Search

Author/Creator Nafissi, S.

2. Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population. Issue 3 (21st July 2016)

Authors:
Fattahi, Z.; Kalhor, Z.; Fadaee, M.; Vazehan, R.; Parsimehr, E.; Abolhassani, A.; Beheshtian, M.; Zamani, G.; Nafissi, S.; Nilipour, Y.; Akbari, M.R.; Kahrizi, K.; Kariminejad, A.; Najmabadi, H.
Journal:
Clinical genetics
Issue:
Volume 91:Issue 3(2017)
Page Start:
386
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies. (26th March 2018)

Authors:
Nilipour, Y.; Nafissi, S.; Tjust, A. E.; Ravenscroft, G.; Hossein Nejad Nedai, H.; Taylor, R. L.; Varasteh, V.; Pedrosa Domellöf, F.; Zangi, M.; Tonekaboni, S. H.; Olivé, M.; Kiiski, K.; Sagath, L.; Davis, M. R.; Laing, N. G.; Tajsharghi, H.
Journal:
European journal of neurology
Issue:
Volume 25:Number 6(2018)
Page Start:
841
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies. (26th March 2018)

Authors:
Nilipour, Y.; Nafissi, S.; Tjust, A. E.; Ravenscroft, G.; Hossein Nejad Nedai, H.; Taylor, R. L.; Varasteh, V.; Pedrosa Domellöf, F.; Zangi, M.; Tonekaboni, S. H.; Olivé, M.; Kiiski, K.; Sagath, L.; Davis, M. R.; Laing, N. G.; Tajsharghi, H.
Journal:
European journal of neurology
Issue:
Volume 25:Number 6(2018)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗