Search Results - "BINDL, Lutz"
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Birth mode is associated with earliest strain-conferred gut microbiome functions and immunostimulatory potential
Published in Nature communications (30-11-2018)“…The rate of caesarean section delivery (CSD) is increasing worldwide. It remains unclear whether disruption of mother-to-neonate transmission of microbiota…”
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Colonization and Succession within the Human Gut Microbiome by Archaea, Bacteria, and Microeukaryotes during the First Year of Life
Published in Frontiers in microbiology (02-05-2017)“…Perturbations to the colonization process of the human gastrointestinal tract have been suggested to result in adverse health effects later in life. Although…”
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Phenotypic and Genetic Heterogeneity in Congenital Generalized Lipodystrophy
Published in The journal of clinical endocrinology and metabolism (01-10-2003)“…Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by near complete absence of adipose tissue from birth…”
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Incidence of acute respiratory distress syndrome in German children and adolescents: A population-based study
Published in Critical care medicine (01-01-2005)“…OBJECTIVE:The objective of this study was to determine the epidemiology of acute respiratory distress syndrome (ARDS) in children and adolescents aged 1 mo to…”
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Human metapneumovirus RNA in encephalitis patient
Published in Emerging infectious diseases (01-03-2005)“…We describe a fatal case of encephalitis that might be correlated with primary human metapneumovirus (HMPV) encephalitis. Postmortem HMPV RNA was detected in…”
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Plasma levels of 24S-hydroxycholesterol reflect the balance between cerebral production and hepatic metabolism and are inversely related to body surface
Published in Journal of lipid research (01-05-2000)“…We have previously presented evidence that most of the 24S-hydroxycholesterol present in the circulation originates from the brain and that most of the…”
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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 )
Published in European journal of paediatric neurology (01-11-2013)“…Abstract Background Primary coenzyme Q10 (CoQ10) deficiencies are heterogeneous autosomal recessive disorders. CoQ2 mutations have been identified only rarely…”
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International, multicentre, observational study of fluid bolus therapy in neonates
Published in Journal of paediatrics and child health (01-06-2019)“…Aim To assess the prevalence, types and indications for fluid bolus therapy in neonates with haemodynamic compromise. Methods This was a pragmatic,…”
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Successful Use of the New Immune-suppressor Sirolimus in IPEX (Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked Syndrome)
Published in The Journal of pediatrics (01-08-2005)“…IPEX (immune-dysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome is an autoimmune disorder with an often lethal outcome in spite of…”
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Autoimmune enteric leiomyositis: A rare cause of chronic intestinal pseudo-obstruction with specific morphological features
Published in Human pathology (01-05-2005)“…Autoimmune enteric leiomyositis is an extraordinary rare cause of acquired chronic intestinal pseudo-obstruction in children. We report a 5-year-old girl who…”
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Antiviral Drug-Resistance Typing Reveals Compartmentalization and Dynamics of Acyclovir-Resistant Herpes Simplex Virus Type-2 (HSV-2) in a Case of Neonatal Herpes
Published in Journal of the Pediatric Infectious Diseases Society (01-06-2014)“…A neonate suffering from herpes simplex virus type 2 disease with central nervous system involvement developed an early recurrence under acyclovir therapy…”
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Treatment with bovine surfactant in severe acute respiratory distress syndrome in children: a randomized multicenter study
Published in Intensive care medicine (01-03-2003)“…To determine whether bovine surfactant given in cases of severe pediatric acute respiratory distress syndrome (ARDS) improves oxygenation. Single-center study…”
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4G/5G promoter polymorphism in the plasminogen-activator-inhibitor-1 gene in children with systemic meningococcaemia
Published in European journal of pediatrics (01-08-2005)“…Meningococcal disease may present as sepsis, meningitis or a combination of both. Impaired fibrinolysis and massive elevation of the plasminogen activator…”
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Gender-based differences in children with sepsis and ARDS: The ESPNIC ARDS Database Group
Published in Intensive care medicine (01-10-2003)“…Male gender predisposes to severe sepsis and septic shock. This effect has been ascribed to higher levels of testosterone. The ESPNIC ARDS database was…”
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Congenital cystic adenomatoid malformation type 0-a rare cause of neonatal death
Published in Pediatric critical care medicine (01-11-2007)“…We give the first account of failure of extracorporeal membrane oxygenation therapy secondary to congenital cystic malformation of the lung (CCAM) type 0. Case…”
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Induction of Adipocyte Differentiation by a Thiazolidinedione in Cultured, Subepidermal, Fibroblast-Like Cells of an Infant with Congenital Generalized Lipodystrophy
Published in The journal of clinical endocrinology and metabolism (01-05-2002)“…Congenital generalized lipodystrophy (CGL) is characterized by the absence of adipose tissue from birth due to a hypothetical differentiation block. The…”
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High Plasma Levels of Phytosterols in Patients on Parenteral Nutrition: A Marker of Liver Dysfunction
Published in Journal of pediatric gastroenterology and nutrition (01-09-2000)Get full text
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High Plasma Levels of Phytosterols in Patients on Parenteral Nutrition: A Marker of Liver Dysfunction
Published in Journal of pediatric gastroenterology and nutrition (01-09-2000)Get full text
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Dual versus triple therapy of Helicobacter pylori infection: results of a multicentre trial
Published in Archives of disease in childhood (01-07-1999)“…OBJECTIVE To compare dual therapy (omeprazole and amoxicillin) with triple therapy (omeprazole, amoxicillin, and clarithromycin) in the treatment…”
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