(Q47439293)

16 January 2018

title

Low molecular weight urinary peptides in ceroid-lipofuscinoses: Potential biochemical markers for the juvenile subtype (English)

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320370434

2 November 2022

author name string

LaBadie GU

1

1 reference

16 January 2018

G. U. LaBadie

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1701959

2 November 2022

R. K. Pullarkat

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1701959

2 November 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=1701959

2 November 2022

publication date

1 December 1990

1 reference

16 January 2018

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320370434

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320370434

https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320370434

2 November 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320370434

American Journal of Medical Genetics Part A

2 November 2022

published in

1 reference

16 January 2018

volume

37

1 reference

16 January 2018

issue

4

1 reference

16 January 2018

page(s)

592-599

1 reference

16 January 2018

Neuronal storage disorder with chorea and curvilinear bodies

cites work

1 reference

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Diagnostic significance of myeloperoxidase assay in neuronal ceroid-lipofuscinoses (Batten-Vogt syndrome)

21 January 2018

1 reference

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Leukocyte peroxidase deficiency in a family with a dominant form of Kuf's disease

21 January 2018

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Studies in batten disease. I. Peroxidase deficiency in granulocytes

2 November 2022

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Urinary sediment dolichol excretion in patients with Batten disease and other neurodegenerative and storage disorders

2 November 2022

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Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease)

2 November 2022

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High-performance liquid chromatographic and field desorption mass spectrometric measurement of picomole amounts of endogenous neuropeptides in biologic tissue

2 November 2022

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Batten disease (Spielmeyer-Sjøgren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16

2 November 2022

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Increased non-protein-bound iron and decreased protection against superoxide-radical damage in cerebrospinal fluid from patients with neuronal ceroid lipofuscinoses

2 November 2022

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Accumulation of dolichol-linked oligosaccharides in ceroid-lipofuscinosis (Batten disease).

2 November 2022

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

2 November 2022

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

2 November 2022

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Protein measurement with the Folin phenol reagent

2 November 2022

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Ultrasensitive stain for proteins in polyacrylamide gels shows regional variation in cerebrospinal fluid proteins

2 November 2022

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Primary structure of three mannosyl-glycoasparagines and nine sialyl-oligosaccharides isolated from the urine of two patients with Gaucher's disease (infantile form)

2 November 2022

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A micromethod for the estimation of blood dolichol

2 November 2022

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High levels of brain dolichols in neuronal ceroid-lipofuscinosis and senescence

2 November 2022

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Presence of abnormal amounts of dolichols in the urinary sediment of Batten disease patients

2 November 2022

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Elevated urinary dolichol levels in chronic alcoholics

2 November 2022

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Neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency

2 November 2022

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Leukocyte PPD-peroxidase activity with polyunsaturated fatty acid hydroperoxides: normal values in Batten's disease

2 November 2022

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4-Hydroxynonenal: a specific indicator for canine neuronal-retinal ceroidosis

2 November 2022

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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

2 November 2022

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Structural analysis of O-glycosidic type of sialyloligosaccharide-alditols derived from urinary glycopeptides of a sialidosis patient

2 November 2022

37

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Clinico-pathological variability in the childhood neuronal ceroid-lipofuscinoses and new observations on glycoprotein abnormalities

2 November 2022

38

1 reference

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Dolichol and dolichyl phosphate in the neuronal ceroid-lipofuscinoses and other diseases

2 November 2022

39

1 reference

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Dolichols in brain and urinary sediment in neuronal ceroid lipofuscinosis

2 November 2022

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1 reference

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Identification of retinoyl complexes as the autofluorescent component of the neuronal storage material in Batten disease

2 November 2022

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Presidential address: Studies in the neuronal ceroid-lipofuscinoses

2 November 2022

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1 reference

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2 November 2022

Identifiers

1 reference

16 January 2018

1 reference

16 January 2018