1-nitrohydroxyphenyl-n-benzoylalanine and Classic Galactosemia

1-nitrohydroxyphenyl-n-benzoylalanine has been researched along with Classic Galactosemia in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Bhatia, KP; Burke, D; Carecchio, M; Chandrashekar, HS; Edwards, MJ; Footitt, EJ; Kojovic, M; Lachmann, RH; Murphy, E; Parees, I; Rubio-Agusti, I	1
ROBINSON, A	1

Other Studies

2 other study(ies) available for 1-nitrohydroxyphenyl-n-benzoylalanine and Classic Galactosemia

Article	Year
Movement disorders in adult patients with classical galactosemia. Movement disorders : official journal of the Movement Disorder Society, 2013, Volume: 28, Issue:6 Topics: Adult; Anti-Dyskinesia Agents; Benzamides; Botulinum Toxins; Brain; Cross-Sectional Studies; Databases, Factual; Female; Galactosemias; Humans; Magnetic Resonance Imaging; Male; Movement Disorders; Muscarinic Antagonists; Retrospective Studies; Severity of Illness Index; Trihexyphenidyl; Tyrosine; Young Adult	2013
THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT. The Journal of experimental medicine, 1963, Sep-01, Volume: 118 Topics: Benzamides; Carrier State; Clinical Enzyme Tests; Erythrocytes; Galactokinase; Galactosemias; Galactosephosphates; Heterozygote; Humans; Phosphotransferases; Tyrosine; UDPglucose-Hexose-1-Phosphate Uridylyltransferase; UTP-Hexose-1-Phosphate Uridylyltransferase	1963

Article

Year

Movement disorders in adult patients with classical galactosemia.

Movement disorders : official journal of the Movement Disorder Society, 2013, Volume: 28, Issue:6

Topics: Adult; Anti-Dyskinesia Agents; Benzamides; Botulinum Toxins; Brain; Cross-Sectional Studies; Databases, Factual; Female; Galactosemias; Humans; Magnetic Resonance Imaging; Male; Movement Disorders; Muscarinic Antagonists; Retrospective Studies; Severity of Illness Index; Trihexyphenidyl; Tyrosine; Young Adult

2013

THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT.

The Journal of experimental medicine, 1963, Sep-01, Volume: 118

Topics: Benzamides; Carrier State; Clinical Enzyme Tests; Erythrocytes; Galactokinase; Galactosemias; Galactosephosphates; Heterozygote; Humans; Phosphotransferases; Tyrosine; UDPglucose-Hexose-1-Phosphate Uridylyltransferase; UTP-Hexose-1-Phosphate Uridylyltransferase

1963