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Acta Paediatrica, Volume 93 Issue 9 2004

ISSN: 1651-2227 (electronic) 0803-5253 (paper)
Publication Frequency: 12 issues per year

The circumstances under which this title is published have changed:

Reason for change: Changed Publisher
Now published by: Blackwell
Date of change: 31 December 2006

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Commentary
Flawed reports of immunization complications: consequences for child health
R. Zetterström
Pages 1140 – 1143
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Annotation
The Nils Rosén von Rosenstein Award 2004
G. Sedin
Pages 1144 – 1145
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Review Article
Evidence-based therapy in neonatology: distilling the evidence and applying it in practice
JC Sinclair
Pages 1146 – 1152
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Commentary
Midazolam and amplitude-integrated EEG
L. Hellström-Westas
Pages 1153 – 1154
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A genetic reason for male excess in infant respiratory mortality?
Orvar Finnström
Pages 1154 – 1155
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Low-cost intervention to decrease mastitis among lactating women
S. Filteau
Pages 1156 – 1158
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Article
Extensively and partially hydrolysed preterm formulas in the prevention of allergic diseases in preterm infants: a randomized, double-blind trial
H. Szajewska;  JZ Mrukowicz;  B. Stoińska; A. Prochowska
Pages 1159 – 1165
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A novel technique to measure position-dependent resistance changes in the vertebral arteries postmortem: new insights into the aetiology of SIDS?
M. Wald;  N. Klupp;  K. Lawrenz;  S. Puig;  K. Heimberger;  C. Reiter;  A. Pollak; O. Ipsiroglu
Pages 1166 – 1171
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Necrotizing pneumonia in children
M. Hacimustafaoglu;  S. Celebi;  H. Sarimehmet;  A. Gurpinar; I. Ercan
Pages 1172 – 1177
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Expression of neurotrophic factors in cerebrospinal fluid and plasma of children with viral and bacterial meningoencephalitis
A. Chiaretti;  A. Antonelli;  M. Piastra;  O. Genovese;  G. Polidori; L. Aloe
Pages 1178 – 1184
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Reduced gains in fat and fat-free mass, and elevated leptin levels in children and adolescents with cystic fibrosis
ML Ahmed;  KK Ong;  AH Thomson; DB Dunger
Pages 1185 – 1191
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Prevalence of germline mutations in the TSH receptor gene as a cause of juvenile thyrotoxicosis
L. Lavard;  B Brock Jacobsen;  H. Perrild;  G. Vassart; J. Parma
Pages 1192 – 1194
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Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature
S. Iyer;  M. Korada;  L. Rainbow;  J. Kirk;  RM Brown;  N. Shaw; TG Barrett
Pages 1195 – 1201
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