scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1046850113 |
P356 | DOI | 10.1007/S10545-005-0252-1 |
P698 | PubMed publication ID | 16763893 |
P2093 | author name string | Philip J Lee | |
P2860 | cites work | Increased fertility in a woman with classic galactosaemia | Q77390646 |
Spontaneous pregnancy in a patient with classical galactosaemia | Q78205343 | ||
Generalized glutathione synthetase deficiency and pregnancy | Q78205351 | ||
Successful pregnancy after combined renal-hepatic transplantation in glycogen storage disease type Ia | Q80502795 | ||
Pregnancy in a patient with mucopolysaccharidosis type IH homozygous for the W402X mutation | Q81317460 | ||
Inborn errors of metabolism and pregnancy | Q33948549 | ||
Reproductive fitness in maternal homocystinuria due to cystathionine beta-synthase deficiency | Q34527090 | ||
Two successful pregnancies in pyridoxine-nonresponsive homocystinuria | Q34553684 | ||
Pregnancy and inherited metabolic disorders: maternal and fetal complications | Q34847379 | ||
Intermediate metabolism in normal pregnancy and in gestational diabetes. | Q35184288 | ||
Sex-specific mutation rates for x-linked disorders: estimation and application | Q35188785 | ||
The Maternal Phenylketonuria International Study: 1984-2002. | Q35599969 | ||
Pregnancies in Gaucher disease: a 5-year study | Q35674478 | ||
Pregnancy and delivery after stimulation with rFSH of a galatosemia patient suffering hypergonadotropic hypogonadism: case report | Q36270301 | ||
Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies | Q40364201 | ||
The prevalence of polycystic ovaries in the hepatic glycogen storage diseases: its association with hyperinsulinism | Q42481343 | ||
Successful pregnancy outcome in atypical hyperglycinaemia | Q43834254 | ||
Successful pregnancy outcome in a patient with severe chylomicronemia due to compound heterozygosity for mutant lipoprotein lipase | Q43975953 | ||
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 acidaemia | Q44410025 | ||
Maternal methionine adenosyltransferase I/III deficiency: reproductive outcomes in a woman with four pregnancies | Q44602086 | ||
Acute postpartum mental status change and coma caused by previously undiagnosed ornithine transcarbamylase deficiency | Q44648397 | ||
Maternal histidinaemia: pregnancies and offspring outcomes | Q44908124 | ||
Ornithine transcarbamylase deficiency in pregnancy | Q44910435 | ||
Successful pregnancy in a treated patient with biotinidase deficiency. | Q46694255 | ||
Social outcome in treated individuals with inherited metabolic disorders: UK study | Q46910563 | ||
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia | Q47628935 | ||
Successful pregnancy outcome in a patient with Fabry disease receiving enzyme replacement therapy with agalsidase alfa. | Q51841502 | ||
Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia | Q52040555 | ||
Long‐term prognosis in galactosaemia: Results of a survey of 350 cases | Q52243798 | ||
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 coma | Q68791245 | ||
Cardiac involvement in glycogen storage disease III: morphologic and biochemical characterization with endomyocardial biopsy | Q70932663 | ||
Pregnancy and argininosuccinic aciduria | Q71726850 | ||
Successful pregnancy in severe methylmalonic acidaemia | Q73075713 | ||
Postpartum death with maple syrup urine disease | Q73216870 | ||
A successful pregnancy in a heterozygote for OTC deficiency treated with sodium phenylbutyrate | Q73484239 | ||
Second spontaneous pregnancy in a galactosaemic woman homozygous for the Q188R mutation | Q73710259 | ||
The HELLP syndrome associated wiht fetal medium-chain acyl-CoA dehydrogenase deficiency | Q74185820 | ||
Growing older: the adult metabolic clinic | Q74509684 | ||
Successful pregnancy in a patient with type III glycogen storage disease managed with cornstarch supplements | Q74731094 | ||
Mitochondrial acetoacetyl-CoA thiolase (beta-ketothiolase) deficiency and pregnancy | Q77075830 | ||
P433 | issue | 2-3 | |
P304 | page(s) | 311-316 | |
P577 | publication date | 2006-04-01 | |
P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
P1476 | title | Pregnancy issues in inherited metabolic disorders | |
P478 | volume | 29 |
Q36757409 | A practical approach to maternal phenylketonuria management. |
Q63363508 | A series of pregnancies in women with inherited metabolic disease |
Q36433340 | Biochemical Monitoring and Management During Pregnancy in Patients with Isovaleric Acidaemia is Helpful to Prevent Metabolic Decompensation |
Q51624513 | Long-term needs of adult patients with organic acidaemias: outcome and prognostic factors. |
Q48687288 | Maternal tetrahydrobiopterin deficiency: the course of two pregnancies and follow-up of two children in a mother with 6-pyruvoyl-tetrahydropterin synthase deficiency |
Q30487009 | Nutrition management guideline for maple syrup urine disease: an evidence- and consensus-based approach |
Q92420420 | Nutrition management guideline for propionic acidemia: An evidence- and consensus-based approach |
Q48092089 | Outcome of three cases of untreated maternal glutaric aciduria type I. |
Q30592032 | Preconception care: screening and management of chronic disease and promoting psychological health |
Q37938787 | Pregnancy and its management in women with GSD type III - a single centre experience |
Q37070481 | Pregnancy in women with inherited metabolic disease |
Q26865440 | Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia |
Q33800670 | Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community |
Q37127656 | The management of pregnancy in maple syrup urine disease: experience with two patients |
Q46886256 | Urea cycle disorders in adult patients |
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