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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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