histamine has been researched along with HbS Disease in 7 studies
Excerpt | Relevance | Reference |
---|---|---|
"Histamine level was elevated in 18% of patients in steady state and in 61% during VOC." | 1.51 | Plasma histamine elevation in a large cohort of sickle cell disease patients. ( Allali, S; Arlet, JB; Bachmeyer, C; Brousse, V; Callebert, J; Chalumeau, M; de Montalembert, M; Georgin-Lavialle, S; Grateau, G; Hermine, O; Launay, JM; Lionnet, F; Maciel, TT; Mattioni, S; Stankovic Stojanovic, K, 2019) |
"Some sickle cell anemia (SCA) patients suffer significantly worse phenotypes than others." | 1.40 | Mast cell activation syndrome as a significant comorbidity in sickle cell disease. ( Afrin, LB, 2014) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (28.57) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 2 (28.57) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Allali, S | 1 |
Lionnet, F | 1 |
Mattioni, S | 1 |
Callebert, J | 1 |
Stankovic Stojanovic, K | 1 |
Bachmeyer, C | 1 |
Arlet, JB | 1 |
Brousse, V | 1 |
de Montalembert, M | 1 |
Chalumeau, M | 1 |
Grateau, G | 1 |
Maciel, TT | 1 |
Launay, JM | 1 |
Hermine, O | 1 |
Georgin-Lavialle, S | 1 |
Afrin, LB | 1 |
Wagner, MC | 1 |
Eckman, JR | 1 |
Wick, TM | 1 |
Manodori, AB | 1 |
Barabino, GA | 1 |
Lubin, BH | 1 |
Kuypers, FA | 1 |
Enwonwu, CO | 1 |
Lu, M | 1 |
Ballas, SK | 1 |
Mohandas, N | 1 |
Clark, MR | 1 |
Embury, SH | 1 |
Smith, ED | 1 |
Marton, LJ | 1 |
Shohet, SB | 1 |
Wosornu, L | 1 |
Konotey-Ahulu, FI | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Sickle Cell Disease (SCD) Biochip': Towards a Simple and Reliable Way to Monitor Sickle Cell Disease[NCT02824471] | 100 participants (Anticipated) | Observational | 2014-10-31 | Recruiting | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
7 other studies available for histamine and HbS Disease
Article | Year |
---|---|
Plasma histamine elevation in a large cohort of sickle cell disease patients.
Topics: Adult; Anemia, Sickle Cell; Child; Cohort Studies; Female; Histamine; Humans; Male; Mast Cells; Pros | 2019 |
Mast cell activation syndrome as a significant comorbidity in sickle cell disease.
Topics: Adult; Anemia, Sickle Cell; Antisickling Agents; Caseins; Chromogranin A; Cohort Studies; Female; He | 2014 |
Histamine increases sickle erythrocyte adherence to endothelium.
Topics: Analysis of Variance; Anemia, Sickle Cell; Cell Adhesion; Cells, Cultured; Endothelial Cells; Endoth | 2006 |
Adherence of phosphatidylserine-exposing erythrocytes to endothelial matrix thrombospondin.
Topics: Anemia, Sickle Cell; Anion Exchange Protein 1, Erythrocyte; Antigens, CD; CD36 Antigens; Cell Adhesi | 2000 |
Elevated plasma histamine in sickle cell anaemia.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Child; Histamine; Histidine; Humans; Middle Aged | 1991 |
Reduced transglutaminase-catalyzed cross-linking of exogenous amines to membrane proteins in sickle erythrocytes.
Topics: Acyltransferases; Anemia, Sickle Cell; Calcimycin; Calcium; Cell Membrane Permeability; Erythrocyte | 1985 |
Gastric acid secretion in sickle-cell anaemia.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Body Weight; Child; Digestion; Duodenal Ulcer; Gastric Juice | 1971 |