Letrozole-Loaded Nano-formulations as a Drug Delivery System for Cancer Therapy: Recent Developments von Pourmadadi, Mehrab, Hosseini, Seyede Mahtab, Parvaneh, Sahand, Ahmadi, Hamed, Abdouss, Majid, Rahdar, Abbas, Ghotekar, Suresh, Tehrani, Fatemeh Soltani

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Carboxymethyl cellulose/starch/reduced graphene oxide composite as a pH-sensitive nanocarrier for curcumin drug delivery von Parvaneh, Sahand, Pourmadadi, Mehrab, Abdouss, Majid, Pourmousavi, Seied Ali, Yazdian, Fatemeh, Rahdar, Abbas, Díez-Pascual, Ana M.

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Novel TECPR2 variant in two cases of hereditary sensory and autonomic neuropathy type 9: insights from genetic characterization and comprehensive literature review von Moeinafshar, Aysan, Tehrani Fateh, Sahand, Hashemi-Gorji, Farzad, Karimzadeh, Parvaneh, Gholibeglou, Elham, Rostami, Masoumeh, Sadeghi, Hossein, Miryounesi, Mohammad, Ghasemi, Mohammad-Reza

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Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene von Moeinafshar, Aysan, Tehrani Fateh, Sahand, Sadeghi, Hossein, Karimzadeh, Parvaneh, Mirfakhraie, Reza, Hashemi-Gorji, Farzad, Larki, Pegah, Miryounesi, Mohammad, Ghasemi, Mohammad-Reza

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Cell-Penetrating Peptide Functionalized ZIF-8 (Zn, Fe)/Doxorubicin/Chitosan-Grafted-Polycaprolactone/Curcumin Against A549 Lung Cancer Cells von Kordbacheh, Hananeh, Eslami, Sahand, Rezaee, Aryan, Abadi, Parvaneh Ghaderi-shekhi, Bybordi, Sara, Ehsanfar, Niloufar, Goleij, Pouya, SharifianJazi, Fariborz, Irani, Mohammad

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Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review von Ghasemi, Mohammad-Reza, Tehrani Fateh, Sahand, Moeinafshar, Aysan, Sadeghi, Hossein, Karimzadeh, Parvaneh, Mirfakhraie, Reza, Rezaei, Mitra, Hashemi-Gorji, Farzad, Rezvani Kashani, Morteza, Fazeli Bavandpour, Fatemehsadat, Bagheri, Saman, Moghimi, Parinaz, Rostami, Masoumeh, Madannejad, Rasoul, Roudgari, Hassan, Miryounesi, Mohammad

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Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome von Norouzi Rostami, Fatemeh, Sadeghi, Hossein, Hashemi-Gorji, Farzad, Tehrani Fateh, Sahand, Mirfakhraie, Reza, Karimzadeh, Parvaneh, Davarpanah, Milad, Jamshidi, Sanaz, Madannejad, Rasoul, Moghimi, Parinaz, Ekrami, Mahdis, Miryounesi, Mohammad, Ghasemi, Mohammad-Reza

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