Page last updated: 2024-08-23

amikacin and Amino Acid Metabolism Disorders, Inborn

amikacin has been researched along with Amino Acid Metabolism Disorders, Inborn 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	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abdenur, JE; Appadurai, V; Besse, A; Bonnen, PE; Cambray-Forker, EJ; Ferdinandusse, S; Leydiker, KB; Stiles, AR	1

Other Studies

1 other study(ies) available for amikacin and Amino Acid Metabolism Disorders, Inborn

Article	Year
Successful diagnosis of HIBCH deficiency from exome sequencing and positive retrospective analysis of newborn screening cards in two siblings presenting with Leigh's disease. Molecular genetics and metabolism, 2015, Volume: 115, Issue:4 Topics: Abnormalities, Multiple; Adolescent; Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Cohort Studies; Exome; Female; Fibroblasts; Humans; Infant; Infant, Newborn; Leigh Disease; Male; Mass Spectrometry; Neonatal Screening; Prognosis; Retrospective Studies; Sequence Analysis, DNA; Siblings; Thiolester Hydrolases	2015

Article

Year

Successful diagnosis of HIBCH deficiency from exome sequencing and positive retrospective analysis of newborn screening cards in two siblings presenting with Leigh's disease.

Molecular genetics and metabolism, 2015, Volume: 115, Issue:4

Topics: Abnormalities, Multiple; Adolescent; Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Cohort Studies; Exome; Female; Fibroblasts; Humans; Infant; Infant, Newborn; Leigh Disease; Male; Mass Spectrometry; Neonatal Screening; Prognosis; Retrospective Studies; Sequence Analysis, DNA; Siblings; Thiolester Hydrolases

2015