Pregnancy issues in inherited metabolic disorders

scientific article published on 01 April 2006

Pregnancy issues in inherited metabolic disorders is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1046850113
P356DOI10.1007/S10545-005-0252-1
P698PubMed publication ID16763893

P2093author name stringPhilip J Lee
P2860cites workIncreased fertility in a woman with classic galactosaemiaQ77390646
Spontaneous pregnancy in a patient with classical galactosaemiaQ78205343
Generalized glutathione synthetase deficiency and pregnancyQ78205351
Successful pregnancy after combined renal-hepatic transplantation in glycogen storage disease type IaQ80502795
Pregnancy in a patient with mucopolysaccharidosis type IH homozygous for the W402X mutationQ81317460
Inborn errors of metabolism and pregnancyQ33948549
Reproductive fitness in maternal homocystinuria due to cystathionine beta-synthase deficiencyQ34527090
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Pregnancy and inherited metabolic disorders: maternal and fetal complicationsQ34847379
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Sex-specific mutation rates for x-linked disorders: estimation and applicationQ35188785
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Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnanciesQ40364201
The prevalence of polycystic ovaries in the hepatic glycogen storage diseases: its association with hyperinsulinismQ42481343
Successful pregnancy outcome in atypical hyperglycinaemiaQ43834254
Successful pregnancy outcome in a patient with severe chylomicronemia due to compound heterozygosity for mutant lipoprotein lipaseQ43975953
Successful pregnancy in a woman with mut- methylmalonic acidaemia.Q44064404
Pregnancy and tyrosinaemia type II.Q44134537
Case Report: Second case of a successful pregnancy in maternal isovaleric acidaemiaQ44410025
Maternal methionine adenosyltransferase I/III deficiency: reproductive outcomes in a woman with four pregnanciesQ44602086
Acute postpartum mental status change and coma caused by previously undiagnosed ornithine transcarbamylase deficiencyQ44648397
Maternal histidinaemia: pregnancies and offspring outcomesQ44908124
Ornithine transcarbamylase deficiency in pregnancyQ44910435
Successful pregnancy in a treated patient with biotinidase deficiency.Q46694255
Social outcome in treated individuals with inherited metabolic disorders: UK studyQ46910563
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemiaQ47628935
Successful pregnancy outcome in a patient with Fabry disease receiving enzyme replacement therapy with agalsidase alfa.Q51841502
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Long‐term prognosis in galactosaemia: Results of a survey of 350 casesQ52243798
Pregnancy in a woman with maple syrup urine disease.Q53704187
Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum comaQ68791245
Cardiac involvement in glycogen storage disease III: morphologic and biochemical characterization with endomyocardial biopsyQ70932663
Pregnancy and argininosuccinic aciduriaQ71726850
Successful pregnancy in severe methylmalonic acidaemiaQ73075713
Postpartum death with maple syrup urine diseaseQ73216870
A successful pregnancy in a heterozygote for OTC deficiency treated with sodium phenylbutyrateQ73484239
Second spontaneous pregnancy in a galactosaemic woman homozygous for the Q188R mutationQ73710259
The HELLP syndrome associated wiht fetal medium-chain acyl-CoA dehydrogenase deficiencyQ74185820
Growing older: the adult metabolic clinicQ74509684
Successful pregnancy in a patient with type III glycogen storage disease managed with cornstarch supplementsQ74731094
Mitochondrial acetoacetyl-CoA thiolase (beta-ketothiolase) deficiency and pregnancyQ77075830
P433issue2-3
P304page(s)311-316
P577publication date2006-04-01
P1433published inJournal of Inherited Metabolic DiseaseQ6295359
P1476titlePregnancy issues in inherited metabolic disorders
P478volume29

Reverse relations

cites work (P2860)
Q36757409A practical approach to maternal phenylketonuria management.
Q63363508A series of pregnancies in women with inherited metabolic disease
Q36433340Biochemical Monitoring and Management During Pregnancy in Patients with Isovaleric Acidaemia is Helpful to Prevent Metabolic Decompensation
Q51624513Long-term needs of adult patients with organic acidaemias: outcome and prognostic factors.
Q48687288Maternal tetrahydrobiopterin deficiency: the course of two pregnancies and follow-up of two children in a mother with 6-pyruvoyl-tetrahydropterin synthase deficiency
Q30487009Nutrition management guideline for maple syrup urine disease: an evidence- and consensus-based approach
Q92420420Nutrition management guideline for propionic acidemia: An evidence- and consensus-based approach
Q48092089Outcome of three cases of untreated maternal glutaric aciduria type I.
Q30592032Preconception care: screening and management of chronic disease and promoting psychological health
Q37938787Pregnancy and its management in women with GSD type III - a single centre experience
Q37070481Pregnancy in women with inherited metabolic disease
Q26865440Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
Q33800670Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community
Q37127656The management of pregnancy in maple syrup urine disease: experience with two patients
Q46886256Urea cycle disorders in adult patients

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