Galanello R - Search Results

1

Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.

Galanello R, Cipollina MD, Carboni G, Perseu L, Barella S, Corrias A, Cao A. Galanello R, et al. Eur J Pediatr. 1999 Nov;158(11):914-6. doi: 10.1007/s004310051241. Eur J Pediatr. 1999. PMID: 10541948 Clinical Trial.

2

Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.

Galanello R, Perseu L, Melis MA, Cipollina L, Barella S, Giagu N, Turco MP, Maccioni O, Cao A. Galanello R, et al. Br J Haematol. 1997 Nov;99(2):433-6. doi: 10.1046/j.1365-2141.1997.3703182.x. Br J Haematol. 1997. PMID: 9375768 Free article.

3

Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia.

Galanello R, Cipollina MD, Dessì C, Giagu N, Lai E, Cao A. Galanello R, et al. Haematologica. 1999 Feb;84(2):103-5. Haematologica. 1999. PMID: 10091405 Clinical Trial.

4

Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.

Galanello R, Piras S, Barella S, Leoni GB, Cipollina MD, Perseu L, Cao A. Galanello R, et al. Br J Haematol. 2001 Dec;115(4):926-8. doi: 10.1046/j.1365-2141.2001.03200.x. Br J Haematol. 2001. PMID: 11843828 Free article.

5

Percentile curves for red cell indices of beta zero-thalassaemia heterozygotes in infancy and childhood.

Galanello R, Lilliu F, Bertolino F, Cao A. Galanello R, et al. Eur J Pediatr. 1991 Apr;150(6):413-5. doi: 10.1007/BF02093721. Eur J Pediatr. 1991. PMID: 2040350

6

Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNA.

Galanello R, Gasperini D, Perseu L, Barella S, Ideo A, Cao A. Galanello R, et al. Hemoglobin. 1994 Nov;18(6):437-9. doi: 10.3109/03630269409045776. Hemoglobin. 1994. PMID: 7713748 No abstract available.

7

A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia.

Filosa S, Cai W, Galanello R, Cao A, de Mattia D, Schettini F, Martini G. Filosa S, et al. Among authors: galanello r. Hum Genet. 1994 Nov;94(5):560-2. doi: 10.1007/BF00211027. Hum Genet. 1994. PMID: 7959695

8

Simultaneous automated determination of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities in whole blood.

Mosca A, Paleari R, Rosti E, Luzzana M, Barella S, Sollaino C, Galanello R. Mosca A, et al. Among authors: galanello r. Eur J Clin Chem Clin Biochem. 1996 May;34(5):431-8. doi: 10.1515/cclm.1996.34.5.431. Eur J Clin Chem Clin Biochem. 1996. PMID: 8790979

9

Relationship between genotype and phenotype. Thalassemia intermedia.

Galanello R, Cao A. Galanello R, et al. Ann N Y Acad Sci. 1998 Jun 30;850:325-33. doi: 10.1111/j.1749-6632.1998.tb10489.x. Ann N Y Acad Sci. 1998. PMID: 9668554 Review.

10

A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. Online.

Galanello R, Loi D, Sollaino C, Dessì S, Cao A, Melis MA. Galanello R, et al. Hum Mutat. 1998;12(1):72-3. doi: 10.1002/(SICI)1098-1004(1998)12:1<72::AID-HUMU19>3.0.CO;2-T. Hum Mutat. 1998. PMID: 10627140

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