Gait Patterns in Patients with Hereditary Spastic Paraparesis.

about

Profiling walking dysfunction in multiple sclerosis: characterisation, classification and progression over time.

P2860

Q55323826-87F2C882-C22E-4815-B4ED-7844D8D52A03

P2860

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

Item

http://www.wikidata.org/entity/Q36161484

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

@ast

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

@en

type

Item

label

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

@ast

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

@en

prefLabel

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

@ast

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

@en

P1476

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

@en

P2093

Alberto Ranavolo

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

Carlo Casali

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

Carmela Conte

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

Francesco Draicchio

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

Francesco Lacquaniti

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

Francesco Pierelli

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

Gianluca Coppola

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

Luca Leonardi

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

Mariano Serrao

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

Martina Rinaldi

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

P2860

Clinical features and management of hereditary spastic paraplegia

Hereditary spastic paraplegia SPG4: what is known and not known about the disease.

Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions

Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study

Is it time to rethink how neuropsychological tests are used to diagnose mild forms of HIV-associated neurocognitive disorders? Impact of false-positive rates on prevalence and power.

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.

Hereditary spastic paraparesis: a review of new developments.

Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia.

Younger is not always better: development of locomotor adaptation from childhood to adulthood

The impact of non-traumatic hip and knee disorders on health-related quality of life as measured with the SF-36 or SF-12. A systematic review.

P304

e0164623

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

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0164623

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

P407

English

P433

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

P478

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

P50

Giovanni Martino

P577

2016-10-12T00:00:00Z

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

P698

27732632

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

P932

5061421

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

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

about

P2860

P2860

Gait Patterns in Patients with Hereditary Spastic Paraparesis.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932