| Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort KM Flanigan, DM Dunn, A Von Niederhausern, P Soltanzadeh, ... Human mutation 30 (12), 1657-1666, 2009 | 384 | 2009 |
| LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy KM Flanigan, E Ceco, KM Lamar, Y Kaminoh, DM Dunn, JR Mendell, ... Annals of neurology 73 (4), 481-488, 2013 | 254 | 2013 |
| Clinical and genetic characterization of manifesting carriers of DMD mutations P Soltanzadeh, MJ Friez, D Dunn, A von Niederhausern, OL Gurvich, ... Neuromuscular Disorders 20 (8), 499-504, 2010 | 191 | 2010 |
| Nonsense mutation‐associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene KM Flanigan, DM Dunn, A Von Niederhausern, P Soltanzadeh, ... Human mutation 32 (3), 299-308, 2011 | 124 | 2011 |
| Wilson’s disease: a great masquerader A Soltanzadeh, P Soltanzadeh, S Nafissi, A Ghorbani, H Sikaroodi, J Lotfi European Neurology 57 (2), 80-85, 2007 | 66 | 2007 |
| A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia A Ben Ammar, P Soltanzadeh, S Bauché, P Richard, E Goillot, R Herbst, ... PloS one 8 (1), e53826, 2013 | 58 | 2013 |
| Zilucoplan in immune-mediated necrotising myopathy: a phase 2, randomised, double-blind, placebo-controlled, multicentre trial AL Mammen, AA Amato, MM Dimachkie, H Chinoy, Y Hussain, JB Lilleker, ... The Lancet Rheumatology 5 (2), e67-e76, 2023 | 35 | 2023 |
| Heterozygous CAPN3 missense variants causing autosomal‐dominant calpainopathy in seven unrelated families L González‐Mera, G Ravenscroft, M Cabrera‐Serrano, N Ermolova, ... Neuropathology and Applied Neurobiology, 2020 | 34 | 2020 |
| Giant congenital melanocytic nevus with neurofibroma‐like changes and spina bifida occulta H Ansarin, R Soltani‐Arabshahi, D Mehregan, N Shayanfar, ... International journal of dermatology 45 (11), 1347-1350, 2006 | 31 | 2006 |
| Myotonic Dystrophies: A Genetic Overview P Soltanzadeh Genes 13 (2), 367, 2022 | 29 | 2022 |
| United Dystrophinopathy Project Consortium Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort KM Flanigan, DM Dunn, A von Niederhausern, P Soltanzadeh, ... Hum Mutat 30 (12), 1657-1666, 2009 | 25 | 2009 |
| Anti–3‐hydroxy‐3‐methylglutaryl‐coenzyme a reductase autoantibody‐positive necrotizing autoimmune myopathy with dermatomyositis‐like eruption P Parikh, J Tavee, P Soltanzadeh, AL Mammen, P McKeever, Y Li Wiley Periodicals, Inc., 2018 | 20 | 2018 |
| Diagnostic challenges in POEMS syndrome presenting with polyneuropathy: a case series Y Li, J Valent, P Soltanzadeh, N Thakore, B Katirji Journal of the neurological sciences 378, 170-174, 2017 | 13 | 2017 |
| Intravascular T‐cell lymphoma: a rare, poorly characterized entity with cytotoxic phenotype TL Sharma, GA Yeaney, P Soltanzadeh, Y Li, CV Cotta Neuropathology 37 (4), 365-370, 2017 | 12 | 2017 |
| United Dystrophinopathy Project C, Weiss RB. Nonsense mutationassociated Becker muscular dystrophy: Interplay between exon definition and splicing regulatory elements within … KM Flanigan, DM Dunn, A von Niederhausern, P Soltanzadeh, ... Human Mutation 32 (3), 299-308, 2011 | 7 | 2011 |
| An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X) P Soltanzadeh, JS Müller, A Ghorbani, A Abicht, H Lochmüller, ... Journal of Neurology, Neurosurgery & Psychiatry 76 (7), 1039-1040, 2005 | 6 | 2005 |
| In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane F Ghanavatinejad, Z Pourteymourfard‐Tabrizi, K Mahnam, A Doosti, ... Cell Biology International 44 (2), 671-683, 2020 | 5 | 2020 |
| Study Design of AOC 1001-CS1, a Phase 1/2 Clinical Trial Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AOC 1001 Administered Intravenously to … N Johnson, J Day, J Hamel, J Statland, SH Subramony, WD Arnold, ... Neurology 98 (18 Supplement), 2711, 2022 | 4 | 2022 |
| Unilateral tensor fascia lata muscle mass as a presentation of lumbosacral radiculopathy P Soltanzadeh, B Pierce, S Lietman, H Ilaslan Neuromuscular Disorders 25, S242-S243, 2015 | 3 | 2015 |
| Phenotypic Heterogeneity in Limb-girdle Muscular Dystrophy Type 2L (Anoctaminopathy)(P5. 446) K Shouman, J Morren, P Soltanzadeh Neurology 90 (15_supplement), P5. 446, 2018 | 2 | 2018 |
Katherine MathewsProfessor of Pediatrics and Neurology, University of IowaEmail yang diverifikasi di uiowa.edu