Paediatric Haematology Research Unit
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- 1997
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Mark
High prevalence of thyroid autoantibodies at diagnosis of insulin-dependent diabetes mellitus in Swedish children
(
- Contribution to journal › Article
- 1996
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Mark
Detection of virus in vertically exposed HIV-antibody-negative children
(
- Contribution to journal › Article
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Mark
Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia
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- Contribution to journal › Article
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Mark
Four novel mutations in deficiency of coagulation factor XIII: Consequences to expression and structure of the A-subunit
(
- Contribution to journal › Article
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Mark
Rätt och fel om talassemidiagnostik : Kommentar
(
- Contribution to specialist publication or newspaper › Specialist publication article
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Mark
Talassemi på väg in i landet : Ny patientgrupp på svenska barnkliniker
(
- Contribution to specialist publication or newspaper › Specialist publication article
- 1995
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Mark
Inversions of the factor VIII gene in Swedish patients with severe haemophilia A
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- Contribution to journal › Article
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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
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Mark
Prophylactic treatment of severe hemophilia A and B can prevent joint disability
(
- Contribution to journal › Article
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Mark
Normal vaginal delivery is to be recommended for haemophilia carrier gravidae
(
- Contribution to journal › Article
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Mark
Haemoglobin Koln as de novo mutations in Sweden : Diagnosis by PCR and specific enzymatic cleavage
(
- Contribution to journal › Article
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Mark
Genetic diagnosis of hemophilia a
(
- Contribution to journal › Article
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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
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Mark
The feasibility of long-term venous access in children with hemophilia
(
- Contribution to journal › Article
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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
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Mark
Piebaldism in a mentally retarded girl with rare deletion of the long arm of chromosome 4
(
- Contribution to journal › Article
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Mark
HIV infection in haemophilia - A European cohort
(
- Contribution to journal › Article
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Mark
Report of a joint WHO/WFH meeting on the control of haemophilia: Carrier detection and prenatal diagnosis
(
- Contribution to journal › Article
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Mark
Haemophilia : strategies for carrier detection and prenatal diagnosis
(
- Contribution to journal › Article