Imaging alterations in skeletal muscle channelopathies: a study in 15 patients

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Imaging alterations in skeletal muscle channelopathies: a study in 15 patients

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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Imaging alterations in skeletal muscle channelopathies: a study in 15 patients

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Imaging alterations in skeletal muscle channelopathies: a study in 15 patients

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Imaging alterations in skeletal muscle channelopathies: a study in 15 patients

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P1476

Imaging alterations in skeletal muscle channelopathies: a study in 15 patients

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P2093

Eleonora Canioni

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Elio Maccagnano

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Lorenzo Maggi

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Lucia Morandi

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Pia Bernasconi

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Raffaella Brugnoni

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P2860

Extraocular muscle hypertrophy in myotonia congenita

Correlating phenotype and genotype in the periodic paralyses

In vivo 35Cl MR imaging in humans: a feasibility study.

Muscle Na+ channelopathies: MRI detects intracellular 23Na accumulation during episodic weakness.

Neuromuscular imaging in inherited muscle diseases

Prevalence study of genetically defined skeletal muscle channelopathies in England.

Distinct muscle imaging patterns in myofibrillar myopathies.

Muscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotonias.

Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation.

Hyperkalemic periodic paralysis and permanent weakness: 3-T MR imaging depicts intracellular 23Na overload--initial results.

P304

109-115

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P31

scholarly article

P433

2-3

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P478

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P577

2015-12-01T00:00:00Z

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P698

27199537

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P932

4859077

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