Sialuria: a second case (Q28306022)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Sialuria: a second case	scientific article

Statements

instance of

scholarly article

0 references

title

Sialuria: a second case (English)

0 references

author name string

B Wilcken

series ordinal

1

0 references

N Don

series ordinal

2

0 references

R Greenaway

series ordinal

3

0 references

J Hammond

series ordinal

4

0 references

L Sosula

series ordinal

5

0 references

language of work or name

English

0 references

publication date

1987

0 references

published in

Journal of Inherited Metabolic Disease

0 references

volume

10

0 references

issue

2

0 references

page(s)

97-102

0 references

cites work

Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile type.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sialuria: an original metabolic disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generalized N-acetylneuraminic acid storage disease: quantitation and identification of the monosaccharide accumulating in brain and other tissues

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and laboratory diagnosis of Salla disease in infancy and childhood

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Salla disease": a new lysosomal storage disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligosaccharides in urine of patients with glycoprotein storage diseases. I. Rapid detection by thin-layer chromatography

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overproduction of N-acetylneuraminic acid (sialic acid) by sialuria fibroblasts.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile form of sialic acid storage disorder: clinical, ultrastructural, and biochemical studies in two siblings

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved thin-layer chromatographic method for urinary oligosaccharide screening

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2443758

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF01800030

0 references

Dimensions Publication ID

1028740820

0 references

PubMed publication ID

2443758

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28306022&oldid=2175232769"