78 related articles for article (PubMed ID: 932535)
1. Chromosomal breakage and scleroderma: studies in family members.
Emerit I; Housset E; Feingold J
J Lab Clin Med; 1976 Jul; 88(1):81-6. PubMed ID: 932535
[TBL] [Abstract][Full Text] [Related]
2. Chromosomal alterations in scleroderma.
Constantin M; Leucuţia M; Purice S
Med Interne; 1987; 25(4):245-9. PubMed ID: 3423700
[TBL] [Abstract][Full Text] [Related]
3. Spontaneous and clastogen induced chromosomal breakage in scleroderma.
Wolff DJ; Needleman BW; Wasserman SS; Schwartz S
J Rheumatol; 1991 Jun; 18(6):837-40. PubMed ID: 1716681
[TBL] [Abstract][Full Text] [Related]
4. Chromosome changes in lymphocytes of patients with scleroderma.
Casalone R; Granata P; Minelli E; Righi R; Meroni E; Mazzola D; Sammarelli G; Baratelli E; Broggini M
Ann Genet; 1995; 38(3):145-50. PubMed ID: 8540685
[TBL] [Abstract][Full Text] [Related]
5. Chromosome studies in scleroderma with consideration of anticentromere antibody status and assessment of possible in vitro clastogenic activity.
Powell FC; Schroeter AL; Winkelmann RK; Dewald GW
Acta Derm Venereol; 1986; 66(5):414-8. PubMed ID: 2431579
[TBL] [Abstract][Full Text] [Related]
6. [Cytogenetic findings in acute myelogenous leukemias (FAB M 1 to M 6)].
Prösch U; Stobbe H
Folia Haematol Int Mag Klin Morphol Blutforsch; 1985; 112(4):481-94. PubMed ID: 2414178
[TBL] [Abstract][Full Text] [Related]
7. [Familial scleroderma with Sjogren's syndrome and lymphocyte and chromosome abnormalities].
Camus JP; Emerit I; Reinert P; Guillien P; Crouzet J; Fourot J
Ann Med Interne (Paris); 1970 Feb; 121(2):149-61. PubMed ID: 5491196
[No Abstract] [Full Text] [Related]
8. [Chromosome abnormalities in systemic scleroderma].
Emerit I; Camus JP
Rev Rhum Mal Osteoartic; 1972 Nov; 39(11):731-4. PubMed ID: 4654971
[No Abstract] [Full Text] [Related]
9. [Generalized scleroderma and chromosome breakage. Demonstration of a breaking factor in patients serum].
Emerit I; Levy A; Housset E
Ann Genet; 1973 Jun; 16(2):135-8. PubMed ID: 4541907
[No Abstract] [Full Text] [Related]
10. Spontaneous chromosome damage (micronuclei) in systemic sclerosis and Raynaud's phenomenon.
Porciello G; Scarpato R; Ferri C; Storino F; Cagetti F; Morozzi G; Bellisai F; Migliore L; Marcolongo R; Galeazzi M
J Rheumatol; 2003 Jun; 30(6):1244-7. PubMed ID: 12784397
[TBL] [Abstract][Full Text] [Related]
11. Chromosomal breakage in systemic sclerosis and related disorders.
Emerit I
Dermatologica; 1976; 153(3):145-56. PubMed ID: 14037
[TBL] [Abstract][Full Text] [Related]
12. Chromosomal breakage in diffuse scleroderma. A study of 27 patients.
Emerit I; Housset E; de Grouchy J; Camus JP
Rev Eur Etud Clin Biol; 1971; 16(7):684-94. PubMed ID: 5125548
[No Abstract] [Full Text] [Related]
13. Chromosome instability in human and murine autoimmune disease: anticlastogenic effect of superoxide dismutase.
Emerit I; Michelson AM
Acta Physiol Scand Suppl; 1980; 492():59-65. PubMed ID: 6939306
[TBL] [Abstract][Full Text] [Related]
14. A cytogenetic analysis of twenty cases of systemic scleroderma.
Romani F; Viguie F; Siffroi JP; Fiessenger JN
Ann Genet; 1986; 29(4):240-5. PubMed ID: 3495226
[TBL] [Abstract][Full Text] [Related]
15. Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes.
Rittner G; Schwanitz G; Baur MP; Black CM; Welsh KI; Kühnl P; Rittner C
Hum Genet; 1988 Dec; 81(1):64-70. PubMed ID: 3198128
[TBL] [Abstract][Full Text] [Related]
16. Deficient DNA repair capacity: a predisposing factor and high risk predictive marker in familial colorectal cancer.
Ankathil R; Jyothish B; Madhavan J; Nair MK
J Exp Clin Cancer Res; 1999 Mar; 18(1):33-7. PubMed ID: 10374674
[TBL] [Abstract][Full Text] [Related]
17. Chromosome aberrations in Raynaud's phenomenon.
Porciello G; Scarpato R; Storino F; Migliore L; Ferri C; Cagetti F; Morozzi G; Bellisai F; Marcolongo R; Galeazzi M
Eur J Dermatol; 2004; 14(5):327-31. PubMed ID: 15358572
[TBL] [Abstract][Full Text] [Related]
18. Analysis of naturally occurring and radiation-induced breakpoint locations in human chromosomes 1, 2 and 4.
Tucker JD; Senft JR
Radiat Res; 1994 Oct; 140(1):31-6. PubMed ID: 7938452
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of anticentromere antibody in blood relatives of anticentromere positive patients.
Ruffatti A; Artifoni L; Glorioso S; Calligaro A; Doria A; Gambari P; Todesco S
J Rheumatol; 1985 Oct; 12(5):940-3. PubMed ID: 3878881
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal aberrations in peripheral blood lymphocytes from patients with dermatomyositis and their first-degree relatives.
Severin E
Rom J Morphol Embryol; 1995; 41(1-2):49-53. PubMed ID: 8680025
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]