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European Journal of Pediatrics

Ausgabe 10/2003

Inhalt (21 Artikel)

Original Paper

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

Original Paper

Chronic eosinophilic ascites in a very young child

Arrigo Vittorio Barabino, Emanuela Castellano, Paolo Gandullia, Franco Torrente, Alessandra Guida, Gian Michele Magnano

Original Paper

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

Original Paper

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

Original Paper

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

Original Paper

Surfactant therapy in neonates with respiratory failure due to haemorrhagic pulmonary oedema

Takasuke Amizuka, Hiroshi Shimizu, Yuichi Niida, Yunosuke Ogawa

Original Paper

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

Original Paper

Acquired angioedema and Helicobacter pylori infection in a child

Jana Varvarovska, Josef Sykora, Frantisek Stozicky, Ivan Chytra

Original Paper

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

Original Paper

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

Research Letter

Fructose 1,6 diphosphatase deficiency in a Turkish infant

Betül Tavil, Tansu Sipahi

Short Report

Continuous subcutaneous insulin infusion in toddlers

Birgit Rami, Edith Nachbaur, Thomas Waldhoer, Edith Schober

Short Report

Paroxetine withdrawal in a neonate with historical and laboratory confirmation

Sanjay Jaiswal, Robert C. Coombs, Geoffrey K. Isbister

Short Report

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

Short Report

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

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