Payam Soltanzadeh

Title(s)	HS Associate Clinical Professor, Neurology
School	Medicine
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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.

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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:
Neu Neurology Phy Physiology
Translation:Humans
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:
Myotonic Dystrophies: A Genetic Overview. Genes (Basel). 2022 02 17; 13(2). Soltanzadeh P. PMID: 35205411; PMCID: PMC8872148.

View in: PubMed Mentions: 3 Fields:
Gen Genetics
Translation:Humans
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:
Bio Biology Neu Neurology Pat Pathology
Translation:Humans
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:
Cel Cell Biology
Translation:Humans Cells
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:
Neu Neurology Phy Physiology
Translation:Humans
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:
Neu Neurology
Translation:Humans
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:
Neu Neurology Pat Pathology
Translation:Humans
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:
Gen Genetics
Translation:Humans Cells
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:
Med Medicine (General)Sci Science
Translation:Humans Animals Cells
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:
Gen Genetics
Translation:Humans Cells
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:
Neu Neurology
Translation:Humans
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:
Gen Genetics
Translation:Humans Cells
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:
Neu Neurology
Translation:Humans
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:
Der Dermatology
Translation:Humans
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:
Neu Neurology Neu Neurosurgery Psy Psychiatry
Translation:Humans