Retraction Note: The toxicity and therapeutic effects of single-and multi-wall carbon nanotubes on mice breast cancer von Kavosi, Arghavan, Noei, Saeideh Hosseini Ghale, Madani, Samaneh, Khalighfard, Solmaz, Khodayari, Saeed, Khodayari, Hamid, Mirzaei, Malihe, Kalhori, Mohammad Reza, Yavarian, Majid, Alizadeh, Ali Mohammad, Falahati, Mojtaba

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia von Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt C., Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Tournev, Ivailo, Chamova, Teodora, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali

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The association of Q472H variant in the KDR gene with recurrent pregnancy loss in Southern Iran: A case-control study von Keshavarz, Leila, Yavarian, Majid

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Genotype–phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in Iran von Karimi, Mehran, Haghpanah, Sezaneh, Farhadi, Ali, Yavarian, Majid

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A novel stop-gain mutation in DPYS gene causing Dihidropyrimidinase deficiency, a case report von Mirzaei, Malihe, Kavosi, Arghavan, Sharifzadeh, Mahboobeh, Mahjoub, Ghazale, Faghihi, Mohammad Ali, Habibzadeh, Parham, Yavarian, Majid

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Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder von Polla, Daniel L., Farazi Fard, Mohammad Ali, Tabatabaei, Zahra, Habibzadeh, Parham, Levchenko, Olga A., Nikuei, Pooneh, Makrythanasis, Periklis, Hussain, Mureed, von Hardenberg, Sandra, Zeinali, Sirous, Fallah, Mohammad-Sadegh, Schuurs-Hoeijmakers, Janneke H.M., Shahzad, Mohsin, Fatima, Fareeha, Fatima, Neelam, Kaat, Laura Donker, Bruggenwirth, Hennie T., Fleming, Leah R., Condie, John, Ploski, Rafal, Pollak, Agnieszka, Pilch, Jacek, Demina, Nina A., Chukhrova, Alena L., Sergeeva, Vasilina S., Venselaar, Hanka, Masri, Amira T., Hamamy, Hanan, Santoni, Federico A., Linda, Katrin, Ahmed, Zubair M., Nadif Kasri, Nael, de Brouwer, Arjan P.M., Bergmann, Anke K., Hethey, Sven, Yavarian, Majid, Ansar, Muhammad, Riazuddin, Saima, Riazuddin, Sheikh, Silawi, Mohammad, Ruggeri, Gaia, Pirozzi, Filomena, Eftekhar, Ebrahim, Taghipour Sheshdeh, Afsaneh, Bahramjahan, Shima, Mirzaa, Ghayda M., Lavrov, Alexander V., Antonarakis, Stylianos E., Faghihi, Mohammad Ali, van Bokhoven, Hans

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Role of the 820 A/G variant in the IGF-2 gene and recurrent spontaneous abortion in southern Iran: A cross-sectional study von Ardeshir, Farzaneh, Keshavarz, Leila, Asadian, Fatemeh, Omidmokhtarkhanloo, Gohar, Yavarian, Majid

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Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy von Habibzadeh, Parham, Silawi, Mohammad, Dastsooz, Hassan, Bahramjahan, Shima, Ezzatzadegan Jahromi, Shahrokh, Ostovan, Vahid Reza, Yavarian, Majid, Mofatteh, Mohammad, Faghihi, Mohammad Ali

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A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment von Habibzadeh, Parham, Inaloo, Soroor, Silawi, Mohammad, Dastsooz, Hassan, Farazi Fard, Mohammad Ali, Sadeghipour, Forough, Faghihi, Zahra, Rezaeian, Mohaddeseh, Yavarian, Majid, Böhm, Johann, Faghihi, Mohammad Ali

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Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report von Amanati, Ali, Badiee, Parisa, Lotfi, Mehrzad, Monabati, Ahmad, Faghihi, Mohammad Ali, Yavarian, Majid, Hatami Mazinani, Nazafarin

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A novel PCDH19 gene mutation in a hemizygous male with epilepsy, new insight to the pathophysiology von Kowkabi, Safoura, Mohammadi, Mahmood, Kaboodkhani, Reza, Yavarian, Majid

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PCDH19-clustering epilepsy, pathophysiology and clinical significance von Kowkabi, Safoura, Yavarian, Majid, Kaboodkhani, Reza, Mohammadi, Mahmood, Shervin Badv, Reza

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The toxicity and therapeutic effects of single-and multi-wall carbon nanotubes on mice breast cancer von Kavosi, Arghavan, Hosseini Ghale Noei, Saeideh, Madani, Samaneh, Khalighfard, Solmaz, Khodayari, Saeed, Khodayari, Hamid, Mirzaei, Malihe, Kalhori, Mohammad Reza, Yavarian, Majid, Alizadeh, Ali Mohammad, Falahati, Mojtaba

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Non-hodgkin lymphoma in a child with schimke immuno-osseous dysplasia von Basiratnia, Mitra, Baradaran-Heravi, Alireza, Yavarian, Majid, Geramizadeh, Bita, Karimi, Mehran

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Multi Centric Origin of Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA] von Yavarian, Majid, Karimi, Mehran, Paran, Farideh, Neven, Catherine, Harteveld, Cornelis L., Giordano, Piero C.

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Association of the functional genetic variants of TOX3 gene with breast cancer in Iran: A case-control study von Jamali, Nehle, Nasiri, Mahboobeh, Yavarian, Majid

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A novel splice-site mutation in the LRP5 gene causing Familial Exudative Vitreoretinopathy von Shafienia, Shohreh, Mirzaei, Malihe, Kavosi, Arghavan, Yavarian, Majid

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MRI Phenotyping of COL9A2/Trp2 and COL9A3/Trp3 Alleles in Lumbar Disc Disease: A Case-control Study in South-Western Iranian Population Reveals a Significant Trp3-Disease Associati... von Bagheri, Mohammad H., Honarpisheh, Amir P., Yavarian, Majid, Alavi, Zahra, Siegelman, Jenifer, Valtchinov, Vladimir I.

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FoxO3a Gene Down-regulation in Pathogenesis of Pediatric Acute Lymphoblastic Leukemia von Mirzaie, Malihe, Nasiri, Mahboobeh, Karimi, Mehran, Yavarian, Majid, Kavosi, Arghavan

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MRI Phenotyping of COL9A2/Trp2 and COL9A3/Trp3 Alleles in Degenerative Disc Disease: a Case-Control Study in Southwestern Iranian Population Reveals a Significant Trp3-Disease Asso... von Bagheri, Mohammad H, Honarpisheh, Amir P, Yavarian, Majid, Alavi, Zahra, Siegelman, Jenifer, Valtchinov, Vladimir I

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