Rösen-Wolff A - Search Results

1

Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease.

Chapgier A, Boisson-Dupuis S, Jouanguy E, Vogt G, Feinberg J, Prochnicka-Chalufour A, Casrouge A, Yang K, Soudais C, Fieschi C, Santos OF, Bustamante J, Picard C, de Beaucoudrey L, Emile JF, Arkwright PD, Schreiber RD, Rolinck-Werninghaus C, Rösen-Wolff A, Magdorf K, Roesler J, Casanova JL. Chapgier A, et al. PLoS Genet. 2006 Aug 18;2(8):e131. doi: 10.1371/journal.pgen.0020131. PLoS Genet. 2006. PMID: 16934001 Free PMC article.

2

Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD).

Gentsch M, Kaczmarczyk A, van Leeuwen K, de Boer M, Kaus-Drobek M, Dagher MC, Kaiser P, Arkwright PD, Gahr M, Rösen-Wolff A, Bochtler M, Secord E, Britto-Williams P, Saifi GM, Maddalena A, Dbaibo G, Bustamante J, Casanova JL, Roos D, Roesler J. Gentsch M, et al. Hum Mutat. 2010 Feb;31(2):151-8. doi: 10.1002/humu.21156. Hum Mutat. 2010. PMID: 19953534 Free article.

3

Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-gamma-receptor (IFNgammaR1) deficiency: mutational analysis and evaluation of therapeutic options.

Roesler J, Kofink B, Wendisch J, Heyden S, Paul D, Friedrich W, Casanova JL, Leupold W, Gahr M, Rösen-Wolff A. Roesler J, et al. Exp Hematol. 1999 Sep;27(9):1368-74. doi: 10.1016/s0301-472x(99)00077-6. Exp Hematol. 1999. PMID: 10480427 Free article. Review.

4

Redundant ability of phagocytes to kill Aspergillus species.

Roesler J, Rösen-Wolff A. Roesler J, et al. J Allergy Clin Immunol. 2011 Sep;128(3):686-7; author reply 687-8. doi: 10.1016/j.jaci.2011.05.018. J Allergy Clin Immunol. 2011. PMID: 21689849 No abstract available.

5

A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD).

Rump A, Rösen-Wolff A, Gahr M, Seidenberg J, Roos C, Walter L, Günther V, Roesler J. Rump A, et al. Gene. 2006 Apr 26;371(2):174-81. doi: 10.1016/j.gene.2005.11.036. Epub 2006 Mar 3. Gene. 2006. PMID: 16516412

6

Meningoencephalitis caused by varicella-zoster virus reactivation in a child with dominant partial interferon-gamma receptor-1 deficiency.

Roesler J, Hedrich C, Laass MW, Heyne K, Rösen-Wolff A. Roesler J, et al. Pediatr Infect Dis J. 2011 Mar;30(3):265-6. doi: 10.1097/INF.0b013e3181f6f78a. Pediatr Infect Dis J. 2011. PMID: 20842068

7

CARD15 genotype and phenotype analysis in 55 pediatric patients with Crohn disease from Saxony, Germany.

Sun L, Roesler J, Rösen-Wolff A, Winkler U, Koch R, Thürigen A, Henker J. Sun L, et al. J Pediatr Gastroenterol Nutr. 2003 Oct;37(4):492-7. doi: 10.1097/00005176-200310000-00017. J Pediatr Gastroenterol Nutr. 2003. PMID: 14508222

8

X-linked chronic granulomatous disease (CGD) caused by an intra-exonic splice mutation (CYBB exon 3, c.262G->A) is mimicking juvenile sarcoidosis.

Brunner J, Dockter G, Rösen-Wolff A, Roesler J. Brunner J, et al. Clin Exp Rheumatol. 2007 Mar-Apr;25(2):336-8. Clin Exp Rheumatol. 2007. PMID: 17543165

9

Successful elimination of an invasive Aspergillus nidulans lung infection by voriconazole after failure of a combination of caspofungin and liposomal amphotericin B in a boy with chronic granulomatous disease.

Rösen-Wolff A, Koch A, Friedrich W, Hahn G, Gahr M, Roesler J. Rösen-Wolff A, et al. Pediatr Infect Dis J. 2004 Jun;23(6):584-6. doi: 10.1097/01.inf.0000130741.01940.ff. Pediatr Infect Dis J. 2004. PMID: 15194848

10

Influence of CARD15 mutations on disease activity and response to therapy in 65 pediatric Crohn patients from Saxony, Germany.

Roesler J, Thürigen A, Sun L, Koch R, Winkler U, Laass MW, Gahr M, Rösen-Wolff A, Henker J. Roesler J, et al. J Pediatr Gastroenterol Nutr. 2005 Jul;41(1):27-32. doi: 10.1097/01.mpg.0000165017.00562.27. J Pediatr Gastroenterol Nutr. 2005. PMID: 15990626

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