Narrow- versus broad-spectrum parenteral antimicrobials against common infections of childhood: a prospective and randomised comparison between penicillin and cefuroxime Elina Vuori-HolopainenHeikki Peltolafor the SE-TU Study Group ORIGINAL PAPER Pages: 878 - 884
Xerostomia in patients with triple A syndrome – a newly recognised finding Miroslav DumićMarinka Mravak-StipetićMarijana Cvitanović ORIGINAL PAPER Pages: 885 - 888
Pericardial cyst in a child treated with video-assisted thoracoscopic surgery Akiko EtoTohru ArimaAkira Nagashima ORIGINAL PAPER Pages: 889 - 891
Genetic and long-term data on a patient with permanent isolated proximal renal tubular acidosis Masaaki ShioharaTakashi IgarashiAtsushi Komiyama ORIGINAL PAPER Pages: 892 - 894
Near fatal acute colchicine intoxication in a child. A case report Aviv GoldbartJoseph PressJoseph Kapelushnik ORIGINAL PAPER Pages: 895 - 897
Early infantile pertussis; increasingly prevalent and potentially fatal Craig SmithHarish Vyas ORIGINAL PAPER Pages: 898 - 900
3-Methylcrotonyl-CoA carboxylase deficiency in an infant with cardiomyopathy, in her brother with developmental delay and in their asymptomatic father Gepke VisserTerttu SuormalaE. Regula Baumgartner ORIGINAL PAPER Pages: 901 - 904
A 6-year-old boy with hyperammonaemia: partial N-acetylglutamate synthase deficiency or portosystemic encephalopathy? Daniel BroereWim G. van GemertMarjo S. van der Knaap ORIGINAL PAPER Pages: 905 - 907
Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boy Toshiaki DoiWataru AboNaoto Terada ORIGINAL PAPER Pages: 908 - 911
Familial disorder of sex determination in seven individuals from three related sibships Nadim JarrahHatem El-ShantiKamel Ajlouni ORIGINAL PAPER Pages: 912 - 918
Continuous infusion of ceftazidime with a portable pump is as effective as thrice-a-day bolus in cystic fibrosis children Isabelle RappazLaurent A. DecosterdMichel Roulet ORIGINAL PAPER Pages: 919 - 925
A 17-month-old with extreme prenatal-onset growth delay Mustafa TekinJanice NgJoann Bodurtha YOUR DIAGNOSIS? Pages: 926 - 928
Preaxial polydactyly type 1 and severe language deficit in maternal uniparental disomy of chromosome 7 Steph PotgieterGert MatthijsJean-Pierre Fryns CORRESPONDENCE Pages: 929 - 929
Mental retardation, developmental delay, and partial psychomotor deficits in maternal uniparental disomy 7 Dieter Kotzot CORRESPONDENCE Pages: 930 - 930
The reactogenicity and immunogenicity of commercial Haemophilus influenzae type b conjugate vaccines Joseph F. HeyseKaren M. Kaplan CORRESPONDENCE Pages: 932 - 932
Thyrotoxic periodic paralysis in a 14-year-old boy Gary Wing-Kin WongTing Fan LeungPik Shun Cheng RESEARCH LETTERS Pages: 934 - 934
A rapid technique for detecting chromosomal aneuploidy in early childhood by fluorescence in situ hybridisation Erika P. TardyAndrás Tóth RESEARCH LETTERS Pages: 935 - 935
Tuberous breast deformity in an adolescent girl with Hurler-Scheie syndrome Rita BaronePiero PavoneEnrico Parano RESEARCH LETTERS Pages: 936 - 937
Growth hormone treatment of children with human immunodeficiency virus-associated growth failure Graziella PintoStéphane BlancheRaja Brauner RESEARCH LETTERS Pages: 937 - 938
Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiency Tom J de KoningMarinus DuranBwee-Tien Poll-The RESEARCH LETTERS Pages: 939 - 940
Real-time monitoring of Helicobacter pylori eradication therapy by testing stool antigen Toshiaki ShimizuYukiko YaritaYuichiro Yamashiro RESEARCH LETTERS Pages: 940 - 941
Factor V 1691G-A mutation and high factor VIII levels in a patient with intracardiac thrombosis Nejat AkarEmine SuskanHafize Gökçe RESEARCH LETTERS Pages: 941 - 941
