Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M C, Bruin"'
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 144(33)
In two neonates, girls, persistent thrombocytopenia was found, which afterwards proved to be caused by a megakaryocytosis. Congenital amegakaryocytic thrombocytopenia is a rare bone marrow failure in young children that is defined as thrombocytopenia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::01b6d4829fb0b44e9c6466fbe3f9b128
https://pubmed.ncbi.nlm.nih.gov/10965369
https://pubmed.ncbi.nlm.nih.gov/10965369
Publikováno v:
Blood. 94(5)
Autoimmune neutropenia (AIN) in children can be divided into 2 forms. In primary AIN, neutropenia is the sole abnormality, and although neutrophil counts are generally below 500 microL(-1), mild bacterial infections occur. Primary AIN is mostly seen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4bfbf61cfc7b185482981bcbf0d9fb63
https://pubmed.ncbi.nlm.nih.gov/10477706
https://pubmed.ncbi.nlm.nih.gov/10477706
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 142(7)
Three children (girls) suffered from neutropenia mediated by anti-neutrophil IgG-Fc receptor type III (Fc gamma RIII) antibodies. The first patient (newborn) had asymptomatic and transient neutropenia caused by maternal Fc gamma RIII iso-antibodies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b2381d1588b621e819047270c4735e1
https://pubmed.ncbi.nlm.nih.gov/9562743
https://pubmed.ncbi.nlm.nih.gov/9562743
Autor:
C L, Harteveld, P C, Giordano, M, Losekoot, J G, Heister, D, Batelaan, P, van Delft, M C, Bruin, L F, Bernini
Publikováno v:
British journal of haematology. 94(3)
We describe a new alpha 2-globin gene point mutation found in six individuals of a three-generation Dutch family. The mutant, which is associated with a mild alpha-thalassaemic phenotype, is not detectable at the protein level. The alpha 2 cd129 (CTG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa405f2d247ae6362a410db004afdd31
https://pubmed.ncbi.nlm.nih.gov/8790146
https://pubmed.ncbi.nlm.nih.gov/8790146
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 138(9)
Vitamin B12 deficiency is an uncommon disorder in a prosperous western country. In two children a nutritional vitamin B12 deficiency was observed. The first was a 2-year-old girl with neurodevelopmental regression and macrocytic anaemia, a result of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b272edfffa0eed4680ac5c0df37ef16e
https://pubmed.ncbi.nlm.nih.gov/8133949
https://pubmed.ncbi.nlm.nih.gov/8133949
Publikováno v:
Tijdschrift voor kindergeneeskunde. 59(6)
Congenital hypoplastic anemia (CHA; syn: Diamond-Blackfan syndrome) is a rare disorder with one of two patients a year in the Netherlands. To get a better understanding of this disorder in the Netherlands we conducted a national retrospective study o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f67ef8e5152d0ef1f961deb241e6cee
https://pubmed.ncbi.nlm.nih.gov/1776145
https://pubmed.ncbi.nlm.nih.gov/1776145