Paediatric Haematology Research Unit
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- 1997
-
Mark
High prevalence of thyroid autoantibodies at diagnosis of insulin-dependent diabetes mellitus in Swedish children
(
- Contribution to journal › Article
- 1996
-
Mark
Detection of virus in vertically exposed HIV-antibody-negative children
(
- Contribution to journal › Article
-
Mark
Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Four novel mutations in deficiency of coagulation factor XIII: Consequences to expression and structure of the A-subunit
(
- Contribution to journal › Article
-
Mark
Rätt och fel om talassemidiagnostik : Kommentar
(
- Contribution to specialist publication or newspaper › Specialist publication article
-
Mark
Talassemi på väg in i landet : Ny patientgrupp på svenska barnkliniker
(
- Contribution to specialist publication or newspaper › Specialist publication article
- 1995
-
Mark
Inversions of the factor VIII gene in Swedish patients with severe haemophilia A
(
- Contribution to journal › Article
-
Mark
Gene mutations and inhibitor formation in patients with hemophilia B
(
- Contribution to journal › Article
-
Mark
The impact of prenatal diagnosis on the incidence of haemophilia in Sweden
(
- Contribution to journal › Article
- 1994
-
Mark
Prophylactic treatment of severe hemophilia A and B can prevent joint disability
(
- Contribution to journal › Article
-
Mark
Normal vaginal delivery is to be recommended for haemophilia carrier gravidae
(
- Contribution to journal › Article
-
Mark
Haemoglobin Koln as de novo mutations in Sweden : Diagnosis by PCR and specific enzymatic cleavage
(
- Contribution to journal › Article
-
Mark
Genetic diagnosis of hemophilia a
(
- Contribution to journal › Article
-
Mark
High titer inhibitors in severe haemophilia A. A meta-analysis based on eight long-term follow-up studies concerning inhibitors associated with crude or intermediate purity factor VIII products [4]
(
- Contribution to journal › Letter
-
Mark
The feasibility of long-term venous access in children with hemophilia
(
- Contribution to journal › Article
-
Mark
Kartläggning av familjer i Sverige med hemofili B : Nästan alla undersökta har unika mutationer
(
- Contribution to specialist publication or newspaper › Specialist publication article
- 1993
-
Mark
Piebaldism in a mentally retarded girl with rare deletion of the long arm of chromosome 4
(
- Contribution to journal › Article
-
Mark
HIV infection in haemophilia - A European cohort
(
- Contribution to journal › Article
-
Mark
Report of a joint WHO/WFH meeting on the control of haemophilia: Carrier detection and prenatal diagnosis
(
- Contribution to journal › Article
-
Mark
Haemophilia : strategies for carrier detection and prenatal diagnosis
(
- Contribution to journal › Article
- 1992
-
Mark
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden
(
- Contribution to journal › Article
-
Mark
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion
(
- Contribution to journal › Article
-
Mark
Factor VIII and factor IX inhibitors in haemophiliacs
(
- Contribution to journal › Letter
-
Mark
Gaucher's disease in an infant diagnosed by fine needle aspiration of the liver and spleen : A case report
(
- Contribution to journal › Article
-
Mark
Haplotype analysis of identical factor IX mutants using PCR
(
- Contribution to journal › Article
-
Mark
Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A
(
- Contribution to journal › Letter
-
Mark
Implantable central venous catheter facilitates prophylactic treatment in children with haemophilia
(
- Contribution to journal › Article
-
Mark
Origin of mutation in sporadic cases of haemophilia-B
(
- Contribution to journal › Article
-
Mark
Cholelithiasis during the first year of life : Case reports and literature review
(
- Contribution to journal › Article
- 1991
-
Mark
Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome
(
- Contribution to journal › Article
-
Mark
More than half the sporadic cases of Hemophilia A in Sweden are due to a recent mutation
(
- Contribution to journal › Article
-
Mark
Population genetics of the Malmö polymorphism of coagulation factor IX
(
- Contribution to journal › Article
-
Mark
Haemophilia B mutations in a complete Swedish population sample : a test of new strategy for the genetic counselling of diseases with high mutational heterogeneity
(
- Contribution to journal › Article
-
Mark
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
- 1990
-
Mark
Hepatitis C virus transmission by monoclonal antibody purified factor VIII concentrate
(
- Contribution to journal › Letter
-
Mark
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspots
(
- Contribution to journal › Article
-
Mark
Two factor IX mutations in the family of an isolated haemophilia B patient : direct carrier diagnosis by amplification mismatch detection (AMD)
(
- Contribution to journal › Article
-
Mark
Diagnostic symptoms of severe and moderate haemophilia A and B. A survey of 140 cases
(
- Contribution to journal › Article
- 1989
-
Mark
How do carriers of hemophilia experience prenatal diagnosis (PND)? : Carriers' Immediate and later reactions to amniocentesis and fetal blood sampling
(
- Contribution to journal › Article
- 1988
-
Mark
The Malmo polymorphism of coagulation factor IX, an immunologic polymorphism due to dimorphism of residue 148 that is in linkage disequilibrium with two other F.IX polymorphisms
(
- Contribution to journal › Article
-
Mark
Neutropenia and congenital cytomegalovirus infection
(
- Contribution to journal › Letter
-
Mark
Hemofilivården i Sverige. Centraliserat ansvar ger hög vårdkvalitet.
(
- Contribution to specialist publication or newspaper › Specialist publication article
- 1987
-
Mark
Prenataldiagnostik av hemofili A och B genom chorionvillus-biopsi och DNA-analys.
(
- Contribution to journal › Article
-
Mark
How do carriers of hemophilia experience prenatal diagnosis by fetal blood sampling?
(
- Contribution to journal › Article
- 1986
-
Mark
Two allotypes of factor IX present in haemophilia B
(
- Contribution to journal › Article
-
Mark
Platelet-associated IgG in childhood idiopathic thrombocytopenic purpura : measurements on intact and solubilized platelets and after gammaglobulin treatment
(
- Contribution to journal › Article
-
Mark
Carrier detection in hemophilia A : a cooperative international study. II. The efficacy of a universal discriminant
(
- Contribution to journal › Article
-
Mark
Carrier detection in hemophilia A : a cooperative international study. I. The carrier phenotype
(
- Contribution to journal › Article
- 1985
-
Mark
High-dose intravenous gammaglobulin : a cautionary note
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Polymorphism of normal factor IX detected by mouse monoclonal antibodies
1985) In Proceedings of the National Academy of Sciences of the United States of America 82(11). p.3839-3843(
- Contribution to journal › Article
- 1984
-
Mark
Ganglioneuroma with an uncommon location in a six-year-old girl
(
- Contribution to journal › Article
- 1983
-
Mark
Suppression of Secondary Antibody Response by Intravenous Immunoglobulin in a Patient with Haemophilia B and Antibodies
(
- Contribution to journal › Article
-
Mark
The effects of plasmin and protein Ca on factor VIII:C and VIII:CAg
(
- Contribution to journal › Article
-
Mark
Detection of factor IX inhibitors by immunoradiometric assay
(
- Contribution to journal › Article
- 1982
-
Mark
Haemophilia A and B--two years experience of genetic counselling and prenatal diagnosis
(
- Contribution to journal › Article
-
Mark
Hemophilia B Leyden and a similar variant of hemophilia A.
(
- Contribution to journal › Letter
-
Mark
Immunoradiometric assay of inhibitors of antihaemophilic factor A
(
- Contribution to journal › Article
-
Mark
Genetic variants of haemophilia B detected by immunoradiometric assay : implications for prenatal diagnosis
(
- Contribution to journal › Article
- 1981
-
Mark
F VIII:CAg in Haemophilia A. A comparison between IRMA:s using haemophilic and spontaneous antibodies
(
- Contribution to journal › Article
-
Mark
Inheritable molecular variants of moderate and mild hemophilia A
(
- Contribution to journal › Article
- 1980
-
Mark
Prenatal diagnosis of hemophilia B by an immunoradiometric assay of factor IX
(
- Contribution to journal › Article
- 1979
-
Mark
Measurement of antihaemophilic factor A antigen (VII:CAg) with a solid phase immunoradiometric method based on homologous non-haemophilic antibodies.
(
- Contribution to journal › Article
-
Mark
Fanconi's anaemia associated with haemophilia A
(
- Contribution to journal › Article
- 1978
-
Mark
Purification of F.VIII:C by antigen-antibody chromatography
(
- Contribution to journal › Article
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