Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention.

Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention.

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Compound Heterozygous Pathogenic Variants of the 15-Hydroxyprostaglandin Dehydrogenase Gene in a Patient With Hypertrophic Osteoarthropathy: First Case in Korea A male Korean who was diagnosed with chronic enteropathy associated with (CEAS): case report with literature review

P2860

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P2860

Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention.

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http://www.wikidata.org/entity/Q50714947

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Clinical, Biochemical, and Gen ...... pective Clinical Intervention.

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Clinical, Biochemical, and Gen ...... pective Clinical Intervention.

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type

Item

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Clinical, Biochemical, and Gen ...... pective Clinical Intervention.

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Clinical, Biochemical, and Gen ...... pective Clinical Intervention.

@nl

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Clinical, Biochemical, and Gen ...... pective Clinical Intervention.

@en

Clinical, Biochemical, and Gen ...... pective Clinical Intervention.

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P1476

Clinical, Biochemical, and Gen ...... pective Clinical Intervention.

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P2093

Jin-We He

http://www.w3.org/2001/XMLSchema#string

Shan-Shan Li

http://www.w3.org/2001/XMLSchema#string

Wen-Zhen Fu

http://www.w3.org/2001/XMLSchema#string

Yu-Juan Liu

http://www.w3.org/2001/XMLSchema#string

Yun-Qiu Hu

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy

Pachydermoperiostosis: an update

A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter

Prostaglandins in bone: bad cop, good cop?

Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistance.

Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy

Prostaglandin catabolizing enzymes.

Mendelian disorders deserve more attention.

Establishing reference intervals for bone turnover markers in the healthy shanghai population and the relationship with bone mineral density in postmenopausal women

Prostaglandin-mediated inhibition of PTH-stimulated β-catenin signaling in osteoblasts by bone marrow macrophages.

P304

1659-1666

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scholarly article

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10.1002/JBMR.3157

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P478

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Z-L Zhang

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2017-04-20T00:00:00Z

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28425581

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P921

primary hypertrophic osteoarthropathy

Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention.

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P2860

P2860

Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention.

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