Adverse reactions of prophylactic intravenous immunoglobulin infusions in Iranian patients with primary immunodeficiency

Blood Cell Parameters, Hemoglobin Electorphoresis, and Thalassemia Gene Types of Patient and His Parents

Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations

Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary Intervention

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Exploring Vitamin D in Children with Febrile Seizure: A Preliminary Study

A novel missense mutation of the HGD gene causes Alkaptonuria

Frequency and Type of Hepatic and Gastrointestinal Involvement in Juvenile Systemic Lupus Erythematosus

Frequency and Type of Hepatic and Gastrointestinal Involvement in Juvenile Systemic Lupus Erythematosus

Prevalence of Acanthosis nigricans and Related Factors in Iranian Obese Children

Comparison of Adenosine Deaminase Level in Serum and Synovial Fluid in Patients with Juvenile Idiopathic Arthritis and Its Relation to Inflammatory Acute Phase Reactants

Status of Bone Mineral Density in Children with Type 1 Diabetes Mellitus and Its Related Factors

Two Novel Mutations in the Argininosuccinate Lyase Gene in Iranian Patients and Literature Review

The Relationship Between Sonographic Findings, and Clinical and Paraclinical Symptoms in Henoch Schonlein Purpura

Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome

Single nucleotide polymorphisms of the genes encoding IL-10 and TGF-1 in Iranian children with atopic dermatitis

A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Patients with Neonatal Diabetes

PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus

Prevalence of Acanthosis nigricans and Related Factors in Iranian Obese Children

The Efficacy of Oral Immunotherapy in Patients with Cow's Milk Allergy

Detection of Mycobacterium avium subsp. paratuberculosis in Iranian patients with type 1 diabetes mellitus by PCR and ELISA

Autoimmune polyendocrinopathy-candidiasisectodermal dystrophy: report of three cases from Iran

Hydroxycitric acid ameliorates inflammation and oxidative stress in mouse models of multiple sclerosis

Hydroxycitric acid ameliorates inflammation and oxidative stress in mouse models of multiple sclerosis

Nicolau Syndrome due to Penicillin Injection: A Report of 3 Cases without Long-Term Complication

Nicolau Syndrome due to Penicillin Injection: A Report of 3 Cases without Long-Term Complication

Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East

Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East

Inborn Errors of Metabolism-Clinical Findings and Laboratory Tests at the Children’s Medical Center, Tehran, Iran

Assessment of Sexual Maturation Among Girls With Special Needs in Tehran, Iran

Evaluation of Serum Adenosine Deaminase in Cystic Fibrosis Patients in an Iranian Referral Hospital

Evaluation of Serum Adenosine Deaminase in Cystic Fibrosis Patients in an Iranian Referral Hospital

Detection of Mycobacterium avium subsp. paratuberculosis in Iranian patients with type 1 diabetes mellitus by PCR and ELISA

The efficacy of the ketogenic diet in infants and young children with refractory epilepsies using a formula-based powder

Monogenic Auto-inflammatory Syndromes: A Review of the Literature

Tetrahydrobiopterin responsiveness in a series of 53 cases of phenylketonuria and hyperphenylalaninemia in Iran

Assessment of Vitamin D Status and Response to Vitamin D3 in Obese and Non-Obese Iranian Children

Assessment of Vitamin D Status and Response to Vitamin D3 in Obese and Non-Obese Iranian Children

Children with Autism Spectrum Disorder and Patterns of Participation in Daily Physical and Play Activities

Intellectual and Developmental Status in Children With Hyperphenylalaninemia and PKU Who Were Screened in a National Program

Altered Suppressor Function of Regulatory T Cells in Type 1 Diabetes

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Biological Motion Perception Is Affected by Age and Cognitive Style in Children Aged 8–15

Hyperostosis-hyperphosphatemia syndrome (HHS): report of two cases with a recurrent mutation and review of the literature

Intellectual and Developmental Status in Children With Hyperphenylalaninemia and PKU Who Were Screened in a National Program

Segregation of a novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi–Bickel syndrome family

Association Between Single Nucleotide Polymorphisms of the Interleukin-4 Gene and Atopic Dermatitis

Morbidity and Mortality in Iranian Children with Juvenile Systemic Lupus erythematosus

Interleukin-4 and Transforming Growth Factor-Beta Single Nucleotide Genes Polymorphisms Confer Susceptibility To Atopic Dermatitis

Effects of visual search vs. auditory tasks on postural control in children with autism spectrum disorder

Effects of visual search vs. auditory tasks on postural control in children with autism spectrum disorder

Clinical course and outcomes of Iranian children with juvenile dermatomyositis and polymyositis

Interleukin-4 and Transforming Growth Factor-Beta Single Nucleotide Genes Polymorphisms Confer Susceptibility To Atopic Dermatitis

Neonatal Lupus erythematosus Following Rheumatoid Arthritis: Case Report and Literature Review

Morbidity and Mortality in Iranian Children with Juvenile Systemic Lupus erythematosus

Periodic Fever: A Review on Clinical, Management and Guideline for Iranian Patients - Part II

Periodic Fever: A Review on Clinical, Management and Guideline for Iranian Patients - Part II

A Randomized Clinical Trial of Insulin Glargine and Aspart, Compared to NPH and Regular Insulin in Children with Type 1 Diabetes Mellitus

Evaluation of Physicians’ Awareness of Pediatric Diseases in Iran

Filaggrin Single Nucleotide Polymorphisms in Atopic Dermatitis

Insulin adherence in patients with diabetes: Risk factors for injection omission

Clinical course and outcomes of Iranian children with juvenile dermatomyositis and polymyositis

Association of single nucleotide polymorphisms of interleukin-1 family with atopic dermatitis

Neonatal Lupus erythematosus Following Rheumatoid Arthritis: Case Report and Literature Review

Periodic Fever: A Review on Clinical, Management and Guideline for Iranian Patients - Part II

Periodic Fever: A Review on Clinical, Management and Guideline for Iranian Patients - Part I

A new missense mutation in FGF23 gene in a male with hyperostosis–hyperphosphatemia syndrome (HHS)

A Randomized Clinical Trial of Insulin Glargine and Aspart, Compared to NPH and Regular Insulin in Children with Type 1 Diabetes Mellitus

Filaggrin Single Nucleotide Polymorphisms in Atopic Dermatitis

Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia

AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndrome

Cognitive flexibility impairments in children with autism spectrum disorders: Links to age, gender and child outcomes

Hypophosphatemic Rickets and its Dental Significance

Cardiac Malformations in Fetuses of Gestational and Pre Gestational Diabetic Mothers

Clinical Trial of Vigabatrin as Adjunctive Therapy in Children with Refractory Epilepsy

Clinical Trial of Vigabatrin as Adjunctive Therapy in Children with Refractory Epilepsy

The Effect of Positive Family History of Autoimmunity in Juvenile Idiopathic Arthritis Characteristics; a Case Control Study

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An Overview of Mutation Detection Methods in Genetic Disorders

Acanthosis nigricans, Abnormal Facial Appearance and Dentition in an Insulin Resistance Syndrome

Reliability of Pubertal Self Assessment Method: An Iranian Study

GCK Mutation in a Child with Maturity Onset Diabetes of the Young, Type 2

The Effects of SPARK Physical Education Program on Fundamental Motor Skills in 4-6 Year-Old Children

Pseudotumor Cerebri in a Case of Ulcerative Colitis with Sagittal Sinus Thrombosis

Probiotics for the Treatment of Pediatric Helicobacter Pylori Infection: A Randomized Double Blind Clinical Trial

Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect

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