Page last updated: 2024-09-02

1-hexadecyl-2-acetyl-glycero-3-phosphocholine and Gasser Syndrome

1-hexadecyl-2-acetyl-glycero-3-phosphocholine has been researched along with Gasser Syndrome in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19903 (42.86)18.7374
1990's2 (28.57)18.2507
2000's2 (28.57)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boster, DR; Ciol, MA; Henderson, WR; Jelacic, S; Jones, F; Smith, JM; Tarr, PI; Watkins, SL; Williams, GD1
Sills, RH1
Naruse, T1
Iijima, K; Kawamura, N; Miwa, M; Nakamura, H; Shiozawa, S; Shirakawa, T; Xu, H; Yamaoka, K; Yoshikawa, N1
Benigni, A; Boccardo, P; Noris, M; Remuzzi, G; Siegler, RL1
Baumgardt, A; Gill, JC; Leichter, HE; Sheth, KJ1
Langenhuysen, C; Monnens, L; van de Meer, W; van Munster, P; van Oostrom, C1

Reviews

2 review(s) available for 1-hexadecyl-2-acetyl-glycero-3-phosphocholine and Gasser Syndrome

ArticleYear
Thrombotic thrombocytopenic purpura. I. Pathophysiology and clinical manifestations.
    The American journal of pediatric hematology/oncology, 1984,Winter, Volume: 6, Issue:4

    Topics: Anemia, Hemolytic; Blood Coagulation Factors; Blood Platelets; Child; Diagnosis, Differential; Endothelium; Epoprostenol; Factor VIII; Female; Fever; Fibrinolytic Agents; Hemolytic-Uremic Syndrome; Humans; Kidney Diseases; Male; Neurologic Manifestations; Platelet Activating Factor; Purpura; Purpura, Thrombotic Thrombocytopenic; Thromboxane A2

1984
[Hemolytic uremic syndrome (HUS): pathophysiology--with reference to the differentiation between HUS and thrombotic thrombocytopenic purpura].
    Nihon rinsho. Japanese journal of clinical medicine, 1993, Volume: 51, Issue:1

    Topics: Autoantibodies; Endothelium, Vascular; Endotoxins; Epoprostenol; Hemolytic-Uremic Syndrome; Hemostasis; Humans; Platelet Activating Factor; Purpura, Thrombotic Thrombocytopenic; von Willebrand Factor

1993

Other Studies

5 other study(ies) available for 1-hexadecyl-2-acetyl-glycero-3-phosphocholine and Gasser Syndrome

ArticleYear
Platelet-activating factor and Escherichia coliO157:H7 infections.
    Pediatric nephrology (Berlin, Germany), 2002, Volume: 17, Issue:12

    Topics: Blood Cell Count; Child, Preschool; DNA; Escherichia coli Infections; Escherichia coli O157; Female; Genotype; Hemolytic-Uremic Syndrome; Humans; Logistic Models; Male; Mutation; Platelet Activating Factor; Prospective Studies; Risk Assessment

2002
Platelet-activating factor acetylhydrolase gene mutation in Japanese children with Escherichia coli O157-associated hemolytic uremic syndrome.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2000, Volume: 36, Issue:1

    Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Adult; Alleles; Child; Child, Preschool; Escherichia coli Infections; Escherichia coli O157; Female; Genotype; Hemolytic-Uremic Syndrome; Heterozygote; Humans; Infant; Japan; Male; Middle Aged; Phospholipases A; Platelet Activating Factor; Point Mutation; Polymerase Chain Reaction

2000
Urinary excretion of platelet-activating factor in haemolytic uraemic syndrome.
    Lancet (London, England), 1992, Apr-04, Volume: 339, Issue:8797

    Topics: Child; Hemolytic-Uremic Syndrome; Humans; Platelet Activating Factor

1992
Reversal of central nervous system involvement in hemolytic uremic syndrome by use of plasma exchanges.
    Clinical pediatrics, 1987, Volume: 26, Issue:12

    Topics: Antigens; Child; Factor VIII; Female; Hemiplegia; Hemolytic-Uremic Syndrome; Humans; Plasma Exchange; Platelet Activating Factor; Seizures; von Willebrand Factor

1987
Platelet aggregating factor in the epidemic form of hemolytic-uremic syndrome in childhood.
    Clinical nephrology, 1985, Volume: 24, Issue:3

    Topics: Blood Coagulation Factors; Child; Child, Preschool; Female; Hemolytic-Uremic Syndrome; Humans; Immunoglobulin G; Infant; Male; Platelet Activating Factor; Platelet Aggregation; Purpura, Thrombotic Thrombocytopenic

1985