Compounds > adenosine monophosphate

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adenosine monophosphate and Intellectual Disability

adenosine monophosphate has been researched along with Intellectual Disability in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	3 (50.00)	18.7374
1990's	2 (33.33)	18.2507
2000's	1 (16.67)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Jaeken, J; Van den Bergh, F; Van den Berghe, G; Vincent, MF	2
Marie, S; Race, V; Van den Berghe, G; Vincent, MF	1
Clausen, J; Dyggve, HV; Jensen, GE; Melchior, JC; Rastogi, SC	1
Balis, ME; Cox, RP; Dancis, J; Silvers, DN	1
Henningsen, K; Moller, B; Therkelsen, AJ	1

Other Studies

6 other study(ies) available for adenosine monophosphate and Intellectual Disability

Article	Year
Residual adenylosuccinase activities in fibroblasts of adenylosuccinase-deficient children: parallel deficiency with adenylosuccinate and succinyl-AICAR in profoundly retarded patients and non-parallel deficiency in a mildly retarded girl. Journal of inherited metabolic disease, 1993, Volume: 16, Issue:2 Topics: Adenosine Monophosphate; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Binding, Competitive; Cells, Cultured; Child; Chromatography, Ion Exchange; Female; Fibroblasts; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Kinetics; Nucleotides; Potassium Chloride; Ribonucleotides; Substrate Specificity	1993
Functional studies in fibroblasts of adenylosuccinase-deficient children. Journal of inherited metabolic disease, 1993, Volume: 16, Issue:2 Topics: Adenosine Monophosphate; Adenosine Triphosphate; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Cells, Cultured; Child; Fibroblasts; Formates; Humans; Hypoxanthine; Hypoxanthines; Intellectual Disability; Ribonucleotides	1993
Clinical, biochemical and molecular genetic correlations in adenylosuccinate lyase deficiency. Human molecular genetics, 2000, Sep-01, Volume: 9, Issue:14 Topics: 5' Untranslated Regions; Adenosine Monophosphate; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Chromatography, Gel; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Genotype; Homozygote; Humans; Intellectual Disability; Kinetics; Metabolism, Inborn Errors; Mutation; Mutation, Missense; Recombinant Fusion Proteins; Recombinant Proteins; Ribonucleosides; Temperature; Time Factors	2000
Lysosomal (leucocyte) proteinase and sulfatase levels in Dyggve-Melchior-Clausen (DMC) syndrome. Acta neurologica Scandinavica, 1977, Volume: 56, Issue:5 Topics: Adenosine Monophosphate; Adolescent; Adult; alpha 1-Antitrypsin; alpha-Macroglobulins; Amidohydrolases; Arylsulfatases; Cathepsins; Female; Humans; Hyaluronic Acid; Intellectual Disability; Leukocytes; Lysosomes; Male; Middle Aged; Mucopolysaccharidoses; Pancreatic Elastase; Sulfatases; Syndrome	1977
Detection of the heterozygote in Lesch-Nyhan disease by hair-root analysis. The New England journal of medicine, 1972, 02-24, Volume: 286, Issue:8 Topics: Adenosine Monophosphate; Athetosis; Clinical Enzyme Tests; Culture Techniques; Female; Fibroblasts; Hair; Heterozygote; Humans; Hypoxanthines; Intellectual Disability; Lesch-Nyhan Syndrome; Male; Mosaicism; Pentosyltransferases; Phosphoric Acids; Purine-Pyrimidine Metabolism, Inborn Errors; Ribose; Scalp; Self Mutilation; Tritium	1972
A group-C ring chromosome in a mentally deficient male. Journal of medical genetics, 1971, Volume: 8, Issue:2 Topics: Acid Phosphatase; Adenosine Monophosphate; Adolescent; Blood Group Antigens; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; Dermatoglyphics; Genetic Linkage; Humans; Intellectual Disability; Karyotyping; Male; Phosphotransferases	1971