Resultats de la cerca - Nikuei, Pooneh

Predictive value of miR-210 as a novel biomarker for pre-eclampsia: a systematic review protocol per Nikuei, Pooneh, Davoodian, Nahid, Tahamtan, Iman, Keshtkar, Abbas Ali

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The imbalance in expression of angiogenic and anti-angiogenic factors as candidate predictive biomarker in preeclampsia per Nikuei, Pooneh, Malekzadeh, Kianoosh, Rajaei, Minoo, Nejatizadeh, Azim, Ghasemi, Nasrin

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Effect of predictive value of progesterone level on the day of HCG injection for IVF success in women with infertility due to tubal factor or polycystic ovarian syndrome referred t... per Ghaseminejad, Azizeh, Rezaee, Zahra, Forootan, Mitra, Hosseinipoor, Taraneh, Forghani, Forough, Nikuei, Pooneh

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Accuracy of Soluble Endoglin for Diagnosis of Preeclampsia and its Severity per Nikuei, Pooneh, Rajaei, Minoo, Malekzadeh, Kianoosh, Nejatizadeh, Azim, Mohseni, Fatemeh, AtashAbParvar, Ali

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Diagnostic accuracy of sFlt1/PlGF ratio as a marker for preeclampsia per Nikuei, Pooneh, Rajaei, Minoo, Roozbeh, Nasibeh, Mohseni, Fatemeh, Poordarvishi, Fatemeh, Azad, Mohsen, Haidari, Solmaz

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Expression of placental growth factor mRNA in preeclampsia per Nikuei, Pooneh, Rajaei, Minoo, Malekzadeh, Kianoosh, Nejatizadeh, Azim, Mohseni, Fatemeh, Poordarvishi, Fatemeh, ghashghaeezadeh, Nasrin, Mohtarami, Mehrdad

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A Pediatric Parathyroid Carcinoma: An Unusual Clinical Presentation and Mini-review per Rahimi, Abbas, Shahbazi, Roghayeh, Nikuei, Pooneh, Soleimani, Sanaz, Moradkhani, Azadeh, Atashabparvar, Ali, Khajehrahimi, Farnaz, Zoghi, Ghazal, Kheirandish, Masoumeh

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Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene per Habibzadeh, Parham, Tabatabaei, Zahra, Farazi Fard, Mohammad Ali, Jamali, Laila, Hafizi, Aazam, Nikuei, Pooneh, Salarian, Leila, Nasr Esfahani, Mohammad Hossein, Anvar, Zahra, Faghihi, Mohammad Ali

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Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia per Kariminejad, Ariana, Szenker-Ravi, Emmanuelle, Lekszas, Caroline, Tajsharghi, Homa, Moslemi, Ali-Reza, Naert, Thomas, Tran, Hong Thi, Ahangari, Fatemeh, Rajaei, Minoo, Nasseri, Mojila, Haaf, Thomas, Azad, Afrooz, Superti-Furga, Andrea, Maroofian, Reza, Ghaderi-Sohi, Siavash, Najmabadi, Hossein, Abbaszadegan, Mohammad Reza, Vleminckx, Kris, Nikuei, Pooneh, Reversade, Bruno

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Distinct genetic variation and heterogeneity of the Iranian population per Mehrjoo, Zohreh, Fattahi, Zohreh, Beheshtian, Maryam, Mohseni, Marzieh, Poustchi, Hossein, Ardalani, Fariba, Jalalvand, Khadijeh, Arzhangi, Sanaz, Mohammadi, Zahra, Khoshbakht, Shahrouz, Najafi, Farid, Nikuei, Pooneh, Haddadi, Mohammad, Zohrehvand, Elham, Oladnabi, Morteza, Mohammadzadeh, Akbar, Jafari, Mandana Hadi, Akhtarkhavari, Tara, Gooshki, Ehsan Shamsi, Haghdoost, Aliakbar, Najafipour, Reza, Niestroj, Lisa-Marie, Helwing, Barbara, Gossmann, Yasmina, Toliat, Mohammad Reza, Malekzadeh, Reza, Nürnberg, Peter, Kahrizi, Kimia, Najmabadi, Hossein, Nothnagel, Michael

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Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder per Polla, Daniel L., Fard, Mohammad Ali Farazi, 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., Kasri, Nael Nadif, 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, Sheshdeh, Afsaneh Taghipour, Bahramjahan, Shima, Mirzaa, Ghayda M., Lavrov, Alexander V., Antonarakis, Stylianos E., Faghihi, Mohammad Ali, van Bokhoven, Hans

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