Page last updated: 2024-10-18

glutaric acid and Dyskinesia Syndromes

glutaric acid has been researched along with Dyskinesia Syndromes in 7 studies

glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.

Research Excerpts

ExcerptRelevanceReference
"A 9-month-old patient was admitted with encephalopathy and acute loss of acquired motor skills during the course of COVID-19 disease."1.62COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1. ( Ahmadzada, S; Aktuglu-Zeybek, C; Kiykim, E; Yalcinkaya, C; Zubarioglu, T, 2021)
"Cerebral MRI revealed regressive subdural hematoma, but marked frontotemporal atrophy as well."1.29Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall. ( Emons, D; Haverkamp, F; Kreft, B; Woelfle, J, 1996)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's3 (42.86)18.2507
2000's2 (28.57)29.6817
2010's0 (0.00)24.3611
2020's1 (14.29)2.80

Authors

AuthorsStudies
Zubarioglu, T1
Ahmadzada, S1
Yalcinkaya, C1
Kiykim, E1
Aktuglu-Zeybek, C1
Hellström, B1
Kyllerman, M1
Skjeldal, OH1
Lundberg, M1
Holme, I1
Jellum, E1
von Döbeln, U1
Fossen, A1
Carlsson, G1
Woelfle, J1
Kreft, B1
Emons, D1
Haverkamp, F1
Hauser, SE1
Peters, H1
Prats Viñas, J1
Corral, I1
Martínez Castrillo, JC1
Martínez-Pardo, M1
Gimeno, A1

Other Studies

7 other studies available for glutaric acid and Dyskinesia Syndromes

ArticleYear
COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1.
    Journal of pediatric endocrinology & metabolism : JPEM, 2021, Dec-20, Volume: 34, Issue:12

    Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Brain Diseases, Metabolic; Carnitine; C

2021
Progressive dystonia and dyskinesia in childhood. A review of some recent advances.
    Acta paediatrica Scandinavica, 1982, Volume: 71, Issue:2

    Topics: Child; Dystonia; Dystonia Musculorum Deformans; Glutarates; Humans; Infant; Movement Disorders

1982
Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations.
    Movement disorders : official journal of the Movement Disorder Society, 1994, Volume: 9, Issue:1

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Brain; Child; Child, Preschool; Combined Modality

1994
Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall.
    Pediatric radiology, 1996, Volume: 26, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Cisterna Magna; Developmental Disabilities; Diagnosis

1996
Glutaric aciduria type 1: an underdiagnosed cause of encephalopathy and dystonia-dyskinesia syndrome in children.
    Journal of paediatrics and child health, 1998, Volume: 34, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Cerebral Palsy; Child, Preschool; Diagnosis, Differential; Dys

1998
[Glutaric aciduria type I: an organic acidemia without acidosis with severe movement disorders].
    Neurologia (Barcelona, Spain), 2001, Volume: 16, Issue:8

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Carnitine; Child, Preschool;

2001
[Glutaric aciduria type I: diagnosis in adulthood and phenotypic variability].
    Neurologia (Barcelona, Spain), 2001, Volume: 16, Issue:8

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic; Carnitine

2001