Issue 2/2010
Content (22 Articles)
Significance of long-chain polyunsaturated fatty acids (PUFAs) for the development and behaviour of children
Jan Philipp Schuchardt, Michael Huss, Manuela Stauss-Grabo, Andreas Hahn
Rupture of the papillary muscle of the tricuspid valve — echocardiographic diagnosis of a rare anomaly leading to critical tricuspid valve regurgitation in the newborn
F. T. Riede, I. Dähnert, V. Razek, M. Kostelka
Fulminant hepatitis B and acute hepatitis B due to intrafamilial transmission of HBV after chemotherapy for non-Hodgkin’s lymphoma in an HBV carrier
Tomoki Aomatsu, Haruki Komatsu, Atsushi Yoden, Akiko Hosomi, Hiroshi Miyazaki, Tsuyoshi Sogo, Ayano Inui, Tomoo Fujisawa, Hiroshi Tamai
Characteristics associated with maltreatment types in children referred to a hospital protection team
Andreas Jud, Ulrich Lips, Markus A. Landolt
Programmed death-1 (PD-1) gene polymorphisms lodged in the genetic predispositions of Kawasaki Disease
Jin-Kyong Chun, Dong Won Kang, Byung Won Yoo, Jeon-Soo Shin, Dong Soo Kim
Does lack of routine postnatal examination on maternity unit increase the risk of hospital admission in the first week of life?
Arthur Abelian, Jim Turner, Jonathan Cusack
Maternal bariatric surgery: adverse outcomes in neonates
A. Eerdekens, A. Debeer, G. Van Hoey, C. De Borger, V. Sachar, I. Guelinckx, R. Devlieger, M. Hanssens, C. Vanhole
Favourable long-term outcome after immediate treatment of neonatal hyperammonemia due to N-acetylglutamate synthase deficiency
Peter Gessler, Peter Buchal, Hans U. Schwenk, Bendicht Wermuth
A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria
Elsebet Ostergaard, Marianne Schwartz, Mustafa Batbayli, Ernst Christensen, Ola Hjalmarson, Gittan Kollberg, Elisabeth Holme
DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins
Lene Bjerke Laborie, Deborah J. G. Mackay, I. Karen Temple, Anders Molven, Oddmund Søvik, Pål Rasmus Njølstad
Increased type 3 iodothyronine deiodinase activity in a regrown hepatic hemangioma with consumptive hypothyroidism
Kazuhiko Bessho, Yuri Etani, Hiroaki Ichimori, Yoko Miyoshi, Noriyuki Namba, Akihiro Yoneda, Takaharu Ooue, Tsuyoshi Chihara, Eiichi Morii, Tomoyuki Aoki, Masami Murakami, Sotaro Mushiake, Keiichi Ozono
A heritable cause of cleft lip and palate—Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis
Giovanni Battista Ferrero, Giuseppina Baldassarre, Emanuele Panza, Mariella Valenzise, Tommaso Pippucci, Alessandro Mussa, Ernesto Pepe, Marco Seri, Margherita Cirillo Silengo
Surveillance study of apparent life-threatening events (ALTE) in the Netherlands
Ben A. Semmekrot, Bregje E. van Sleuwen, Adele C. Engelberts, Koen F. M. Joosten, Jaap C. Mulder, K. Djien Liem, Rob Rodrigues Pereira, Rob P. G. M. Bijlmer, Monique P. L’Hoir
Streptococcus pneumoniae-associated haemolytic uremic syndrome following influenza A virus infection
Tzu-Hui Lei, Shao-Hsuan Hsia, Chang-Teng Wu, Jainn-Jim Lin
Titration of betaine therapy to optimize therapy in an infant with 5,10-methylenetetrahydrofolate reductase deficiency
Sema Kalkan Ucar, Özge Altun Koroğlu, Ömer Berk, Mehmet Yalaz, Nilgün Kültürsay, Henk J. Blom, Mahmut Coker
Long-term treatment with recombinant insulin-like growth factor 1 (IGF-1) in a child with IGF-1 gene mutation
Daniela Concolino, Gianluca Muzzi, Simona Sestito, Giovanna Vega, Giuseppe Bonapace, Pietro Strisciuglio
A 4-year-old boy presenting with recurrent croup
Chien-Yu Lin, Hsin Chi, Shin-Lin Shih, Kuo-Sheng Lee, Jin-Cherng Sheu, Nan-Chang Chiu, Fu-Yuan Huang
WHO child growth standards
Mrinal Kanti Das, Nabanita Bhattacharyya, Amiya Kumar Bhattacharyya
Reply to correspondence letter by M. Das et al.: WHO Child Growth Standards
Jan Van den Broeck, Douladel Willie, Novie Younger