Addis M - Search Results

1

Cytogenetic and molecular characterization of a variant translocation associated with acute promyelocytic leukemia and involving chromosomes 11, 15 and 17.

Casula L, Archidiacono N, Grazia Pau M, Addis M, Mura R, Galanello R, Biddau P, Cao A, Nucaro A. Casula L, et al. Among authors: addis m. Leukemia. 1996 Oct;10(10):1655-7. Leukemia. 1996. PMID: 8847902 No abstract available.

2

Pitfalls in genetic counselling for beta-thalassemia: an individual with 4 different thalassemia mutations.

Galanello R, Paglietti ME, Addis M, Melis MA, Tuveri T, Furbetta M, Cao A. Galanello R, et al. Among authors: addis m. Clin Genet. 1988 Mar;33(3):151-5. doi: 10.1111/j.1399-0004.1988.tb03430.x. Clin Genet. 1988. PMID: 3359676

3

Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene.

Galanello R, Paglietti E, Melis MA, Crobu MG, Addis M, Moi P, Cao A. Galanello R, et al. Among authors: addis m. Am J Hematol. 1988 Oct;29(2):63-6. doi: 10.1002/ajh.2830290202. Am J Hematol. 1988. PMID: 3189303

4

Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype.

Galanello R, Monne MI, Paderi L, Paglietti E, Atzori G, Addis M, Limongelli O, Macciotta A, Cao A. Galanello R, et al. Among authors: addis m. Br J Haematol. 1991 Sep;79(1):117-9. doi: 10.1111/j.1365-2141.1991.tb08018.x. Br J Haematol. 1991. PMID: 1911369 No abstract available.

5

Interferon-alpha 2a therapy in CML: disappearance of BCR/ABL transcript in a case of long-lasting continuous cytogenetic conversion.

Pardini S, Addis M, Dore F, Bonfigli S, Nieddu RM, Galanello R, Longinotti M, Pau MG. Pardini S, et al. Among authors: addis m. Haematologica. 1994 Nov-Dec;79(6):540-1. Haematologica. 1994. PMID: 7896213 Review.

6

Genetic counseling and genetic heterogeneity in the thalassemias.

Paglietti E, Galanello R, Addis M, Cao A. Paglietti E, et al. Among authors: addis m. Clin Genet. 1985 Jul;28(1):1-7. doi: 10.1111/j.1399-0004.1985.tb01209.x. Clin Genet. 1985. PMID: 2992852

7

Molecular analysis of beta zero-thalassemia intermedia in Sardinia.

Galanello R, Dessi E, Melis MA, Addis M, Sanna MA, Rosatelli C, Argiolu F, Giagu N, Turco MP, Cacace E, et al. Galanello R, et al. Among authors: addis m. Blood. 1989 Aug 1;74(2):823-7. Blood. 1989. PMID: 2473806 Free article.

8

Hemoglobin A2 in iron deficient beta-thalassemia heterozygotes.

Galanello R, Ruggeri R, Addis M, Paglietti E, Cao A. Galanello R, et al. Among authors: addis m. Hemoglobin. 1981;5(6):613-8. doi: 10.3109/03630268108991694. Hemoglobin. 1981. PMID: 7319832 No abstract available.

9

A strategy for fragile-X carrier screening.

Melis MA, Addis M, Lepiani C, Congeddu E, Cossu P, Cao A. Melis MA, et al. Among authors: addis m. Genet Test. 1999;3(3):301-4. doi: 10.1089/109065799316635. Genet Test. 1999. PMID: 10495931

10

A novel interstitial deletion in Xq25, identified by array-CGH in a patient with Lowe syndrome.

Addis M, Meloni C, Congiu R, Santaniello S, Emma F, Zuffardi O, Ciccone R, Cao A, Melis MA, Cau M. Addis M, et al. Eur J Med Genet. 2007 Jan-Feb;50(1):79-84. doi: 10.1016/j.ejmg.2006.10.003. Epub 2006 Nov 10. Eur J Med Genet. 2007. PMID: 17142121

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