Ásgeir Haraldsson
Ásgeir Haraldsson
Professor of Paediatrics, Faculty of Medicine, University of Iceland and Chair and Faculty Chairman
Verified email at lsh.is
Cited by
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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
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
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
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
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
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
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
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
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
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
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
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
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
Thyrotoxicosis in Iceland 1980–1982: An epidemiological survey
Acta Medica Scandinavica 217 (3), 253-258, 1985
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
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
Griscelli disease with cerebral involvement
A Haraldsson, CMR Weemaes, J Bakkeren, R Happle
European journal of pediatrics 150 (6), 419-422, 1991
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
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
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
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