A 5-year-old girl with muscle atrophy lacking motor developments after spontaneous sitting

Neuropathology

Volumn 24, Issue 4, 2004, Pages 347-349

  Hayashi, Masaharu ^a  

^a TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE; GENE PRODUCT; SURVIVAL MOTOR NEURON PROTEIN;

ARTICLE; CASE REPORT; CHILD; CHILDHOOD MORTALITY; DEVELOPMENTAL DELAY; DEVELOPMENTAL DISORDER; ELECTROMYOGRAPHY; ENZYME BLOOD LEVEL; FASCICULATION; FEMALE; FOOD POISONING; GENE; GENE DELETION; HUMAN; HUMAN TISSUE; HYPOREFLEXIA; MOTOR DEVELOPMENT; MUSCLE ATROPHY; MUSCLE HYPOTONIA; NEUROLOGIC EXAMINATION; PRIORITY JOURNAL; SITTING; SMN GENE; SPINAL MUSCULAR ATROPHY; SPINAL MUSCULAR ATROPHY TYPE II; STANDING; TENDON REFLEX; TONGUE DISEASE; TONGUE FASCICULATION; WALKING;

CHILD, PRESCHOOL; FEMALE; HUMANS; MOTOR SKILLS DISORDERS; MUSCULAR ATROPHY; POSTURE; SPINAL MUSCULAR ATROPHIES OF CHILDHOOD;

EID: 10844252230     PISSN: 09196544     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1440-1789.2004.00581.x     Document Type: Article

References (3)

1. Araki S, Hayashi M, Tamagawa K et al. Neuropathological analysis in spinal muscular atrophy type II. Acta Neuropathol (Berl) 2003; 106: 441-448.
2. Schmalbruch H, Haase G. Spinal muscular atrophy: present state. Brain Pathol 2001; 11: 231-247.
3. Osawa M, Shishikura K. Werdnig-Hoffmann disease and variants. In: de Jong JMBD (ed.) Handbook of Clinical Neurology, Vol 15. Amsterdam: Elsevier, 1991; 51-80.