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Pediatric Rheumatology Online Journal|September 19, 2023
Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositisTimmy Strauss, Claudia Günther, Anja Schnabel, et al.Journal of Pediatric Hematology/Oncology|March 8, 2005
Mucoepidermoid carcinoma as an unusual cause for recurrent respiratory infections in a childChristian Vogelberg, Brigitte Mohr, Guido Fitze, et al.Pediatric Nephrology (Berlin, Germany)|March 10, 2004
Tuberous sclerosis and polycystic kidney disease in a 3-month-old infantMartin W Laass, Miriam Spiegel, Anna Jauch, et al.The Journal of General Virology|January 22, 2005
Dendritic-cell infection by human cytomegalovirus is restricted to strains carrying functional UL131-128 genes and mediates efficient viral antigen presentation to CD8+ T cellsGiuseppe Gerna, Elena Percivalle, Daniele Lilleri, et al.Clinical Rheumatology|October 2, 2010
Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment optionsChristian Michael Hedrich, Hildegard Zappel, Simon Straub, et al.Journal of Pediatric Hematology/Oncology|January 10, 2009
Chronic granulomatous disease (CGD) mimicking neoplasms: a suspected mediastinal teratoma unmasking as thymic granulomas due to X-linked CGD, and 2 related casesFabian Hauck, Sabine Heine, Rita Beier, et al.The Pediatric Infectious Disease Journal|March 5, 2003
Capofungin therapy for Aspergillus lung infection in a boy with chronic granulomatous diseaseSvea Sallmann, Antje Heilmann, Frank Heinke, et al.Pediatric Radiology|April 5, 2016
Safety of gadobutrol in more than 1,000 pediatric patients: subanalysis of the GARDIAN study, a global multicenter prospective non-interventional studyKatja Glutig, Ravi Bhargava, Gabriele Hahn, et al.Journal of Child Neurology|August 12, 2006
Selenoprotein N muscular dystrophy: differential diagnosis for early-onset limited mobility of the spineStefanie Sponholz, Maja von der Hagen, Gabriele Hahn, et al.Neuropediatrics|March 9, 2016
Novel Mutation in the DKC1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome As a Rare Differential Diagnosis in Pontocerebellar Hypoplasia, Primary Microcephaly, and Progressive Bone Marrow FailureMaria Dehmel, Sebastian Brenner, Meinolf Suttorp, et al.Pageof 8