Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation (Q55670371)

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English	Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation	No description defined

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instance of

scholarly article

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title

Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation (English)

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main subject

Charcot-Marie-Tooth disease type 2

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based on heuristic

inferred from title

author name string

Elena Gallardo

series ordinal

1

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Kristl G Claeys

series ordinal

2

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Eva Nelis

series ordinal

3

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Antonio García

series ordinal

4

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Ana Canga

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5

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Onofre Combarros

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6

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Vincent Timmerman

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7

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Peter De Jonghe

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8

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José Berciano

series ordinal

9

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language of work or name

English

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publication date

July 2008

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published in

Journal of Neurology

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volume

255

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issue

7

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page(s)

986-92

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cites work

Abnormal signal intensity in skeletal muscle at MR imaging: patterns, pearls, and pitfalls

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00415-008-0808-8

retrieved

21 January 2018

Magnetic resonance imaging signal changes in denervated muscles after peripheral nerve injury

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5th Workshop of the European CMT Consortium, 69th ENMC International Workshop: therapeutic approaches in CMT neuropathies and related disorders 23-25 April 1999, Soestduinen, The Netherlands.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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136th ENMC International Workshop: Charcot-Marie-Tooth disease type 1A (CMT1A)8-10 April 2005, Naarden, The Netherlands

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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Quantitative MR evaluation of body composition in patients with Duchenne muscular dystrophy

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of hereditary motor and sensory neuropathy in Cantabria

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Denervated human skeletal muscle: MR imaging evaluation

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

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12 December 2020

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Patterns of muscle atrophy in the lower limbs in patients with Charcot-Marie-Tooth disease as measured by magnetic resonance imaging

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

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Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

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Characterization of the muscle involvement in dynamin 2-related centronuclear myopathy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18560793

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12 December 2020

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Charcot-Marie-Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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Immunological study of hereditary motor and sensory neuropathy type 1a (HMSN1a).

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

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Coexistent hereditary and inflammatory neuropathy

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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Mutations in dynamin 2 cause dominant centronuclear myopathy

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Molecular genetics of autosomal-dominant axonal Charcot-Marie-Tooth disease

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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Fatty muscle degeneration in cuff ruptures. Pre- and postoperative evaluation by CT scan

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18560793

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Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18560793

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12 December 2020

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Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with charcot-marie-tooth disease 1A duplication

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

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12 December 2020

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Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18560793

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12 December 2020

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Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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MRI in DNM2-related centronuclear myopathy: Evidence for highly selective muscle involvement

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

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inferred from PubMed ID database lookup

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

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12 December 2020

based on heuristic

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Lower limb manual muscle testing in the early stages of Charcot-Marie-Tooth disease type 1A

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The dominantly inherited motor and sensory neuropathies: clinical and molecular advances

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

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12 December 2020

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inferred from PubMed ID database lookup

Intermediate forms of Charcot-Marie-Tooth neuropathy: a review

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18560793

retrieved

12 December 2020

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Identifiers

DOI

10.1007/S00415-008-0808-8

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Dimensions Publication ID

1043728565

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PubMed publication ID

18560793

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