Payam Soltanzadeh

Title(s)HS Associate Clinical Professor, Neurology
vCardDownload vCard

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Myofibrillar myopathy presenting with an inclusion body myositis-like phenotype. Muscle Nerve. 2023 05; 67(5):E15-E17. Diaz F, Soltanzadeh P, Khosa S, Khanlou N, Freundlich R, Mishra SK. PMID: 36815757.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Using Intensity Modulated Radiation Therapy for the Treatment of Sialorrhea in Amyotrophic Lateral Sclerosis. Adv Radiat Oncol. 2023 Jan-Feb; 8(1):101116. Ati S, Chhetri D, Wiedau M, Soltanzadeh P, Bordelon Y, Chin RK, Savjani RR. PMID: 36420480; PMCID: PMC9676140.
      View in: PubMed   Mentions:
    3. Myotonic Dystrophies: A Genetic Overview. Genes (Basel). 2022 02 17; 13(2). Soltanzadeh P. PMID: 35205411; PMCID: PMC8872148.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    4. Heterozygous CAPN3 missense variants causing autosomal-dominant calpainopathy in seven unrelated families. Neuropathol Appl Neurobiol. 2021 02; 47(2):283-296. González-Mera L, Ravenscroft G, Cabrera-Serrano M, Ermolova N, Domínguez-González C, Arteche-López A, Soltanzadeh P, Evesson F, Navas C, Mavillard F, Clayton J, Rodrigo P, Servián-Morilla E, Cooper ST, Waddell L, Reardon K, Corbett A, Hernandez-Laín A, Sanchez A, Esteban Perez J, Paradas-Lopez C, Rivas-Infante E, Spencer M, Laing N, Olivé M. PMID: 32896923.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    5. In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane. Cell Biol Int. 2020 Feb; 44(2):671-683. Ghanavatinejad F, Pourteymourfard-Tabrizi Z, Mahnam K, Doosti A, Mehri-Ghahfarrokhi A, Pourhadi M, Azimeh Hosseini S, Hashemzadeh Chaleshtori M, Soltanzadeh P, Jami MS. PMID: 31769568.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    6. Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase autoantibody-positive necrotizing autoimmune myopathy with dermatomyositis-like eruption. Muscle Nerve. 2018 06; 57(6):E135-E136. Parikh P, Tavee J, Soltanzadeh P, Mammen AL, McKeever P, Li Y. PMID: 29346706.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    7. Diagnostic challenges in POEMS syndrome presenting with polyneuropathy: A case series. J Neurol Sci. 2017 Jul 15; 378:170-174. Li Y, Valent J, Soltanzadeh P, Thakore N, Katirji B. PMID: 28566158.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    8. Intravascular T-cell lymphoma: A rare, poorly characterized entity with cytotoxic phenotype. Neuropathology. 2017 Aug; 37(4):365-370. Sharma TL, Yeaney GA, Soltanzadeh P, Li Y, Cotta CV. PMID: 28317291.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    9. Hereditary inclusion body myopathy in Persian Jews: a case report from Iran. Clin Genet. 2014 Jun; 85(6):595-7. Miryounesi M, Soltanzadeh P, Modarressi MH. PMID: 23841835.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    10. A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia. PLoS One. 2013; 8(1):e53826. Ben Ammar A, Soltanzadeh P, Bauché S, Richard P, Goillot E, Herbst R, Gaudon K, Huzé C, Schaeffer L, Yamanashi Y, Higuchi O, Taly A, Koenig J, Leroy JP, Hentati F, Najmabadi H, Kahrizi K, Ilkhani M, Fardeau M, Eymard B, Hantaï D. PMID: 23326516; PMCID: PMC3541344.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimalsCells
    11. Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene. Hum Mutat. 2011 Mar; 32(3):299-308. Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Howard MT, Sampson JB, Swoboda KJ, Bromberg MB, Mendell JR, Taylor LE, Anderson CB, Pestronk A, Florence JM, Connolly AM, Mathews KD, Wong B, Finkel RS, Bonnemann CG, Day JW, McDonald C, United Dystrophinopathy Project Consortium, Weiss RB. PMID: 21972111; PMCID: PMC3724403.
      View in: PubMed   Mentions: 59     Fields:    Translation:HumansCells
    12. Clinical and genetic characterization of manifesting carriers of DMD mutations. Neuromuscul Disord. 2010 Aug; 20(8):499-504. Soltanzadeh P, Friez MJ, Dunn D, von Niederhausern A, Gurvich OL, Swoboda KJ, Sampson JB, Pestronk A, Connolly AM, Florence JM, Finkel RS, Bönnemann CG, Medne L, Mendell JR, Mathews KD, Wong BL, Sussman MD, Zonana J, Kovak K, Gospe SM, Gappmaier E, Taylor LE, Howard MT, Weiss RB, Flanigan KM. PMID: 20630757; PMCID: PMC2944769.
      View in: PubMed   Mentions: 58     Fields:    Translation:Humans
    13. Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort. Hum Mutat. 2009 Dec; 30(12):1657-66. Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Gappmaier E, Howard MT, Sampson JB, Mendell JR, Wall C, King WM, Pestronk A, Florence JM, Connolly AM, Mathews KD, Stephan CM, Laubenthal KS, Wong BL, Morehart PJ, Meyer A, Finkel RS, Bonnemann CG, Medne L, Day JW, Dalton JC, Margolis MK, Hinton VJ, United Dystrophinopathy Project Consortium, Weiss RB. PMID: 19937601; PMCID: PMC3404892.
      View in: PubMed   Mentions: 156     Fields:    Translation:HumansCells
    14. Wilson's disease: a great masquerader. Eur Neurol. 2007; 57(2):80-5. Soltanzadeh A, Soltanzadeh P, Nafissi S, Ghorbani A, Sikaroodi H, Lotfi J. PMID: 17179709.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    15. Giant congenital melanocytic nevus with neurofibroma-like changes and spina bifida occulta. Int J Dermatol. 2006 Nov; 45(11):1347-50. Ansarin H, Soltani-Arabshahi R, Mehregan D, Shayanfar N, Soltanzadeh P. PMID: 17076723.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    16. An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X). J Neurol Neurosurg Psychiatry. 2005 Jul; 76(7):1039-40. Soltanzadeh P, Müller JS, Ghorbani A, Abicht A, Lochmüller H, Soltanzadeh A. PMID: 15965226; PMCID: PMC1739705.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    Payam's Networks
    Concepts (111)
    Derived automatically from this person's publications.
    Co-Authors (7)
    People in Profiles who have published with this person.
    Similar People (60)
    People who share similar concepts with this person.
    Same Department
    Search Department