Page last updated: 2024-10-17

salicylic acid and HbS Disease

salicylic acid has been researched along with HbS Disease in 7 studies

Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).

Research Excerpts

ExcerptRelevanceReference
"Impairment of nitric oxide bioavailability secondary to increased arginase activity and overproduction of reactive oxygen species (ROS) is thought to be a major cause of vascular complications in sickle cell disease (SCD)."1.35Cysteine-iron promotes arginase activity by driving the Fenton reaction. ( Iyamu, EW; Perdew, H; Woods, GM, 2008)
"We suggest that reperfusion injury physiology may contribute to the evolution of the chronic organ damage characteristic of sickle cell disease."1.31Reperfusion injury pathophysiology in sickle transgenic mice. ( Belcher, JD; Choong, S; Hebbel, RP; Osarogiagbon, UR; Paller, MS; Vercellotti, GM, 2000)
"We report a black girl with sickle cell anemia."1.29Encephaloduroarterio-synangiosis in a child with sickle cell anemia and moyamoya disease. ( Baruchel, S; Farmer, JP; Montes, JL; O'Gorman, AM; Vernet, O, 1996)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's1 (14.29)18.2507
2000's4 (57.14)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Iyamu, EW1
Perdew, H1
Woods, GM1
Osarogiagbon, UR1
Choong, S1
Belcher, JD1
Vercellotti, GM1
Paller, MS1
Hebbel, RP1
Nelson, CE1
Scarfone, RJ1
Dahdaleh, NS1
Lindley, TE1
Kirby, PA1
Oya, H1
Howard, MA1
Yildirim, T1
Agildere, AM1
Oguzkurt, L1
Barutcu, O1
Kizilkilic, O1
Kocak, R1
Alp Niron, E1
Vernet, O1
Montes, JL1
O'Gorman, AM1
Baruchel, S1
Farmer, JP1
Ndugwa, CM1
Mukidi, F1

Reviews

1 review available for salicylic acid and HbS Disease

ArticleYear
A "neurosurgical crisis" of sickle cell disease.
    Journal of neurosurgery. Pediatrics, 2009, Volume: 4, Issue:6

    Topics: Acute Disease; Adolescent; Anemia, Sickle Cell; Craniotomy; Follow-Up Studies; Hematoma; Hematoma, E

2009

Other Studies

6 other studies available for salicylic acid and HbS Disease

ArticleYear
Cysteine-iron promotes arginase activity by driving the Fenton reaction.
    Biochemical and biophysical research communications, 2008, Nov-07, Volume: 376, Issue:1

    Topics: Anemia, Sickle Cell; Arginase; Cysteine; Enzyme Activation; Erythrocytes; Humans; Iron; Salicylic Ac

2008
Reperfusion injury pathophysiology in sickle transgenic mice.
    Blood, 2000, Jul-01, Volume: 96, Issue:1

    Topics: Allopurinol; Anemia, Sickle Cell; Animals; Biomarkers; Enzyme Inhibitors; Ethane; Hemoglobin, Sickle

2000
A Teenager With Sickle Cell Disease and Scalp Swelling.
    Pediatric emergency care, 2018, Volume: 34, Issue:9

    Topics: Adolescent; Anemia, Sickle Cell; Diagnosis, Differential; Drainage; Emergency Service, Hospital; Hum

2018
MRI evaluation of cranial bone marrow signal intensity and thickness in chronic anemia.
    European journal of radiology, 2005, Volume: 53, Issue:1

    Topics: Adult; Age Factors; Aged; alpha-Thalassemia; Anemia; Anemia, Hemolytic, Congenital; Anemia, Iron-Def

2005
Encephaloduroarterio-synangiosis in a child with sickle cell anemia and moyamoya disease.
    Pediatric neurology, 1996, Volume: 14, Issue:3

    Topics: Anemia, Sickle Cell; Cerebral Angiography; Cerebral Arteries; Child, Preschool; Female; Humans; Moya

1996
Sickle cell cephalohaematoma.
    East African medical journal, 1976, Volume: 53, Issue:9

    Topics: Adolescent; Anemia, Sickle Cell; Child; Child, Preschool; Cysts; Female; Head; Hematoma; Humans; Mal

1976