(Q33672071)

28 July 2017

title

Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder (English)

1 reference

28 July 2017

Pagon RA

1

1 reference

28 July 2017

Bird TD

series ordinal

2

1 reference

28 July 2017

Detter JC

series ordinal

3

1 reference

28 July 2017

Pierce I

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 August 1985

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

22

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28 July 2017

issue

4

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28 July 2017

page(s)

267-273

1 reference

A sex-linked recessive form of spastic paraplegia

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Sideroblastic anaemia. A review of seven paediatric cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Pyridoxine-responsive anaemia determined by an X-linked gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Hereditary, X-linked, sideroachrestic anemia. The isolation of two erythrocyte populations differing in Xga blood type and porphyrin content

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Hereditary sideroblastic anemia and glucose-6-phosphate dehydrogenase deficiency in a Negro family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Sideroblasts, Siderocytes, and Sideroblastic Anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Haem Synthesis in Sideroblastic Anaemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

A spinocerebellar degeneration with X-linked inheritance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Porphyrin and iron metabolism in sideroblastic anemia,

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Hereditary cerebral palsy; a preliminary report

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049446

Haema synthesis during pyridoxine therapy in two families with different types of hereditary sideroblastic anaemia

30 October 2018

1 reference

12 December 2020

An hereditary anemia with hemochromatosis; studies of an unusual hemopathic syndrome resembling thalassemia

1 reference

12 December 2020

Hereditary iron-loading anemia with secondary hemochromatosis

1 reference

12 December 2020

Hereditary hypochromic anemia with transfusion hemosiderosis treated with pyridoxine: report of a case

1 reference

12 December 2020

Unusual form of cerebellar ataxia with sex-linked inheritance

1 reference

12 December 2020

Iron-loading anemia. Treatment with repeated phlebotomies and pyridoxine

1 reference

12 December 2020

Sex-linked spastic paraplegia

1 reference

12 December 2020

Porphyrin synthesis and heme synthetase activity in pyridoxine-responsive anemia

1 reference

12 December 2020

Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation

1 reference

12 December 2020

Two kindreds with a sex-linked recessive form of spastic paraplegia

1 reference

12 December 2020

Chondrodysplasia punctata (rhizomelic type): case report and pathologic findings

1 reference

12 December 2020

Identifiers

PMC publication ID

1049446

1 reference

28 July 2017

1 reference