Primary Sjögren syndrome in the paediatric age: a multicentre survey Rolando CimazAnnachiara CasadeiAlexandros A. Drosos Original Paper 29 July 2003 Pages: 661 - 665
Chronic eosinophilic ascites in a very young child Arrigo Vittorio BarabinoEmanuela CastellanoGian Michele Magnano Original Paper 12 August 2003 Pages: 666 - 668
Chronic infantile neurological cutaneous articular syndrome: CD10 over-expression in neutrophils is a possible key to the pathogenesis of the disease Valentina LeoneGianni PresaniLoredana Lepore Original Paper 20 August 2003 Pages: 669 - 673
Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene Guy MassaNele JaenenWim Wuyts Original Paper 15 August 2003 Pages: 674 - 677
Infant stroke and beta-2-glycoprotein 1 antibodies: six cases Freja EbelingJari PetäjäVesa Rasi Original Paper 12 August 2003 Pages: 678 - 681
Chronic illness, life style and emotional health in adolescence: results of a cross-sectional survey on the health of 15-20-year-olds in Switzerland Lise MiautonFrançoise NarringPierre-André Michaud Original Paper 12 August 2003 Pages: 682 - 689
The late consequences of anthracycline treatment on left ventricular function after treatment for childhood cancer Lubomir ElblHana HrstkovaVaclav Chaloupka Original Paper 07 August 2003 Pages: 690 - 696
Surfactant therapy in neonates with respiratory failure due to haemorrhagic pulmonary oedema Takasuke AmizukaHiroshi ShimizuYunosuke Ogawa Original Paper 29 July 2003 Pages: 697 - 702
Congenital toxoplasmosis: assessment of risk to newborns in confirmed and uncertain maternal infection Mariangela MombròCristina PerathonerClaudio Fabris Original Paper 11 July 2003 Pages: 703 - 706
Acquired angioedema and Helicobacter pylori infection in a child Jana VarvarovskaJosef SykoraIvan Chytra Original Paper 01 August 2003 Pages: 707 - 709
Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation Luitgard M. NeumannArpad von MoersThorsten Marquardt Original Paper 02 August 2003 Pages: 710 - 713
Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation Olga GrafakouKonrad OexleJan Smeitink Original Paper 19 August 2003 Pages: 714 - 718
Fructose 1,6 diphosphatase deficiency in a Turkish infant Betül TavilTansu Sipahi Research Letter 25 July 2003 Pages: 719 - 720
Continuous subcutaneous insulin infusion in toddlers Birgit RamiEdith NachbaurEdith Schober Short Report 20 August 2003 Pages: 721 - 722
Paroxetine withdrawal in a neonate with historical and laboratory confirmation Sanjay JaiswalRobert C. CoombsGeoffrey K. Isbister Short Report 07 August 2003 Pages: 723 - 724
An unspecific immunostimulating agent and juvenile dermatomyositis: enhanced T-cell proliferation and reverse immunosuppression as a severe adverse drug reaction Gerd M. LackmannJenny NdagijimanaTim Niehues Short Report 07 August 2003 Pages: 725 - 726
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting Carmelo Damiano SalpietroSilvana BriugliaLuciana Rigoli Short Report 02 August 2003 Pages: 727 - 728
Experience of continuous haemodiafiltration in a male neonate with ornithine transcarbamylase deficiency Shigehiro EnkaiMasaki YamamotoWataru Abo Short Report 01 August 2003 Pages: 729 - 730
An 8-year-old boy with a 4-day history of fever, cough and malaise, and a 2-day history of painful calves and difficulty walking Paul W. MeierMario G. Bianchetti Your Diagnosis 16 July 2003 Pages: 731 - 732
Smith OP, Hann IM (eds): Essential paediatric haematology Susanne Suter Book Review 24 May 2003 Pages: 733 - 733
A4 Integrin Antibody Successful in Adult Crohn Disease News for the Practitioner 09 September 2003 Pages: 734 - 734
