Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Diego Buriot"'
Autor:
Diego Buriot
Publikováno v:
International Seminar on Nuclear War and Planetary Emergencies — 40th Session.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16379a886df9b46b348405f03a945547
https://doi.org/10.1142/9789814289139_0032
https://doi.org/10.1142/9789814289139_0032
Autor:
Diego Buriot
Publikováno v:
International Seminar on Nuclear War and Planetary Emergencies — 32nd Session.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddac7bfafc1fbec2abb8a712eaef447d
https://doi.org/10.1142/9789812701787_0023
https://doi.org/10.1142/9789812701787_0023
Autor:
Diego Buriot
Publikováno v:
International Seminar on Nuclear War and Planetary Emergencies — 30th Session.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a955aedba135a2b257768d45b8afef95
https://doi.org/10.1142/9789812702753_0023
https://doi.org/10.1142/9789812702753_0023
Publikováno v:
American Journal of Hematology. 5:355-363
Acquired von Willebrand syndrome is reported in a 16-year-old girl with systemic lupus erythematosus. Routine coagulation studies showed a normal platelet count, prolonged bleeding time, and abnormal glass bead retention. Factor VIII molecular comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54df74ef3725f8d8d28388a308fcee03
https://doi.org/10.1002/ajh.2830050411
https://doi.org/10.1002/ajh.2830050411
Publikováno v:
Mutation research. 69(2)
The R-banding of more than 1100 lymphocytes and fibroblasts from 11 patients with ataxia telangiectasia (AT) showed rearrangements of chromosomes 7 and/or 14 in about 7% of the cells. Among these rearrangements, pericentric inversion of chromosome 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e6677c1682c6dc69709f4fdfe34cbd
https://pubmed.ncbi.nlm.nih.gov/7360152
https://pubmed.ncbi.nlm.nih.gov/7360152
Publikováno v:
American journal of diseases of children (1960). 137(9)
• We made clinical and immunologic observations of 30 children with common variable hypogammaglobulinemia. The mean age at diagnosis was 10.5 years, five years after clinical onset. Diagnosis was initially made based on a history of recurrent otobr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeaa1e75fc6fbbdd262569d0974147b1
https://pubmed.ncbi.nlm.nih.gov/6604451
https://pubmed.ncbi.nlm.nih.gov/6604451
Publikováno v:
American journal of hematology. 10(2)
Monocytes from five unrelated children (four boys and a girl) with chronic granulomatous disease were studied for their ability to reduce nitroblue tetrazolium dye after stimulation with zymosan, and for their alpha-naphtyl butyrate esterase activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f45b8b8adddced6d4a20b466c4ba679
https://pubmed.ncbi.nlm.nih.gov/7234863
https://pubmed.ncbi.nlm.nih.gov/7234863
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781468480900
Chronic granulomatous disease (CGD) is by convention defined as a disorder involving a high susceptibility to bacterial infection related to the inability of the patient’s neutrophils to increase oxygen consumption, despite normal phagocytosis and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eb0dee08a25ee13b56331355a0f1e2a
https://doi.org/10.1007/978-1-4684-8088-7_62
https://doi.org/10.1007/978-1-4684-8088-7_62
Autor:
Stéphane-Mircea Dumitresco, Claude Rivat, Diego Buriot, Claude Griscelli, Liliane Rivat-Peran, Jean-Philippe Salier
Publikováno v:
Clinical immunology and immunopathology. 20(1)
Twenty-five ataxia-telangiectasia patients, as well as 17 of their families, have been investigated for serum immunoglobulin patterns. Severe IgA2 deficiencies and/or IgG4 deficiencies (associated in three cases with IgG2 deficiencies) which frequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::587c9d7b16a2015482ffec5925b041bd
https://pubmed.ncbi.nlm.nih.gov/6973438
https://pubmed.ncbi.nlm.nih.gov/6973438