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phosphoribosyl pyrophosphate and Autotomy Human

phosphoribosyl pyrophosphate has been researched along with Autotomy Human in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mitev, VI; Neychev, VK1
Seegmiller, JE1

Reviews

1 review(s) available for phosphoribosyl pyrophosphate and Autotomy Human

ArticleYear
Inherited deficiency of hypoxanthine-guanine phosphoribosyltransferase in X-linked uric aciduria (the Lesch-Nyhan syndrome and its variants).
    Advances in human genetics, 1976, Volume: 6

    Topics: Adolescent; Adult; Anemia, Megaloblastic; Child; Child, Preschool; Chromosome Mapping; Erythrocytes; Genes; Genetic Linkage; Humans; Hypoxanthine Phosphoribosyltransferase; Infant; Infant, Newborn; Lesch-Nyhan Syndrome; Male; Mutation; Pedigree; Phenotype; Phosphoribosyl Pyrophosphate; Prenatal Diagnosis; Self Mutilation; Sex Chromosomes; Uric Acid

1976

Other Studies

1 other study(ies) available for phosphoribosyl pyrophosphate and Autotomy Human

ArticleYear
The biochemical basis of the neurobehavioral abnormalities in the Lesch-Nyhan syndrome: a hypothesis.
    Medical hypotheses, 2004, Volume: 63, Issue:1

    Topics: Animals; Biochemistry; Brain; Humans; Hypoxanthine Phosphoribosyltransferase; Intellectual Disability; Lesch-Nyhan Syndrome; Mental Disorders; Models, Biological; Movement Disorders; Neurons; Phosphoribosyl Pyrophosphate; Self Mutilation; Uric Acid

2004