AMYOTONIA congenita.
Explore the source record for details and available documents.
Neuromuscular Diseases↗
SEARCH · Search PubMed
Results for “AMYOTONIA CONGENITA”
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
The problem of amyotonia congenita.
Explore the source record for details and available documents.
Neuromuscular Diseases↗
[Two cases of amyotonia congenita].
Explore the source record for details and available documents.
Neuromuscular Diseases↗
The amyotonia congenita syndrome.
Explore the source record for details and available documents.
Neuromuscular Diseases↗
The relationship between progressive muscular atrophy of spinal origin and amyotonia congenita.
Explore the source record for details and available documents.
Muscular Atrophy, Spinal↗
[MARFAN'S SYNDROME ASSOCIATED WITH AMYOTONIA CONGENITA].
Explore the source record for details and available documents.
Arachnodactyly↗
Amyotonia congenita with pyloric stenosis. (A case report).
Explore the source record for details and available documents.
Neuromuscular Diseases↗
[AMYOTONIA CONGENITA: (AMYOTONIC SYNDROME)].
Explore the source record for details and available documents.
Neuromuscular Diseases↗
Amyotonia congenita: a follow-up study.
Explore the source record for details and available documents.
Follow-Up Studies↗
[Amyotonia congenita in two brothers (Oppenheim's disease)].
Explore the source record for details and available documents.
Humans↗
[Follow-up examination of children with spinal muscular atrophy of the Werdning-Hoffmann type; at the same time a critical contribution to the problem of amyotonia congenita Oppenheim].
Explore the source record for details and available documents.
Child↗
[Case of Oppenheim's disease (amyotonia congenita) in a 15 month-old infant].
Explore the source record for details and available documents.
Humans↗
[CONSIDERATIONS ON SOME CASES OF AMYOTONIA CONGENITA].
Explore the source record for details and available documents.
Classification↗
Studies in disorders of muscle. IX. Glycogen storage disease primarily affecting skeletal muscle and clinically resembling amyotonia congenita.
Explore the source record for details and available documents.
Disease↗
A case of amyotonia congenita associated with bilateral subdural hygroma and occlusion of the sagittal sinus; demonstration of occlusion by diodrast sinography.
Explore the source record for details and available documents.
Dental Occlusion↗
Amyotonia congenita syndrome, with the report of a case of Werdnig-Hoffmann disease.
Explore the source record for details and available documents.
Neuromuscular Diseases↗
[Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children].
Explore the source record for details and available documents.
Atrophy↗
[Case of amyotonia congenita].
Explore the source record for details and available documents.
Medical Records↗