A Dominant ABCC8-Related Hyperinsulinism: Familial Case Report Moreira et al. ABCC8-Related Hyperinsulinism

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dc.contributor Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.author MOREIRA, M. C.
PIAZZON, F. B. FMUSP-HC
CARVALHO, M. D. F.
QUAIO, C. R. D. C. FMUSP-HC
DUTRA, A. B.
CECCON, M. E. FMUSP-HC
DELLA-MANNA, T. FMUSP-HC
TANNURI, U. FMUSP-HC
LEE, J. H.
ZERBINI, M. C. N. FMUSP-HC
BELLANNE-CHANTELOT, C.
LONLAY, P.
BERTOLA, D. R. FMUSP-HC
KIM, C. A. FMUSP-HC
dc.date.issued 2013
dc.identifier.citation FETAL AND PEDIATRIC PATHOLOGY, v.32, n.5, p.384-386, 2013
dc.identifier.issn 1551-3815
dc.identifier.uri http://observatorio.fm.usp.br/handle/OPI/4172
dc.language.iso eng
dc.publisher INFORMA HEALTHCARE
dc.relation.ispartof Fetal and Pediatric Pathology
dc.rights restrictedAccess
dc.subject.other congenital hyperinsulinism; abcc8; mutations; gene
dc.title A Dominant ABCC8-Related Hyperinsulinism: Familial Case Report Moreira et al. ABCC8-Related Hyperinsulinism
dc.type article
dc.rights.holder Copyright INFORMA HEALTHCARE
dc.description.group LIM/36
dc.description.group LIM/14
dc.description.group LIM/30
dc.identifier.doi 10.3109/15513815.2012.754531
dc.identifier.pmid 23301914
dc.type.category letter
dc.type.version publishedVersion
hcfmusp.author PIAZZON, F. B.:FM:
hcfmusp.author QUAIO, C. R. D. C.:HC:ICR
hcfmusp.author CECCON, M. E.:HC:ICR
hcfmusp.author DELLA-MANNA, T.:HC:ICR
hcfmusp.author TANNURI, U.:FM:MPE
hcfmusp.author ZERBINI, M. C. N.:FM:MPT
hcfmusp.author BERTOLA, D. R.:HC:ICR
hcfmusp.author KIM, C. A.:HC:ICR
hcfmusp.author.external · MOREIRA, M. C.:Univ Sao Paulo, Fac Med, Hosp Clin, Inst Crianca, Sao Paulo, Brazil
· CARVALHO, M. D. F.:Univ Sao Paulo, Fac Med, Hosp Clin, Inst Crianca, Sao Paulo, Brazil
· DUTRA, A. B.:Univ Sao Paulo, Fac Med, Hosp Clin, Inst Crianca, Sao Paulo, Brazil
· LEE, J. H.:Univ Sao Paulo, Fac Med, Dept Pathol, Sao Paulo, Brazil
· BELLANNE-CHANTELOT, C.:Grp Hosp Pitie Salpetriere, Dept Genet, F-75634 Paris, France
· LONLAY, P.:Univ Paris 05, Hop Necker Enfants Malad, Reference Ctr Inherited Metab Dis, Paris, France
hcfmusp.origem.id 2-s2.0-84883028322
hcfmusp.origem.id WOS:000323487700012
hcfmusp.publisher.city LONDON
hcfmusp.publisher.country ENGLAND
hcfmusp.relation.reference · Arnoux JB, 2011, ORPHANET J RARE DIS, V6, DOI 10.1186/1750-1172-6-63
· Babenko AP, 2006, NEW ENGL J MED, V355, P456, DOI 10.1056/NEJMoa055068
· Bellanne-Chantelot C, 2010, J MED GENET, V47, P752, DOI 10.1136/jmg.2009.075416
· Beltrand J, 2012, DIABETES CARE, V35, P198, DOI 10.2337/dc11-1296
· Park SE, 2011, EUR J ENDOCRINOL, V164, P919, DOI 10.1530/EJE-11-0160
dc.description.index MEDLINE
hcfmusp.citation.scopus 0
hcfmusp.citation.wos 0
hcfmusp.affiliation.country Brasil
hcfmusp.affiliation.country França


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