Histochemical and ultrastructural findings in a case of centronuclear myopathy.

A case of late onset lipid storage myopathy. Electromyographic, histochemical and ultrastructural findings.

Centronuclear myopathy.

gemfibrozil myopathy: a clinical, histochemical, and ultrastructural study.

Myotonia in centronuclear myopathy.

Muscular pseudohypertrophy in an adult case with centronuclear myopathy.

[Histological, histochemical, and ultrastructural findings in malignant hyperthermia (author's transl)].

Neuropathy in myotubular or centronuclear myopathy.

Neonatal respiratory insufficiency due to centronuclear myopathy.

Familial centronuclear myopathy associated with 'cardiomyopathy'.

Dynamin 2 the rescue for centronuclear myopathy.

Phospholamban overexpression in mice causes a centronuclear myopathy-like phenotype.

Crural hypertrophy associated with centronuclear myopathy.

A rare case of centronuclear myopathy with DNM2 mutation: genotype-phenotype correlation.

Postnatal centralization of muscle fibre nuclei in centronuclear myopathy.

A case of progressive external ophthalmoplegia (Kiloh-Nevin type) with abnormal mitochondria. Clinical, histochemical and ultrastructural findings.

Contraction versus contracture and centronuclear myopathy versus central part myopathy in malignant hyperthermia.

Maternal muscle biopsy in X-linked recessive centronuclear (myotubular) myopathy.

[Centronuclear myopathy with autosomal dominant inheritance(author's transl)].

Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations.

Reducing dynamin 2 expression rescues X-linked centronuclear myopathy.

X-linked centronuclear myopathy: mapping the gene to Xq28.

Mucolipidosis IV. Clinical, ultrastructural, histochemical, and chemical studies of a case, including a brain biopsy.

Identification of the mutation causing centronuclear myopathy in a border collie.

DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy.

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A case of late onset lipid storage myopathy. Electromyographic, histochemical and ultrastructural findings.

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Myotonia in centronuclear myopathy.

Muscular pseudohypertrophy in an adult case with centronuclear myopathy.

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Neuropathy in myotubular or centronuclear myopathy.

Neonatal respiratory insufficiency due to centronuclear myopathy.

Familial centronuclear myopathy associated with 'cardiomyopathy'.

Dynamin 2 the rescue for centronuclear myopathy.

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A rare case of centronuclear myopathy with DNM2 mutation: genotype-phenotype correlation.

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A case of progressive external ophthalmoplegia (Kiloh-Nevin type) with abnormal mitochondria. Clinical, histochemical and ultrastructural findings.

Contraction versus contracture and centronuclear myopathy versus central part myopathy in malignant hyperthermia.

Maternal muscle biopsy in X-linked recessive centronuclear (myotubular) myopathy.

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Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations.

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Identification of the mutation causing centronuclear myopathy in a border collie.

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