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Familial case of piebaldism with regression of white forelock

Author
MATSUNAGA, H1 ; TANIOKA, M1 ; UTANI, A1 ; MIYACHI, Y1
[1] Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, 606-8507, Japan
Source

Clinical and experimental dermatology (Print). 2008, Vol 33, Num 4, pp 511-512, 2 p ; ref : 6 ref

CODEN
CEDEDE
ISSN
0307-6938
Scientific domain
Dermatology
Publisher
Blackwell, London / Blackwell, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Albinisme Dermatologie Localisé Mélatonine Régression Aminoacidopathie Enzymopathie Hormone épiphysaire Maladie héréditaire Maladie métabolique Pathologie de l'oeil Pathologie de l'uvée Pathologie de la peau Trouble de la pigmentation
Keyword (en)
Albinism Dermatology Localized Melatonin Regression Aminoacid disorder Enzymopathy Pineal hormone Genetic disease Metabolic diseases Eye disease Uvea disease Skin disease Pigmentation disorder
Keyword (es)
Albinismo Dermatología Localizado Melatonina Regresión Aminoacido alteración Enzimopatía Hormona epifisaria Enfermedad hereditaria Metabolismo patología Ojo patología Uvea patología Piel patología Trastorno pigmentación
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B08 Dermatology / 002B08F Pigmentary diseases of the skin

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D01 Aminoacid disorders

Discipline
Dermatology Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
20453226

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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