Schulz A - Search Results

1

Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API).

Speckmann C, Nennstiel U, Hönig M, Albert MH, Ghosh S, Schuetz C, Brockow I, Hörster F, Niehues T, Ehl S, Wahn V, Borte S, Lehmberg K, Baumann U, Beier R, Krüger R, Bakhtiar S, Kuehl JS, Klemann C, Kontny U, Holzer U, Meinhardt A, Morbach H, Naumann-Bartsch N, Rothoeft T, Kreins AY, Davies EG, Schneider DT, Bernuth HV, Klingebiel T, Hoffmann GF, Schulz A, Hauck F. Speckmann C, et al. Among authors: schulz a. J Clin Immunol. 2023 Jul;43(5):965-978. doi: 10.1007/s10875-023-01450-6. Epub 2023 Feb 27. J Clin Immunol. 2023. PMID: 36843153 Free PMC article.

2

Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning.

Classen CF, Schulz AS, Sigl-Kraetzig M, Hoffmann GF, Simmonds HA, Fairbanks L, Debatin KM, Friedrich W. Classen CF, et al. Among authors: schulz as. Bone Marrow Transplant. 2001 Jul;28(1):93-6. doi: 10.1038/sj.bmt.1703100. Bone Marrow Transplant. 2001. PMID: 11498751

3

Immune reconstitution in congenital disorders after HLA-haploidentical hemopoietic stem cell transplantation.

Friedrich W, Hönig M, Schulz A, Müller SM. Friedrich W, et al. Among authors: schulz a. Blood Cells Mol Dis. 2004 Nov-Dec;33(3):291-3. doi: 10.1016/j.bcmd.2004.08.020. Blood Cells Mol Dis. 2004. PMID: 15528147 No abstract available.

4

A novel mutation in the interleukin-2 receptor gamma gene as the cause of lymphopenia in a neonate vertically exposed to human immunodeficiency virus.

Neubert J, Meindl A, Theisen A, Adams O, Schulz A, Feyen O, Niehues T. Neubert J, et al. Among authors: schulz a. Pediatr Infect Dis J. 2005 Feb;24(2):187-9. doi: 10.1097/01.inf.0000148934.36915.5d. Pediatr Infect Dis J. 2005. PMID: 15702055

5

Stem cell transplantation in children with infantile osteopetrosis is associated with a high incidence of VOD, which could be prevented with defibrotide.

Corbacioglu S, Hönig M, Lahr G, Stöhr S, Berry G, Friedrich W, Schulz AS. Corbacioglu S, et al. Among authors: schulz as. Bone Marrow Transplant. 2006 Oct;38(8):547-53. doi: 10.1038/sj.bmt.1705485. Epub 2006 Sep 4. Bone Marrow Transplant. 2006. PMID: 16953210 Clinical Trial.

6

Schuetz C, Hoenig M, Schulz A, Lee-Kirsch MA, Roesler J, Friedrich W, von Bernuth H. Schuetz C, et al. Among authors: schulz a. Eur J Pediatr. 2007 Aug;166(8):785-8. doi: 10.1007/s00431-006-0317-7. Epub 2006 Nov 14. Eur J Pediatr. 2007. PMID: 17103189

7

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: schulz a. 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.

8

An immunodeficiency disease with RAG mutations and granulomas.

Schuetz C, Huck K, Gudowius S, Megahed M, Feyen O, Hubner B, Schneider DT, Manfras B, Pannicke U, Willemze R, Knüchel R, Göbel U, Schulz A, Borkhardt A, Friedrich W, Schwarz K, Niehues T. Schuetz C, et al. Among authors: schulz a. N Engl J Med. 2008 May 8;358(19):2030-8. doi: 10.1056/NEJMoa073966. N Engl J Med. 2008. PMID: 18463379 Free article.

9

Results and long-term outcome in 39 patients with Wiskott-Aldrich syndrome transplanted from HLA-matched and -mismatched donors.

Friedrich W, Schütz C, Schulz A, Benninghoff U, Hönig M. Friedrich W, et al. Among authors: schulz a. Immunol Res. 2009;44(1-3):18-24. doi: 10.1007/s12026-008-8063-8. Immunol Res. 2009. PMID: 18846321

10

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: schulz a. Nat Genet. 2009 Jan;41(1):101-5. doi: 10.1038/ng.265. Epub 2008 Nov 30. Nat Genet. 2009. PMID: 19043417

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