(Q35004125)

5 August 2017

title

High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria (English)

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5 August 2017

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Melissa P Wasserstein

3

object named as

Melissa P Wasserstein

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5 August 2017

Laurie E Profitlich

1

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5 August 2017

Brian Kirmse

2

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5 August 2017

George A Diaz

4

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5 August 2017

Shubhika Srivastava

5

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5 August 2017

publication date

12 August 2009

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Molecular Genetics and Metabolism

5 August 2017

published in

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5 August 2017

volume

98

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5 August 2017

issue

4

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5 August 2017

page(s)

344-348

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Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: a meta-analysis

5 August 2017

cites work

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Hyperhomocysteinemia in patients with symptomatic chronic heart failure: prevalence and prognostic importance--pilot study

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Elevated Homocysteine Is Associated With Reduced Regional Left Ventricular Function

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

7 January 2021

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Decyanation of vitamin B12 by a trafficking chaperone

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

7 January 2021

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Long-term outcome in treated combined methylmalonic acidemia and homocystinemia

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Ventricular septal defect closure in a neonate with combined methylmalonic aciduria/homocystinuria

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CblC/D defect combined with haemodynamically highly relevant VSD.

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Fetal dilated cardiomyopathy: an unsuspected presentation of methylmalonic aciduria and hyperhomocystinuria, cblC type

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Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy

7 January 2021

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7 January 2021

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The methyl donor S-Adenosylmethionine inhibits active demethylation of DNA: a candidate novel mechanism for the pharmacological effects of S-Adenosylmethionine

7 January 2021

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Methionine synthase reductase deficiency results in adverse reproductive outcomes and congenital heart defects in mice

7 January 2021

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Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolism

7 January 2021

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Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

7 January 2021

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Folic acid for the prevention of congenital anomalies

7 January 2021

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Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease.

7 January 2021

1 reference

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The relationship between maternal and neonatal umbilical cord plasma homocyst(e)ine suggests a potential role for maternal homocyst(e)ine in fetal metabolism

7 January 2021

1 reference

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Targeted disruption of the methionine synthase gene in mice

7 January 2021

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Homocysteine metabolism in cardiovascular cells and tissues: implications for hyperhomocysteinemia and cardiovascular disease

7 January 2021

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Meta-analysis of hyperhomocysteinemia as a risk factor for venous thromboembolic disease.

7 January 2021

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10.1016/J.YMGME.2009.07.017

7 January 2021

Identifiers

DOI

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5 August 2017

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