Patient reported outcomes in GNE myopathy: incorporating a valid assessment of physical function in a rare disease.

about

GNE myopathy: from clinics and genetics to pathology and research strategies.

P2860

Q55268638-5E349F81-6D61-4944-AF0C-20380D82E578

P2860

Patient reported outcomes in GNE myopathy: incorporating a valid assessment of physical function in a rare disease.

Item

http://www.wikidata.org/entity/Q38668420

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Patient reported outcomes in G ...... al function in a rare disease.

@en

type

Item

label

Patient reported outcomes in G ...... al function in a rare disease.

@en

prefLabel

Patient reported outcomes in G ...... al function in a rare disease.

@en

P1476

Patient reported outcomes in G ...... cal function in a rare disease

@en

P2093

Christina Slota

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

Galen Joe

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

Joseph Shrader

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

Li Yang

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

Margaret Bevans

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

P2860

Functional Reach: A New Clinical Measure of Balance

Measures of physical performance assessments: Self-Paced Walk Test (SPWT), Stair Climb Test (SCT), Six-Minute Walk Test (6MWT), Chair Stand Test (CST), Timed Up & Go (TUG), Sock Test, Lift and Carry Test (LCT), and Car Task

Measures of adult and juvenile dermatomyositis, polymyositis, and inclusion body myositis: Physician and Patient/Parent Global Activity, Manual Muscle Testing (MMT), Health Assessment Questionnaire (HAQ)/Childhood Health Assessment Questionnaire (C-

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene

Hereditary inclusion body myopathy: the Middle Eastern genetic cluster

Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance

Nationwide patient registry for GNE myopathy in Japan

GNE myopathy: new name and new mutation nomenclature.

Assessing function and endurance in adults with spinal and bulbar muscular atrophy: validity of the adult myopathy assessment tool.

P304

1206-1213

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

P31

scholarly article

P356

10.1080/09638288.2017.1283712

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

P433

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

P478

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

P50

Nuria Carrillo-Carrasco

P577

2017-02-07T00:00:00Z

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

P698

28637129

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

P921

rare disease

P932

6166247

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

Patient reported outcomes in GNE myopathy: incorporating a valid assessment of physical function in a rare disease.

about

P2860

P2860

Patient reported outcomes in GNE myopathy: incorporating a valid assessment of physical function in a rare disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932