for guanidine and Syndrome
| Article | Year |
|---|---|
[Guanidine and azotemic intoxication: clinical value of the correlation between guanidine and urea in uremic and eclamptic syndromes].
Topics: Blood; Guanidine; Guanidines; Syndrome; Urea | 1949 |
Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman-Diamond Syndrome.
Topics: Alleles; Amino Acid Sequence; Archaeoglobus fulgidus; Blotting, Western; Cell Cycle; Crystallography | 2005 |
Congenital Lambert-Eaton myasthenic syndrome.
Topics: Action Potentials; Biopsy; Child, Preschool; Electromyography; Female; Guanidine; Guanidines; Humans | 1987 |