Document Detail


[Multifocal epithelial hyperplasia: a familial case].
MedLine Citation:
PMID:  20833119     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONCLUSION: We present two members of an ecuadorian family with MEH. Although it is a rare disease in Spain, we must take this disease into account, given the increase in the immigrant population in Spain.
Authors:
C A Villanueva Álvarez-Santullano; A Hernández-Núñez; A Castaño; R Miñano Medrano; S Córdoba Guijarro; J Borbujo Martínez
Publication Detail:
Type:  Case Reports; English Abstract; Journal Article     Date:  2010-09-15
Journal Detail:
Title:  Anales de pediatría (Barcelona, Spain : 2003)     Volume:  73     ISSN:  1695-9531     ISO Abbreviation:  An Pediatr (Barc)     Publication Date:  2010 Dec 
Date Detail:
Created Date:  2010-12-06     Completed Date:  2011-04-06     Revised Date:  2013-05-20    
Medline Journal Info:
Nlm Unique ID:  101162596     Medline TA:  An Pediatr (Barc)     Country:  Spain    
Other Details:
Languages:  spa     Pagination:  357-60     Citation Subset:  IM    
Copyright Information:
Copyright © 2010 Asociación Española de Pediatría. Published by Elsevier Espana. All rights reserved.
Affiliation:
Hospital Universitario de Fuenlabrada, Madrid, España. cvillanueva.hflr@salud.madrid.org
Vernacular Title:
Hiperplasia epitelial multifocal: un caso familiar.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Family Health
Female
Focal Epithelial Hyperplasia / pathology*
Humans
Male

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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