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Patient with unusual Hutchinson-Gilford syndrome (Progeria)

Author
MATSUO, S1 ; TAKEUCHI, Y1 ; HAYASHI, S; KINUGASA, A1 ; SAWADA, T1
[1] Kyoto prefectural univ. medicine, childen's res. hosp., dep. pediatrics, Kamigyo-ku Kyoto 602, Japan
Source

Pediatric neurology. 1994, Vol 10, Num 3, pp 237-240 ; ref : 17 ref

ISSN
0887-8994
Scientific domain
Neurology; Pediatrics
Publisher
Elsevier, New York, NY
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Enfant Etude cas Mâle Progéria Ramollissement cérébral Appareil circulatoire pathologie Cérébrovasculaire pathologie Encéphale pathologie Homme Maladie héréditaire Peau pathologie Syndrome complexe Système nerveux central pathologie Système nerveux pathologie Vaisseau sanguin pathologie
Keyword (en)
Child Case study Male Progeria Cerebral infarction Cardiovascular disease Cerebrovascular disease Cerebral disorder Human Genetic disease Skin disease Complex syndrome Central nervous system disease Nervous system diseases Vascular disease
Keyword (es)
Niño Estudio caso Macho Progería Infarto cerebral Aparato circulatorio patología Vaso sanguíneo encéfalo patología Encéfalo patología Hombre Enfermedad hereditaria Piel patología Síndrome complejo Sistema nervosio central patología Sistema nervioso patología Vaso sanguíneo patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23E Complex syndromes

Discipline
Medical genetics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4107982

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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