1. Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012. Issue 4 (June 2014) Authors: Jalali, Hossein; Mahdavi, Mohammad Reza; Roshan, Payam; Kosaryan, Mehrnoush; Karami, Hosein; Mahdavi, Mehrad Journal: Hematology Issue: Volume 19:Issue 4(2014) Page Start: 192 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comparison of human‐induced pluripotent stem cells and mesenchymal stem cell differentiation potential to insulin producing cells in 2D and 3D culture systems in vitro. Issue 5 (15th October 2019) Authors: Abazari, Mohammad Foad; Nasiri, Navid; Nejati, Fatemeh; Zare Karizi, Shohreh; Amini Faskhodi, Mojdeh; Saburi, Ehsan; Aghapur, Nasrin; Mahdavi, Mohammad Reza; Ardeshirylajimi, Abdolreza; Enderami, Seyed Ehsan; Soleimanifar, Fatemeh Journal: Journal of cellular physiology Issue: Volume 235:Issue 5(2020:May) Page Start: 4239 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Detection of Rare Beta Globin Gene Mutation [+22 5UTR(G>A)] in an Infant, Despite Prenatal Screening. (14th April 2013) Authors: Mahdavi, Mohammad Reza; Karami, Hosein; Akbari, Mohammad Taghi; Jalali, Hosein; Roshan, Payam Other Names: Singh M. Academic Editor.; Storti S. Academic Editor. Journal: Case reports in hematology Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. First report of c.425-1G>A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia. Issue 5 (September 2021) Authors: Jalali, Hossein; Najafi, Mojtaba; Khoshaeen, Atefeh; Mahdavi, Mohammad Reza; Mahdavi, Mahan Journal: European journal of ophthalmology Issue: Volume 31:Issue 5(2021) Page Start: NP23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. First report of novel mutation (c.790del) on SQSTM1 gene on a family with childhood onset of progressive cerebellar ataxia with vertical gaze palsy. Issue 8 (9th August 2022) Authors: Jalali, Hossein; Khoshaeen, Atefeh; Mahdavi, Mohammad Reza; Mahdavi, Mahan Journal: Clinical case reports Issue: Volume 10:Issue 8(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Improved biological behaviours and osteoinductive capacity of the gelatin nanofibers while composites with GO/MgO. (3rd February 2022) Authors: Mahdavi, Mohammad Reza; Kehtari, Mousa; Mellati, Amir; Mansour, Reyhaneh Nassiri; Mahdavi, Mehrad; Mahdavi, Mahan; Enderami, Seyed Ehsan Journal: Cell biochemistry and function Issue: Volume 40:Number 2(2022) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Why does the Iranian National Program of Screening Newborns for G6PD Enzyme Deficiency Miss a Large Number of Affected Infants?. (1st February 2014) Authors: Kosaryan, Mehrnoush; Mahdavi, Mohammad Reza; Jalali, Hossein; Roshan, Payam Journal: Pediatric hematology and oncology Issue: Volume 31:Number 1(2014:Feb.) Page Start: 95 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗