Randomised clinical trial of Berberis vulgaris root extract on glycemic and lipid parameters in type 2 diabetes mellitus patients von Tahmasebi, Ladan, Zakerkish, Mehrnoosh, Golfakhrabadi, Fereshteh, Namjoyan, Foroogh

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Recent advances of therapeutic targets based on the molecular signature in breast cancer: genetic mutations and implications for current treatment paradigms von Lima, Zeinab Safarpour, Ghadamzadeh, Mostafa, Arashloo, Farzad Tahmasebi, Amjad, Ghazaleh, Ebadi, Mohammad Reza, Younesi, Ladan

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PastoCovac and PastoCovac Plus as protein subunit COVID-19 vaccines led to great humoral immune responses in BBIP-CorV immunized individuals von Ramezani, Amitis, Sorouri, Rahim, Haji Maghsoudi, Saiedeh, Dahmardeh, Sarah, Doroud, Delaram, Sadat Larijani, Mona, Eybpoosh, Sana, Mostafavi, Ehsan, Olyaeemanesh, Alireza, Salehi-Vaziri, Mostafa, Bavand, Anahita, Zarghani, Ghazaleh, Moradi, Ladan, Ashrafian, Fatemeh, Bagheri Amiri, Fahimeh, Mashayekhi, Parisa, Tahmasebi, Zahra, Biglari, Alireza

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Association of Human Leukocyte Antigen Alleles with Carbamazepine- or Lamotrigine-Induced Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in an Iranian Population: A Case-c... von Dastgheib, Ladan, Rostami, Farima, Gharesi-Fard, Behrouz, Asadi-Pooya, Ali Akbar, Namjoo, Saba, Tahmasebi, Foroozan, Hadibarhaghtalab, Maryam

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Long-term assessment of anti-SARS-CoV-2 antibody levels post-pandemic: Tracking the dynamics after two, three, and four COVID-19 vaccine doses von Ashrafian, Fatemeh, Salehi-Vaziri, Mostafa, Mostafavi, Ehsan, Maghsoudi, Saiedeh Haji, Dahmardeh, Sarah, Bavand, Anahita, Moradi, Ladan, Namini, Parinaz Tajmehrabi, Zali, Mahsan, Tahmasebi, Zahra, Larijani, Mona Sadat, Ramezani, Amitis

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Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred von Sadeghian, Ladan, Tabatabaiefar, Mohammad Amin, Fattahi, Najmeh, Pourreza, Mohammad Reza, Tahmasebi, Parisa, Alavi, Zahra, Hashemzadeh Chaleshtori, Morteza

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Efficacy of diffusion-weighted imaging in symptomatic and asymptomatic multiple sclerotic plaques von Arashloo, Farzad, Hanzaei, Farnaz, Sedighi, Behnaz, Amjad, Ghazaleh, Younesi, Ladan

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Identification a novel mononucleotide deletion mutation in GAA in pompe disease patients von Ebrahimi, Milad, Behnam, Mahdieh, Behranvand-jazi, Nafiseh, Yari, Ladan, Sheikh-kanlomilan, Sajad, Salehi, Mansoor, Tahmasebi, Pardis, Amini, Mohaddeseh, Behjati, Mohaddeseh, Hosseini, Nafisehsadat

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Frequency of GJB2 mutations in families with autosomal recessive non-syndromic hearing loss in Khuzestan province von Tahmasebi, Parisa, Chaleshtori Hashemzadeh, Morteza, Abdollahnejad, Fatemeh, Alavi, Zahra, Sadeghian, Ladan, Talebi, Farah, Mohammadi-Asl, Javad, Saki, Nader, Nezhad, Seyed, Tabatabaiefar, Mohammad

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