Zobrazeno 1 - 10
of 61
pro vyhledávání: '"B. Sölder"'
Publikováno v:
Lung. 176:337-344
Neopterin is produced and released by human macrophages in response to stimulation with interferon-gamma and changes in neopterin concentrations indicate cellular immune activation. Pulmonary infection with Mycobacterium tuberculosis is also associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b2dc9c9bb7018df27e1c75dfb7237e
https://doi.org/10.1007/pl00007615
https://doi.org/10.1007/pl00007615
Publikováno v:
Clinical Pediatrics. 37:521-530
Dyskeratosis congenita (DC) is a rare, predominantly X-linked multisystemic disorder. It demonstrates a wide spectrum of clinical manifestations and typically presents with dermatologic symptoms during the first decade of life. This review of the lit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0175dbb15fb88b5cbccc9661099be300
https://doi.org/10.1177/000992289803700901
https://doi.org/10.1177/000992289803700901
Autor:
Bernd H. Belohradsky, Josef Eberle, Theoni Petropoulou, Florian Hoffmann, Uwe Wintergerst, Gundula Notheis, Lutz Gürtler, B. Sölder
Publikováno v:
The Pediatric Infectious Disease Journal. 17:495-499
Objective. The effects of two antiretroviral triple combinations including the protease inhibitor indinavir on the surrogate markers, viral load and CD4 cells were evaluated. Methods. Fifteen patients with high viral load or disease progression under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2d81ef906600d56e1bd279973ba54d8
https://doi.org/10.1097/00006454-199806000-00012
https://doi.org/10.1097/00006454-199806000-00012
Autor:
A. Malcolm R. Taylor, Pamela S. Karnes, Karen M. Cerosaletti, Michael Boehnke, Patrick Concannon, Kenshi Komatsu, Dominique Smeets, Heather M. Stringham, Richard A. Gatti, Ethan M. Lange, B. Sölder, Bernd H. Belohradsky, Alison M. Elliott, Corry M.R. Weemaes
Publikováno v:
American Journal of Human Genetics, 63, 125-135
American Journal of Human Genetics, 63, pp. 125-135
American Journal of Human Genetics, 63, pp. 125-135
Summary Nijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by microcephaly, a birdlike face, growth retardation, immunodeficiency, lack of secondary sex characteristics in females, and increased incidence of lymphoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8145020406e55c1095e49a75e8c72f49
https://doi.org/10.1086/301927
https://doi.org/10.1086/301927
Publikováno v:
World Journal of Surgery. 21:520-523
Although its protective effect is contested and the risk of contracting tuberculosis is rather low nowadays, BCG vaccination is frequently performed. Changes of strain repeatedly led to an increased complication rate. In Austria between 1990 and 1991
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33bb53aed32b20d9bc725e83f3d23198
https://doi.org/10.1007/pl00012279
https://doi.org/10.1007/pl00012279
Autor:
H. Jäger, Boris Rolinski, Johannes R. Bogner, Bernd H. Belohradsky, Uwe Wintergerst, E. Wolf, Adelbert A. Roscher, B. Sölder
Publikováno v:
Europe PubMed Central
The feasibility of rectal administration of didanosine (DDI) was studied in six human immunodeficiency virus-infected patients. After oral intake of a DDI solution (100 mg/m 2 of body surface area) combined with an antacid (Maalox), pharmacokinetic p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09c21732cd3cc0b53e8b7da5bdc04b04
https://doi.org/10.1128/aac.43.3.699
https://doi.org/10.1128/aac.43.3.699
Autor:
Satoru Endo, Kenshi Komatsu, Yusuke Nakamura, Minoru Isomura, Shinya Matsuura, Asako Nakamura, Bernd H. Belohradsky, B. Sölder, Dominique Smeets, Shuichi Sakamoto, Mitsuo Oshimura, Noriko Kondo, Hiroshi Tauchi, Vazken M. Der Kaloustian
Publikováno v:
Nature Genetics, 19, 179-181
Nature Genetics, 19, pp. 179-181
Nature Genetics, 19, pp. 179-181
Nijmegen breakage syndrome (NBS), also known as ataxia-telangiectasia (AT) variant, is an autosomal recessive disorder characterized by microcephaly, growth retardation, severe combined immunodeficiency and a high incidence of lymphoid cancers. Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3877b73e83251303ac05020d1e66974
https://doi.org/10.1038/549
https://doi.org/10.1038/549
Autor:
B, Sölder
Publikováno v:
Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege. 15(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df8e44ca22619e84ed2262d4c0e5b427
https://pubmed.ncbi.nlm.nih.gov/8715185
https://pubmed.ncbi.nlm.nih.gov/8715185
Publikováno v:
Infection. 22(1)
Several European countries report a decreasing prevalence of antibodies to hepatitis A virus (anti-HAV). This trend is most pronounced in the youngest age groups. In 1979, however, 58% of young Austrians aged 20 to 30 years were shown to possess anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc57c8e658ae9e20facef2e1fa677387
https://pubmed.ncbi.nlm.nih.gov/8181844
https://pubmed.ncbi.nlm.nih.gov/8181844
Publikováno v:
Zeitschrift fur Geburtshilfe und Perinatologie. 196(3)
The influence of serotonine, a vasoactive neurotransmitter, on the spontaneous motility of uterine strips was investigated. A highly significant (p less than 0.001) increase of uterine activity was observed when serotonine 10(-6) M was added to the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9a421fdb935a637702f95f2951eee33d
https://pubmed.ncbi.nlm.nih.gov/1496845
https://pubmed.ncbi.nlm.nih.gov/1496845