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   International Journal Of Pediatrics   
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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