Spontaneous resolution of Chiari I malformation and syringomyelia : Case report and review of the literature. Commentaries
- Author
- KLEKAMP, Jörg1 ; IACONETTA, Giorgio1 ; SAMII, Madjid1 ; BATZDORF, Ulrich (Commentator)
; DE WITTE, Olivier (Commentator)
; BROTCHI, Jacques (Commentator)
; MILHORAT, Thomas H (Commentator)
[1] Department of Neurosurgery, Nordstadt Krankenhaus, Medizinische Hochschule, Hannover, Germany - Source
Neurosurgery. 2001, Vol 48, Num 3, pp 664-667 ; ref : 35 ref
- Publisher
- Lippincott Williams & Wilkins, Hagerstown, MD
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Adulte Arnold Chiari syndrome Etude cas Evolution Femelle Pronostic Spontané Syringomyélie Encéphale pathologie Homme Maladie congénitale Malformation Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Adult Arnold Chiari malformation Case study Evolution Female Prognosis Spontaneous Syringomyelia Cerebral disorder Human Congenital disease Malformation Central nervous system disease Nervous system diseases
- Keyword (es)
- Adulto Arnold Chiari síndrome Estudio caso Evolución Hembra Pronóstico Espontáneo Siringomielia Encéfalo patología Hombre Enfermedad congénita Malformación Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17D Malformations of the nervous system
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 971821
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
10.1097/00006123-200103000-00044 
https://dx.doi.org/10.1097/00006123-200103000-00044
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