(Q82928015)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

Camptocormia phenotype of FSHD: a clinical and MRI study on six patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

Berit Jordan

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Katharina Eger

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Sabrina Koesling

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Stephan Zierz

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

publication date

17 December 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

volume

258

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

page(s)

866-873

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165637%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00415-010-5858-z

18 January 2020

exact match

0 references

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12 December 2020

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12 December 2020

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Axial myopathy due to primary amyloidosis.

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Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene

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Leg muscle involvement in facioscapulohumeral muscular dystrophy assessed by MRI

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12 December 2020

Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement.

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12 December 2020

Beevor's sign in facioscapulohumeral muscular dystrophy: an old sign with new implications

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12 December 2020

Control of the upper body movements during level walking in patients with facioscapulohumeral dystrophy

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12 December 2020

Disorders of paravertebral lumbar muscles: from pathology to cross-sectional imaging.

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12 December 2020

Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophy

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12 December 2020

Atypical Phenotypes in Patients With Facioscapulohumeral Muscular Dystrophy 4q35 Deletion

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12 December 2020

Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH Consortium

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12 December 2020

Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathy

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12 December 2020

Head drop and camptocormia

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12 December 2020

Epidemiology and pathophysiology of falls in facioscapulohumeral disease

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12 December 2020

Assessment of thoracic paraspinal muscles in the diagnosis of ALS

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12 December 2020

Clinical and histopathological heterogeneity in patients with 4q35 facioscapulohumeral muscular dystrophy (FSHD)

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12 December 2020

Camptocormia: pathogenesis, classification, and response to therapy

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12 December 2020

Inclusion body myositis presenting with isolated erector spinae paresis

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12 December 2020

An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1

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12 December 2020

Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia

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12 December 2020

Teaching NeuroImage: Axial muscle atrophy in adult-onset Pompe disease

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12 December 2020

Myopathy causing camptocormia in idiopathic Parkinson's disease: a multidisciplinary approach.

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12 December 2020

Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2 : a whole body highfield MRI study

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12 December 2020

40th ENMC Sponsored International Workshop: Nemaline Myopathy. 2-4 February 1996, Naarden, The Netherlands

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12 December 2020

Fatty replacement of lower paraspinal muscles: normal and neuromuscular disorders

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12 December 2020

Facioscapulohumeral muscular dystrophy presenting with isolated axial myopathy and bent spine syndrome

1 reference

12 December 2020

Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy

1 reference

12 December 2020

Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures

1 reference

12 December 2020

Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1).

1 reference

12 December 2020

Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases

1 reference

12 December 2020

Muscle MRI in inherited neuromuscular disorders: past, present, and future

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12 December 2020

[Value of x-ray computed tomography in muscular pathology. Personal cases and review of the literature]

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12 December 2020

Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs

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12 December 2020

Early-onset facioscapulohumeral muscular dystrophy - significance of pelvic extensors in sagittal spinal imbalance

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12 December 2020

De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).

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12 December 2020

Camptocormia as a presentation of generalized inflammatory myopathy

1 reference

12 December 2020

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)

1 reference

12 December 2020

Magnetic Resonance Imaging Assessment of Trunk Muscles During Prolonged Bed Rest

1 reference

12 December 2020

Unusual clinical presentations in patients harboring the facioscapulohumeral dystrophy 4q35 deletion

1 reference

12 December 2020

Facioscapulohumeral muscular dystrophy

1 reference

12 December 2020

Involvement patterns in myotilinopathy and desminopathy detected by a novel neuromuscular whole-body MRI protocol.

1 reference

12 December 2020

Severe forward flexion of the trunk in Parkinson's disease: focal myopathy of the paraspinal muscles mimicking camptocormia.

1 reference

12 December 2020