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 in rivista

5 Citazioni (Scopus)

Abstract

No abstract

Lingua originale	English
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 in rivista

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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