(Q37080235)

English

Brief report: genotype, phenotype, and clinical course in five patients with PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne).

scientific article published on 12 December 2011

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Brief report: genotype, phenotype, and clinical course in five patients with PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne). (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

0 references

pyoderma gangrenosum

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

Ivona Aksentijevich

4

object named as

Ivona Aksentijevich

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Daniel L. Kastner

7

object named as

Daniel L Kastner

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Douglas B Kuhns

3

object named as

Douglas B Kuhns

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

author name string

Andrew P Demidowich

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Alexandra F Freeman

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

John I Gallin

5

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Maria L Turner

6

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Steven M Holland

8

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

publication date

12 December 2011

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Arthritis & Rheumatology

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

64

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

2022-2027

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Inflammatory bowel disease and mutations affecting the interleukin-10 receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

Pyrin Modulates the Intracellular Distribution of PSTPIP1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

Pyrin activates the ASC pyroptosome in response to engagement by autoinflammatory PSTPIP1 mutants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

CD2BP1 modulates CD2-dependent T cell activation via linkage to protein tyrosine phosphatase (PTP)-PEST.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

Peculiarities of PAPA syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

Resolution of severe pyoderma gangrenosum in a patient with streaking leukocyte factor disease after treatment with tacrolimus (FK 506).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3737487

29 September 2017

Variable expression and treatment of PAPA syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A New Autosomal Dominant Disorder of Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne: PAPA Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal production of tumor necrosis factor (TNF) -- alpha and clinical efficacy of the TNF inhibitor etanercept in a patient with PAPA syndrome [corrected]

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anakinra for flares of pyogenic arthritis in PAPA syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dramatic improvement of pyoderma gangrenosum with infliximab in a patient with PAPA syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyogene Arthritis, Pyoderma gangraenosum und Akne-Syndrom (PAPA-Syndrom)

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted treatment of pyoderma gangrenosum in PAPA (pyogenic arthritis, pyoderma gangrenosum and acne) syndrome with the recombinant human interleukin-1 receptor antagonist anakinra

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical efficacy of etanercept for treatment of PAPA syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22161697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ART.34332

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

ResearchGate publication ID

0 references

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