Schroeder-Kurth T - Search Results

1

Variable response to the diepoxybutane test in two dizygotic twins with Fanconi's anemia and flow cytometry for diagnosis confirmation.

Toraldo R, Canino G, Tolone C, D'Avanzo M, Porfirio B, Hoehn H, Schroeder-Kurth T, Pistoia V. Toraldo R, et al. Among authors: schroeder kurth t. Pediatr Hematol Oncol. 1998 Jan-Feb;15(1):45-54. doi: 10.3109/08880019809009507. Pediatr Hematol Oncol. 1998. PMID: 9509505

2

Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia.

Seyschab H, Friedl R, Sun Y, Schindler D, Hoehn H, Hentze S, Schroeder-Kurth T. Seyschab H, et al. Among authors: schroeder kurth t. Blood. 1995 Apr 15;85(8):2233-7. Blood. 1995. PMID: 7718895 Free article.

3

Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience.

Altay C, Alikaşifoglu M, Kara A, Tunçbilek E, Ozbek N, Schroeder-Kurth TM. Altay C, et al. Among authors: schroeder kurth tm. Clin Genet. 1997 May;51(5):296-302. doi: 10.1111/j.1399-0004.1997.tb02477.x. Clin Genet. 1997. PMID: 9212176

4

International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity.

Auerbach AD, Rogatko A, Schroeder-Kurth TM. Auerbach AD, et al. Blood. 1989 Feb;73(2):391-6. Blood. 1989. PMID: 2917181 Free article.

5

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype.

Joenje H, Lo ten Foe JR, Oostra AB, van Berkel CG, Rooimans MA, Schroeder-Kurth T, Wegner RD, Gille JJ, Buchwald M, Arwert F. Joenje H, et al. Among authors: schroeder kurth t. Blood. 1995 Sep 15;86(6):2156-60. Blood. 1995. PMID: 7662964 Free article.

6

Fanconi anemia complementation group E: clinical and cytogenetic data of the first patient.

Wegner RD, Henrichs I, Joenje H, Schroeder-Kurth T. Wegner RD, et al. Among authors: schroeder kurth t. Clin Genet. 1996 Dec;50(6):479-82. doi: 10.1111/j.1399-0004.1996.tb02716.x. Clin Genet. 1996. PMID: 9147877

7

[Treatment of Fanconi anemia by bone marrow transplantation].

Friedrich W, Ebell W, Blütters-Sawatzki R, Junker A, Hübener KH, Schroeder-Kurth T, Kohne E, Kleihauer E. Friedrich W, et al. Monatsschr Kinderheilkd. 1987 May;135(5):253-8. Monatsschr Kinderheilkd. 1987. PMID: 3302684 German.

8

Position of chromosomes in the human interphase nucleus. An analysis of nonhomologous chromatid translocations in lymphocyte cultures after Trenimon treatment and from patients with Fanconi's anemia and Bloom's syndrome.

Hager HD, Schroeder-Kurth TM, Vogel F. Hager HD, et al. Hum Genet. 1982;61(4):342-56. doi: 10.1007/BF00276599. Hum Genet. 1982. PMID: 7152519

9

Clinical, cytogenetic and molecular investigations in three patients with Wolf-Hirschhorn syndrome.

Thies U, Back E, Wolff G, Schroeder-Kurth T, Hager HD, Schröder K. Thies U, et al. Clin Genet. 1992 Oct;42(4):201-5. doi: 10.1111/j.1399-0004.1992.tb03238.x. Clin Genet. 1992. PMID: 1424245

10

Quality of life of adults with trisomy 21 living in mental retardation homes compared with those staying under parental care.

Schroeder-Kurth TM, Schaffert G, Koeckritz W, Kernich M. Schroeder-Kurth TM, et al. Am J Med Genet Suppl. 1990;7:317-21. doi: 10.1002/ajmg.1320370763. Am J Med Genet Suppl. 1990. PMID: 2149970

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