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19 in total

1. Vigabatrin in the treatment of glutaric aciduria type I.

Authors: B Francois; J Jaeken; P Gillis
Journal: J Inherit Metab Dis Date: 1990 Impact factor: 4.982

2. Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management.

Authors: A A Monavari; E R Naughten
Journal: Arch Dis Child Date: 2000-01 Impact factor: 3.791

3. Caspase-3 mediates apoptosis of striatal cells in GA I rat model.

Authors: Fengyan Tian; Xi Fu; Jinzhi Gao; Cai Zhang; Qin Ning; Xiaoping Luo
Journal: J Huazhong Univ Sci Technolog Med Sci Date: 2012-01-27

4. Infant mice with glutaric acidaemia type I have increased vulnerability to 3-nitropropionic acid toxicity.

Authors: K B Bjugstad; L S Crnic; S I Goodman; C R Freed
Journal: J Inherit Metab Dis Date: 2006-08-30 Impact factor: 4.982

Review 5. The salience of Garrod's 'molecular groupings' and 'Inborn Factors in Disease'.

Authors: C R Scriver
Journal: J Inherit Metab Dis Date: 1989 Impact factor: 4.982

6. Favourable outcome in a child with symptomatic diagnosis of Glutaric aciduria type 1 despite vertical HIV infection and minor head trauma.

Authors: Angeline Thomas; Els F M Dobbels; Priscilla E Springer; Christelle Ackermann; Mark F Cotton; Barbara Laughton
Journal: Metab Brain Dis Date: 2018-02-09 Impact factor: 3.584

Glutaric aciduria: inherited deficiency of glutaryl-CoA dehydrogenase activity.

1. Vigabatrin in the treatment of glutaric aciduria type I.

2. Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management.

3. Caspase-3 mediates apoptosis of striatal cells in GA I rat model.

4. Infant mice with glutaric acidaemia type I have increased vulnerability to 3-nitropropionic acid toxicity.

Review 5. The salience of Garrod's 'molecular groupings' and 'Inborn Factors in Disease'.

6. Favourable outcome in a child with symptomatic diagnosis of Glutaric aciduria type 1 despite vertical HIV infection and minor head trauma.

7. Diffusion-weighted MR imaging and MR spectroscopy in glutaric aciduria type 1.

8. Implication of a peroxisomal enzyme in the catabolism of glutaryl-CoA.

9. Specific glutaryl-CoA dehydrogenating activity is deficient in cultured fibroblasts from glutaric aciduria patients.

Review 10. The biochemical basis of mitochondrial diseases.