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- 2019
- Management and outcome of TaG3 tumours of the urinary bladder in the nationwide, population-based bladder cancer database Sweden (BladderBaSe)
- 2016
- Carl-Gustaf Bergstrand (1914–2011), former Managing Editor of Acta Paediatrica
- 2009
- Brain tumours in children.
- 2008
- Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD)
- Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD
- Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)
- N1421K mutation in the glycoprotein Ib binding domain impairs ristocetin- and botrocetin-mediated binding of von Willebrand factor to platelets.
- Characterization of a novel mutation in the von Willebrand factor propeptide in a distinct subtype of recessive von Willebrand disease.
- Asn1421Lys mutation in the glycoprotein Ib binding domain impairs - ristocetin and botrocetin - mediated binding of von Willebrand factor to platelets
- 2007
- Residual adverse changes in arterial endothelial function and LDL oxidation after a mild systemic inflammation induced by influenza vaccination
-
ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura.
Manea Hedström, Minola LU ; Kristoffersson, Ann-Charlotte LU ; Tsai, Han-Mou ; Zhou, Wenhua ; Winqvist, Ingemar ; Oldaeus, Goran ; Billstrom, Rolf ; Björk, Peter LU ; Holmberg, Lars LU and Karpman, Diana LU
(2007)
In European Journal of Pediatrics
166(3).
p.249-257
Mark
- Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1VWD)
- Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
-
Podocytes express ADAMTS13 in normal renal cortex and in patients with thrombotic thrombocytopenic purpura
Manea Hedström, Minola LU ; Kristoffersson, Ann-Charlotte LU ; Schneppenheim, Reinhard ; Saleem, Moin A. ; Mathieson, Peter W. ; Mörgelin, Matthias LU ; Björk, Peter LU ; Holmberg, Lars LU and Karpman, Diana LU
(2007)
In British Journal of Haematology
138(5).
p.651-662
Mark
- 2006
-
Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.
Vaziri-Sani, F ; Holmberg, Lars LU ; Sjöholm, Anders LU ; Kristoffersson, Ann-Charlotte LU ; Manea Hedström, Minola LU ; Frémeaux-Bacchi, V ; Fehrman-Ekholm, I ; Raafat, R and Karpman, Diana LU
(2006)
In Kidney International
69(6).
p.981-988
Mark
- Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor
- A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD)
- Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
- 2005
- VWF-cleaving protease (ADAMTS13) in premature infants.
- 2004
- Sorting of Von Willebrand factor to lysosome-related granules of haematopoietic cells
- 2003
- Desmopressin (DDAVP) and factor VIII
- 2002
- Predictors of deterioration of lung function in cystic fibrosis.
- Von Willebrand's disease caused by compound heterozygosity for a substitution mutation (T1156M) in the D3 domain of the von Willebrand factor and a stop mutation (Q2470X).
- 2001
- Symposium in memory of Professor Inga Marie Nilsson
- 1997
-
von Willebrand factor mediates increased platelet retention in recurrent thrombotic thrombocytopenic purpura
Karpman, D LU
; Lethagen, S
LU
; Kristoffersson, Anne
LU
; Isaksson, C.
and Holmberg, Lars
LU
(1997)
In Thrombosis and Haemostasis
78(6).
p.62-1456
Mark
-
Bernard-Soulier syndrome Karlstad : Trp 498-->Stop mutation resulting in a truncated glycoprotein Ib alpha that contains part of the transmembranous domain
Holmberg, Lars LU ; Karpman, D LU
; Nilsson, Ingemar
and Olofsson, Tor
LU
(1997)
In British Journal of Haematology
98(1).
p.57-63
Mark
- 1996
-
Increased platelet retention in familial recurrent thrombotic thrombocytopenic purpura
Karpman, D LU
; Holmberg, Lars
LU
; Jirgård, Lena
and Lethagen, S
LU
(1996)
In Kidney International
49(1).
p.9-190
Mark
- 1992
- Cerebral infarction in a girl who developed anticardiolipin syndrome after acute lymphoblastic leukemia
- 1991
-
Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome
Kling, S. LU ; Coffey, A. J. ; Ljung, R. LU
; Sjörin, Elsy
LU
; Nilsson, Inga Marie
; Holmberg, L.
LU
and Giannelli, F.
(1991)
In European Journal of Haematology
47(4).
p.257-261
Mark
- 1990
- Platelet surface-bound IgG and platelet-specific IgG in plasma in childhood thrombocytopenia
- 1987
-
Prenataldiagnostik av hemofili A och B genom chorionvillus-biopsi och DNA-analys.
Holmberg, L. LU ; Ljung, R. LU
; Nilsson, Inga Marie
and Gustavii, B.
LU
(1987)
In Läkartidningen
84(38).
p.2967-2968
Mark
- 1986
-
Platelet-associated IgG in childhood idiopathic thrombocytopenic purpura : measurements on intact and solubilized platelets and after gammaglobulin treatment
Ljung, R. LU
; Nilsson, Inga Marie
; Frohm, B.
and Holmberg, Lars
LU
(1986)
In Scandinavian Journal of Haematology
36(4).
p.402-407
Mark
- 1985
-
Polymorphism of normal factor IX detected by mouse monoclonal antibodies
Wallmark, Anders LU ; Ljung, Rolf LU
; Nilsson, Inga.Marie
; Holmberg, Lars
LU
; Hedner, Ulla
LU
; Lindvall, Magnus
LU
and Sjögren, Hans Olov
LU
(1985)
In Proceedings of the National Academy of Sciences of the United States of America
82(11).
p.3839-3843
Mark
- 1983
-
Suppression of Secondary Antibody Response by Intravenous Immunoglobulin in a Patient with Haemophilia B and Antibodies
Nilsson, I. M. ; Sundqvist, S. ‐B ; Ljung, R. LU
; Holmberg, L.
LU
; Freiburghaus, Catja
LU
and Björlin, G.
(1983)
In Scandinavian Journal of Haematology
30(5).
p.458-464
Mark
-
The effects of plasmin and protein Ca on factor VIII:C and VIII:CAg
Holmberg, Lars LU ; Ljung, R LU
and Nilsson, Inga Marie
(1983)
In Thrombosis Research
31(1).
p.41-50
Mark
- Detection of factor IX inhibitors by immunoradiometric assay
- 1982
-
Haemophilia A and B--two years experience of genetic counselling and prenatal diagnosis
Ljung, R LU
; Holmberg, Lars
LU
; Gustavii, B
LU
; Philip, J
and Bang, J
(1982)
In Clinical Genetics
22(2).
p.70-75
Mark
-
Immunoradiometric assay of inhibitors of antihaemophilic factor A
Ljung, Rolf LU
and Holmberg, Lars
LU
(1982)
In Acta Paediatrica Scandinavica
71(6).
p.1019-1023
Mark
- Genetic variants of haemophilia B detected by immunoradiometric assay : implications for prenatal diagnosis
- 1981
- F VIII:CAg in Haemophilia A. A comparison between IRMA:s using haemophilic and spontaneous antibodies
-
Inheritable molecular variants of moderate and mild hemophilia A
Ljung, R LU
; Holmberg, Lars
LU
and Nilsson, Inga Marie
(1981)
In Acta Medica Scandinavica
209(1-2).
p.11-16
Mark
- 1980
-
Prenatal diagnosis of hemophilia B by an immunoradiometric assay of factor IX
Holmberg, Lars LU ; Gustavii, B LU ; Cordesius, E ; Kristoffersson, A C LU ; Ljung, R LU
; Löfberg, L
; Strömberg, P
and Nilsson, Inga Marie
(1980)
In Blood
56(3).
p.397-401
Mark
- 1979
-
Fanconi's anaemia associated with haemophilia A
Ljung, R LU
; Holmberg, Lars
LU
; Nilsson, K O
LU
and Thilén, A
(1979)
In Clinical Genetics
16(5).
p.8-364
Mark
-
Measurement of antihaemophilic factor A antigen (VII:CAg) with a solid phase immunoradiometric method based on homologous non-haemophilic antibodies.
Holmberg, Lars LU ; Borge, L. ; Ljung, R. LU
and Nilsson, Inga Marie
(1979)
In Scandinavian Journal of Haematology
23(1).
p.17-24
Mark
- 1978
- Purification of F.VIII:C by antigen-antibody chromatography