Schwarz K - Search Results

1

Successful hematopoietic stem-cell transplantation in a patient with chronic granulomatous disease and McLeod phenotype sensitized to Kx and K antigens.

Hönig M, Flegel WA, Schwarz K, Freihorst JF, Baumann U, Seltsam A, Debatin KM, Schulz AS, Friedrich W. Hönig M, et al. Among authors: schwarz k. Bone Marrow Transplant. 2010 Jan;45(1):209-11. doi: 10.1038/bmt.2009.115. Epub 2009 Jun 8. Bone Marrow Transplant. 2010. PMID: 19503108 Free PMC article. No abstract available.

2

Definition of a critical T cell threshold for prevention of GVHD after HLA non-identical PBPC transplantation in children.

Müller S, Schulz A, Reiss U, Schwarz K, Schreiner T, Wiesneth M, Debatin KM, Friedrich W. Müller S, et al. Among authors: schwarz k. Bone Marrow Transplant. 1999 Sep;24(6):575-81. doi: 10.1038/sj.bmt.1701970. Bone Marrow Transplant. 1999. PMID: 10490721

3

Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients.

Müller SM, Ege M, Pottharst A, Schulz AS, Schwarz K, Friedrich W. Müller SM, et al. Among authors: schwarz k. Blood. 2001 Sep 15;98(6):1847-51. doi: 10.1182/blood.v98.6.1847. Blood. 2001. PMID: 11535520 Free article.

4

Congenital erythrocytosis and polycythemia vera in childhood and adolescence.

Cario H, Schwarz K, Debatin KM, Kohne E. Cario H, et al. Among authors: schwarz k. Klin Padiatr. 2004 May-Jun;216(3):157-62. doi: 10.1055/s-2004-822628. Klin Padiatr. 2004. PMID: 15175960

5

Omenn syndrome: a lack of tolerance on the background of deficient lymphocyte development and maturation.

Hönig M, Schwarz K. Hönig M, et al. Among authors: schwarz k. Curr Opin Rheumatol. 2006 Jul;18(4):383-8. doi: 10.1097/01.bor.0000231907.50290.6f. Curr Opin Rheumatol. 2006. PMID: 16763459 Review.

6

Patients with adenosine deaminase deficiency surviving after hematopoietic stem cell transplantation are at high risk of CNS complications.

Hönig M, Albert MH, Schulz A, Sparber-Sauer M, Schütz C, Belohradsky B, Güngör T, Rojewski MT, Bode H, Pannicke U, Lippold D, Schwarz K, Debatin KM, Hershfield MS, Friedrich W. Hönig M, et al. Among authors: schwarz k. Blood. 2007 Apr 15;109(8):3595-602. doi: 10.1182/blood-2006-07-034678. Epub 2006 Dec 21. Blood. 2007. PMID: 17185467 Free article.

7

Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2.

Pannicke U, Hönig M, Hess I, Friesen C, Holzmann K, Rump EM, Barth TF, Rojewski MT, Schulz A, Boehm T, Friedrich W, Schwarz K. Pannicke U, et al. Among authors: schwarz k. Nat Genet. 2009 Jan;41(1):101-5. doi: 10.1038/ng.265. Epub 2008 Nov 30. Nat Genet. 2009. PMID: 19043417

8

The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events.

Pannicke U, Hönig M, Schulze I, Rohr J, Heinz GA, Braun S, Janz I, Rump EM, Seidel MG, Matthes-Martin S, Soerensen J, Greil J, Stachel DK, Belohradsky BH, Albert MH, Schulz A, Ehl S, Friedrich W, Schwarz K. Pannicke U, et al. Among authors: schwarz k. Hum Mutat. 2010 Feb;31(2):197-207. doi: 10.1002/humu.21168. Hum Mutat. 2010. PMID: 19953608

9

Congenital null mutations of the FOLR1 gene: a progressive neurologic disease and its treatment.

Cario H, Bode H, Debatin KM, Opladen T, Schwarz K. Cario H, et al. Among authors: schwarz k. Neurology. 2009 Dec 15;73(24):2127-9. doi: 10.1212/WNL.0b013e3181c679df. Neurology. 2009. PMID: 20018644 No abstract available.

10

Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation.

Gatz SA, Benninghoff U, Schütz C, Schulz A, Hönig M, Pannicke U, Holzmann KH, Schwarz K, Friedrich W. Gatz SA, et al. Among authors: schwarz k. Bone Marrow Transplant. 2011 Apr;46(4):552-6. doi: 10.1038/bmt.2010.169. Epub 2010 Jul 12. Bone Marrow Transplant. 2011. PMID: 20622910

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