P. Rostami

发表

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

N. Rezaei, A. Rabbani, P. Rostami, 2013, Annales d'endocrinologie.

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

V. Ziaee, F. Sayarifard, A. Rabbani, 2017 .

Hepato-Protection Effect of Curcumin Against Methylphenidate-Induced Hepatotoxicity: Histological and Biochemical Evidences

P. Rostami, M. Motevalian, M. Motaghinejad, 2022, International journal of preventive medicine.

Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review

M. Garshasbi, A. Tavasoli, P. Rostami, 2019, Acta Neurologica Belgica.

Role of vitamin D and vitamin D receptor gene polymorphisms on residual beta cell function in children with type 1 diabetes mellitus

A. Alipour, M. Amoli, F. Sayarifard, 2019, Pharmacological reports : PR.

Comparison of Once-daily versus Twice-daily Injection of Insulin Detemir in Children with Type 1 Diabetes Mellitus

F. Sayarifard, A. Rabbani, A. Sayarifard, 2022, Iranian Journal of Pediatrics.

Molecular investigation of mutations in androgen receptor and 5‐alpha‐reductase‐2 genes in 46,XY Disorders of Sex Development with normal testicular development

Abdolmohamad Kajbafzadeh, A. Setoodeh, J. Tavakkoly-Bazzaz, 2019, Andrologia.

The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry System

M. Qorbani, M. Mohammadi, Z. Rezaei, 2018, Journal of child neurology.

Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variants

N. Parvaneh, H. Akhavan-Niaki, F. Sayarifard, 2022, Orphanet Journal of Rare Diseases.

Apolipoprotein E genotype does not associate with disease severity measured by Multiple Sclerosis Severity Score

Á. Guerrero, P. Rostami, F. Iglesias, 2007, Acta neurologica Scandinavica.

Inborn errors of metabolism underlying primary immunodeficiencies

J. Casanova, P. Quartier, P. Lonlay, 2014, Journal of Clinical Immunology.

Epidermal nevus in association with some uncommon manifestations.

E. Zwarthoff, N. Rezaei, I. Lurkin, 2013, Acta dermatovenerologica Croatica : ADC.

Stimulated and Unstimulated Saliva Glucose Levels in Children Suffer Insulin-Dependent Diabetes Mellitus

I. Mirzaii-Dizgah, M. Kharazifard, P. Rostami, 2017 .

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

J. Zschocke, N. Parvaneh, Z. Rezaei, 2018, Orphanet Journal of Rare Diseases.

Placenta derived Mesenchymal Stem Cells transplantation in Type 1 diabetes: preliminary report of phase 1 clinical trial

B. Larijani, B. Arjmand, H. Aghayan, 2021, Journal of Diabetes & Metabolic Disorders.

Pericentric Inversion of Chromosome 9 in an Infant With Ambiguous Genitalia.

N. Rezaei, Reihaneh Mohsenipour, P. Rostami, 2017, Acta medica Iranica.

Trisomy 9 Syndrome in an Infant with Ambiguous Genitalia

P. Rostami, 2016 .

Insulin edema in a child with diabetes mellitus type 1.

N. Rezaei, A. Rabbani, P. Rostami, 2012, The Turkish journal of pediatrics.

Hypothalamic hamartoma in an unusual case with delayed puberty.

Ameneh Zare-Shahabadi, N. Rezaei, M. Mehdizadeh, 2013, Acta medica Iranica.

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

J. Zschocke, J. Häberle, F. Sayarifard, 2017 .

Pediatric endocrinopathies related to COVID-19: an update

Reihaneh Mohsenipour, P. Rostami, E. Memar, 2022, World Journal of Pediatrics.

Neurological and Vascular Manifestations of Ethylmalonic Encephalopathy

A. Tavasoli, P. Karimzadeh, P. Rostami, 2017, Iranian journal of child neurology.

The Cost-effectiveness of Analogue Insulin Pens in Comparison with Human Insulin Pens for Controlling Type 1, Type 2, and Gestational Diabetes: A Systematic Review Article

M. Pakdaman, P. Rostami, R. Akbari, 2019, Health Technology Assessment in Action.

Relationship Between Body Mass Index, Fatty Liver, Lipids Profile, Carotid Intima-Media Thickness and Subcutaneous and Visceral Fat Determined by Ultrasound

M. Mehdizadeh, F. Sayarifard, A. Sayarifard, 2020, Iranian Journal of Pediatrics.

Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature review

J. Zschocke, A. Tavasoli, P. Rostami, 2017, Brain and Development.

OUTPATIENT PARENTERAL ANTIMICROBIAL THERAPY IN CHILDREN WITH FEBRILE URINARY TRACT INFECTION: A PROSPECTIVE RANDOMIZED CLINICAL TRIAL

P. Salamati, P. Rostami, D. Fahimi, 2009 .

Prevalence of dental abnormalities in different calcium metabolism disorders in a group of Iranian children

P. Rahmani, P. Rostami, A. Mohebi, 2017 .

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

F. Sayarifard, A. Rabbani, F. Abbasi, 2016 .

K. Mirnia, P. Rostami, Sedra Mohammadi, 2022, Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo.

Methylmalonic acidemia with emergency hypertension.

N. Rezaei, P. Rostami, Behnaz Bazargani, 2016, Nefrología.

Beta-Ketothiolase Deficiency as A Treatable Neurometabolic Disorder: A Case Report Due to A Novel Compound Heterozygote Mutations in ACAT1 Gene

M. Garshasbi, A. Tavasoli, P. Rostami, 2019, Biomedical Journal of Scientific & Technical Research.

Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b)

M. Abiri, M. Shakiba, M. Modarressi, 2020, Orphanet Journal of Rare Diseases.

Vitamin D Deficiency Induced Hypocalcemia as a Leading Cause of Dilated Cardiomyopathy: A Rare Report

P. Rostami, A. Salimi, A. Ghamari, 2019, Global Journal of Pediatrics & Neonatal Care.