Ausgabe 5/2005
Inhalt (18 Artikel)
Vascular rings—presentation, investigation and outcome
Alastair Turner, Gil Gavel, Jonathan Coutts
Prevalence of fat redistribution and metabolic disorders in human immunodeficiency virus-infected children
Ana María Sánchez Torres, Raquel Munoz Muniz, Rosario Madero, Clementina Borque, María Jesús García-Miguel, María Isabel De José Gómez
Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia
Toshimi Michigami, Takayuki Uchihashi, Akira Suzuki, Kanako Tachikawa, Shigeo Nakajima, Keiichi Ozono
Tight skin and limited joint movements as early presentation of Hutchinson-Gilford progeria in a 7-week-old infant
Lieve Sevenants, Carine Wouters, Annachiara De Sandre-Giovannoli, Hugo Devlieger, Koen Devriendt, Joost J. van den Oord, Karel Marien, Nicolas Lévy, Marie-Anne Morren
Idiopathic male pseudohermaphroditism is associated with prenatal growth retardation
Francisco de Andrade Machado Neto, André Moreno Morcillo, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior
Population-based study of bronchopulmonary dysplasia in very low birth weight infants in Switzerland
Juliane Hentschel, Thomas M. Berger, Alois Tschopp, Martina Müller, Mark Adams, Hans-Ulrich Bucher
Biotinidase deficiency: the importance of adequate follow-up for an inconclusive newborn screening result
Trevor L. Hoffman, Erin M. Simon, Can Ficicioglu
A case of idiopathic sclerosing mediastinitis in a 7-year-old Japanese boy
Tomoko Shinkawa, Mitsuru Nakajima, Tomoko Kishimoto, Jiro Inagaki, Young-Dong Park, Keiji Kushibe, Shigeki Taniguchi, Atsuko Nakagawa, Akira Yoshioka
Colorectal cancer in two pre-teenage siblings with familial adenomatous polyposis
Silvija Jerkic, Hendrik Rosewich, Jens-Gerd Scharf, Christina Perske, Laszlo Füzesi, Ekkehard Wilichowski, Jutta Gärtner
Severe combined immunodeficiency caused by a splicing abnormality of the CD3δ gene
Hidetoshi Takada, Akihiko Nomura, Chaim M. Roifman, Toshiro Hara
Occurrence of haemophagocytic lymphohistiocytosis at less than 1 year of age: analysis of 96 patients
Shinsaku Imashuku, Ikuyo Ueda, Tomoko Teramura, Kanako Mori, Akira Morimoto, Masahiro Sako, Eiichi Ishii
Acceptance and timeliness of standard vaccination in children with chronic neurological deficits in north-western Switzerland
Bettina Ute Tillmann, Hanns-Christian Tillmann, Ulrich Heininger, Jürg Lütschg, Peter Weber
Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation
Gabriele Wohlrab, Goekhan Uyanik, Claudia Gross, Ute Hehr, Jürgen Winkler, Bernhard Schmitt, Eugen Boltshauser
Prevention and management of meconium aspiration syndrome—assessment of evidence based practice
Anne Greenough, Ashok Pulikot, Gabriel Dimitriou
Surfactant lavage for extracorporeal membrane oxygenation-requiring meconium aspiration syndrome —a cheap alternative
Thierry Lejeune, Riccardo E. Pfister
Rituximab treatment in refractory idiopathic thrombocytopenic purpura in children
Jelena Roganovic
Life-threatening complications of transient abnormal myelopoiesis in neonates with Down syndrome
Sabine Dormann, Marcus Krüger, Roland Hentschel, Regina Rasenack, Brigitte Strahm, Udo Kontny, Charlotte Niemeyer