Showing results (231-240 of 2,449) with videos related to
Sort By:
Pageof 245
Italian Journal of Pediatrics|September 29, 2011
Inhaled surfactant in the treatment of accidental talc powder inhalation: a new case reportFederico Matina, Mirella Collura, Maria Cristina Maggio, et al.Italian Journal of Pediatrics|September 24, 2011
New advances in leukaemia immunotherapy by the use of Chimeric Artificial Antigen Receptors (CARs): state of the art and perspectives for the near futureEttore Biagi, Virna Marin, Greta Maria Paola Giordano Attianese, et al.Italian Journal of Pediatrics|May 19, 2011
18q deletion in a cystic fibrosis infant, increased morbidity and challenge for correct treatment choices: a case reportElide Spinelli, Silviana Timpano, Annalisa Fogazzi, et al.Italian Journal of Pediatrics|December 2, 2011
Pediatric febrile urinary tract infections: the current state of playIan K Hewitt, Giovanni MontiniItalian Journal of Pediatrics|July 21, 2011
Obesity modulate serum hepcidin and treatment outcome of iron deficiency anemia in children: a case control studyMohammed Sanad, Mohammed Osman, Amal GharibItalian Journal of Pediatrics|November 13, 2010
Comparison of health related quality of life of primary school deaf children with and without motor impairmentVenkadesan Rajendran, Finita Glory RoyItalian Journal of Pediatrics|December 15, 2010
Body fluids and salt metabolism - part IIMattia Peruzzo, Gregorio P Milani, Luca Garzoni, et al.Italian Journal of Pediatrics|October 1, 2011
A randomized, double-blind, placebo-controlled trial of paracetamol and ketoprofren lysine salt for pain control in children with pharyngotonsillitis cared by family pediatriciansNicolino Ruperto, Luigi Carozzino, Roberto Jamone, et al.Italian Journal of Pediatrics|October 6, 2011
Immune-related disorders in families of children with inflammatory bowel disease--a prospective cohort studyAlyzée M Sibtain, Donald Spady, Wael El-MataryItalian Journal of Pediatrics|March 20, 2012
Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiencyNecil Kutukculer, Nesrin Gulez, Neslihan Edeer Karaca, et al.Pageof 245