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Mirna Lechpammer

TitleASSOC PROF-HCOMP
InstitutionUniversity of California Davis
DepartmentPathology and Laboratory Medicine
Address4400 V St
CA 95817
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    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.
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    1. Ghorbani-Aghbolaghi A, Lechpammer M, Ali SF, Ku NK, Dwyre DM, Rashidi HH. An extremely rare case of concurrent BRAF V600E mutation driven hairy cell leukemia and melanoma: case report and review of literature. Autops Case Rep. 2017 Jul-Sep; 7(3):13-19. PMID: 29043205.
      View in: PubMed
    2. Lechpammer M, Martínez Cerdeno V, Hunsaker MR, Hah M, Gonzales H, Tisch S, Joffe R, Pamphlett R, Tassone F, Hagerman PJ, Bolitho SJ, Hagerman RJ. Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: report of two cases. Croat Med J. 2017 Aug 31; 58(4):310-315. PMID: 28857524.
      View in: PubMed
    3. Aghbolaghi AG, Lechpammer M. A rare case of centronuclear myopathy with DNM2 mutation: genotype-phenotype correlation. Autops Case Rep. 2017 Apr-Jun; 7(2):43-48. PMID: 28740838.
      View in: PubMed
    4. Martínez-Cerdeño V, Lechpammer M, Hagerman PJ, Hagerman R. Two FMR1 premutation cases without nuclear inclusions. Mov Disord. 2017 Sep; 32(9):1328-1329. PMID: 28568317.
      View in: PubMed
    5. Martínez-Cerdeño V, Lechpammer M, Noctor S, Ariza J, Hagerman P, Hagerman R. FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome. Clin Case Rep. 2017 May; 5(5):625-629. PMID: 28469864.
      View in: PubMed
    6. Lechpammer M, Tran YP, Wintermark P, Martínez-Cerdeño V, Krishnan VV, Ahmed W, Berman RF, Jensen FE, Nudler E, Zagzag D. Upregulation of cystathionine ß-synthase and p70S6K/S6 in neonatal hypoxic ischemic brain injury. Brain Pathol. 2017 07; 27(4):449-458. PMID: 27465493.
      View in: PubMed
    7. Hashemi E, Ariza J, Lechpammer M, Noctor SC, Martínez-Cerdeño V. Abnormal white matter tracts resembling pencil fibers involving prefrontal cortex (Brodmann area 47) in autism: a case report. J Med Case Rep. 2016 Aug 26; 10(1):237. PMID: 27562638; PMCID: PMC5000439.
    8. Arzamendi AE, Shahlaie K, Latchaw RE, Lechpammer M, Arzumanyan H. Ectopic Acromegaly Arising from a Pituitary Adenoma within the Bony Intersphenoid Septum of a Patient with Empty Sella Syndrome. J Neurol Surg Rep. 2016 Jul; 77(3):e113-7. PMID: 27468406; PMCID: PMC4958022.
    9. Liu J, Ahmadpour A, Bewley AF, Lechpammer M, Bobinski M, Shahlaie K. Chondroblastoma of the Clivus: Case Report and Review. J Neurol Surg Rep. 2015 Nov; 76(2):e258-64. PMID: 26623238; PMCID: PMC4648736.
    10. Martínez-Cerdeño V, Lechpammer M, Lott A, Schneider A, Hagerman R. Fragile X-Associated Tremor/Ataxia Syndrome in a Man in His 30s. JAMA Neurol. 2015 Sep; 72(9):1070-3. PMID: 26368352; PMCID: PMC4629842.
    11. Lechpammer M, Wintermark P, Merry KM, Jackson MC, Jantzie LL, Jensen FE. Dysregulation of FMRP/mTOR Signaling Cascade in Hypoxic-Ischemic Injury of Premature Human Brain. J Child Neurol. 2016 Mar; 31(4):426-32. PMID: 26239490; PMCID: PMC4740274 [Available on 03/01/17].
    12. Kim E, Camacho J, Combs Z, Ariza J, Lechpammer M, Noctor SC, Martínez-Cerdeño V. Preliminary findings suggest the number and volume of supragranular and infragranular pyramidal neurons are similar in the anterior superior temporal area of control subjects and subjects with autism. Neurosci Lett. 2015 Mar 04; 589:98-103. PMID: 25582788; PMCID: PMC4336808.
    13. Lechpammer M, Clegg MS, Muzar Z, Huebner PA, Jin LW, Gospe SM. Pathology of inherited manganese transporter deficiency. Ann Neurol. 2014 Apr; 75(4):608-12. PMID: 24599576.
      View in: PubMed
    14. Budimlija ZM, Lechpammer M, Popiolek D, Fogt F, Prinz M, Bieber FR. Forensic applications of laser capture microdissection: use in DNA-based parentage testing and platform validation. Croat Med J. 2005 Aug; 46(4):549-55. PMID: 16100757.
      View in: PubMed