Ausgabe 12/2000
Inhalt (27 Artikel)
Xerostomia in patients with triple A syndrome – a newly recognised finding
Miroslav Dumić, Marinka Mravak-Stipetić, Zvonimir Kaić, Jasenka Ille, Vesna Plavšić, Stipe Batinica, Marijana Cvitanović
Narrow- versus broad-spectrum parenteral antimicrobials against common infections of childhood: a prospective and randomised comparison between penicillin and cefuroxime
Elina Vuori-Holopainen, Heikki Peltola, Markku JT Kallio
Genetic and long-term data on a patient with permanent isolated proximal renal tubular acidosis
Masaaki Shiohara, Takashi Igarashi, Tetsuo Mori, Atsushi Komiyama
Pericardial cyst in a child treated with video-assisted thoracoscopic surgery
Akiko Eto, Tohru Arima, Akira Nagashima
Near fatal acute colchicine intoxication in a child. A case report
Aviv Goldbart, Joseph Press, Shaul Sofer, Joseph Kapelushnik
Early infantile pertussis; increasingly prevalent and potentially fatal
Craig Smith, Harish Vyas
3-Methylcrotonyl-CoA carboxylase deficiency in an infant with cardiomyopathy, in her brother with developmental delay and in their asymptomatic father
Gepke Visser, Terttu Suormala, G. Peter A. Smit, Dirk-Jan Reijngoud, Margreet Th. E. Bink-Boelkens, Klary E. Niezen-Koning, E. Regula Baumgartner
A 6-year-old boy with hyperammonaemia: partial N-acetylglutamate synthase deficiency or portosystemic encephalopathy?
Daniel Broere, Wim G. van Gemert, C. M. Frank Kneepkens, Diana M. Neele, Radu A. Manoliu, Jan A. Rauwerda, Marjo S. van der Knaap
Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boy
Toshiaki Doi, Wataru Abo, Masaru Tateno, Kaori Hayashi, Tsukasa Hori, Toshimasa Nakada, Toshiyuki Fukao, Yukitoshi Takahashi, Naoto Terada
Familial disorder of sex determination in seven individuals from three related sibships
Nadim Jarrah, Hatem El-Shanti, Ahmad Khier, Fatima Nouri Obeidat, Azmi Haddidi, Kamel Ajlouni
Continuous infusion of ceftazidime with a portable pump is as effective as thrice-a-day bolus in cystic fibrosis children
Isabelle Rappaz, Laurent A. Decosterd, Jacques Bille, Marianne Pilet, Nicole Bélaz, Michel Roulet
A 17-month-old with extreme prenatal-onset growth delay
Mustafa Tekin, Janice Ng, Joann Bodurtha
Preaxial polydactyly type 1 and severe language deficit in maternal uniparental disomy of chromosome 7
Steph Potgieter, Gert Matthijs, Paul De Cock, Jean-Pierre Fryns
Mental retardation, developmental delay, and partial psychomotor deficits in maternal uniparental disomy 7
Dieter Kotzot
The reactogenicity and immunogenicity of commercial Haemophilus influenzae type b conjugate vaccines
Joseph F. Heyse, Karen M. Kaplan
Thyrotoxic periodic paralysis in a 14-year-old boy
Gary Wing-Kin Wong, Ting Fan Leung, Amy Fung-Cheung Lo, Anil T. Ahuja, Pik Shun Cheng
Tuberous breast deformity in an adolescent girl with Hurler-Scheie syndrome
Rita Barone, Piero Pavone, Rosario R. Trifiletti, Enrico Parano
Growth hormone treatment of children with human immunodeficiency virus-associated growth failure
Graziella Pinto, Stéphane Blanche, Ingrid Thiriet, Jean Claude Souberbielle, Olivier Goulet, Raja Brauner
A rapid technique for detecting chromosomal aneuploidy in early childhood by fluorescence in situ hybridisation
Erika P. Tardy, András Tóth
Real-time monitoring of Helicobacter pylori eradication therapy by testing stool antigen
Toshiaki Shimizu, Yukiko Yarita, Ryuyo Suzuki, Kazunari Kaneko, Yuichiro Yamashiro
Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiency
Tom J de Koning, Marinus Duran, Lambertus Dorland, Cornelis Jakobs, Ron A Wevers, Ruud Berger, Bwee-Tien Poll-The
Factor V 1691G-A mutation and high factor VIII levels in a patient with intracardiac thrombosis
Nejat Akar, Emine Suskan, Hafize Gökçe