Strategy to prevent neonatal early-onset group B streptococcal (GBS) disease in the Netherlands

Autor: Leo J. Gerards, Jan L. L. Kimpen, Albert H. Adriaanse, Monique A. J. M. Trijbels-Smeulders

Publikováno v: Reviews in Medical Microbiology. 14:35-39

Early-onset group B streptococcal (GBS) infection can be prevented by intrapartum antibiotic prophylaxis. In the USA the effectiveness of this strategy was demonstrated after the introduction of formal guidelines in 1996. In Europe prevention strateg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b76182ad0b9d7aa6d50d2e1a99012ef7
https://doi.org/10.1097/00013542-200301000-00004

Serotypes, genotypes, and antibiotic susceptibility profiles of group B streptococci causing neonatal sepsis and meningitis before and after introduction of antibiotic prophylaxis

Autor: Monique A. J. M. Trijbels-Smeulders, Jan L. L. Kimpen, Judith M. J. E. Bakkers, Wim J B Wannet, Louis A.A. Kollée, Willem J. G. Melchers, Lodewijk Spanjaard, Mieke Hoogkamp-Korstanje

Publikováno v: Pediatric Infectious Disease Journal, 25(10), 945-948. Lippincott Williams & Wilkins
Pediatric Infectious Disease Journal, 25, 10, pp. 945-8
Pediatric infectious disease journal, 25(10), 945-948. Lippincott Williams and Wilkins
Pediatric Infectious Disease Journal, 25, 945-8

Contains fulltext : 35391.pdf (Publisher’s version ) (Closed access) We studied the characteristics of strains isolated from neonates with group B streptococci sepsis and meningitis, before and after the introduction of antibiotic prophylaxis in Th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44748b8d6900c7259366076daaaf1c79
https://doi.org/10.1097/01.inf.0000237821.65559.08

Metabolic studies in older mentally retarded patients: significance of metabolic testing and correlation with the clinical phenotype

Autor: G J, Van Buggenhout, J M, Trijbels, R, Wevers, J C, Trommelen, B C, Hamel, H G, Brunner, J P, Fryns

Publikováno v: Genetic counseling (Geneva, Switzerland). 12(1)

In 471 adult mentally retarded adult patients (mean age 46 years; 92.6% males) living in an institution for the mentally retarded, a clinical examination, cytogenetic and molecular studies were done. 306 patients were screened for metabolic disorders

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::37ce482acb866166d72e48845326e4ba
https://pubmed.ncbi.nlm.nih.gov/11332972

Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I

Autor: R H, Triepels, L P, van den Heuvel, J L, Loeffen, C A, Buskens, R J, Smeets, M E, Rubio Gozalbo, S M, Budde, E C, Mariman, F A, Wijburg, P G, Barth, J M, Trijbels, J A, Smeitink

Publikováno v: Annals of neurology. 45(6)

Leigh syndrome is the phenotypical expression of a genetically heterogeneous cluster of disorders, with pyruvate dehydrogenase complex deficiency and respiratory chain disorders as the main biochemical causes. We report the first missense mutation wi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f68c71cf99f7a0d5893c072f9d589dd4
https://pubmed.ncbi.nlm.nih.gov/10360760

Detection and identification of 6-methylmercapto-8-hydoxypurine, a major metabolite of 6-mercaptopurine, in plasma during intravenous administration

Autor: C W, Keuzenkamp-Jansen, J M, van Baal, R A, De Abreu, J G, de Jong, R, Zuiderent, J M, Trijbels

Publikováno v: Clinical chemistry. 42(3)

6-Mercaptopurine, a hypoxanthine antimetabolite, is used in the treatment of acute lymphoblastic leukemia (ALL) in children. Extensively metabolized before it exerts cytotoxic action, it is catabolized into 6-mercapto-2,8-dihydroxypurine (thiouric ac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::42cc7e44a3aacc60a7347a748976ad15
https://pubmed.ncbi.nlm.nih.gov/8598099