Cerebrospinal fluid levels of cytokines and soluble tumour necrosis factor receptor in acute disseminated encephalomyelitis Takashi IchiyamaHiroshi ShojiSusumu Furukawa Original Paper 19 January 2002 Pages: 133 - 137
Tuberculous pericarditis in an infant evolving during triple chemotherapy Jochen MeyburgKlaus G. SchmidtMarkus Bettendorf Original Paper 19 January 2002 Pages: 138 - 141
Long-term clinical effectiveness of an acellular pertussis component vaccine and a whole cell pertussis component vaccine Siegfried LugauerUlrich HeiningerKlemens Stehr Original Paper 24 January 2002 Pages: 142 - 146
Acute rheumatic fever in a patient with glycogen storage disease type Ib: causal or coincidental simultaneous occurrence? Jennifer NdagijimanaTim NiehuesHorst Schroten Original Paper 24 January 2002 Pages: 147 - 148
The effectiveness of octreotide in the treatment of post-operative chylothorax Luca RostiRoberta M. BiniMario Carminati Original Paper 19 January 2002 Pages: 149 - 150
Growth, developmental milestones and health problems in the first 2 years in very preterm infants compared with term infants: a population based study Hans BucherChrista KillerJean-Claude Fauchère Original Paper 30 January 2002 Pages: 151 - 156
Congenital hemihypertrophy and pheochromocytoma, not a coincidental combination? Erica L. van den AkkerRonald R. de KrijgerStenvert L. Drop Original Paper 24 January 2002 Pages: 157 - 160
Acute myeloid leukemia presenting with diabetes insipidus Willi WössmannArndt BorkhardtAlfred Reiter Research Letter 29 January 2002 Pages: 161 - 162
Hyperammonaemic encephalopathy in a 13-year-old boy Guido F. LaubeAndrea Superti-FurgaThomas J. Neuhaus Your Diagnosis 09 January 2002 Pages: 163 - 164
Epidemiology of Streptococcus pneumoniae pharyngeal carriage among healthy Turkish infants and children Mustafa BakirAysegul YagciGuner Soyletir Correspondence 16 January 2002 Pages: 165 - 166
Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype Barry Wolf Correspondence 24 January 2002 Pages: 167 - 168
Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype Sylvia Stöckler-IpsirogluWolfgang StroblDorothea Möslinger Correspondence 29 January 2002 Pages: 169 - 169
Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome” Dana HiyasatMunir A. DehyyatKamel M. Ajlouni Research Letter 25 January 2002 Pages: 170 - 172
Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot Tadahiko ItoTadashi OkuboHiroshi Sato Research Letter 08 January 2002 Pages: 173 - 174
Clinical heterogeneity in eyelid myoclonia, with absences, and epilepsy Gemma IncorporaVito SofiaEnrico Parano Research Letter 12 January 2002 Pages: 175 - 177
Mydriasis due to self-administered inhaled ipratropium bromide David W. BondHarish VyasHelen E. Venning Research Letter 11 January 2002 Pages: 178 - 178