Issue 1-2/2000
Content (40 Articles)
Failure of IGF-A and IGFBP-3 to diagnose growth-hormone insufficiency
Prognosis for vesicoureteral reflux
Postoperative Mycobacterium avium osteomyelitis confirmed by polymerase chain reaction
J. A. I. Weigl, W. H. Haas
Brown tumour as a complication of secondary hyperparathyroidism in severe long-lasting vitamin D deficiency rickets
A. Bereket, Y. Casur, P. Firat, N. Yordam
Accelerated phase in partial albinism with immunodeficiency (Griscelli syndrome): genetics and stem cell transplantation in a 2-month-old girl
F. A. M. Baumeister, D. Stachel, F. Schuster, I. Schmid, M. Schaller, H. Wolff, M. Weiss, B. H. Belohradsky
Vallecular cyst: an uncommon cause of stridor in newborn infants
W. -S. Hsieh, P. -H. Yang, K. -S. Wong, H. -Y. Li, E. C.-R. Wang, T. -F. Yeh
Familial neonatal SIDS revealing carnitine-acylcarnitine translocase deficiency
J. -M. Nuoffer, P. de Lonlay, C. Costa, C. R. Roe, N. Chamoles, M. Brivet, J. M. Saudubray
Carotenoid supply in breast-fed and formula-fed neonates
Olaf Sommerburg, Kristina Meissner, Mathias Nelle, Henning Lenhartz, Michael Leichsenring
Presence of metabolic cardiovascular syndrome in obese children
Györgyi Csábi, Katalin Török, Sára Jeges, Dénes Molnár
Diagnostic approach to primary ciliary dyskinesia: a review
D. Holzmann, P. M. Ott, H. Felix
Buccal cell DNA analysis in premature and term neonates: screening for mutations of the complete coding region for the cystic fibrosis transmembrane conductance regulator
L. -C. Bennett, R. Kraemer, S. Liechti-Gallati
Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature
C. F. Boerkoel, S. O'Neill, J. L. André, P. J. Benke, R. Bogdanovíć, M. Bulla, A. Burguet, S. Cockfield, I. Cordeiro, J. H. H. Ehrich, S. Fründ, D. F. Geary, A. Ieshima, F. Illies, M. W. Joseph, I. Kaitila, G. Lama, B. Leheup, M. D. Ludman, D. R. McLeod, A. Medeira, D. V. Milford, T. Örmälä, Z. Rener-Primec, A. Santava, H. G. Santos, B. Schmidt, G. C. Smith, J. Spranger, N. Zupancic, R. Weksberg
Persistent acquired lobar overinflation complicating bronchopulmonary dysplasia
C. Murray, D. W. Pilling, N. J. Shaw
Diagnosis and molecular analysis of an atypical case of holocarboxylase synthetase deficiency
O. Sakamoto, Y. Suzuki, X. Li, Y. Aoki, M. Hiratsuka, E. Holme, J. Kudoh, N. Shimizu, K. Narisawa
Novel mutations, no detectable mRNA and familial genetic analysis of the Wiskott-Aldrich syndrome protein gene in six Japanese patients with Wiskott-Aldrich syndrome
Y. Sasahara, S. Kawai, S. Kumaki, Y. Ohashi, M. Minegishi, S. Tsuchiya
Pubertal development and growth after total-body irradiation and bone marrow transplantation for haematological malignancies
B. Bakker, G. G. Massa, W. Oostdijk, M. H. Van Weel-Sipman, J. M. Vossen, J. M. Wit
Primary infantile hypomagnesaemia: outcome after 21 years and treatment with continuous nocturnal nasogastric magnesium infusion
D. E. C. Cole, S. W. Kooh, R. Vieth
Neonatal renal venous thrombosis in Germany between 1992 and 1994: epidemiology, treatment and outcome
A. Bökenkamp, R. von Kries, U. Nowak-Göttl, U. Göbel, P. F. Hoyer
Erythrocyte fatty acid composition in term infants fed human milk or a formula enriched with a low eicosapentanoic acid fish oil for 4 months
A. Lapillonne, N. Brossard, O. Claris, B. Reygrobellet, B. L. Salle
Odd-numbered long-chain fatty acids in propionic acidaemia
W. Sperl, C. Murr, D. Skladal, J. O. Sass, T. Suormala, R. Baumgartner, U. Wendel
Low serum inhibin B levels as a marker of testicular damage after treatment for a childhood malignancy
A. Cicognani, E. Cacciari, A. Pasini, R. Burnelli, R. De Iasio, P. Pirazzoli, G. Paolucci
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings
L. Van Maldergem, D. Tuerlinckx, R. J. Wanders, C. Vianey-Saban, F. Van Hoof, J. -J. Martin, C. Fourneau, Y. Gillerot, A. Bachy
Sclerosing cholangitis associated to cryptosporidiosis in liver-transplanted children
M. Campos, E. Jouzdani, C. Sempoux, J. P. Buts, R. Reding, J. B. Otte, E. M. Sokal
A child with abnormal features and expressive dysphasia
R. Kishore Kumar, S. P. Nagi
An infant with chronic diarrhoea and failure to thrive
H. Narchi, M. R. El Jamil, S. S. Amr
Decreased bone mineral density in short normal children: normalization with growth-hormone therapy
Cosmetic sequelae of thoraco-amniotic shunting
R. D. Webb, S. A. Walkinshaw, N. J. Shaw
One hundred courses of high frequency oscillatory ventilation: what have we learned?
S. J. Watkins, M. J. Peters, R. C. Tasker
Myocarditis associated with parvovirus B19 infection in two siblings with merosin-deficient congenital muscular dystrophy
Maurice Beghetti, Alain Gervaix, Charles Antoine, Haenggeli, Michel Berner, Peter C. Rimensberger
Transient heart block in a newborn due to maternal antipsychotic treatment during pregnancy
E. Ergenekon, Y. Atalay, S. Tunaoglu, E. Koc
The infection risk of oesophageal dilatations
F. Andiran, F. Cahit Tanyel, S. Özsoylu