(Q71910195)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5597051%20AND%20SRC:MED&resulttype=core&format=json

reason for deprecated rank

22 October 2019

title

Alpha-Thalassämie mit HbH und Hb Bart's in einer deutschen Familie (German)

marking inconsistent with the registered/official identifier/name

1 reference

reason for deprecated rank

7 June 2023

Alpha-thalassemia with HbH and Hb Bart's in a German family (English)

marking inconsistent with the registered/official identifier/name

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5597051

7 June 2023

1 reference

7 June 2023

author name string

P. Rönisch

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5597051

7 June 2023

E. Kleihauer

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5597051

7 June 2023

language of work or name

German

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5597051

7 June 2023

publication date

1 December 1967

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5597051%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

22 October 2019

http://link.springer.com/content/pdf/10.1007/BF01727633.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF01727633/fulltext.html

7 June 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF01727633

7 June 2023

1 reference

7 June 2023

published in

Klinische Wochenschrift

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5597051%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

volume

45

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5597051%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

issue

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5597051%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

page(s)

1193-1200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5597051%20AND%20SRC:MED&resulttype=core&format=json

Genetic basis of the thalassaemia diseases

22 October 2019

cites work

1 reference

12 December 2020

HEMOGLOBIN SYNTHESIS IN HUMAN RETICULOCYTES: A DEFECT IN GLOBIN FORMATION IN THALASSEMIA MAJOR

1 reference

12 December 2020

Mediterranean anemia; a study of thirty-two cases in Thailand

1 reference

12 December 2020

Types of Thalassaemia‐Trait Carriers as Revealed by a Study of their Incidence in Greece

1 reference

12 December 2020

HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IN GREECE. A STUDY AND A COMPARISON.

1 reference

12 December 2020

HAEMOGLOBIN H DISEASE IN AN ENGLISH FAMILY

1 reference

12 December 2020

Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin.

1 reference

12 December 2020

New fast hemoglobin associated with thalassemia

1 reference

12 December 2020

Hemoglobin H disease. A family study

1 reference

12 December 2020

Regulation of haemoglobin synthesis at the polysome level

1 reference

12 December 2020

THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS

1 reference

12 December 2020

ABNORMALITIES OF HEME AND PYRROLE METABOLISM IN THALASSEMIA

1 reference

12 December 2020

Hemoglobin H disease in Thailand. Clinical and hematological studies in 138 cases

1 reference

12 December 2020

New hemoglobin possessing a higher electrophoretic mobility than normal adult hemoglobin

1 reference

12 December 2020

THE DISTRIBUTION OF HEMOGLOBIN TYPES IN THALASSEMIC ERYTHROCYTES

1 reference

12 December 2020

Estimation of Small Percentages of Fœtal Hæmoglobin

1 reference

12 December 2020

A MOLECULAR MODEL FOR THALASSEMIA

1 reference

12 December 2020

The abnormal haemoglobins in haemoglobin-H disease

1 reference

12 December 2020

Globin Synthesis in Thalassaemia: An in vitro Study

1 reference

12 December 2020

Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore

1 reference

12 December 2020

[Fetal and residual hemoglobin in the erythrocytes and erythroblasts of human fetuses and newborn infants]

1 reference

12 December 2020

[A simple staining test for the determination of glucose-6-phosphate dehydrogenase in human erythrocytes. (Modification of the "Motulsky test")]

1 reference

12 December 2020

Inclusions of hemoglobin erythroblasts and erythrocytes of thalassemia

1 reference

12 December 2020

Determination of low percentages of fetal hemoglobin in blood of normal children

1 reference

12 December 2020

HUMORAL REGULATION OF ERYTHROPOIESIS XIV: A MODEL FOR ABNORMAL ERYTHROPOIESIS IN THALASSEMIA

1 reference

12 December 2020

Ontogenesis of erythrocytes and hemoglobin formation

1 reference

12 December 2020

[Heat lability and acid stability of hemoglobin H]

1 reference

12 December 2020

Protein synthesis in a cell free human reticulocyte system: ribosome function in thalassemia

1 reference

12 December 2020

Hæmoglobin H Disease in Thailand: a Genetical Study

1 reference

12 December 2020

Decreased erythrocyte survival in hemoglobin H disease as a result of the abnormal properties of hemoglobin H: the benefit of splenectomy

1 reference

12 December 2020

RELATIONSHIP OF HEMOGLOBIN BART'S AND H TO ALPHA THALASSEMIA

1 reference

12 December 2020

CURRENT CONCEPTS OF THE GENETICS OF THALASSEMIA.

1 reference

12 December 2020

Alpha, beta and gamma hemoglobin polypeptide chains during the neonatal period with description of a fetal form of hemoglobin Da-St. Louis

1 reference

12 December 2020

HAEMOGLOBIN BART'S AND H IN A SWEDISH BOY.

1 reference

12 December 2020

THE METABOLISM OF THE INDIVIDUAL C14 LABELED HEMOGLOBINS IN PATIENTS WITH H-THALASSEMIA, WITH OBSERVATIONS ON RADIOCHROMATE BINDING TO THE HEMOGLOBINS DURING RED CELL SURVIVAL.

1 reference

12 December 2020

Observations on some fast haemoglobins: K, J, N, and Bart's.

1 reference

12 December 2020

Hemoglobin H and the red cell

1 reference

12 December 2020

[Studies on the mechanical resistance of erythrocytes.]

1 reference

12 December 2020

Abnormal Human Hæmoglobins: Hæmoglobin ‘Bart's’: a Fœtal Hæmoglobin without α-Chains

1 reference

12 December 2020

The sidero-achrestic anemias

1 reference

12 December 2020

Occurrence of Hæmoglobin H and Hæmoglobin Bart's in Alpha-thalassæmia: a Family with Two Possible Homozygous Cases and with G-6-PD-deficiency

1 reference

12 December 2020

Persistence of haemoglobin "Bart's" beyond infancy in a child with thalassaemia

1 reference

12 December 2020

[Description of a new variety of congenital hemolytic anemia; hematologic study, electrophoretic and genetic]

1 reference

12 December 2020

THALASSEMIAS, ABNORMAL HEMOGLOBINS AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN THE ARTA AREA OF GREECE: DIAGNOSTIC AND GENETIC ASPECTS OF COMPLETE VILLAGE STUDIES.

1 reference

12 December 2020

Abnormal haemoglobins in the neonatal period and their relationship to thalassaemia

1 reference

12 December 2020

NORMAL AND ABNORMAL HUMAN HEMOGLOBINS.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01727633

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5597051%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference