(Q48599029)

13 February 2018

title

Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12. (English)

1 reference

13 February 2018

author name string

Sharon E Smith

1

1 reference

13 February 2018

Hannah C Kinney

2

1 reference

13 February 2018

Kathryn J Swoboda

3

1 reference

13 February 2018

Harvey L Levy

4

1 reference

13 February 2018

publication date

30 March 2006

1 reference

13 February 2018

Molecular Genetics and Metabolism

published in

1 reference

13 February 2018

volume

88

1 reference

13 February 2018

issue

2

1 reference

13 February 2018

page(s)

138-145

1 reference

13 February 2018

A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduria.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

A derangement in B 12 metabolism leading to homocystinemia, cystathioninemia and methylmalonic aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Ocular histopathologic characteristics of cobalamin C type vitamin B12 defect with methylmalonic aciduria and homocystinuria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Neuropsychiatric Disturbances in Presumed Late-Onset Cobalamin C Disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Adult-onset combined methylmalonic aciduria and homocystinuria (cblC).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

An Ultrastructural Study of Subacute Combined Degeneration of the Spinal Cord in Vitamin B12-Deficient Rhesus Monkeys

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Sensory peripheral neuropathy of vitamin B12 deficiency: a primary demyelinating disease?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

The peripheral neuropathy of vitamin B12 deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Coma and axonal degeneration in vitamin B12 deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Long-term outcome in treated combined methylmalonic acidemia and homocystinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Pathogenesis of subacute combined degeneration: a result of methyl group deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Methylation deficiency causes vitamin B12-associated neuropathy in the pig.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Disorders of intermediary metabolism: toxic leukoencephalopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Biochemical pathogenesis of subacute combined degeneration of the spinal cord and brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Creatine metabolism in combined methylmalonic aciduria and homocystinuria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Influence of vitamin B12 on brain methionine adenosyltransferase activity in senile dementia of the Alzheimer's type.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Methionine adenosyltransferase: structure and function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Cobalamin E (cblE) disease: a severe neurological disorder with megaloblastic anaemia, homocystinuria and low serum methionine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

CblE type of homocystinuria: mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

An inborn error of vitamin B12 metabolism associated with cellular deficiency of coenzyme forms of the vitamin. Pathological and neurochemical findings in one case

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Spinal MRI supporting myelopathic origin of early symptoms in unsuspected cobalamin deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalamin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria and sulfur amino acid abnormalities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.02.007

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YMGME.2006.02.007

1 reference

13 February 2018

1 reference

13 February 2018