Zobrazeno 1 - 10
of 614
pro vyhledávání: '"Titus H.J. Huisman"'
Publikováno v:
Scandinavian Journal of Haematology. 16:81-89
The clinical, haematological and biochemical findings in a person with delta beta-thalassaemia and Hb-Lepore are described. The patient was a 24-year-old student who suffered from anaemia of intermediate severity with late onset of the clinical manif
Publikováno v:
Animal Blood Groups and Biochemical Genetics. 2:159-177
Summary Bovine serum transferrin (type Tf-A) was isolated by a series of four techniques; (a) precipitation with Rivanol; (b) chromatography of the soluble protein fraction on a column of Sephadex G-150; (c) chromatography of the transferrin containi
Autor:
E. George, T. A. Stoming, G. Petkov, K. G. Yang, Titus H.J. Huisman, L. Jankovic, Georgi D. Efremov, Christos Kattamis
Publikováno v:
British Journal of Haematology. 75:122-126
In an ongoing effort to identify point mutations causing beta-thalassaemia, we have found two previously unreported mutations which are located in the Poly A site of the beta-globin gene. The screening programme used amplified DNA and dot-blot hybrid
Publikováno v:
American Journal of Hematology. 59:181-184
Unexpectedly low hemoglobin oxygen saturation as determined by pulse-oximeter analysis was observed in a patient who underwent an elective surgical procedure. Specific hemoglobin derivatives such as carboxyhemoglobin, methemoglobin, and reduced hemog
Publikováno v:
Genomics. 47:429-437
Autor:
Titus H.J. Huisman, M. F. H. Carver
Publikováno v:
Hemoglobin. 22:169-195
Autor:
Titus H.J. Huisman, M. F. H. Carver
Publikováno v:
Hemoglobin. 22:287-310
(1998). The Thalassemia Repository (Ninth Edition; Part II) Hemoglobin: Vol. 22, No. 3, pp. 287-310.
Autor:
H. Landman, Titus H.J. Huisman
Publikováno v:
Hemoglobin. 22:53-63
We describe a Black female who has suffered for many years from an (often) severe anemia (Hb 5-9 g/dl) with iron deficiency (serum Fe 8 microg/dl; TIBC 462 microg/dl; ferritin 7 ng/ml or less) and folate deficiency. The patient had hypermenorrhea whi
Autor:
Titus H.J. Huisman
Publikováno v:
Hemoglobin. 22:267-272
Publikováno v:
Acta Haematologica. 100:4-8
We have studied the relative levels of γ-mRNA [%γ/(γ + β)], Gγ- and Aγ-mRNAs [%Gγ/(Gγ + Aγ)], hemoglobin (Hb) F, and the Gγ and Aγ chains in some 50 patients with sickle cell anemia (SS) and with different haplotypes. As expected, the Hb F