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Expert Opinion on Biological Therapy|November 24, 2007
Gene therapy for chronic granulomatous diseaseMartin F Ryser, Joachim Roesler, Marcus Gentsch, et al.Molecular and Cellular Pediatrics|October 14, 2020
A case of recurrent herpes simplex 2 encephalitis, VZV reactivations, and dominant partial interferon-gamma-receptor-1 deficiency supports relevance of IFNgamma for antiviral defense in humansJulia Körholz, Nicole Richter, Jochen Schäfer, et al.The Pediatric Infectious Disease Journal|September 16, 2010
Meningoencephalitis caused by varicella-zoster virus reactivation in a child with dominant partial interferon-gamma receptor-1 deficiencyJoachim Roesler, Christian Hedrich, Martin W Laass, et al.The Pediatric Infectious Disease Journal|June 15, 2004
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 diseaseAngela Rösen-Wolff, Anne Koch, Wilhelm Friedrich, et al.European Journal of Haematology|August 22, 2003
Two German CINCA (NOMID) patients with different clinical severity and response to anti-inflammatory treatmentAngela Rösen-Wolff, Jürgen Quietzsch, Heinz Schröder, et al.Frontiers in Genetics|October 16, 2018
Genetic Diagnostic Elucidation of a Patient With Multiorgan Granulomas, Facial Peculiarities, and Psychomotor RetardationDaniel Soukup, Alma Kuechler, Joachim Roesler, et al.Journal of Pediatric Gastroenterology and Nutrition|September 26, 2003
CARD15 genotype and phenotype analysis in 55 pediatric patients with Crohn disease from Saxony, GermanyLiping Sun, Joachim Roesler, Angela Rösen-Wolff, et al.Plos One|April 20, 2012
P67-phox (NCF2) lacking exons 11 and 12 is functionally active and leads to an extremely late diagnosis of chronic granulomatous disease (CGD)Joachim Roesler, Florian Segerer, Henner Morbach, et al.European Journal of Pediatrics|November 15, 2006
Successful unrelated bone marrow transplantation in a child with chronic granulomatous disease complicated by pulmonary and cerebral granuloma formationCatharina Schuetz, Manfred Hoenig, Ansgar Schulz, et al.Gene|March 7, 2006
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)Andreas Rump, Angela Rösen-Wolff, Manfred Gahr, et al.Pageof 6