Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease. (Q51009002)

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scientific article published in November 2013

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English	Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.	scientific article published in November 2013

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scholarly article

1 reference

Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease. (English)

1 reference

Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Luis Corral-Gudino

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

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27 March 2018

http://europepmc.org/abstract/MED/23658060

Daniela Merlotti

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Daniela Merlotti

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Fernando Gianfrancesco

object named as

Fernando Gianfrancesco

9

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Teresa Esposito

object named as

Teresa Esposito

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Maria Luisa Brandi

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object named as

Maria Luisa Brandi

1 reference

Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Stuart H Ralston

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object named as

Stuart H Ralston

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

author name string

Omar M E Albagha

1

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Micaela Rios Visconti

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Nerea Alonso

3

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Sachin Wani

4

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Kirsteen Goodman

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

William D Fraser

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Luigi Gennari

7

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Domenico Rendina

11

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Marco di Stefano

12

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Giancarlo Isaia

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Francesca Giusti

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Javier Del Pino-Montes

16

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Rogelio Gonzalez-Sarmiento

18

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Lynley Ward

19

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Thomas Ratajczak

21

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

publication date

1 November 2013

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Journal of Bone and Mineral Research

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

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27 March 2018

http://europepmc.org/abstract/MED/23658060

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http://europepmc.org/abstract/MED/23658060

2338-2346

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

Incidence and natural history of Paget's disease of bone in England and Wales.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Clinical determinants of quality of life in Paget's disease of bone.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Paget's disease of bone and quality of life.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Mutation of the sequestosome 1 (p62) gene increases osteoclastogenesis but does not induce Paget disease

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Genetic epidemiology of Paget's disease of bone in italy: sequestosome1/p62 gene mutational test and haplotype analysis at 5q35 in a large representative series of sporadic and familial Italian cases of Paget's disease of bone

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Three Novel Mutations in SQSTM1 Identified in Familial Paget's Disease of Bone

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Familial Paget's disease in The Netherlands: occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Randomized trial of intensive bisphosphonate treatment versus symptomatic management in Paget's disease of bone.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Secular changes in Paget's disease: contrasting changes in the number of new referrals and in disease severity in two neighboring regions of Spain.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Sequestosome 1 mutations in Paget's disease of bone in Australia: prevalence, genotype/phenotype correlation, and a novel non-UBA domain mutation (P364S) associated with increased NF-kappaB signaling without loss of ubiquitin binding.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Overview of the SF-36 Health Survey and the International Quality of Life Assessment (IQOLA) Project.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Paget's disease of bone in New Zealand: continued decline in disease severity.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Pathogenesis of Paget disease of bone.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Comparison of a single infusion of zoledronic acid with risedronate for Paget's disease.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

A single infusion of zoledronic acid produces sustained remissions in Paget disease: data to 6.5 years

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Clinical practice. Paget's disease of bone

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1975

21 January 2018

Identifiers

10.1002/JBMR.1975

1 reference

Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

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https://api.fatcat.wiki/v0/release/hzz6ku67uzaanek2mq3gm3yq2a

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Europe PubMed Central

27 March 2018

http://europepmc.org/abstract/MED/23658060

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