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Items: 1 to 20 of 44

1.

The molecular oncology of bilateral high-grade thalamic astrocytomas in children.

Goodarzi A, Garza N, Lechpammer M, Anthony R, Zwienenberg M.

Childs Nerv Syst. 2019 Nov;35(11):2047-2054. doi: 10.1007/s00381-019-04372-0. Epub 2019 Sep 14.

PMID:
31522255
2.

Real-time augmented reality for delineation of surgical margins during neurosurgery using autofluorescence lifetime contrast.

Alfonso-Garcia A, Bec J, Sridharan Weaver S, Hartl B, Unger J, Bobinski M, Lechpammer M, Girgis F, Boggan J, Marcu L.

J Biophotonics. 2020 Jan;13(1):e201900108. doi: 10.1002/jbio.201900108. Epub 2019 Aug 9.

PMID:
31304655
3.

Microglial cell activation and senescence are characteristic of the pathology FXTAS.

Martínez Cerdeño V, Hong T, Amina S, Lechpammer M, Ariza J, Tassone F, Noctor SC, Hagerman P, Hagerman R.

Mov Disord. 2018 Dec;33(12):1887-1894. doi: 10.1002/mds.27553. Epub 2018 Dec 10.

4.

Induction and Assessment of Hypoxia in Glioblastoma Cells In Vitro.

Gagner JP, Lechpammer M, Zagzag D.

Methods Mol Biol. 2018;1741:111-123. doi: 10.1007/978-1-4939-7659-1_9.

PMID:
29392695
5.

Expression Levels and Localizations of DVL3 and sFRP3 in Glioblastoma.

Kafka A, Tomas D, Lechpammer M, Gabud T, Pažanin L, Pećina-Šlaus N.

Dis Markers. 2017;2017:9253495. doi: 10.1155/2017/9253495. Epub 2017 Oct 19.

6.

Microscopy with ultraviolet surface excitation for rapid slide-free histology.

Fereidouni F, Harmany ZT, Tian M, Todd A, Kintner JA, McPherson JD, Borowsky AD, Bishop J, Lechpammer M, Demos SG, Levenson R.

Nat Biomed Eng. 2017 Dec;1(12):957-966. doi: 10.1038/s41551-017-0165-y. Epub 2017 Dec 4.

PMID:
31015706
7.

An extremely rare case of concurrent BRAF V600E mutation driven hairy cell leukemia and melanoma: case report and review of literature.

Ghorbani-Aghbolaghi A, Lechpammer M, Ali SF, Ku NK, Dwyre DM, Rashidi HH.

Autops Case Rep. 2017 Sep 30;7(3):13-19. doi: 10.4322/acr.2017.032. eCollection 2017 Jul-Sep.

8.

Intradural Chordoma of Cerebellopontine Angle: Case Report and Review.

Goodarzi A, Toussi A, Lechpammer M, Lee D, Shahlaie K.

World Neurosurg. 2017 Nov;107:1052.e11-1052.e16. doi: 10.1016/j.wneu.2017.08.124. Epub 2017 Sep 1. Review.

PMID:
28866065
9.

Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: report of two cases.

Lechpammer M, Martínez Cerdeńo V, Hunsaker MR, Hah M, Gonzales H, Tisch S, Joffe R, Pamphlett R, Tassone F, Hagerman PJ, Bolitho SJ, Hagerman RJ.

Croat Med J. 2017 Aug 31;58(4):310-315.

10.

A rare case of centronuclear myopathy with DNM2 mutation: genotype-phenotype correlation.

Aghbolaghi AG, Lechpammer M.

Autops Case Rep. 2017 Jun 30;7(2):43-48. doi: 10.4322/acr.2017.020. eCollection 2017 Apr-Jun. Review.

11.

Two FMR1 premutation cases without nuclear inclusions.

Martínez-Cerdeño V, Lechpammer M, Hagerman PJ, Hagerman R.

Mov Disord. 2017 Sep;32(9):1328-1329. doi: 10.1002/mds.27060. Epub 2017 Jun 1. No abstract available.

12.

Embolic Foreign Material in the Central Nervous System of Pediatric Autopsy Patients With Instrumented Heart Disease.

Torre M, Lechpammer M, Paulson V, Prabhu S, Marshall AC, Juraszek AL, Padera RF, Bundock EA, Vargas SO, Folkerth RD.

J Neuropathol Exp Neurol. 2017 Jul 1;76(7):571-577. doi: 10.1093/jnen/nlx037.

PMID:
28525615
13.

FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome.

Martínez-Cerdeño V, Lechpammer M, Noctor S, Ariza J, Hagerman P, Hagerman R.

Clin Case Rep. 2017 Mar 23;5(5):625-629. doi: 10.1002/ccr3.834. eCollection 2017 May.

14.

Microscopy with ultraviolet surface excitation for rapid slide-free histology.

Fereidouni F, Harmany ZT, Tian M, Todd A, Kintner JA, McPherson JD, Borowsky AD, Lechpammer M, Bishop J, Demos SG, Levenson R.

Nat Biomed Eng. 2017;1:957-966. Epub 2017 Dec 4.

15.

Abnormal white matter tracts resembling pencil fibers involving prefrontal cortex (Brodmann area 47) in autism: a case report.

Hashemi E, Ariza J, Lechpammer M, Noctor SC, Martínez-Cerdeño V.

J Med Case Rep. 2016 Aug 26;10(1):237. doi: 10.1186/s13256-016-1020-6.

16.

Ectopic Acromegaly Arising from a Pituitary Adenoma within the Bony Intersphenoid Septum of a Patient with Empty Sella Syndrome.

Arzamendi AE, Shahlaie K, Latchaw RE, Lechpammer M, Arzumanyan H.

J Neurol Surg Rep. 2016 Jul;77(3):e113-7. doi: 10.1055/s-0036-1585091.

17.

Upregulation of cystathionine β-synthase and p70S6K/S6 in neonatal hypoxic ischemic brain injury.

Lechpammer M, Tran YP, Wintermark P, Martínez-Cerdeño V, Krishnan VV, Ahmed W, Berman RF, Jensen FE, Nudler E, Zagzag D.

Brain Pathol. 2017 Jul;27(4):449-458. doi: 10.1111/bpa.12421. Epub 2016 Aug 28. Erratum in: Brain Pathol. 2017 Nov;27(6):856.

PMID:
27465493
18.

Molecular Genetics of Intracranial Meningiomas with Emphasis on Canonical Wnt Signalling.

Pećina-Šlaus N, Kafka A, Lechpammer M.

Cancers (Basel). 2016 Jul 15;8(7). pii: E67. doi: 10.3390/cancers8070067. Review.

19.

Chondroblastoma of the Clivus: Case Report and Review.

Liu J, Ahmadpour A, Bewley AF, Lechpammer M, Bobinski M, Shahlaie K.

J Neurol Surg Rep. 2015 Nov;76(2):e258-64. doi: 10.1055/s-0035-1564601. Epub 2015 Oct 9.

20.

Fragile X-Associated Tremor/Ataxia Syndrome in a Man in His 30s.

Martínez-Cerdeño V, Lechpammer M, Lott A, Schneider A, Hagerman R.

JAMA Neurol. 2015 Sep;72(9):1070-3. doi: 10.1001/jamaneurol.2015.1138. No abstract available.

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