Bahareh Rabbani

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 11

Top Topics

Transcranial Magnetic Stimulation

Staphylococcus Aureus

Top Venues

International journal of genomics

International journal of endocrinology

American journal of medical genetics. Part A

Clinical case reports

This page only lists publications with an associated author ORCID identifier.

Publications

Bahareh Rabbani, Mohadeseh Aghli Moghadam, Shiva Esmaeili, Amirhassan Rabbani, Bahman Akbari, Nejat Mahdieh
Pancreatitis as a Main Consequence of APOC2 -Related Hypertriglyceridemia: The Role of Nonsense and Frameshift Variants. International journal of genomics 2024 (2024)
Bahareh Rabbani, Mohadeseh Aghli Moghadam, Shiva Esmaeili, Amirhassan Rabbani, Bahman Akbari, Nejat Mahdieh
Pancreatitis as a Main Consequence of APOC2 -Related Hypertriglyceridemia: The Role of Nonsense and Frameshift Variants. International journal of genomics 2024 (2024)
Shohreh Maleknejad, Setila Dalili, Ameneh Sharifi, Afagh Hassanzadeh Rad, Reza Bayat, Bahareh Rabbani, Nejat Mahdieh
Expanding the Phenotype of Congenital Glucocorticoid Deficiency: An Iranian Patient with Cholestasis due to Pathogenic Variants in the MC2R Gene. International journal of endocrinology 2024 (2024)
Shohreh Maleknejad, Setila Dalili, Ameneh Sharifi, Afagh Hassanzadeh Rad, Reza Bayat, Bahareh Rabbani, Nejat Mahdieh
Expanding the Phenotype of Congenital Glucocorticoid Deficiency: An Iranian Patient with Cholestasis due to Pathogenic Variants in the MC2R Gene. International journal of endocrinology 2024 (2024)
Bahareh Rabbani, Mohadeseh Aghli Moghadam, Shiva Esmaeili, Amirhassan Rabbani, Bahman Akbari, Nejat Mahdieh
Pancreatitis as a Main Consequence of APOC2 -Related Hypertriglyceridemia: The Role of Nonsense and Frameshift Variants. International journal of genomics 2024 (2024)
Bahareh Rabbani, Mohadeseh Aghli Moghadam, Shiva Esmaeili, Amirhassan Rabbani, Bahman Akbari, Nejat Mahdieh
Pancreatitis as a Main Consequence of APOC2 -Related Hypertriglyceridemia: The Role of Nonsense and Frameshift Variants. International journal of genomics 2024 (2024)
Bahareh Rabbani, Mohammadrafi Khorgami, Mohammad Dalili, Nasrin Zamani, Nejat Mahdieh, Michael H Gollob
Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome. American journal of medical genetics. Part A 185 (11) (2021)
Mahdieh Soveizi, Nejat Mahdieh, Aria Setoodeh, Fatemeh Sayarifard, Farzaneh Abbasi, Himangshu S Bose, Bahareh Rabbani, Ali Rabbani
p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche. International journal of endocrinology 2020 (2020)
Katayoun Heshmatzad, Nejat Mahdieh, Ali Rabbani, Abdolah Didban, Bahareh Rabbani
The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel Variants. International journal of endocrinology 2020 (2020)
Setilla Dalili, Bahareh Rabbani, Afagh Hassanzadeh Rad, Shaahin Koohmanaee, Nejat Mahdieh
A novel pathogenic variant of SRD5A2 in an Iranian psuedohermaphrodite male. Clinical case reports 8 (10) (2020)
Nejat Mahdieh, Maryam Hosseini Moghaddam, Mahsa Motavaf, Ahmad Rabbani, Mahdieh Soveizi, Majid Maleki, Bahareh Rabbani, Azin Alizadeh-Asl
Genotypic effect of a mutation of the MYBPC3 gene and two phenotypes with different patterns of inheritance. Journal of clinical laboratory analysis 32 (6) (2018)