Type 1 early infantile epileptic encephalopathy: A case report and literature review von Zaker, Erfan, Nouri, Negar, Movahedinia, Mojtaba, Dadbinpour, Ali, Vahidi Mehrjardi, Mohammad Yahya

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Circulating microRNA-122, microRNA-126-3p and microRNA-146a are associated with inflammation in patients with pre-diabetes and type 2 diabetes mellitus: A case control study von Zeinali, Fahime, Aghaei Zarch, Seyed Mohsen, Jahan-Mihan, Alireza, Kalantar, Seyed Mehdi, Vahidi Mehrjardi, Mohammad Yahya, Fallahzadeh, Hossein, Hosseinzadeh, Mahdieh, Rahmanian, Masoud, Mozaffari-Khosravi, Hassan

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Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1 von Appelhof, Bart, Wagner, Matias, Hoefele, Julia, Heinze, Anja, Roser, Timo, Koch-Hogrebe, Margarete, Roosendaal, Stefan D, Dehghani, Mohammadreza, Mehrjardi, Mohammad Yahya Vahidi, Torti, Erin, Houlden, Henry, Maroofian, Reza, Rajabi, Farrah, Sticht, Heinrich, Baas, Frank, Wieczorek, Dagmar, Jamra, Rami Abou

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Plasma miR‐21 as a potential predictor in prediabetic individuals with a positive family history of type 2 diabetes mellitus von Yazdanpanah, Zakieh, Kazemipour, Nasrin, Kalantar, Seyed Mehdi, Vahidi Mehrjardi, Mohammad Yahya

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Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families von Moudi, Mahdiyeh, Vahidi Mehrjardi, Mohammad Yahya, Hozhabri, Hossein, Metanat, Zahra, Kalantar, Seyed Mehdi, Taheri, Mohsen, Ghasemi, Nasrin, Dehghani, Mohammadreza

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Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder von Christensen, Maria B., Levy, Amanda M., Mohammadi, Nazanin A., Niceta, Marcello, Kaiyrzhanov, Rauan, Dentici, Maria Lisa, Al Alam, Chadi, Alesi, Viola, Benoit, Valérie, Bhatia, Kailash P., Bierhals, Tatjana, Boßelmann, Christian M., Buratti, Julien, Callewaert, Bert, Ceulemans, Berten, Charles, Perrine, De Wachter, Matthias, Dehghani, Mohammadreza, D'haenens, Erika, Doco‐Fenzy, Martine, Geßner, Michaela, Gobert, Cyrielle, Guliyeva, Ulviyya, Haack, Tobias B., Hammer, Trine B., Heinrich, Tilman, Hempel, Maja, Herget, Theresia, Hoffmann, Ute, Horvath, Judit, Houlden, Henry, Keren, Boris, Kresge, Christina, Kumps, Candy, Lederer, Damien, Lermine, Alban, Magrinelli, Francesca, Maroofian, Reza, Vahidi Mehrjardi, Mohammad Yahya, Moudi, Mahdiyeh, Müller, Amelie J., Oostra, Anna J., Pletcher, Beth A., Ros‐Pardo, David, Samarasekera, Shanika, Tartaglia, Marco, Van Schil, Kristof, Vogt, Julie, Wassmer, Evangeline, Winkelmann, Juliane, Zaki, Maha S., Zech, Michael, Lerche, Holger, Radio, Francesca Clementina, Gomez‐Puertas, Paulino, Møller, Rikke S., Tümer, Zeynep

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Effects of synbiotic supplementation on gut microbiome, serum level of TNF-α, and expression of microRNA-126 and microRNA-146a in patients with type 2 diabetes mellitus: study prot... von Zeinali, Fahime, Aghaei Zarch, Seyed Mohsen, Vahidi Mehrjardi, Mohammad Yahya, Kalantar, Seyed Mehdi, Jahan-Mihan, Alireza, Karimi-Nazari, Elham, Fallahzadeh, Hossein, Hosseinzadeh-Shamsi-Anar, Mahdieh, Rahmanian, Masoud, Fazeli, Mohammad Reza, Mozaffari-Khosravi, Hassan

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Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes von Sadeghzadeh, Salman, Dehghani Ashkezari, Mahmood, Seifati, Seyed Morteza, Vahidi Mehrjardi, Mohammad Yahya, Dehghan Tezerjani, Masoud, Sadeghzadeh, Sara, Ladan, Seyed Amir Behtash

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Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy von McMillan, Hugh J, Telegrafi, Aida, Singleton, Amanda, Cho, Megan T, Lelli, Daniel, Lynn, Francis C, Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E, Koolen, David A, Haaxma, Charlotte A, Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J, Henderson, Lindsay B, McLaughlin, Heather, Molday, Laurie L, Molday, Robert S, Yoon, Grace

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Joint effects of paraoxonase 1 rs662 polymorphism and vitamins C/E intake on coronary artery disease severity (Gensini and SYNTAX scores) and lipid profile in patients undergoing c... von Darand, Mina, Salehi-Abargouei, Amin, Vahidi Mehrjardi, Mohammad Yahya, Feizi, Awat, Seyedhossaini, Seyed Mustafa, Askari, Gholamreza

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Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease von Dehghanian, Mehran, Yarahmadi, Ghafour, Sandoghsaz, Reyhaneh Sadat, Khodadadian, Ali, Shamsi, Farimah, Vahidi Mehrjardi, Mohammad Yahya

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Evaluation of NF1 and RASA1 gene expression in endometriosis von Yarahmadi, Ghafour, Dehghanian, Mehran, Sandoghsaz, Reyhaneh Sadat, Savaee, Mohamadreza, Shamsi, Farimah, Vahidi Mehrjardi, Mohammad Yahya

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Co-segregation of variant NSUN2 Lue198Arg among Iranian family with intellectual disability: a case report von Moudi, Mahdiyeh, Vahidi Mehrjardi, Mohammad Yahya, Kalantar, Seyed Mehdi, Taheri, Mohsen, Metanat, Zahra, Ghasemi, Nasrin, Dehghani, Mohammadreza

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Is there any relationship between mutation in CPS1 Gene and pregnancy loss? von Talebi, Mehrdad, Yahya Vahidi Mehrjardi, Mohammad, Kalhor, Kambiz, Dehghani, Mohammadreza

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A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II) von Dehghan Tezerjani, Masoud, Vahidi Mehrjardi, Mohammad Yahya, Hozhabri, Hossein, Rahmanian, Masoud

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Association of NFKB1 gene polymorphism (rs28362491) with cardiometabolic risk factor in patients undergoing coronary angiography von Darabi, Zahra, Jambarsang, Sara, Vahidi Mehrjardi, Mohammad Yahya, Seyed Hosseini, Seyed Mostafa, Sarebanhassanabadi, Mohammadtaghi, Hosseinzadeh, Mahdieh, Beigrezaei, Sara, Ahmadi Vasmehjani, Azam, Taftian, Marzieh, Arabi, Vahid, Motallaei, Maryam, Golvardi Yazdi, Faezeh, Salehi-Abargouei, Amin, Nadjarzadeh, Azadeh

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A novel mutation in CYP17A1 gene leads to congenital adrenal hyperplasia: A case report von Nazari, Majid, Yahya Vahidi Mehrjardi, Mohammad, Neghab, Nosrat, Aghabagheri, Mahdi, Ghasemi, Nasrin

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GGPS1‐associated muscular dystrophy with and without hearing loss von Kaiyrzhanov, Rauan, Perry, Luke, Rocca, Clarissa, Zaki, Maha S., Hosny, Heba, Araujo Martins Moreno, Cristiane, Phadke, Rahul, Zaharieva, Irina, Camelo Gontijo, Clara, Beetz, Christian, Pini, Veronica, Movahedinia, Mojtaba, Zanoteli, Edmar, DiTroia, Stephanie, Vuillaumier‐Barrot, Sandrine, Isapof, Arnaud, Mehrjardi, Mohammad Yahya Vahidi, Ghasemi, Nasrin, Sarkozy, Anna, Muntoni, Francesco, Whalen, Sandra, Vona, Barbara, Houlden, Henry, Maroofian, Reza

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MiR-194-5p might be a Potential Biomarker for Type 2 Diabetes Mellitus von Dadbinpour, Ali, Dehghanian, Mehran, Vahidi Mehrjardi, Mohammad Yahya

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Whole-exome sequencing revealed a novel ERCC8 variant in an Iranian large family with Cockayne syndrome von Ashrafzadeh, Hamidreza, Tafvizi, Farzaneh, Ghasemi, Nasrin, Vahidi Mehrjardi, Mohammad Yahya, Naseh, Vahid

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