(Q42946955)

11 November 2017

The hereditary anemias (English)

1 reference

11 November 2017

WATSON RJ

1

1 reference

PMCID

1804395

11 November 2017

language of work or name

1 reference

1 February 1954

1 reference

Bulletin of the New York Academy of Medicine

11 November 2017

1 reference

11 November 2017

30

1 reference

11 November 2017

106-121

1 reference

11 November 2017

2

1 reference

A Third Abnormal Hemoglobin Associated with Hereditary Hemolytic Anemia

11 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Studies with inagglutinable erythrocyte counts; analysis of mechanism of Cooley's anemia

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Fetal hemoglobin in the human; a review.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Sickle cell anemia, a molecular disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Studies on thalassemia. I. An extracorpuscular defect in thalassemia major. II. The effects of splenectomy in thalassemia major with an associated acquired hemolytic anemia

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Filter paper electrophoresis of human hemoglobins with special reference to the incidence and clinical significance of hemoglobin C.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

The Inheritance of Sickle Cell Anemia.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

A new inherited abnormality of hemoglobin and its interaction with sickle cell hemoglobin.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Hereditary spherocytosis. II. Observations on the role of the spleen.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

X-ray and solubility studies of the haemoglobin of sickle-cell anaemia patients.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

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

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Studies on the destruction of red blood cells. VIII. Molecular orientation in sickle cell hemoglobin solutions.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1804395

Perspectives in the genetics of sickle cell disease

16 August 2018

1 reference

12 December 2020

1 reference

12 December 2020

EXPERIMENTAL AND CLINICAL OBSERVATIONS ON INCREASED MECHANICAL FRAGILITY OF ERYTHROCYTES

1 reference

12 December 2020

1 reference

12 December 2020

The destruction of thyroid tissue in the rat by the halogen, astatine

1 reference

12 December 2020

Studies on abnormal hemoglobins. VI. Electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon

1 reference

12 December 2020

Sickle cell anemia; a composite study and survey

1 reference

12 December 2020

Two cases of sickle cell disease presumably due to the combination of the genes for thalassemia and sickle cell hemoglobin

1 reference

12 December 2020

Identifiers

PMCID

1804395

1 reference

11 November 2017

1 reference

PMCID

1804395