Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria. (Q40127118)

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2 January 2020

title

Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria (English)

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2 January 2020

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5

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author name string

Martina Huemer

1

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2 January 2020

Manuela Födinger

2

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2 January 2020

Olaf A Bodamer

3

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2 January 2020

Adolf Mühl

4

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2 January 2020

Claudia Weigmann

6

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2 January 2020

Hanno Ulmer

7

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2 January 2020

Sylvia Stöckler-Ipsiroglu

8

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Dorothea Möslinger

9

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publication date

14 January 2008

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Molecular Genetics and Metabolism

2 January 2020

published in

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volume

94

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issue

1

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page(s)

46-51

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Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997.

2 January 2020

cites work

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DACH-LIGA homocystein (german, austrian and swiss homocysteine society): consensus paper on the rational clinical use of homocysteine, folic acid and B-vitamins in cardiovascular and thrombotic diseases: guidelines and recommendations

7 January 2021

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Homozygous thermolabile variant of the methylenetetrahydrofolate reductase gene: a potential risk factor for hyperhomocysteinaemia, CVD, and stroke in childhood

7 January 2021

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Hyperhomocysteinemia: a risk factor for ischemic stroke in children

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Vitamin B12 deficiency in adolescents and young adults with phenylketonuria

7 January 2021

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Increased risk of vitamin B12 deficiency in patients with phenylketonuria on an unrestricted or relaxed diet

7 January 2021

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Vitamin B12 and vitamin B6 supplementation is needed among adults with phenylketonuria (PKU)

7 January 2021

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Molecular genetics of homocysteine metabolism.

7 January 2021

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Biological and environmental determinants of plasma homocysteine

7 January 2021

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Phenotypic expression of the methylenetetrahydrofolate reductase 677C-->T polymorphism and flavin cofactor availability in thyroid dysfunction

7 January 2021

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The C677T mutation in the methylenetetrahydrofolate reductase gene contributes to hyperhomocysteinemia in patients taking anticonvulsants

7 January 2021

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Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome

7 January 2021

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Genetic determinants of the homocysteine level

7 January 2021

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Total homocysteine, folate, and cobalamin, and their relation to genetic polymorphisms, lifestyle and body mass index in healthy children and adolescents

7 January 2021

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Hyperhomocysteinemia in children with renal transplants

7 January 2021

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Plasma homocysteine concentration in a Belgian school-age population

7 January 2021

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Dietary vitamin B-6 restriction does not alter rates of homocysteine remethylation or synthesis in healthy young women and men

7 January 2021

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Effects of valproate and carbamazepine on serum levels of homocysteine, vitamin B12, and folic acid

7 January 2021

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Reduced total plasma homocyst(e)ine in children and adolescents with type 1 diabetes

7 January 2021

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Total homocysteine and its predictors in Dutch children

7 January 2021

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Common mutations at the homocysteine metabolism pathway and pediatric stroke

7 January 2021

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Protein insufficiency and linear growth restriction in phenylketonuria

7 January 2021

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Nutrient intakes and physical growth of children with phenylketonuria undergoing nutrition therapy

7 January 2021

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Dependence of the utilization of a phenylalanine-free amino acid mixture on different amounts of single dose ingested. A case report

7 January 2021

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Plasma thiols and their determinants in phenylketonuria

7 January 2021

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Efficacy of folic acid supplementation in stroke prevention: a meta-analysis

7 January 2021

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10.1016/J.YMGME.2007.12.001

7 January 2021

Identifiers

DOI

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2 January 2020

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