Issue 8/1997
Content (19 Articles)
A new classification for pericarditis associated with meningococcal infection
Y. Finkelstein, Y. Adler, M. Nussinovitch, I. Varsano, J. Amir
Effect of growth hormone therapy on bone metabolism of growth hormone deficient children
L. Stamoyannou, F. Karachaliou, E. Gioureli, E. Voskaki, C. Mengreli, C. S. Bartsocas, A. Koutselinis
Auxological and endocrinological evaluation of children with hydrocephalus and /or meningomyelocele
F. Hochhaus, O. Butenandt, H.-P. Schwarz, E. Ring-Mrozik
Iron overload and urinary lysosomal enzyme levels in β-thalassaemia major
H. Michelakakis, E. Dimitriou, H. Georgakis, F. Karabatsos, C. Fragodimitri, J. Saraphidou, E. Premetis, M. Karagiorga-Lagana
Glucose phosphate isomerase deficiency: biochemical and molecular genetic studies on the enzyme variants of two patients with severe haemolytic anaemia
P. Huppke, D. Wünsch, A. Pekrun, R. Kind, H. Winkler, W. Schröter, M. Lakomek
Diagnostic imaging in abdominal neuroblastoma: Is there a complementary role of MIBG-scintigraphy and ultrasonography?
M. Petjak, M. M. C. Tiel-van Buul, C. R. Staalman, J. C. Greve, J. de Kraker, E. A. van Royen
Frequency and correlates of severe hypoglycaemia in children and adolescents with diabetes mellitus
E. Bognetti, A. Brunelli, F. Meschi, M. Viscardi, R. Bonfanti, G. Chiumello
Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosis
Ü. Saatçi, S. Ozen, S. Özdemir, A. Bakkaloglu, N. Besbas, R. Topaloglu, S. Arslan
Anti-endomysium antibody on human umbilical cord vein tissue: an inexpensive and sensitive diagnostic tool for the screening of coeliac disease
T. Not, A. Città, A. Lucchesi, G. Torre, S. Martelossi, A. Ventura
Chronic infantile neurological cutaneous articular syndrome in a patient from Japan
M. Miura, T. Okabe, S. Tsubata, N. Takizawa, T. Sawaguchi
Axial spondylometaphyseal dysplasia
S. Ehara, O. H. Kim, S. Maisawa, Y. Takasago, G. Nishimura
Osteopathia striata, short stature, and characteristic facies: a previously unknown skeletal dysplasia
G. Nishimura, T. Okada, K. Tachibana, M. Adachi, M. Masuno, K. Imaizumi, N. Aida
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion
K. E. Chandler, C. E. M. de Die-Smulders, J. J. M. Engelen, J. J. P. Schrander, C. E. M. de Die-Smulders
Response to nitric oxide in term and preterm infants
B. Laubscher, A. Greenough, V. Kavvadia, S. P. Devane
The in vivo effect of recombinant human granulocyte-colony stimulating factor in neutropenic neonates with sepsis
Y. Barak, E. Leibovitz, B. Mogilner, A. Juster-Reicher, M. Amitay, A. Ballin, A. Koren, M. Goebel
Pulmonary thrombo-embolism in nephrotic syndrome treated with tissue plasminogen activator
C. J. D. Reid, T. Segal
Selective screening of 10,000 high-risk Brazilian patients for the detection of inborn errors of metabolism
J. C. Coelho, M. Wajner, M. G. Burin, C. R. Vargas, R. Giugliani
Epidemiological features of sudden infant death after a German intervention campaign in 1992
J. Schellscheidt, A. Ott, G. Jorch
Case of the month A 3.5-year-old female with developmental delays, hepatomegaly, and coarse facies
S. Yano, R. E. Falk, M. R. Natowicz, J. C. Williams