Kohne E - Search Results

1

Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea.

Allard P, Alhaj N, Lobitz S, Cario H, Jarisch A, Grosse R, Oevermann L, Hakimeh D, Tagliaferri L, Kohne E, Kopp-Schneider A, Kulozik AE, Kunz JB. Allard P, et al. Among authors: kohne e. Haematologica. 2022 Jul 1;107(7):1577-1588. doi: 10.3324/haematol.2021.278952. Haematologica. 2022. PMID: 34706496 Free PMC article.

2

[The molecular basis of hereditary persistence of fetal hemoglobin (HPFH). Clinical importance of the hemoglobin switching mechanism with special reference to Corfu delta beta zero thalassemia].

Kulozik AE, Kohne E, Kleihauer E. Kulozik AE, et al. Among authors: kohne e. Monatsschr Kinderheilkd. 1988 Nov;136(11):751-7. Monatsschr Kinderheilkd. 1988. PMID: 2464759 German.

3

Rapid and non-radioactive prenatal diagnosis of beta thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR).

Kulozik AE, Lyons J, Kohne E, Bartram CR, Kleihauer E. Kulozik AE, et al. Among authors: kohne e. Br J Haematol. 1988 Dec;70(4):455-8. doi: 10.1111/j.1365-2141.1988.tb02516.x. Br J Haematol. 1988. PMID: 3219295

4

[Monitoring pregnant patients from risk countries with sickle cell disease and thalassemia. Clinical aspects, screening and prenatal diagnosis].

Dickerhoff R, Kulozik AE, Kohne E. Dickerhoff R, et al. Among authors: kohne e. Geburtshilfe Frauenheilkd. 1993 Apr;53(4):215-21. doi: 10.1055/s-2007-1023668. Geburtshilfe Frauenheilkd. 1993. PMID: 8491363 Review. German.

5

Thalassemia intermedia: compound heterozygous beta zero/beta(+)-thalassemia and co-inherited heterozygous alpha(+)-thalassemia.

Kulozik AE, Kohne E, Kleihauer E. Kulozik AE, et al. Among authors: kohne e. Ann Hematol. 1993 Jan;66(1):51-4. doi: 10.1007/BF01737689. Ann Hematol. 1993. PMID: 8431522

6

Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis.

Rives S, Pahl HL, Florensa L, Bellosillo B, Neusuess A, Estella J, Debatin KM, Kohne E, Schwarz K, Cario H. Rives S, et al. Among authors: kohne e. Haematologica. 2007 May;92(5):674-7. doi: 10.3324/haematol.10787. Haematologica. 2007. PMID: 17488692 Free article.

7

[Beta thalassemia in Germany: molecular genetics and clinical phenotype in immigrant and in the native population].

Schwarz C, Vetter B, Kohne E, Kulozik AE. Schwarz C, et al. Among authors: kohne e. Klin Padiatr. 1997 Jul-Aug;209(4):172-7. doi: 10.1055/s-2008-1043946. Klin Padiatr. 1997. PMID: 9340427 German.

8

Treatment with hydroxyurea in thalassemia intermedia with paravertebral pseudotumors of extramedullary hematopoiesis.

Cario H, Wegener M, Debatin KM, Kohne E. Cario H, et al. Among authors: kohne e. Ann Hematol. 2002 Aug;81(8):478-82. doi: 10.1007/s00277-002-0501-4. Epub 2002 Aug 15. Ann Hematol. 2002. PMID: 12224008

9

A deletion/inversion rearrangement of the beta-globin gene cluster in a Turkish family with delta beta zero-thalassemia intermedia.

Kulozik AE, Bellan-Koch A, Kohne E, Kleihauer E. Kulozik AE, et al. Among authors: kohne e. Blood. 1992 May 1;79(9):2455-9. Blood. 1992. PMID: 1571556 Free article.

10

Beta-thalassaemia in the immigrant and non-immigrant German populations.

Vetter B, Schwarz C, Kohne E, Kulozik AE. Vetter B, et al. Among authors: kohne e. Br J Haematol. 1997 May;97(2):266-72. doi: 10.1046/j.1365-2141.1997.342674.x. Br J Haematol. 1997. PMID: 9163586 Free article.

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