Results 151 to 160 of about 1,793 (201)
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Myositis Ossificans Progressiva

Acta Rheumatologica Scandinavica, 1967
SummaryA 17-years-old male suffering from myositis ossificans progressiva with ossification in the left hip joint and cervical spine regions and microdactyly of both big toes is described. Electromyographic examination of clinically normal quadriceps and tibialis anterior muscles revealed a myopathic pattern.
G, Korányi, J, Nábrády, E, Vetró
  +7 more sources

Myositis ossificans progressiva

British Journal of Hospital Medicine, 2006
A 23-year-old man with myositis ossificans progressiva was seen in the orthopaedic clinic with pain on sitting as a result of a bony spur extending caudally from the right ischiopubic eminence. The fragment of bone was mobile and exquisitely tender on palpation.
Waller, S. L.   +2 more
openaire   +4 more sources

MYOSITIS OSSIFICANS PROGRESSIVA

Pediatrics, 1951
Four new cases of myositis ossificans progressiva have been presented and the literature on the subject has been reviewed. At the onset typical cases will usually develop palpable masses over the fascial planes of the head and neck.
H D, RILEY, A, CHRISTIE
openaire   +2 more sources

Myositis ossificans progressiva

Indian Journal of Pediatrics, 1958
1. Two cases of myositis ossificans progressiva are reported. 2. A brief review of the literature is presented.
O P, GHAI, B N, SINGH, D P, MUKERJEA
openaire   +2 more sources

Myositis Ossificans Progressiva

Radiology, 1954
In 1692 Patin (1) described the first case of progressive muscle ossification and in 1868 von Dusch (2) gave the disease its present name of myositis ossificans progressiva. A detailed survey of the literature was published by Rosenstirn (3) in 1918, and in 1932 Mair (4) reviewed the subject thoroughly and published two cases of his own.
E B, SINGLETON, J F, HOLT
openaire   +2 more sources

Fibrodysplasia (Myositis) ossificans progressiva

Seminars in Arthritis and Rheumatism, 1994
Fibrodysplasia ossificans progressiva (FOP) is a rare hereditary connective tissue disorder. Patients with FOP develop progressive ossification of muscle and connective tissue associated with pain and disability. Onset is typically in childhood, and congenital anomalies of the feet are an early sign of this condition. Pain and stiffness of the spine or
A J, Bridges   +4 more
openaire   +2 more sources

Myositis ossificans progressiva

Journal of Clinical Anesthesia, 1991
Myositis ossificans progressiva is a rare, incurable disease causing progressive ossification of skeletal muscles leading to total immobility. We report one such case.
D, Ghosh   +4 more
openaire   +3 more sources

Myositis ossificans progressiva

1968
Das seltene und ungewohnliche Krankheitsbild der Myositis ossificans progressiva ist im Jahre 1692 durch Guy Patin erstmals beschrieben worden. Die Bezeichnung „Myositis ossificans progressiva“ stammt von Munchmeyer (1869) jedoch handelt es sich weder um eine echte Entzundung noch um eine eigentliche Myopathie.
P E, Becker, G, von Knorre
openaire   +2 more sources

Myositis Ossificans Progressiva

Archives of Internal Medicine, 1973
The effect of parathyroid extract infusion was studied in a 17-year-old boy with myositis ossificans progressiva to evaluate its effect on excretion of connective tissue components in extensive ectopic ossification and to explore its therapeutic potential. There was an increase in urinary excretion of hydroxyproline, hexosamine, glycosaminoglycans, and
openaire   +1 more source

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