(Q42539521)

2 November 2017

Ahomocysteinemia in molybdenum cofactor deficiency (English)

1 reference

2 November 2017

1 reference

1 reference

Graf WD

1

1 reference

2 November 2017

Oleinik OE

2

1 reference

2 November 2017

Jack RM

3

1 reference

2 November 2017

Weiss AH

4

1 reference

2 November 2017

Johnson JL

5

1 reference

2 November 2017

language of work or name

English

0 references

publication date

1 September 1998

1 reference

2 November 2017

1 reference

2 November 2017

51

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2 November 2017

860-862

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2 November 2017

3

1 reference

An HPLC assay for detection of elevated urinary S-sulphocysteine, a metabolic marker of sulphite oxidase deficiency

2 November 2017

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Plasma homocysteine and methionine concentrations in children with neural tube defects.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Cortical control of movement.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Cerebrospinal fluid S-adenosylmethionine (SAMe) and glutathione concentrations in HIV infection Effect of parenteral treatment with SAMe

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Sulfite oxidase deficiency: clinical, neuroradiologic, and biochemical features in two new patients

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Folic acid--an innocuous means to reduce plasma homocysteine.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Autosomal dominant cerebellar phenotypes: the genotype has settled the issue

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1212/WNL.51.3.860

Identifiers

DOI

10.1212/WNL.51.3.860

1 reference

2 November 2017

1 reference