[PDF][PDF] Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays

S Shojaee, F Sina, SS Banihosseini, MH Kazemi… - The American Journal of …, 2008 - cell.com
Robust SNP genotyping technologies and data analysis programs have encouraged researchers
in recent years to use SNPs for linkage studies. Platforms used to date have been 10 K …

Corticosteroid regimens for treatment of acute and chronic graft versus host disease (GvHD) after allogenic stem cell transplantation

…, M Rohanizadegan, S Banihosseini… - Cochrane Database …, 2010 - cochranelibrary.com
Background Corticosteroids are commonly used in treatment of acute and chronic graft‐versus‐host
disease (GvHD). Nevertheless, there has been no systematic analysis of effects of …

[HTML][HTML] Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype

E Elahi, R Kalhor, SS Banihosseini, N Torabi… - Journal of investigative …, 2006 - Elsevier
Cutis laxa is a rare group of inherited and acquired disorders characterized by loose and
redundant skin with reduced elasticity. Mutations in the elastin coding gene have been shown …

Family physician perspectives on primary care reform priorities: a cross-sectional survey

L Hedden, S Banihosseini, N Strydom… - … Open Access Journal, 2021 - cmajopen.ca
Background: The province of British Columbia is facing a family physician shortage despite
consistent increases in the number of physicians per capita and ongoing reforms to address …

[HTML][HTML] Modern work patterns of “classic” versus millennial family doctors and their effect on workforce planning for community-based primary care: a cross-sectional …

L Hedden, S Banihosseini, N Strydom… - Human Resources for …, 2020 - Springer
Background There are ongoing accessibility challenges in primary care in British Columbia,
Canada, with 17% of the population not having a regular source of care. Anecdotal …

[HTML][HTML] Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients

…, N Rafati, M Chiani, SS Banihosseini… - … & visual science, 2007 - iovs.arvojournals.org
purpose. To perform a mutation screening of TACSTD2 in 13 Iranian Gelatinous Drop-like
Corneal Dystrophy (GDLD) pedigrees. To assess genotype–phenotype correlations. To …

PRKN, DJ‐1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ‐1 mutations

F Ghazavi, Z Fazlali, SS Banihosseini… - Movement …, 2011 - Wiley Online Library
We present results of mutation screening of PRKN gene in 93 Iranian Parkinson's disease (PD)
patients with average age at onset (AAO) of 42.2 years. The gene was screened by direct …

[PDF][PDF] Variation in plasma leptin levels in young Iranian children with cystic fibrosis

…, F Motamed, MN Sani, SS Banihosseini… - Archives of Medical …, 2013 - termedia.pl
Results: Leptin levels and BMI values were significantly different between patients and controls
(p= 0.02, p< 0.001, respectively) but only patients aged 13–48 months had significantly …

Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patients

S Shojaee, Z Fazlali, F Ghazavi, SS Banihosseini… - Neuroscience …, 2009 - Elsevier
The results of mutation screening of 24 exons of LRRK2 in 60 Iranian Parkinson's Disease
patients are presented. The Iranian cohort represents a novel population and was notably …

Applying a neural network to predict the thermodynamic parameters for an expanded nearest-neighbor model

…, H Goodarzi, N Torabi, SS Banihosseini - Journal of theoretical …, 2006 - Elsevier
Predicting the secondary and tertiary structure of RNAs largely depends on our capabilities
in estimating the thermodynamics of RNA duplexes. In this work, an expanded nearest-…