Ásgeir Haraldsson
Ásgeir Haraldsson
Professor of Paediatrics, Faculty of Medicine, University of Iceland and Chair and Faculty Chairman
Verified email at lsh.is
Title
Cited by
Cited by
Year
Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis
KG Ericson, B Fadeel, S Nilsson-Ardnor, C Söderhäll, AC Samuelsson, ...
The American Journal of Human Genetics 68 (3), 590-597, 2001
3012001
Respiratory syncytial virus and other respiratory viruses during the first 3 months of life promote a local TH2-like response
S Kristjansson, SP Bjarnarson, G Wennergren, AH Palsdottir, T Arnadottir, ...
Journal of Allergy and Clinical Immunology 116 (4), 805-811, 2005
1902005
Vernix caseosa as a multi-component defence system based on polypeptides, lipids and their interactions
M Tollin, G Bergsson, Y Kai-Larsen, J Lengqvist, J Sjövall, W Griffiths, ...
Cellular and Molecular Life Sciences CMLS 62 (19), 2390-2399, 2005
1312005
The influence of partial or total thymectomy during open heart surgery in infants on the immune function later in life
JH Eysteinsdottir, J Freysdottir, A Haraldsson, J Stefansdottir, I Skaftadottir, ...
Clinical & Experimental Immunology 136 (2), 349-355, 2004
1172004
Loss-of-function variants in ATM confer risk of gastric cancer
H Helgason, T Rafnar, HS Olafsdottir, JG Jonasson, A Sigurdsson, ...
Nature genetics 47 (8), 906-910, 2015
1042015
Antibody deficiency in patients with ataxia telangiectasia is caused by disturbed B-and T-cell homeostasis and reduced immune repertoire diversity
GJ Driessen, H IJspeert, CMR Weemaes, Á Haraldsson, M Trip, A Warris, ...
Journal of allergy and clinical immunology 131 (5), 1367-1375. e9, 2013
892013
The effects of smoking in pregnancy on factors influencing fetal growth
RF Ingvarsson, AO Bjarnason, A Dagbjartsson, H Hardardottir, ...
Acta Paediatrica 96 (3), 383-386, 2007
792007
Familial predisposition and cosegregation analysis of adult obstructive sleep apnea and the sudden infant death syndrome
T Gislason, JH Johannsson, A Haraldsson, BR Olafsdottir, H Jonsdottir, ...
American journal of respiratory and critical care medicine 166 (6), 833-838, 2002
712002
Congenital cardiac malformations in Iceland from 1990 through 1999
SS Stephensen, G Sigfusson, H Eiriksson, JT Sverrisson, B Torfason, ...
Cardiology in the young 14 (4), 396, 2004
692004
Cutaneous granulomas in ataxia telangiectasia and other primary immunodeficiencies: reflection of inappropriate immune regulation?
LYT Chiam, MMM Verhagen, A Haraldsson, N Wulffraat, GJ Driessen, ...
Dermatology 223 (1), 13-19, 2011
622011
Paediatric burns in Iceland. Hospital admissions 1982-1995, a populations based study.
R Elisdottir, P Lúdvígsson, O Einarsson, S Thorgrímsson, A Haraldsson
Burns 25 (2), 149-151, 1999
621999
Development of immunoglobulin A in infancy and childhood
C Weemaes, I Klasen, J Göertz, M Beldhuis‐Valkis, O Olafsson, ...
Scandinavian journal of immunology 58 (6), 642-648, 2003
612003
Ataxia–telangiectasia patients presenting with hyper-IgM syndrome
JG Noordzij, NM Wulffraat, Á Haraldsson, I Meyts, LJ van’t Veer, ...
Archives of disease in childhood 94 (6), 448-449, 2009
592009
Thyrotoxicosis in Iceland 1980–1982: An epidemiological survey
A HARALDSSON, STH GUDMUNDSSON, G LARUSSON, ...
Acta Medica Scandinavica 217 (3), 253-258, 1985
561985
Increased frequency of C4B* Q0 alleles in patients with Henoch–Schönlein purpura
V Stefansson Thors, R Kolka, SL Sigurdardottir, VO Edvardsson, ...
Scandinavian journal of immunology 61 (3), 274-278, 2005
542005
Immunological studies in the hyper-immunoglobulin D syndrome
A Haraldsson, CMR Weemaes, AW De Boer, J Bakkeren, GBA Stoelinga
Journal of clinical immunology 12 (6), 424-428, 1992
521992
Griscelli disease with cerebral involvement
A Haraldsson, CMR Weemaes, J Bakkeren, R Happle
European journal of pediatrics 150 (6), 419-422, 1991
511991
Evidence for extrathymic T cell maturation after thymectomy in infancy
H Torfadottir, J Freysdóttir, I Skaftadóttir, A Haraldsson, G Sigfusson, ...
Clinical & Experimental Immunology 145 (3), 407-412, 2006
502006
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease
GA Arnadottir, GL Norddahl, S Gudmundsdottir, AB Agustsdottir, ...
Nature communications 9 (1), 1-9, 2018
472018
Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: description of seven patients and review of the literature
IVD Burgt, A Haraldsson, JC Oosterwijk, AJ van Essen, C Weemaes, ...
American journal of medical genetics 41 (3), 371-380, 1991
431991
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