(Q44455222)

3 December 2017

title

Zellweger syndrome in a preterm, small for gestational age infant (English)

1 reference

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11 October 2022

0 references

1 reference

J. F. Samsom

1

1 reference

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11 October 2022

C. Jakobs

2

1 reference

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11 October 2022

J. van de Klei-van Moorsel

3

1 reference

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11 October 2022

L. M. Smit

4

1 reference

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11 October 2022

R. B. Schutgens

5

1 reference

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11 October 2022

R. J. Wanders

6

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11 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1583879

11 October 2022

publication date

1 January 1992

1 reference

Journal of Inherited Metabolic Disease

3 December 2017

published in

1 reference

3 December 2017

volume

15

1 reference

3 December 2017

issue

1

1 reference

3 December 2017

page(s)

75-83

1 reference

https://scigraph.springernature.com/pub.10.1007/bf01800347

3 December 2017

exact match

0 references

cites work

The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblasts

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01800347

Peroxisomal disorders: clinical characterization

21 January 2018

1 reference

12 December 2020

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

1 reference

12 December 2020

Incidence and evolution of subependymal and intraventricular hemorrhage: A study of infants with birth weights less than 1,500 gm

1 reference

12 December 2020

Follow-up of infants receiving cranial ultrasound for intracranial hemorrhage.

1 reference

12 December 2020

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

1 reference

12 December 2020

The inborn errors of peroxisomal beta-oxidation: a review

1 reference

12 December 2020

Stable isotope dilution analysis of very long chain fatty acids in plasma, urine and amniotic fluid by electron capture negative ion mass fragmentography

1 reference

12 December 2020

A milder variant of Zellweger syndrome.

1 reference

12 December 2020

Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals

1 reference

12 December 2020

Peroxisomal disorders in neurology

1 reference

12 December 2020

Diagnosis of impaired fetal growth in newborn infants

1 reference

12 December 2020

Stable isotope dilution analysis of pipecolic acid in cerebrospinal fluid, plasma, urine and amniotic fluid using electron capture negative ion mass fragmentography

1 reference

12 December 2020

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS

1 reference

12 December 2020

Determination of plasma bile acids by capillary gas-liquid chromatography-electron capture negative chemical ionization mass fragmentography.

1 reference

12 December 2020

Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders

1 reference

12 December 2020

Leukocytes as a diagnostic tool for classical galactosaemia

1 reference

12 December 2020

A sibship with a mild variant of Zellweger syndrome.

1 reference

12 December 2020

Peroxisomal dysfunction in a boy with neurologic symptoms and amaurosis (Leber disease): clinical and biochemical findings similar to those observed in Zellweger syndrome.

1 reference

12 December 2020

Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome.

1 reference

12 December 2020

Intrauterine growth of live-born Caucasian infants at sea level: standards obtained from measurements in 7 dimensions of infants born between 25 and 44 weeks of gestation

1 reference

12 December 2020

Effect of neonatal periventricular haemorrhage on neurodevelopmental outcome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01800347

1 reference

3 December 2017

1 reference