Page last updated: 2024-10-18

histamine and Acroosteolysis, Giaccai Type

histamine has been researched along with Acroosteolysis, Giaccai Type in 3 studies

Research Excerpts

ExcerptRelevanceReference
"Congenital insensitivity to pain with anhidrosis is a rare autosomal recessive hereditary disorder that is characterized by having both sensory neuropathy and anhidrosis."1.38Congenital insensitivity to pain with anhidrosis: a case with preserved itch sensation to histamine and partial pain sensation. ( Satoh, T; Tanaka, A; Tanaka, T; Yokozeki, H, 2012)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Tanaka, T1
Satoh, T1
Tanaka, A1
Yokozeki, H1
Sweet, WH1
Axelrod, FB1
Pearson, J1

Reviews

1 review available for histamine and Acroosteolysis, Giaccai Type

ArticleYear
Animal models of chronic pain: their possible validation from human experience with posterior rhizotomy and congenital analgesia (Part I of the second John J. Bonica lecture).
    Pain, 1981, Volume: 10, Issue:3

    Topics: Adolescent; Adult; Animals; Child; Child, Preschool; Chronic Disease; Cordotomy; Disease Models, Ani

1981

Other Studies

2 other studies available for histamine and Acroosteolysis, Giaccai Type

ArticleYear
Congenital insensitivity to pain with anhidrosis: a case with preserved itch sensation to histamine and partial pain sensation.
    The British journal of dermatology, 2012, Volume: 166, Issue:4

    Topics: Child; Hereditary Sensory and Autonomic Neuropathies; Histamine; Histamine Agonists; Humans; Male; M

2012
Congenital sensory neuropathies. Diagnostic distinction from familial dysautonomia.
    American journal of diseases of children (1960), 1984, Volume: 138, Issue:10

    Topics: Bone and Bones; Diagnosis, Differential; Dysautonomia, Familial; Female; Hereditary Sensory and Auto

1984