Works matching IS 03406199 AND DT 2003 AND VI 162 AND IP 2

Results: 13

Two siblings with tyrosinaemia type 2.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 2, p. 81, doi. 10.1007/s00431-002-0962-4

By:

Aydin, Faruk;
Zorlu, Pelin;
Kunak, Benal;
Tezic, Tahsin;
Eken, Alev

Publication type:

Article

Clinical consequences of twin-to-twin transfusion.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 2, p. 68, doi. 10.1007/s00431-002-1107-5

By:

Chiang, Ming-Chou;
Lien, Reyin;
Chao, An-Shine;
Chou, Yi-Hung;
en Chen, Yu-Jen

Publication type:

Article

Serious adverse effects of unconventional therapies for children and adolescents: a systematic review of recent evidence.

Published in:

2003

By:

Ernst, Edzard

Publication type:

journal article

Prolonged ventilation and intact survival in very low birth weight infants.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 2, p. 65, doi. 10.1007/s00431-002-0914-z

By:

Thomas, Mark;
Greenough, Anne;
Morton, Margaret

Publication type:

Article

Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 2, p. 84, doi. 10.1007/s00431-002-1112-8

By:

Klepper, Jörg;
Flörcken, Anne;
Fischbarg, Jorge;
Voit, Thomas

Publication type:

Article

Complete deficiency of mitochondrial trifunctional protein due to a novel mutation within the β-subunit of the mitochondrial trifunctional protein gene leads to failure of long-chain fatty acid β-oxidation with fatal outcome.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 2, p. 90, doi. 10.1007/s00431-002-1035-4

By:

Schwab, Otfried;
Ensenauer, Regina;
Matern, Dietrich;
Uyanik, Gökhan;
Schnieders, Birgit;
Wanders, Ronald A.;
Lehnert, Willy

Publication type:

Article

Diagnosis of juvenile hemochromatosis in an 11-year-old child combining genetic analysis and non-invasive liver iron quantitation.

Published in:

2003

By:

De Gobbi, M.;
Caruso, R.;
Daraio, F.;
Chianale, F.;
Pinto, R. M.;
Longo, F.;
Piga, A.;
Camaschella, C.

Publication type:

journal article

Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.

Published in:

2003

By:

Olivieri, Carla;
Maraschio, Paola;
Caselli, Desiree;
Martini, Carla;
Beluffi, Giampiero;
Maserati, Emanuela;
Danesino, Cesare

Publication type:

journal article

Evaluation of antibody response after vaccination with conjugate Haemophilus influenzae type b vaccine in infants and toddlers in Slovakia.

Published in:

2003

By:

Novakova, Elena;
Kosecka, Gabriela;
Gajdos, Jan;
Olear, Vladimir;
Hudeckova, Henrieta

Publication type:

journal article

Complications of varicella requiring hospitalisation before and after the introduction of varicella vaccine in a children's hospital in Taiwan.

Published in:

2003

By:

Chuang, Yu-Yu;
Huang, Yhu-Chering;
Chang, Luan-Yin;
Chiu, Cheng-Hsun;
Lin, Tzou-Yien

Publication type:

journal article

Hair changes in congenital disorders of glycosylation (CDG type 1).

Published in:

2003

By:

Silengo, Margherita;
Valenzise, Mariella;
Pagliardini, Severo;
Spada, Marco

Publication type:

journal article

Secular trends in body mass index measurements in preschool children from the City of Aachen, Germany.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 2, p. 104, doi. 10.1007/s00431-002-1056-z

By:

Herpertz-Dahlmann, Beate;
Geller, Frank;
Böhle, Corinna;
Khalil, Corinna;
Trost-Brinkhues, Gabriele;
Ziegler, Andreas;
Hebebrand, Johannes

Publication type:

Article

Genetic susceptibility to common disorders.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 2, p. 116, doi. 10.1007/s00431-002-1073-y

By:

J.W.S.

Publication type:

Article