Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Author:

Grohmann Katja,Varon Raymonda,Stolz Piroschka,Schuelke Markus,Janetzki Catrin,Bertini Enrico,Bushby Kate,Muntoni Francesco,Ouvrier Robert,Van Maldergem Lionel,Goemans Nathalie M. L. A.,Lochmüller Hanns,Eichholz Stephan,Adams Coleen,Bosch Friedrich,Grattan-Smith Padraic,Navarro Carmen,Neitzel Heidemarie,Polster Tilman,Topaloğlu Haluk,Steglich Christina,Guenther Ulf P.,Zerres Klaus,Rudnik-Schöneborn Sabine,Hübner Christoph

Funder

German Research Foundation (Deutsche Forschungsgemeinschaft)

“Helft dem muskelkranken Kind,” Hamburg, Germany

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference23 articles.

1. Respiratory distress as the initial manifestation of Werdnig-Hoffmann disease;Mellins;Pediatrics,1974

2. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings;Rudnik-Schöneborn;Neuropediatrics,1996

3. Familial fatal neonatal radiculoneuropathy;Gilmartin;Birth Defects Orig Artic Ser,1977

4. Diaphragmatic paralysis due to spinal muscular atrophy;McWilliam;Arch Dis Child,1985

5. Diaphragmatic paralysis due to spinal muscular atrophy;Murphy;Arch Dis Child,1985

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