Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum von Karamzade, Arezou, Babaei, Meisam, Saberi, Mohammad, Golchin, Neda, Khalil Nejad Sani Banaei, Aysun, Eshaghkhani, Yeganeh, Golchehre, Zahra, Keramatipour, Mohammad

Volltext

Identification of a novel mutation in ARSA gene in three patients of an Iranian family with metachromatic leukodystrophy disorder von Golchin, Neda, Hajjari, Mohammadreza, Malamiri, Reza Azizi, Aminzadeh, Majid, Mohammadi-Asl, Javad

Volltext

Coexistence of p190 BCR/ABL Transcript and CALR 52-bp Deletion in Chronic Myeloid Leukemia Blast Crisis: A Case Report von Seghatoleslami, Mohammad, Ketabchi, Neda, Ordo, Alireza, Asl, Javad Mohammadi, Golchin, Neda, Saki, Najmaldin

Volltext

Whole exome sequencing revealed a novel dystrophin-related protein-2 ( DRP2 ) deletion in an Iranian family with symptoms of polyneuropathy von Tahmasebi-Birgani, Maryam, Hajjari, Mohammadreza, Golchin, Neda, Shalbafan, Bita, Mohammadi-Asl, Javad, Sadeghian, Forouzan

Volltext

Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing von Nikkhah, Emad, Safaralizadeh, Reza, Mohammadiasl, Javad, Tahmasebi Birgani, Maryam, Hosseinpour Feizi, Mohammad Ali, Golchin, Neda

Volltext

Association between microRNA-21, microRNA-150, and micro- RNA-451 expression and clinical outcome of patients with acute lymphoblastic leukemia von Asnafi, Ali Amin, Khodadi, Elahe, Golchin, Neda, Alghasi, Arash, Tavakolifar, Yousef, Saki, Najmaldin

Volltext

Rare Cytogenetic Abnormalities and Alteration of microRNAs in Acute Myeloid Leukemia and Response to Therapy von Shahjahani, Mohammad, Khodadi, Elahe, Seghatoleslami, Mohammad, Asl, Javad Mohammadi, Golchin, Neda, Zaieri, Zeynab Deris, Saki, Najmaldin

Volltext

The Diagnostic Value of Gene Expression of FHL1 in the Differential Diagnosis of Papillary Thyroid Carcinoma and Benign Tumors von Javad Mohammadi-Asl, Gholamabbas Dinarvand, Neda Golchin, Nader Saki, Nastran Ranjberi, Iran Rashidi

Volltext

Lipid profile improvement after four group psychological interventions in combination to nutritional and physical activity instructing among overweight and obese individuals von Agah Heris, Mojgan, Alipour, Ahmad, Janbozorgi, Masoud, Hajihosseini, Reza, Shaghaghi, Farhad, Golchin, Neda, Nouhi, Shahnaz

Volltext

A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis von Tabatabaiefar, Mohammad Amin, Alipour, Paria, Pourahmadiyan, Azam, Fattahi, Najmeh, Shariati, Laleh, Golchin, Neda, Mohammadi-Asl, Javad

Volltext

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant von Helal, Mayada, Mazaheri, Neda, Shalbafan, Bita, Malamiri, Reza Azizi, Dilaver, Nafi, Buchert, Rebecca, Mohammadiasl, Javad, Golchin, Neda, Sedaghat, Alireza, Mehrjardi, Mohammad Yahya Vahidi, Haack, Tobias B., Riess, Olaf, Chung, Wendy K., Galehdari, Hamid, Shariati, Gholamreza, Maroofian, Reza

Volltext

Quantification of viral genome in cord blood donors by real time PCR to investigate human herpesvirus type 8 active infection von Golchin, Neda, Kheirandish, Maryam, Sharifi, Zohreh, Samiee, Shahram, Kokhaei, Parviz, Pourpak, Zahra

Volltext

Immunophenotype, microRNA expression and cytogenetic characterization of acute leukemias of ambiguous lineage von Golchin, Neda, Khodadi, Elahe, Yaghooti, Seyed Hamid, Jaseb, Kaveh, Shahjahani, Mohammad, Tavakolifar, Yousef, Saki, Najmaldin

Volltext

The mechanistic role of epigenetic in multiple myeloma von Hajizamani, Saeideh, Golchin, Neda, Shahjahani, Mohammad, Tamaddon, Gholam Hossein, Vosoughi, Tina, Yousefi, Homayon, Saki, Najmaldin

Volltext

Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing von Nikkhah, Emad, Safaralizadeh, Reza, Mohammadiasl, Javad, Mohammad Ali Hosseinpour Feizi, Golchin, Neda

Volltext

Characterization of Wild-Type and Mutated RET Proto-Oncogene Associated with Familial Medullary Thyroid Cancer von Masbi, Mohammad Hosein, Mohammadiasl, Javad, Galehdari, Hamid, Ahmadzadeh, Ahmad, Tabatabaiefar, Mohammad Amin, Golchin, Neda, Haghpanah, Vahid, Rahim, Fakher

Volltext

A case of chronic lymphoblastic leukemia with an abnormal rare karyotype von Mohammdai-asl, Javad, Hajizamani, Saeideh, Shahjahani, Mohammad, Golchin, Neda, Masbi, Mohammad-hosein, Ahmadzadeh, Ahmad, Saki, Najmaldin

Volltext

Lipid profile improvement after four group psychological interventions in combination to nutritional and physical activity instructing among overweight and obese individuals von Mojgan Agah Heris, Ahmad Alipour, Masoud Janbozorgi, Reza Hajihosseini, Farhad Shaghaghi, Neda Golchin, Shahnaz Nouhi

Volltext

Characterization of Wild-Type and Mutated RET Proto-Oncogene Associated with Familial Medullary Thyroid Cancer von Masbi, Mohammad Hosein, Mohammadiasl, Javad, Galehdari, Hamid, Ahmadzadeh, Ahmad, Tabatabaiefar, Mohammad Amin, Golchin, Neda, Haghpanah, Vahid, Rahim, Fakher

Volltext

بررسی پلی‌مورفیسم ژن سوپراکسید دیسموتاز 1 و ارتباط آن با رتینوپاتی و نفروپاتی در بیماران مبتلا به دیابت نوع 2 در اهواز... von Javad Mohammadi-Asl, Arghavan Soleimanizadeh, Hajieh Bibi Shahbazian, Heshmatollah Shahbazian, Neda Golchin

Volltext