Page last updated: 2024-08-21

aminoimidazole carboxamide and Abnormalities, Congenital

aminoimidazole carboxamide has been researched along with Abnormalities, Congenital in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (100.00)	2.80

Authors

Authors	Studies
Billiemaz, K; Ceballos, I; Denommé-Pichon, AS; Héron, B; Imbard, A; Kuentz, P; Marie, S; Piraud, M; Ramond, F; Rio, M; Touraine, R; Vincent, MF	1

Other Studies

1 other study(ies) available for aminoimidazole carboxamide and Abnormalities, Congenital

Article	Year
AICA-ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long-term update on the first case. Journal of inherited metabolic disease, 2020, Volume: 43, Issue:6 Topics: Aminoimidazole Carboxamide; Child; Child, Preschool; Congenital Abnormalities; Epilepsy; Female; Humans; Hydroxymethyl and Formyl Transferases; Infant; Infant, Newborn; Intellectual Disability; Male; Multienzyme Complexes; Mutation; Nucleotide Deaminases; Phenotype; Ribonucleosides	2020

Article

Year

AICA-ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long-term update on the first case.

Journal of inherited metabolic disease, 2020, Volume: 43, Issue:6

Topics: Aminoimidazole Carboxamide; Child; Child, Preschool; Congenital Abnormalities; Epilepsy; Female; Humans; Hydroxymethyl and Formyl Transferases; Infant; Infant, Newborn; Intellectual Disability; Male; Multienzyme Complexes; Mutation; Nucleotide Deaminases; Phenotype; Ribonucleosides

2020