(Q33948549)

30 July 2017

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title

Inborn errors of metabolism and pregnancy (English)

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30 July 2017

Walter JH

1

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30 July 2017

publication date

1 May 2000

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Journal of Inherited Metabolic Disease

30 July 2017

published in

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30 July 2017

volume

23

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30 July 2017

issue

3

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30 July 2017

page(s)

229-236

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https://scigraph.springernature.com/pub.10.1023/a:1005679928521

30 July 2017

exact match

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cites work

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Methylmalonic aciduria in pregnancy: a case report

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[Simvastatin and pregnancy]

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Placental tyrosine transport and maternal phenylketonuria

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Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma

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Successful pregnancy in a patient with type III glycogen storage disease managed with cornstarch supplements

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Porphyria cutanea tarda and pregnancy

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A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

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Altered follicle stimulating hormone isoforms in female galactosaemia patients

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Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications

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Histidinaemia: a benign metabolic disorder.

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12 December 2020

Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

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The genetics of male infertility in relation to cystic fibrosis

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Effects of dietary mixtures of amino acids on fetal growth and maternal and fetal amino acid pools in experimental maternal phenylketonuria.

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12 December 2020

A successful pregnancy in a patient with homocystinuria and a previous near-fatal postpartum cavernous sinus thrombosis

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12 December 2020

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12 December 2020

Pregnancy and homocystinuria

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12 December 2020

Tyrosine supplementation in the treatment of maternal phenylketonuria

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Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency

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Long‐term prognosis in galactosaemia: Results of a survey of 350 cases

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Pregnancy in a woman with maple syrup urine disease.

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12 December 2020

Ovarian failure in a young woman with galactosaemia

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12 December 2020

Three consecutive pregnancies in a patient with glycogen storage disease type IA (von Gierke's disease).

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12 December 2020

Gonadal function in patients with galactosaemia.

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Maternal tyrosinaemia II: management and successful outcome

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Is the HELLP syndrome due to inherited factors? Report of two cases.

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Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

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Evaluation of the reproductive and developmental safety of cysteamine in the rat: effects on female reproduction and early embryonic development.

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Effect of lactation in a mother with galactosemia

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12 December 2020

Identifiers

DOI

10.1023/A:1005679928521

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Dimensions Publication ID

30 July 2017

1025513450

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1 reference