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   journal of pediatric perspectives   
سال:2022 - دوره:10 - شماره:9


  tick  a novel heterozygous acan variant in an iranian family with short stature: a case report - صفحه:16729-16737

  tick  anaplastic kinase-positive large t-cell lymphoma simultaneous with tuberculosis in a child: a case report - صفحه:16719-16728

  tick  apolipoprotein e serum levels in children with guillain-barre syndrome in northwest of iran - صفحه:16673-16682

  tick  design and validation of a physical education curriculum model for elementary school children based on the fundamental transformation document - صفحه:16683-16698

  tick  differentiation of biliary atresia from the intrahepatic etiology of infantile cholestasis with alagille criteria - صفحه:16699-16704

  tick  dilemma of retained intraorbital fragment of pencil - صفحه:16758-16765

  tick  effects of peer acceptance on participation of children with adhd in physical activity: mediating role of physical self-efficacy - صفحه:16666-16672

  tick  evaluation of proper prescription of antacid agents in a group of critically ill children admitted to picu in 2018-2019 - صفحه:16656-16665

  tick  importance of il-1β in sars-cov-2 infection - صفحه:16745-16757

  tick  pulmonary sequestration infant with unusual presentation: a case report - صفحه:16738-16744

  tick  recurrent seizure during hospitalization in children with the first febrile seizure: incidence and risk factors - صفحه:16650-16655

  tick  the impact of children’s tv shows on the intelligence of children in tehran - صفحه:16631-16640

  tick  the prevalence of celiac disease in children suffering chronic constipation: a study in the western region of iran - صفحه:16705-16711

  tick  the relationship of regimen adherence with family resilience and parenting style among adolescents with type 2 diabetes - صفحه:16620-16630

  tick  the rs6323 and uvntr polymorphisms in the maoa gene are associated with attention deficit hyperactivity disorder in iranian azeri children - صفحه:16712-16718

  tick  whole-exome sequencing identified a novel hemizygous missense variant in the eda gene in an iranian patient causing hypohidrotic ectodermal dysplasia - صفحه:16641-16649
 

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