Articles with public access mandates - Behnaz AnsariLearn more
Available somewhere: 4
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy
AT Pagnamenta, R Kaiyrzhanov, Y Zou, SI Da'as, R Maroofian, ...
Brain 144 (2), 584-600, 2021
Mandates: US National Institutes of Health, German Research Foundation, Swedish …
Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study
M Sedghi, AR Moslemi, M Olive, M Etemadifar, B Ansari, J Nasiri, ...
Annals of Clinical and Translational Neurology 6 (11), 2197-2204, 2019
Mandates: National Health and Medical Research Council, Australia, Swedish Research …
Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP
M Sedghi, AR Moslemi, M Cabrera-Serrano, B Ansari, M Ghasemi, ...
Brain Communications 1 (1), fcz011, 2019
Mandates: Swedish Research Council, Government of Spain
Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review
F Magrinelli, KP Bhatia, M Beiraghi Toosi, F Arab, EG Karimiani, ...
Movement Disorders Clinical Practice 10 (1), 101-108, 2023
Mandates: UK Medical Research Council, National Institute for Health Research, UK …
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