(Q48266568)

10 February 2018

title

A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN. (English)

1 reference

10 February 2018

amyotrophic lateral sclerosis

main subject

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author

Masahiro Nakatochi

5

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10 February 2018

Satoshi Kuwabara

24

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10 February 2018

Gen Sobue

32

Gen Sobue

1 reference

10 February 2018

9

Michiaki Kubo

1 reference

10 February 2018

Daichi Yokoi

10

Daichi Yokoi

1 reference

10 February 2018

Mitsuya Morita

15

Mitsuya Morita

1 reference

10 February 2018

Kazuaki Kanai

16

Kazuaki Kanai

1 reference

10 February 2018

Ikuko Aiba

18

Ikuko Aiba

1 reference

10 February 2018

Osamu Kano

22

Osamu Kano

1 reference

10 February 2018

Kazuko Hasegawa

25

Kazuko Hasegawa

1 reference

10 February 2018

author name string

Hazuki Watanabe

1

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10 February 2018

Naoki Atsuta

2

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10 February 2018

Akihiro Hirakawa

3

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10 February 2018

Ryoichi Nakamura

4

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10 February 2018

Shinsuke Ishigaki

6

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10 February 2018

Aritoshi Iida

7

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10 February 2018

Shiro Ikegawa

8

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10 February 2018

Hirohisa Watanabe

11

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10 February 2018

Mizuki Ito

12

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10 February 2018

Masahisa Katsuno

13

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10 February 2018

Yuishin Izumi

14

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10 February 2018

Akira Taniguchi

17

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10 February 2018

Koji Abe

19

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10 February 2018

Koichi Mizoguchi

20

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10 February 2018

Masaya Oda

21

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10 February 2018

Koichi Okamoto

23

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10 February 2018

Takashi Imai

26

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10 February 2018

Akihiro Kawata

27

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10 February 2018

Masashi Aoki

28

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10 February 2018

Shoji Tsuji

29

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10 February 2018

Kenji Nakashima

30

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10 February 2018

Ryuji Kaji

31

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10 February 2018

language of work or name

English

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publication date

8 January 2016

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10 February 2018

Journal of Neurology, Neurosurgery and Psychiatry

published in

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10 February 2018

volume

87

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10 February 2018

issue

8

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10 February 2018

page(s)

851-858

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10 February 2018

Amyotrophic lateral sclerosis

cites work

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Recent progress in the genetics of motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

State of play in amyotrophic lateral sclerosis genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Disease progression in amyotrophic lateral sclerosis: predictors of survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Amyotrophic lateral sclerosis disease progression model

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Rating the severity of ALS by caregivers over the telephone using the ALSFRS-R.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Early symptom progression rate is related to ALS outcome: a prospective population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Prognosis in amyotrophic lateral sclerosis: a population-based study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Alteration of nutritional status at diagnosis is a prognostic factor for survival of amyotrophic lateral sclerosis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

The giant protein titin: a major player in myocardial mechanics, signaling, and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Muscle assembly: a titanic achievement?

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Titin and nebulin: protein rulers in muscle?

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Disuse-induced preferential loss of the giant protein titin depresses muscle performance via abnormal sarcomeric organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Analysis of factors that modify susceptibility and rate of progression in amyotrophic lateral sclerosis (ALS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Excellent inter‐rater, intra‐rater, and telephone‐administered reliability of the ALSFRS‐R in a multicenter clinical trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

Amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2015-311541

21 January 2018

Identifiers

DOI

10.1136/JNNP-2015-311541

1 reference

10 February 2018

PubMed ID

26746183

1 reference

10 February 2018