Ausgabe 10/2003
Inhalt (21 Artikel)
Primary Sjögren syndrome in the paediatric age: a multicentre survey
Rolando Cimaz, Annachiara Casadei, Carlos Rose, Jirina Bartunkova, Anna Sediva, Fernanda Falcini, Paolo Picco, Marco Taglietti, Francesco Zulian, Rebecca Ten Cate, Flavio R. Sztajnbok, Paraskevi V. Voulgari, Alexandros A. Drosos
Chronic eosinophilic ascites in a very young child
Arrigo Vittorio Barabino, Emanuela Castellano, Paolo Gandullia, Franco Torrente, Alessandra Guida, Gian Michele Magnano
Chronic infantile neurological cutaneous articular syndrome: CD10 over-expression in neutrophils is a possible key to the pathogenesis of the disease
Valentina Leone, Gianni Presani, Sandra Perticarari, Alberto Tommasini, Sergio Crovella, Alessandro Lenhardt, Paolo Picco, Loredana Lepore
Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene
Guy Massa, Nele Jaenen, Sebastien Janssens de Varebeke, Nils Peeters, Wim Wuyts
Infant stroke and beta-2-glycoprotein 1 antibodies: six cases
Freja Ebeling, Jari Petäjä, Soile Alanko, Aune Hirvasniemi, Tarja Holm, Marja Lähde, Auli Nuutila, Helena Pesonen, Elina Vahtera, Vesa Rasi
Chronic illness, life style and emotional health in adolescence: results of a cross-sectional survey on the health of 15-20-year-olds in Switzerland
Lise Miauton, Françoise Narring, Pierre-André Michaud
The late consequences of anthracycline treatment on left ventricular function after treatment for childhood cancer
Lubomir Elbl, Hana Hrstkova, Vaclav Chaloupka
Surfactant therapy in neonates with respiratory failure due to haemorrhagic pulmonary oedema
Takasuke Amizuka, Hiroshi Shimizu, Yuichi Niida, Yunosuke Ogawa
Congenital toxoplasmosis: assessment of risk to newborns in confirmed and uncertain maternal infection
Mariangela Mombrò, Cristina Perathoner, Agata Leone, Vittorina Buttafuoco, Carla Zotti, Maria Alessandra Lievre, Claudio Fabris
Acquired angioedema and Helicobacter pylori infection in a child
Jana Varvarovska, Josef Sykora, Frantisek Stozicky, Ivan Chytra
Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation
Luitgard M. Neumann, Arpad von Moers, Jürgen Kunze, Oliver Blankenstein, Thorsten Marquardt
Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation
Olga Grafakou, Konrad Oexle, Lambert van den Heuvel, Roel Smeets, Frans Trijbels, Hans H. Goebel, Nils Bosshard, Andrea Superti-Furga, Beat Steinmann, Jan Smeitink
Continuous subcutaneous insulin infusion in toddlers
Birgit Rami, Edith Nachbaur, Thomas Waldhoer, Edith Schober
Paroxetine withdrawal in a neonate with historical and laboratory confirmation
Sanjay Jaiswal, Robert C. Coombs, Geoffrey K. Isbister
An unspecific immunostimulating agent and juvenile dermatomyositis: enhanced T-cell proliferation and reverse immunosuppression as a severe adverse drug reaction
Gerd M. Lackmann, Jenny Ndagijimana, Tim Niehues
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting
Carmelo Damiano Salpietro, Silvana Briuglia, Maria Valeria Merlino, Chiara Di Bella, Luciana Rigoli
Experience of continuous haemodiafiltration in a male neonate with ornithine transcarbamylase deficiency
Shigehiro Enkai, Masaki Yamamoto, Kaori Hayashi, Masaki Kobayashi, Tomohiro Sasajima, Takasuke Amizuka, Wataru Abo
An 8-year-old boy with a 4-day history of fever, cough and malaise, and a 2-day history of painful calves and difficulty walking
Paul W. Meier, Mario G. Bianchetti