Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease)
- Author
- CHAN, C. K1 ; MOHSENIN, M; LOKE, J; VIRGULTO, J; LEONIDE SIPSKI, M; FERRANTI, R
[1] Gaylord hosp., pulmonary sect., New Haven CT 06510, United States - Source
Chest. 1987, Vol 91, Num 4, pp 567-570 ; ref : 22 ref
- CODEN
- CHETBF
- ISSN
- 0012-3692
- Scientific domain
- Anesthesia, intensive care; Cardiology, blood circulation, phlebology; Pneumology
- Publisher
- American College of Chest Physicians, Northbrook, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Amyotrophie Charcot Marie Tooth Appareil respiratoire pathologie Diaphragme Homme Hérédodégénération Nerf phrénique Paralysie Système nerveux pathologie
- Keyword (en)
- Charcot Marie Tooth disease Respiratory disease Diaphragm Human Heredodegeneration Phrenic nerve Paralysis Nervous system diseases
- Keyword (es)
- Amiotrofia Charcot Marie Tooth Aparato respiratorio patología Diafragma Hombre Heredodegeneracion Nervio frenico Paralisis Sistema nervioso patologia
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8131896
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1378/chest.91.4.567 
https://dx.doi.org/10.1378/chest.91.4.567
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