Schneider W - Search Results

1

No large deletions of mitochondrial DNA in acquired idiopathic sideroblastic anemia (AISA).

Gattermann N, Lotz H, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Am J Hematol. 1992 Dec;41(4):297. doi: 10.1002/ajh.2830410418. Am J Hematol. 1992. PMID: 1288294 No abstract available.

2

Is acquired idiopathic sideroblastic anemia (AISA) a disorder of mitochondrial DNA?

Gattermann N, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Leukemia. 1993 Dec;7(12):2069-76. Leukemia. 1993. PMID: 8255108 Review. No abstract available.

3

Heteroplasmic point mutations of mitochondrial DNA affecting subunit I of cytochrome c oxidase in two patients with acquired idiopathic sideroblastic anemia.

Gattermann N, Retzlaff S, Wang YL, Hofhaus G, Heinisch J, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Blood. 1997 Dec 15;90(12):4961-72. Blood. 1997. PMID: 9389715 Free article.

4

Two types of acquired idiopathic sideroblastic anaemia (AISA).

Gattermann N, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Br J Haematol. 1990 Jan;74(1):45-52. doi: 10.1111/j.1365-2141.1990.tb02536.x. Br J Haematol. 1990. PMID: 2310696

5

Risk of leukemic transformation in two types of acquired idiopathic sideroblastic anemia.

Gattermann N, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Haematol Blood Transfus. 1990;33:374-81. doi: 10.1007/978-3-642-74643-7_71. Haematol Blood Transfus. 1990. PMID: 2323645 No abstract available.

6

A heteroplasmic point mutation of mitochondrial tRNALeu(CUN) in non-lymphoid haemopoietic cell lineages from a patient with acquired idiopathic sideroblastic anaemia.

Gattermann N, Retzlaff S, Wang YL, Berneburg M, Heinisch J, Wlaschek M, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Br J Haematol. 1996 Jun;93(4):845-55. doi: 10.1046/j.1365-2141.1996.d01-1724.x. Br J Haematol. 1996. PMID: 8703816

7

Detection of the ageing-associated 5-Kb common deletion of mitochondrial DNA in blood and bone marrow of hematologically normal adults. Absence of the deletion in clonal bone marrow disorders.

Gattermann N, Berneburg M, Heinisch J, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Leukemia. 1995 Oct;9(10):1704-10. Leukemia. 1995. PMID: 7564514

8

No improvement of refractory sideroblastic anaemia with ubidecarenone.

Gattermann N, Briviba K, Tsamaloukas A, Aul C, Schneider W. Gattermann N, et al. Among authors: schneider w. Lancet. 1995 Apr 29;345(8957):1121-2. doi: 10.1016/s0140-6736(95)90854-4. Lancet. 1995. PMID: 7715371 No abstract available.

9

Antiphospholipid syndrome complicating chronic graft-versus-host disease after allogeneic bone marrow transplantation.

Sõhngen D, Heyll A, Meckenstock G, Aul C, Wolf HH, Schneider W, Specker C, Withold W. Sõhngen D, et al. Among authors: schneider w. Am J Hematol. 1994 Oct;47(2):143-4. doi: 10.1002/ajh.2830470218. Am J Hematol. 1994. PMID: 8092133 No abstract available.

10

T-cell receptor gamma/delta expressing acute leukemia emerging from sideroblastic anemia: morphological, immunological, and cytogenetic features.

Meckenstock G, Fonatsch C, Heyll A, Schneider EM, Kögler G, Söhngen D, Aul C, Schneider W. Meckenstock G, et al. Among authors: schneider em, schneider w. Leuk Res. 1992;16(4):379-84. doi: 10.1016/0145-2126(92)90140-3. Leuk Res. 1992. PMID: 1373459

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