Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders (Q67653760)

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16 September 2019

title

Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders (English)

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16 September 2019

6

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16 September 2019

author name string

J L Hughes

1

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16 September 2019

A Poulos

2

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16 September 2019

E Robertson

3

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16 September 2019

C W Chow

4

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16 September 2019

L J Sheffield

5

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16 September 2019

R F Carter

7

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16 September 2019

publication date

1 January 1990

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Virchows Archiv. A, Pathological Anatomy and Histopathology

16 September 2019

published in

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volume

416

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16 September 2019

issue

3

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16 September 2019

page(s)

255-264

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Optical diffraction studies of crystalline structures in electron micrographs. II. Crystalline inclusions in mitochondria of human hepatocytes

16 September 2019

cites work

1 reference

12 December 2020

Hepatic peroxisomes are deficient in infantile refsum disease: a cytochemical study of 4 cases

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12 December 2020

Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies

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12 December 2020

Clinical biochemistry of peroxisomal disorders

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12 December 2020

Accumulation and defective beta-oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants

1 reference

12 December 2020

Liver in the cerebro-hepato-renal syndrome: defective bile acid synthesis and abnormal mitochondria

1 reference

12 December 2020

Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data

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12 December 2020

Diffusion artifacts in cytochemistry of catalase

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12 December 2020

Zellweger syndrome: biochemical and morphological studies on two patients treated with clofibrate

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12 December 2020

The cerebro-hepato-renal (Zellweger) syndrome and other peroxisomal disorders

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12 December 2020

The cerebro-hepato-renal (Zellweger) syndrome: lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma.

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12 December 2020

Adrenoleukodystrophy. A clinical and pathological study of 17 cases

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12 December 2020

Treatment of infantile phytanic acid storage disease: clinical, biochemical and ultrastructural findings in two children treated for 2 years

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12 December 2020

Studies on microperoxisomes. V. Are microperoxisomes ubiquitous in mammalian cells?

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12 December 2020

CRYSTALLINE STRUCTURES IN THE MITOCHONDRIA OF NORMAL HUMAN LIVER PARENCHYMAL CELLS

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12 December 2020

Patterns of Refsum's disease. Phytanic acid oxidase deficiency

1 reference

12 December 2020

Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?

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12 December 2020

Disturbances in bile acid metabolism of infants with the Zellweger (cerebro-hepato-renal) syndrome

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12 December 2020

A correlative study of the adrenal cortex in adreno-leukodystrophy--evidence for a fatal intoxication with very long chain saturated fatty acids

1 reference

12 December 2020

Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liver

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12 December 2020

Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies

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12 December 2020

Light and electron microscopic liver changes in the cerebro-hepato-renal syndrome of Zellweger (Peroxisome deficiency) (author's transl)

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12 December 2020

Ultrastructure of the Liver in the Cerebrohepatorenal Syndrome of Zellweger

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12 December 2020

Peroxisomal disorders: clinical commentary and future prospects

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12 December 2020

Absence of hepatic peroxisomes in a case of infantile Refsum's disease

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12 December 2020

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

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12 December 2020

The peroxisomal disorders

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12 December 2020

Cerebro-hepato-renal syndrome of Zellweger: clinical symptoms and relevant laboratory findings in 16 patients

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12 December 2020

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities.

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12 December 2020

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

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12 December 2020

Peroxisomal disorders: a newly recognised group of genetic diseases

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12 December 2020

Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes

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12 December 2020

Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children

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12 December 2020

Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblasts

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12 December 2020

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

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12 December 2020

Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy

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12 December 2020

Identifiers

DOI

10.1007/BF01678985

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16 September 2019

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