(Q42163765)

17 October 2017

A-BETA-LIPOPROTEINAEMIA (BASSEN-KORNZWEIG SYNDROME): REPORT OF A CASE. (English)

1 reference

17 October 2017

BECROFT DM

1

1 reference

17 October 2017

COSTELLO JM

series ordinal

2

1 reference

17 October 2017

SCOTT PJ

series ordinal

3

1 reference

17 October 2017

language of work or name

English

0 references

publication date

1 February 1965

1 reference

Archives of Disease in Childhood

17 October 2017

1 reference

17 October 2017

40

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17 October 2017

40-46

1 reference

Malformation of the erythrocytes in a case of atypical retinitis pigmentosa

17 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

ESTIMATION OF THE LOW-DENSITY (BETA) LIPOPROTEINS OF SERUM IN HEALTH AND DISEASE USING LARGE MOLECULAR WEIGHT DEXTRAN SULPHATE

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

ACQUIRED ACANTHOCYTOSIS AND MYELOPHTHISIS IN A CASE OF EALES'S DISEASE

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

RED-CELL AND PLASMA LIPIDS IN ACANTHOCYTOSIS

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

Microangiopathic haemolytic anaemia: the possible role of vascular lesions in pathogenesis

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

A human lipoprotein polymorphism

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

An unusual syndrome of hemolytic anemia, thrombocytopenic purpura and renal disease.

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

The burr red cell and azotaemia

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

THE DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUM

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

Congenital absence of beta-lipoproteins.

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019261

Infantile pyknocytosis occurring in dissimilar twins

17 August 2018

1 reference

12 December 2020

[The congenital absence of beta-lipoproteins.]

1 reference

12 December 2020

Atypical retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease

1 reference

12 December 2020

Retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease

1 reference

12 December 2020

Hypocholesteremia in idiopathic steatorrhea with report of a case of profound hypocholesteremia of lifelong standing

1 reference

12 December 2020

Atypical congenital haemolytic anaemia

1 reference

12 December 2020

Infantile pyknocytosis; a common erythrocyte abnormality of the first trimester

1 reference

12 December 2020

Acute haemolytic anaemia with distortion and fragmentation of erythrocytes in children

1 reference

12 December 2020

Acanthrocytosis; a genetic erythrocytic malformation

1 reference

12 December 2020

The diagnostic significance of burr red blood cells

1 reference

12 December 2020

Estimation of eight serum proteins by a gel diffusion precipitin technique

1 reference

12 December 2020

Bassen-Kornweig syndrome. Neuromuscular disorder resembling Friedreich's ataxia associated with retinitis pigmentosa, acanthocytosis, steatorrhea, and an abnormality of lipid metabolism

1 reference

12 December 2020

[New case of acanthocytosis: congenital erythrocytic abnormalities with retinitis, neurological disorders & degenerative stigmata]

1 reference

12 December 2020

Quantitative chromatographic analysis of plasma and red blood cell lipids in patients with acanthocytosis

1 reference

12 December 2020

On having no beta-lipoprotein. A syndrome comprising a-beta-lipoproteinaemia, acanthocytosis, and steatorrhoea

1 reference

12 December 2020

Acanthrocytosis, pigmentary degeneration of the retina and ataxic neuropathy: a genetically determined syndrome and associated metabolic disorder

1 reference

12 December 2020

Red-cell fragmentation syndrome: A condition of multiple aetiology?

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.40.209.40

1 reference

17 October 2017

1 reference

17 October 2017

PubMed publication ID

14259270

1 reference