Balassopoulou A - Search Results

1

Cystic fibrosis in Greece: typing with DNA probes and identification of the common molecular defect.

Balassopoulou A, Loukopoulos D, Kollia P, Devoto M, Adam G, Arvanitakis S, Hadjisevastou H. Balassopoulou A, et al. Hum Genet. 1990 Sep;85(4):393-4. doi: 10.1007/BF02428270. Hum Genet. 1990. PMID: 2210741

2

A novel nonsense mutation identified in the first nucleotide binding fold of the CFTR gene in a Greek patient.

Balassopoulou A, Papadakis M, Loukopoulos D. Balassopoulou A, et al. Hum Mol Genet. 1994 Oct;3(10):1887-8. doi: 10.1093/hmg/3.10.1887. Hum Mol Genet. 1994. PMID: 7531541 No abstract available.

3

Haplotypes in cystic fibrosis patients with or without pancreatic insufficiency from four European populations.

Devoto M, De Benedetti L, Seia M, Piceni Sereni L, Ferrari M, Bonduelle ML, Malfroot A, Lissens W, Balassopoulou A, Adam G, et al. Devoto M, et al. Among authors: balassopoulou a. Genomics. 1989 Nov;5(4):894-8. doi: 10.1016/0888-7543(89)90131-6. Genomics. 1989. PMID: 2574150

4

Analysis of 14 cystic fibrosis mutations in five south European populations.

Nunes V, Gasparini P, Novelli G, Gaona A, Bonizzato A, Sangiuolo F, Balassopoulou A, Giménez FJ, Dognini M, Ravnik-Glavac M, et al. Nunes V, et al. Among authors: balassopoulou a. Hum Genet. 1991 Oct;87(6):737-8. doi: 10.1007/BF00201737. Hum Genet. 1991. PMID: 1937479

5

Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics.

Serre JL, Simon-Bouy B, Mornet E, Jaume-Roig B, Balassopoulou A, Schwartz M, Taillandier A, Boué J, Boué A. Serre JL, et al. Among authors: balassopoulou a. Hum Genet. 1990 Apr;84(5):449-54. doi: 10.1007/BF00195818. Hum Genet. 1990. PMID: 1969843

6

Pregnancy in beta-thalassemia intermedia: 20-year experience of a Greek thalassemia center.

Voskaridou E, Balassopoulou A, Boutou E, Komninaka V, Christoulas D, Dimopoulou M, Delaki EE, Loukopoulos D, Terpos E. Voskaridou E, et al. Among authors: balassopoulou a. Eur J Haematol. 2014 Dec;93(6):492-9. doi: 10.1111/ejh.12387. Epub 2014 Jun 26. Eur J Haematol. 2014. PMID: 24889414

7

A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.

Papaioannou M, Bessant D, Payne A, Bellingham J, Rougas C, Loutradis-Anagnostou A, Gregory-Evans C, Balassopoulou A, Bhattacharya S. Papaioannou M, et al. Among authors: balassopoulou a. J Med Genet. 1998 May;35(5):429-31. doi: 10.1136/jmg.35.5.429. J Med Genet. 1998. PMID: 9610810 Free PMC article.

8

Double mutant alleles: are they rare?

Savov A, Angelicheva D, Balassopoulou A, Jordanova A, Noussia-Arvanitakis S, Kalaydjieva L. Savov A, et al. Among authors: balassopoulou a. Hum Mol Genet. 1995 Jul;4(7):1169-71. doi: 10.1093/hmg/4.7.1169. Hum Mol Genet. 1995. PMID: 8528204

9

Coinheritance of Triplicated Alpha-Globin Gene and Beta-Thalassemia Mutations in Adulthood: Ten Years of Referrals in Northern Greece.

Theodoridou S, Balassopoulou A, Boutou E, Delaki EE, Yfanti E, Vyzantiadis TA, Vetsiou E, Voskaridou E, Vlachaki E. Theodoridou S, et al. Among authors: balassopoulou a. J Pediatr Hematol Oncol. 2020 Nov;42(8):e762-e764. doi: 10.1097/MPH.0000000000001730. J Pediatr Hematol Oncol. 2020. PMID: 32032239

10

First Report of a Coincidental Discovery of Hb Antibes-Juan-Les-Pins (HBB: c.349_350insGTGTGCTGGCCC) in a Greek Woman.

Theodoridou S, Boutou E, Vyzantiadis TA, Balassopoulou A, Vlachaki E. Theodoridou S, et al. Among authors: balassopoulou a. Hemoglobin. 2020 Sep;44(5):361-363. doi: 10.1080/03630269.2020.1813160. Epub 2020 Dec 2. Hemoglobin. 2020. PMID: 33267629

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