Migrating atelectasis in Werdnig-Hoffmann Disease: Pulmonary manifestations in two cases of spinal muscular atrophy type 1

Pediatric Pulmonology

Volumn 28, Issue 2, 1999, Pages 149-153

  Leistikow, E A ^a   Jones, N E ^b   Josephson, K D ^b   De Sierra, T M ^c   Costakos, D T ^b   Sprague, D ^a   Gorch, D H ^d   Asonye, U O ^e  

^a PEDIATRIX MEDICAL GROUP   (United States)

^b Franciscan Skemp/Mayo Hlthcare S   (United States)

^c HOSPITAL INFANTIL DE MÉXICO FEDERICO GÓMEZ   (Mexico)

^d MICHIGAN STATE UNIVERSITY   (United States)

^e Midwest NeoPed Associates   (United States)

Author keywords

Atelectasis; Genetics; Neuromuscular disease; Werdnig Hoffmann disease

Indexed keywords

ARTICLE; ATELECTASIS; CASE REPORT; CHILDHOOD DISEASE; CLINICAL FEATURE; DISEASE ASSOCIATION; GENE DELETION; HUMAN; HUMAN TISSUE; INFANT; NEUROMUSCULAR DISEASE; PRIORITY JOURNAL; SYMPTOMATOLOGY; WERDNIG HOFFMANN DISEASE;

ATELECTASIS; HUMANS; INFANT; LUNG; MALE; SPINAL MUSCULAR ATROPHIES OF CHILDHOOD;

EID: 0032769966     PISSN: 87556863     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0496(199908)28:2<149::AID-PPUL12>3.0.CO;2-W     Document Type: Article

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