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17 in total

1. Modifications in the sarcoplasmic reticulum and subcellular calcium distribution in skeletal muscle in a case of Westphal's disease (hypokalemic periodic paralysis).

Authors: A Porte; M E Stoeckel; J Y Ledeaut; S Guez; C Hindelang-Gertner; G Mack
Journal: Virchows Arch A Pathol Anat Histol Date: 1979-08-23

2. The MRL +/+ mouse: a new model of tubular aggregates which are gender- and age-related.

Authors: R W Kuncl; A Pestronk; J Lane; E Alexander
Journal: Acta Neuropathol Date: 1989 Impact factor: 17.088

3. Clinical and ultrastructural observations in a kindred with normo-hyperkalaemic periodic paralysis.

Authors: T S Danowski; E R Fisher; C Vidalon; J W Vester; R Thompson; S Nolan; T Stephan; J H Sunder
Journal: J Med Genet Date: 1975-03 Impact factor: 6.318

4. The syndrome of continuous muscle fibre activity: light and electron microscopic studies in muscle and nerve biopsies.

Authors: S Ono; S Munakata; K Nagao; N Shimizu; N Shimizu
Journal: J Neurol Date: 1989-10 Impact factor: 4.849

Familial hypokalemic periodic paralysis with permanent myopathy. A clinical and ultrastructural study.

1. Modifications in the sarcoplasmic reticulum and subcellular calcium distribution in skeletal muscle in a case of Westphal's disease (hypokalemic periodic paralysis).

2. The MRL +/+ mouse: a new model of tubular aggregates which are gender- and age-related.

3. Clinical and ultrastructural observations in a kindred with normo-hyperkalaemic periodic paralysis.

4. The syndrome of continuous muscle fibre activity: light and electron microscopic studies in muscle and nerve biopsies.

5. Tubular aggregates: their association with myalgia.

6. The cytoplasmic body: another structural anomaly of the Z disk.

7. Pathological changes in skeletal muscle in acromegaly.

8. Light and electron microscopic study of the muscles in hypokalemic periodic paralysis.

9. Histochemistry and electron microscopy of muscle fibres in a case of congenital paramyotonia.

10. Muscle pathology correlates with permanent weakness in hypokalemic periodic paralysis: a case report.