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The first national pediatric immune thrombocytopenia registry in Iran: research protocol and preliminary study results

BMC health services research, 2024-05, Vol.24 (1), p.675-675, Article 675

2024

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Online information-seeking behavior of Iranian web users on Google about Henoch-Schönlein purpura (HSP): an infodemiology study

BMC health services research, 2023-12, Vol.23 (1), p.1389-1389, Article 1389

2023

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Arterial stroke in a child with Seckel syndrome with a pattern of non‐moyamoya vasculopathy

Clinical case reports, 2024-05, Vol.12 (5), p.e8871-n/a

2024

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Development and evaluation of a customized checklist to assess the quality control of disease registry systems of Tehran, the capital of Iran in 2021

BMC health services research, 2023-07, Vol.23 (1), p.726-726, Article 726

2023

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Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control study

Frontiers in molecular biosciences, 2023-06, Vol.10, p.1203019-1203019

2023

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Novel blood and tissue-based mitochondrial D-loop mutations detected in an Iranian NAFLD patient cohort

Mitochondrion, 2024-07, Vol.77, p.101888-101888, Article 101888

2024

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Dehydrogenase (DLD) Deficiency in an Iranian Patient with Recurrent Intractable Vomiting: Successful Treatment with Thiamine Supplementation

Iranian journal of child neurology, 2024, Vol.18 (1), p.131-138

2024

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Etiology, Presenting Features, and Endoscopic Findings of Portal Vein Hypertension in Children

Journal of comprehensive pediatrics, 2023-05, Vol.14 (2)

2023

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The Mitochondrial DNA 4977-bp Deletion in Patients with Colorectal Cancer: a Case-control Study in Iran

Iranian journal of blood and cancer, 2022-12, Vol.14 (4), p.104-110

2022

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COVID-19 Related Multi-System Inflammatory Syndrome in Children (MIS-C): A Systematic Review

Archives of pediatric infectious diseases, 2024-07, Vol.12 (3)

2024

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Clinical and genetic characteristics of hemoglobin H disease in Iran

Pediatric hematology and oncology, 2022-08, Vol.39 (6), p.489-499

2022

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Allogenic hematopoietic stem cell transplantation in an Iranian patient with osteopetrosis caused by carbonic anhydrase II deficiency: A case report

Pediatric transplantation, 2024-05, Vol.28 (3), p.e14689-n/a

2024

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Prevalence of Anemia and its Relation with Shwachman Score in Children with Cystic Fibrosis

Tanaffus, 2023-01, Vol.22 (1), p.160-166

2023

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Liver Mitochondrial DNA Copy Number and Deletion Levels May Contribute to Nonalcoholic Fatty Liver Disease Susceptibility

Hepatitis monthly, 2016-12, Vol.16 (12), p.e40774-e40774

2016

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Analysis of Mitochondrial 4977-bp Deletion and D-Loop Variation in Iranian Non-Alcoholic Fatty Liver Disease Patients

Hepatitis monthly, 2019-02, Vol.In Press (In Press)

2019

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Dehydrogenase (DLD) Deficiency in an Iranian Patient with Recurrent Intractable Vomiting: Successful Treatment with Thiamine Supplementation

Iranian journal of child neurology, 2024, Vol.18 (1), p.131-138

2024

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Pyogenic Arthritis, Pyoderma Gangrenosum and Acne (PAPA) and PAPA-Like Syndromes: Systematic Review of the Literature

Immunology and Genetics Journal, 2023-11

2023

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Arterial stroke in a child with Seckel syndrome with a pattern of non-moyamoya vasculopathy

Clinical case reports, 2024, Vol.12 (5), p.e8871-e8871

2024

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Allogenic hematopoietic stem cell transplantation in an Iranian patient with osteopetrosis caused by carbonic anhydrase II deficiency: A case report

Pediatric transplantation, 2024, Vol.28 (3), p.e14689-e14689

2024

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The first national pediatric immune thrombocytopenia registry in Iran: research protocol and preliminary study results

Online information-seeking behavior of Iranian web users on Google about Henoch-Schönlein purpura (HSP): an infodemiology study

Arterial stroke in a child with Seckel syndrome with a pattern of non‐moyamoya vasculopathy

Development and evaluation of a customized checklist to assess the quality control of disease registry systems of Tehran, the capital of Iran in 2021

Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control study

Novel blood and tissue-based mitochondrial D-loop mutations detected in an Iranian NAFLD patient cohort

Dehydrogenase (DLD) Deficiency in an Iranian Patient with Recurrent Intractable Vomiting: Successful Treatment with Thiamine Supplementation

Etiology, Presenting Features, and Endoscopic Findings of Portal Vein Hypertension in Children

The Mitochondrial DNA 4977-bp Deletion in Patients with Colorectal Cancer: a Case-control Study in Iran

COVID-19 Related Multi-System Inflammatory Syndrome in Children (MIS-C): A Systematic Review

Clinical and genetic characteristics of hemoglobin H disease in Iran

Allogenic hematopoietic stem cell transplantation in an Iranian patient with osteopetrosis caused by carbonic anhydrase II deficiency: A case report

Prevalence of Anemia and its Relation with Shwachman Score in Children with Cystic Fibrosis

Liver Mitochondrial DNA Copy Number and Deletion Levels May Contribute to Nonalcoholic Fatty Liver Disease Susceptibility

Analysis of Mitochondrial 4977-bp Deletion and D-Loop Variation in Iranian Non-Alcoholic Fatty Liver Disease Patients

Dehydrogenase (DLD) Deficiency in an Iranian Patient with Recurrent Intractable Vomiting: Successful Treatment with Thiamine Supplementation

Pyogenic Arthritis, Pyoderma Gangrenosum and Acne (PAPA) and PAPA-Like Syndromes: Systematic Review of the Literature

Arterial stroke in a child with Seckel syndrome with a pattern of non-moyamoya vasculopathy

Allogenic hematopoietic stem cell transplantation in an Iranian patient with osteopetrosis caused by carbonic anhydrase II deficiency: A case report

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