1. Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants. Issue 2 (14th November 2022) Authors: Mianesaz, Hamidreza; Ghalamkari, Safoura; Salehi, Mansoor; Behnam, Mahdiyeh; Hosseinzadeh, Majid; Basiri, Keivan; Ghasemi, Majid; Sedghi, Maryam; Ansari, Behnaz Journal: Molecular genetics & genomic medicine Issue: Volume 11:Issue 2(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical features of the myasthenic syndrome arising from mutations in GMPPB. Issue 8 (4th May 2016) Authors: Rodríguez Cruz, Pedro M; Belaya, Katsiaryna; Basiri, Keivan; Sedghi, Maryam; Farrugia, Maria Elena; Holton, Janice L; Liu, Wei Wei; Maxwell, Susan; Petty, Richard; Walls, Timothy J; Kennett, Robin; Pitt, Matthew; Sarkozy, Anna; Parton, Matt; Lochmüller, Hanns; Muntoni, Francesco; Palace, Jacqueli... Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87:Issue 8(2016) Page Start: 802 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1. (April 2015) Authors: Ganji, Hamid; Nouri, Nayereh; Salehi, Mansoor; Aryani, Omid; Houshmand, Massoud; Basiri, Keivan; Fazel-Najafabadi, Esmat; Sedghi, Maryam Journal: Journal of child neurology Issue: Volume 30:Number 5(2015:Apr.) Page Start: 558 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. How realistic is static traffic assignment? Analyzing automatic number-plate recognition data and image processing of real-time traffic maps for investigation. (March 2021) Authors: Mirzahossein, Hamid; Gholampour, Iman; Sedghi, Maryam; Zhu, Lei Journal: Transportation research interdisciplinary perspectives Issue: Volume 9(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication. (12th November 2015) Authors: Sedghi, Maryam; Abdali, Hossein; Memarzadeh, Mehrdad; Salehi, Mansoor; Nouri, Narges; Hosseinzadeh, Majid; Nouri, Nayereh Other Names: Doggett Norman A. Academic Editor. Journal: Genetics research international Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects. Issue 1 (12th September 2013) Authors: Ganji, Hamid; Salehi, Mansoor; Sedghi, Maryam; Abdali, Hossein; Nouri, Nayereh; Sadri, Leyli; Hosseinzadeh, Majid; Vakili, Bahareh; Lotfi, Mahdi Journal: Heart Asia Issue: Volume 5:Issue 1(2013) Page Start: 200 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study. Issue 11 (27th September 2019) Authors: Sedghi, Maryam; Moslemi, Ali‐Reza; Olive, Montse; Etemadifar, Masoud; Ansari, Behnaz; Nasiri, Jafar; Emrahi, Leila; Mianesaz, Hamid‐Reza; Laing, Nigel G.; Tajsharghi, Homa Journal: Annals of clinical and translational neurology Issue: Volume 6:Issue 11(2019) Page Start: 2197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP. Issue 1 (3rd September 2019) Authors: Sedghi, Maryam; Moslemi, Ali-Reza; Cabrera-Serrano, Macarena; Ansari, Behnaz; Ghasemi, Majid; Baktashian, Mojtaba; Fattahpour, Ali; Tajsharghi, Homa Journal: Brain communications Issue: Volume 1:Issue 1(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP. Issue 1 (3rd September 2019) Authors: Sedghi, Maryam; Moslemi, Ali-Reza; Cabrera-Serrano, Macarena; Ansari, Behnaz; Ghasemi, Majid; Baktashian, Mojtaba; Fattahpour, Ali; Tajsharghi, Homa Journal: Brain communications Issue: Volume 1:Issue 1(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP. Issue 1 (3rd September 2019) Authors: Sedghi, Maryam; Moslemi, Ali-Reza; Cabrera-Serrano, Macarena; Ansari, Behnaz; Ghasemi, Majid; Baktashian, Mojtaba; Fattahpour, Ali; Tajsharghi, Homa Journal: Brain communications Issue: Volume 1:Issue 1(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗