(Q42271250)

English

Morphology and diagnosis of Zellweger syndrome. A contribution to combined cytochemical-finestructural identification of peroxisomes in autopsy material and frozen liver tissue with case report

scientific article published on January 1981

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Morphology and diagnosis of Zellweger syndrome. A contribution to combined cytochemical-finestructural identification of peroxisomes in autopsy material and frozen liver tissue with case report (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

1 reference

based on heuristic

inferred from title

author name string

Müller-Höcker J

1

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Bise K

2

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Endres W

3

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Hübner G

4

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

publication date

1 January 1981

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

number of pages

12

1 reference

based on heuristic

inferred from page(s)

Virchows Archiv. A, Pathological anatomy and histology

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

393

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

103-114

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microbodies and related particles. Morphology, biochemistry, and physiology.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomes (microbodies and related particles)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The renal lesion in syndromes of multiple congenital malformations. Cerebrohepatorenal syndrome; Jeune asphyxiating thoracic dystrophy; tuberous sclerosis; Meckel syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal (Zellweger's) syndrome. Ocular involvement.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal syndrome. Report of a case with histochemical and ultrastructural observations

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropathological considerations in cerebro-hepato-renal syndrome (Zellweger's syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndrome*

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal syndrome. Report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal syndrome of Zellweger. Two patients with islet cell hyperplasia, hypoglycemia, and thymic anomalies, and comments on iron metabolism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microbodies: constituent organelles of animal cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomes: new aspects of cell physiology and biochemistry

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of necrosis in vitro of mouse hepatic parenchymal cells. Ultrastructural and cytochemical alterations of cytosomes, cytosegresomes, multivesicular bodies, and microbodies and their relation to the lysosome concept

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital and Familial Iron Overload

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of zellweger: Comparative pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microbodies in experimentally altered cells. IX. The fate of microbodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cerebro-hepato-renal syndrome (CHRS) (Zellweger's syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal Syndrome of Zellweger

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mechanism of arrest of neuronal migration in the Zellweger malformation: An hypothesis based upon cytoarchitectonic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The kinetics of catalase synthesis and destruction in vivo

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects of Bile Acid Synthesis in Zellweger's Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Disorders of neuronal migration in Zellwegers cerebrohepato-renal syndrome (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal syndrome of Zellweger. Ocular histopathologic findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of Zellweger's cerebro-hepato-renal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Zellweger syndrome: subcellular pathology, neuropathology, and the demonstration of pneumocystis carinii pneumonitis in two siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycogen accumulation in the central nervous system in the cerebro-hepato-renal syndrome. Report of a case with ultrastructural studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cerebro-hepato-renal syndrome (Zellweger's syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Neuropathology of a Peculiar Form of Cerebro-Renal Syndrome in a Child

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Globoid cells, glial nodules, and peculiar fibrillary changes in the cerebro-hepato-renal syndrome of zellweger

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebro-hepato-renal syndrome with parental consanguinity

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical studies in the cerebro-hepato-renal syndrome of Zellweger: a disturbance in the metabolism of pipecolic acid.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Giant cell transformation cerebrohepatorenal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A syndrome of ocular abnormalities, calcification of cartilage, and failure to thrive

1 reference

https://pubmed.ncbi.nlm.nih.gov/7347441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00430874

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42271250&oldid=1940768418"