Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient

Angelo Minucci; Giulia Canu; Ester Tellone; Bruno Giardina; Cecilia Zuppi; Ettore Domenico Capoluongo

doi:10.1016/j.bcmd.2012.05.004

Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient

Angelo Minucci
, Giulia Canu
, Ester Tellone
, Bruno Giardina
, Cecilia Zuppi
, Ettore Domenico Capoluongo

Università Cattolica del Sacro Cuore

University of Messina

Risultato della ricerca: Contributo in rivista › Articolo

5 Citazioni (Scopus)

Abstract

No abstract

Lingua originale	Inglese
pagine (da-a)	118-119
Numero di pagine	2
Rivista	BLOOD CELLS, MOLECULES, & DISEASES
Volume	49
DOI	https://doi.org/10.1016/j.bcmd.2012.05.004
Stato di pubblicazione	Pubblicato - 2012

Keywords

Crigler-Najjar Syndrome type II
hyperbilirubinemia

Accesso al documento

10.1016/j.bcmd.2012.05.004

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Minucci, A., Canu, G., Tellone, E., Giardina, B., Zuppi, C., & Capoluongo, E. D. (2012). Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient. BLOOD CELLS, MOLECULES, & DISEASES, 49, 118-119. https://doi.org/10.1016/j.bcmd.2012.05.004

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title = "Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient",

abstract = "No abstract",

keywords = "Crigler-Najjar Syndrome type II, hyperbilirubinemia, Crigler-Najjar Syndrome type II, hyperbilirubinemia",

author = "Angelo Minucci and Giulia Canu and Ester Tellone and Bruno Giardina and Cecilia Zuppi and Capoluongo, \{Ettore Domenico\}",

year = "2012",

doi = "10.1016/j.bcmd.2012.05.004",

language = "English",

volume = "49",

pages = "118--119",

journal = "BLOOD CELLS, MOLECULES, \& DISEASES",

issn = "1079-9796",

publisher = "Elsevier Science Incorporated / NY Journals:Madison Square Station, PO Box 882:New York, NY 10159:(212)633-3730, EMAIL: [email protected], INTERNET: http://www.elsevier.com, Fax: (212)633-3680",

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Minucci, A, Canu, G, Tellone, E, Giardina, B, Zuppi, C & Capoluongo, ED 2012, 'Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient', BLOOD CELLS, MOLECULES, & DISEASES, vol. 49, pagg. 118-119. https://doi.org/10.1016/j.bcmd.2012.05.004

Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient. / Minucci, Angelo; Canu, Giulia; Tellone, Ester et al.
In: BLOOD CELLS, MOLECULES, & DISEASES, Vol. 49, 2012, pag. 118-119.

Risultato della ricerca: Contributo in rivista › Articolo

TY - JOUR

T1 - Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient

AU - Minucci, Angelo

AU - Canu, Giulia

AU - Tellone, Ester

AU - Giardina, Bruno

AU - Zuppi, Cecilia

AU - Capoluongo, Ettore Domenico

PY - 2012

Y1 - 2012

N2 - No abstract

AB - No abstract

KW - Crigler-Najjar Syndrome type II

KW - hyperbilirubinemia

KW - Crigler-Najjar Syndrome type II

KW - hyperbilirubinemia

UR - http://hdl.handle.net/10807/40067

U2 - 10.1016/j.bcmd.2012.05.004

DO - 10.1016/j.bcmd.2012.05.004

M3 - Article

SN - 1079-9796

VL - 49

SP - 118

EP - 119

JO - BLOOD CELLS, MOLECULES, & DISEASES

JF - BLOOD CELLS, MOLECULES, & DISEASES

ER -

Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient

Abstract

Keywords

Accesso al documento

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