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Human Pathology|June 11, 2005
Autoimmune enteric leiomyositis: a rare cause of chronic intestinal pseudo-obstruction with specific morphological featuresSusanne Haas, Lutz Bindl, Hans-Peter Fischer
Critical Care Medicine|January 13, 2005
Incidence of acute respiratory distress syndrome in German children and adolescents: a population-based studyLutz Bindl, Katja Dresbach, Michael J Lentze
The Journal of Clinical Endocrinology and Metabolism|May 8, 2002
Induction of adipocyte differentiation by a thiazolidinedione in cultured, subepidermal, fibroblast-like cells of an infant with congenital generalized lipodystrophyPamela Fischer, Peter Möller, Lutz Bindl, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|October 5, 2007
Congenital cystic adenomatoid malformation type 0-a rare cause of neonatal deathStefan Stuhrmann, Jörg Sachweh, Lutz Bindl, et al.
The Journal of Pediatrics|August 30, 2005
Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome)Lutz Bindl, Troy Torgerson, Lucia Perroni, et al.
American Journal of Medical Genetics|September 5, 2002
Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrationsHartmut Engels, Kristin Bosse, Antje Ehrbrecht, et al.
Journal of the Pediatric Infectious Diseases Society|December 2, 2015
Antiviral Drug-Resistance Typing Reveals Compartmentalization and Dynamics of Acyclovir-Resistant Herpes Simplex Virus Type-2 (HSV-2) in a Case of Neonatal HerpesManon Bache, Graciela Andrei, Lutz Bindl, et al.
Emerging Infectious Diseases|March 11, 2005
Human metapneumovirus RNA in encephalitis patientOliver Schildgen, Thomas Glatzel, Tilman Geikowski, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 3, 2013
Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2)Emmanuel Scalais, Ronit Chafai, Rudy Van Coster, et al.
Frontiers in Microbiology|May 18, 2017
Colonization and Succession within the Human Gut Microbiome by Archaea, Bacteria, and Microeukaryotes during the First Year of LifeLinda Wampach, Anna Heintz-Buschart, Angela Hogan, et al.
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