(Q36981620)

17 August 2017

Phenotypic Variability in Majeed Syndrome (English)

1 reference

17 August 2017

1 reference

Anand Prahalad Rao

1

1 reference

17 August 2017

Dharmanand Balebail Gopalakrishna

series ordinal

2

1 reference

17 August 2017

Xinyu Bing

series ordinal

3

1 reference

17 August 2017

Polly J Ferguson

series ordinal

4

1 reference

17 August 2017

language of work or name

English

0 references

publication date

1 June 2016

1 reference

The Journal of Rheumatology

17 August 2017

1 reference

17 August 2017

43

1 reference

17 August 2017

6

1 reference

17 August 2017

1258-1259

1 reference

Efficacy of anti-IL-1 treatment in Majeed syndrome

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898189

The lipin family: mutations and metabolism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898189

A splice site mutation confirms the role of LPIN2 in Majeed syndrome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898189

Three mammalian lipins act as phosphatidate phosphatases with distinct tissue expression patterns

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898189

Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898189

The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. Report of a new family and a review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898189

Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis in three related children and the association with Sweet syndrome in two siblings

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898189

On mice and men: An autosomal recessive syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anemia

29 September 2017

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27252506

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3899/JRHEUM.151193

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

27252506

1 reference