Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

Angelo Minucci; Antonio Ruggiero; Giulia Canu; Palma Maurizi; Maria De Bonis; Paola Concolino; Daniele De Luca; Ettore Domenico Capoluongo

doi:10.1002/pbc.25500

Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

Angelo Minucci^*
, Antonio Ruggiero
, Giulia Canu
, Palma Maurizi
, Maria De Bonis
, Paola Concolino
, Daniele De Luca
, Ettore Domenico Capoluongo

^*Autore corrispondente per questo lavoro

Department of Laboratory Medicine, Laboratory of Clinical Molecular and Personalized Diagnostics
Assistance publique – Hôpitaux de Paris

Risultato della ricerca: Contributo in rivista › Articolo

2 Citazioni (Scopus)

Abstract

NO ABSTRACT AVALAIBLE

Lingua originale	Inglese
pagine (da-a)	1680-1681
Numero di pagine	2
Rivista	PEDIATRIC BLOOD & CANCER
Volume	62
Numero di pubblicazione	9
DOI	https://doi.org/10.1002/pbc.25500
Stato di pubblicazione	Pubblicato - 2015

All Science Journal Classification (ASJC) codes

Pediatria, Perinatologia e Salute del Bambino
Ematologia
Oncologia

Keywords

PYRUVATE-KINASE DEFICIENCY
UDP-GLUCURONOSYLTRANSFERASE

Accesso al documento

10.1002/pbc.25500

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title = "Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome",

abstract = "NO ABSTRACT AVALAIBLE",

keywords = "PYRUVATE-KINASE DEFICIENCY, UDP-GLUCURONOSYLTRANSFERASE, PYRUVATE-KINASE DEFICIENCY, UDP-GLUCURONOSYLTRANSFERASE",

author = "Angelo Minucci and Antonio Ruggiero and Giulia Canu and Palma Maurizi and \{De Bonis\}, Maria and Paola Concolino and \{De Luca\}, Daniele and Capoluongo, \{Ettore Domenico\}",

year = "2015",

doi = "10.1002/pbc.25500",

language = "English",

volume = "62",

pages = "1680--1681",

journal = "PEDIATRIC BLOOD \& CANCER",

issn = "1545-5009",

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T1 - Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

AU - Minucci, Angelo

AU - Ruggiero, Antonio

AU - Canu, Giulia

AU - Maurizi, Palma

AU - De Bonis, Maria

AU - Concolino, Paola

AU - De Luca, Daniele

AU - Capoluongo, Ettore Domenico

PY - 2015

Y1 - 2015

N2 - NO ABSTRACT AVALAIBLE

AB - NO ABSTRACT AVALAIBLE

KW - PYRUVATE-KINASE DEFICIENCY

KW - UDP-GLUCURONOSYLTRANSFERASE

KW - PYRUVATE-KINASE DEFICIENCY

KW - UDP-GLUCURONOSYLTRANSFERASE

UR - https://publicatt.unicatt.it/handle/10807/72374

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U2 - 10.1002/pbc.25500

DO - 10.1002/pbc.25500

M3 - Article

SN - 1545-5009

VL - 62

SP - 1680

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JO - PEDIATRIC BLOOD & CANCER

JF - PEDIATRIC BLOOD & CANCER

IS - 9

ER -

Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

Abstract

All Science Journal Classification (ASJC) codes

Keywords

Accesso al documento

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