Hematologically important mutations: Bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler–Najjar syndromes (English)
- New search for: Costa, E. s.
- New search for: Costa, E. s.
In:
BLOOD CELLS MOLECULES AND DISEASES
;
36
, 1
;
77-80
;
2006
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ISSN:
- Article (Journal) / Print
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Title:Hematologically important mutations: Bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler–Najjar syndromes
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Contributors:Costa, E. s. ( author )
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Published in:BLOOD CELLS MOLECULES AND DISEASES ; 36, 1 ; 77-80
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Publisher:
- New search for: Elsevier Science B.V., Amsterdam
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Publication date:2006-01-01
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Size:4 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 616.15
- Further information on Dewey Decimal Classification
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Classification:
DDC: 616.15 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 36, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
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Mechanisms involved in the swelling of erythrocytes caused by Pacific and Caribbean ciguatoxinsSauviat, M. P. / Boydron-Le Garrec, R. l. / Masson, J. B. / Lewis, R. L. / Vernoux, J. P. / Molgó, J. / Laurent, D. / Benoit, E. et al. | 2006
- 10
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The human red cell voltage-dependent cation channel. Part III: Distribution homogeneity and pH dependenceBennekou, P. / Barksmann, T. L. / Christophersen, P. / Kristensen, B. I. et al. | 2006
- 15
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Mild copper deficiency alters gene expression of proteins involved in iron metabolismAuclair, S. / Feillet-Coudray, C. / Coudray, C. / Schneider, S. / Muckenthaler, M. U. / Mazur, A. et al. | 2006
- 21
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Iron chelation treatment with combined therapy with deferiprone and deferioxamine: A 12-month trialKattamis, A. / Ladis, V. / Berdousi, H. / Kelekis, N. L. / Alexopoulou, E. / Papasotiriou, I. / Drakaki, K. / Kaloumenou, I. / Galani, A. / Kattamis, C. et al. | 2006
- 26
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Ferroportin is a monomer in vivo in micePignatti, E. / Mascheroni, L. / Sabelli, M. / Barelli, S. / Biffo, S. / Pietrangelo, A. et al. | 2006
- 33
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Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IREPapanikolaou, G. / Chandrinou, H. / Bouzas, E. / Contopoulos-Ioannidis, D. / Kalotychou, V. / Prentzas, K. / Lilakos, K. / Asproudis, I. / Palaiologou, D. / Premetis, E. et al. | 2006
- 41
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Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in SpainBach, V. / Remacha, A. / Altés, A. / Barceló, M. J. / Molina, M. A. / Baiget, M. et al. | 2006
- 46
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Analysis of nonsense-mediated mRNA decay in mutant alleles identified in Spanish Gaucher disease patientsMontfort, M. / Chabás, A. / Vilageliu, L. s. / Grinberg, D. et al. | 2006
- 53
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Increased incidence of cancer in adult Gaucher disease in Western Europede Fost, M. / vom Dahl, S. / Weverling, G. J. / Brill, N. / Brett, S. / Häussinger, D. / Hollak, C. E. et al. | 2006
- 59
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In vitro dual effect of arsenic trioxide on hemopoiesis: Inhibition of erythropoiesis and stimulation of megakaryocytic maturationSaulle, E. / Riccioni, R. / Pelosi, E. / Stafness, M. / Mariani, G. / De Tuglie, G. / Peschle, C. / Testa, U. et al. | 2006
- 77
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Hematologically important mutations: Bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler–Najjar syndromesCosta, E. s. et al. | 2006
- 81
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Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b5 reductase: An aid to determine recessive congenital methemoglobinemia status in an infantPercy, M. J. / Crowley, L. J. / Roper, D. / Vulliamy, T. J. / Layton, D. M. / Barber, M. J. et al. | 2006
- 91
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Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler–Najjar syndromesCosta, E. s. / Vieira, E. l. / Martins, M. / Saraiva, J. / Cancela, E. n. / Costa, M. / Bauerle, R. / Freitas, T. / Carvalho, J. o. / Santos-Silva, E. et al. | 2006
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Editorial Board| 2006