(Q40884401)

24 September 2017

1 reference

title

Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature review (English)

1 reference

24 September 2017

1 reference

1 reference

1 reference

A N Prasad

1

1 reference

24 September 2017

J C Breen

series ordinal

2

1 reference

24 September 2017

M G Ampola

series ordinal

3

1 reference

24 September 2017

N P Rosman

series ordinal

4

1 reference

24 September 2017

1 August 1997

1 reference

Journal of Child Neurology

24 September 2017

1 reference

24 September 2017

12

1 reference

24 September 2017

5

1 reference

24 September 2017

301-309

1 reference

Inborn errors of urea synthesis

24 September 2017

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Familial hyperargininaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Arginase deficiency in multiple tissues in argininemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

A new case of hyperargininaemia: neurological and biochemical findings prior to and during dietary treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Hyperargininemia: intellectual and motor improvement related to changes in biochemical data

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Guanidino compounds in plasma, urine and cerebrospinal fluid of hyperargininemic patients during therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Guanidino Compound Analysis as a Complementary Diagnostic Parameter for Hyperargininemia: Follow-Up of Guanidino Compound Levels during Therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

A novel neuronal messenger molecule in brain: the free radical, nitric oxide

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Nitric oxide triggers a switch to growth arrest during differentiation of neuronal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

HTLV-I associated myelopathy, a new clinical entity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

A biotinidase Km variant causing late onset bilateral optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Induction of arginase activity with the Shope papilloma virus in tissue culture cells from an argininemic patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharide

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

A new case of arginase deficiency in a Spanish male

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389701200502

10.1177/088307389701200502

21 January 2018

Identifiers

DOI

0 references

1 reference