(Q39728254)

14 September 2017

ERYTHROCYTIC ANOMALIES IN HEREDITARY VITREO-RETINAL DEGENERATION (DEGENERATIO HYALOIDEORETINALIS) (English)

1 reference

14 September 2017

KAHAN A

1

1 reference

14 September 2017

KAHAN IL

series ordinal

2

1 reference

14 September 2017

BENKO A

series ordinal

3

1 reference

14 September 2017

language of work or name

English

0 references

publication date

1 October 1963

1 reference

British Journal of Ophthalmology

14 September 2017

1 reference

14 September 2017

47

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14 September 2017

620-631

1 reference

Malformation of the erythrocytes in a case of atypical retinitis pigmentosa

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505860

Unusual retinal detachment possibly sex-linked

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505860

Ocular complications in thalassaemia minor

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505860

Studies on the blood lipids and lipoproteins in thalassaemia and sickle cell anaemia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505860

CONGENITAL VASCULAR VEILS IN THE VITREOUS

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505860

Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505860

Atypical retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease

20 August 2018

1 reference

12 December 2020

[Practical use of the demonstration of cells containing hemoglobin F in fixed blood smears.]

1 reference

12 December 2020

A new technique for differentiation of hemoglobin

1 reference

12 December 2020

Retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease

1 reference

12 December 2020

The thalassaemia syndromes. II. Intermediate type of Cooley's anaemia. Study of a family

1 reference

12 December 2020

Determination of serum cholesterol

1 reference

12 December 2020

1 reference

12 December 2020

A discontinuous buffer system for paper electrophoresis of human hemoglobins

1 reference

12 December 2020

Rapid estimation of free and total cholesterol

1 reference

12 December 2020

Acanthrocytosis; a genetic erythrocytic malformation

1 reference

12 December 2020

[On the clinical manifestation and pathology of degeneratio hyaloideoretinalis hereditaria (Wagner)]

1 reference

12 December 2020

An improved method for the estimation of small quantities of alkali-resistant hemoglobin in blood

1 reference

12 December 2020

Hereditary retinoschisis

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

[Acanthocytosis. Its relations to the congenital absence of beta-lipoproteins.]

1 reference

12 December 2020

Some remarks on hemoglobinopathies with particular reference to thalassemia

1 reference

12 December 2020

Identifiers

DOI

10.1136/BJO.47.10.620

1 reference

14 September 2017

1 reference

14 September 2017

PubMed publication ID

14198722

1 reference