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Items: 1 to 50 of 88

1.

Increasing value of autopsies in patients with brain tumors in the molecular era.

Ahrendsen JT, Filbin MG, Chi SN, Manley PE, Wright KD, Bandopadhayay P, Clymer JR, Yeo KK, Kieran MW, Jones R, Lidov HG, Ligon KL, Alexandrescu S.

J Neurooncol. 2019 Sep 30. doi: 10.1007/s11060-019-03302-z. [Epub ahead of print]

PMID:
31571114
2.

Perioperatively Inhaled Hydrogen Gas Diminishes Neurologic Injury Following Experimental Circulatory Arrest in Swine.

Cole AR, Perry DA, Raza A, Nedder AP, Pollack E, Regan WL, van den Bosch SJ, Polizzotti BD, Yang E, Davila D, Afacan O, Warfield SK, Ou Y, Sefton B, Everett AD, Neil JJ, Lidov HGW, Mayer JE, Kheir JN.

JACC Basic Transl Sci. 2019 Mar 27;4(2):176-187. doi: 10.1016/j.jacbts.2018.11.006. eCollection 2019 Apr.

3.

Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites.

Bruels CC, Li C, Mendoza T, Khan J, Reddy HM, Estrella EA, Ghosh PS, Darras BT, Lidov HGW, Pacak CA, Kunkel LM, Modave F, Draper I, Kang PB.

Mol Genet Genomic Med. 2019 Mar;7(3):e552. doi: 10.1002/mgg3.552. Epub 2019 Jan 28.

4.

Histopathologic Correlates of Familial Hemophagocytic Lymphohistiocytosis Isolated to the Central Nervous System.

Solomon IH, Li H, Benson LA, Henderson LA, Degar BA, Gorman MP, Duncan CN, Lidov HG, Alexandrescu S.

J Neuropathol Exp Neurol. 2018 Dec 1;77(12):1079-1084. doi: 10.1093/jnen/nly094.

PMID:
30295794
5.

The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles.

Coulter ME, Dorobantu CM, Lodewijk GA, Delalande F, Cianferani S, Ganesh VS, Smith RS, Lim ET, Xu CS, Pang S, Wong ET, Lidov HGW, Calicchio ML, Yang E, Gonzalez DM, Schlaeger TM, Mochida GH, Hess H, Lee WA, Lehtinen MK, Kirchhausen T, Haussler D, Jacobs FMJ, Gaudin R, Walsh CA.

Cell Rep. 2018 Jul 24;24(4):973-986.e8. doi: 10.1016/j.celrep.2018.06.100.

6.

PHOX2B is a reliable immunomarker in distinguishing peripheral neuroblastic tumours from CNS embryonal tumours.

Alexandrescu S, Paulson V, Dubuc A, Ligon A, Lidov HG.

Histopathology. 2018 Sep;73(3):483-491. doi: 10.1111/his.13648. Epub 2018 Jul 4.

PMID:
29758594
7.

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy.

Winawer MR, Griffin NG, Samanamud J, Baugh EH, Rathakrishnan D, Ramalingam S, Zagzag D, Schevon CA, Dugan P, Hegde M, Sheth SA, McKhann GM, Doyle WK, Grant GA, Porter BE, Mikati MA, Muh CR, Malone CD, Bergin AMR, Peters JM, McBrian DK, Pack AM, Akman CI, LaCoursiere CM, Keever KM, Madsen JR, Yang E, Lidov HGW, Shain C, Allen AS, Canoll PD, Crino PB, Poduri AH, Heinzen EL.

Ann Neurol. 2018 Jun;83(6):1133-1146. doi: 10.1002/ana.25243. Epub 2018 May 16.

8.

Mice Expressing Myc in Neural Precursors Develop Choroid Plexus and Ciliary Body Tumors.

Shannon ML, Fame RM, Chau KF, Dani N, Calicchio ML, Géléoc GS, Lidov HGW, Alexandrescu S, Lehtinen MK.

Am J Pathol. 2018 Jun;188(6):1334-1344. doi: 10.1016/j.ajpath.2018.02.009. Epub 2018 Mar 13.

9.

Multiparametric Analysis of Permeability and ADC Histogram Metrics for Classification of Pediatric Brain Tumors by Tumor Grade.

Vajapeyam S, Brown D, Johnston PR, Ricci KI, Kieran MW, Lidov HGW, Poussaint TY.

AJNR Am J Neuroradiol. 2018 Mar;39(3):552-557. doi: 10.3174/ajnr.A5502. Epub 2018 Jan 4.

10.

A novel GIT2-BRAF fusion in pilocytic astrocytoma.

Helgager J, Lidov HG, Mahadevan NR, Kieran MW, Ligon KL, Alexandrescu S.

Diagn Pathol. 2017 Nov 15;12(1):82. doi: 10.1186/s13000-017-0669-5.

11.

GM2 Activator Deficiency Caused by a Homozygous Exon 2 Deletion in GM2A.

Hall PL, Laine R, Alexander JJ, Ankala A, Teot LA, Lidov HGW, Anselm I.

JIMD Rep. 2018;38:61-65. doi: 10.1007/8904_2017_31. Epub 2017 May 25.

12.

AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant.

Morton SU, Prabhu SP, Lidov HGW, Shi J, Anselm I, Brownstein CA, Bainbridge MN, Beggs AH, Vargas SO, Agrawal PB.

Cold Spring Harb Mol Case Stud. 2017 Mar;3(2):a001560. doi: 10.1101/mcs.a001560.

13.

The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States.

Reddy HM, Cho KA, Lek M, Estrella E, Valkanas E, Jones MD, Mitsuhashi S, Darras BT, Amato AA, Lidov HG, Brownstein CA, Margulies DM, Yu TW, Salih MA, Kunkel LM, MacArthur DG, Kang PB.

J Hum Genet. 2017 Feb;62(2):243-252. doi: 10.1038/jhg.2016.116. Epub 2016 Oct 6.

14.

Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations.

Mangum JE, Hardee JP, Fix DK, Puppa MJ, Elkes J, Altomare D, Bykhovskaya Y, Campagna DR, Schmidt PJ, Sendamarai AK, Lidov HG, Barlow SC, Fischel-Ghodsian N, Fleming MD, Carson JA, Patton JR.

Sci Rep. 2016 May 20;6:26202. doi: 10.1038/srep26202.

15.

Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-α protein (PMPCA) cause a severe mitochondrial disease.

Joshi M, Anselm I, Shi J, Bale TA, Towne M, Schmitz-Abe K, Crowley L, Giani FC, Kazerounian S, Markianos K, Lidov HG, Folkerth R, Sankaran VG, Agrawal PB.

Cold Spring Harb Mol Case Stud. 2016 May;2(3):a000786. doi: 10.1101/mcs.a000786.

16.

Sonic Hedgehog promotes proliferation of Notch-dependent monociliated choroid plexus tumour cells.

Li L, Grausam KB, Wang J, Lun MP, Ohli J, Lidov HG, Calicchio ML, Zeng E, Salisbury JL, Wechsler-Reya RJ, Lehtinen MK, Schüller U, Zhao H.

Nat Cell Biol. 2016 Apr;18(4):418-30. doi: 10.1038/ncb3327. Epub 2016 Mar 21.

17.

EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy.

Byrne S, Jansen L, U-King-Im JM, Siddiqui A, Lidov HG, Bodi I, Smith L, Mein R, Cullup T, Dionisi-Vici C, Al-Gazali L, Al-Owain M, Bruwer Z, Al Thihli K, El-Garhy R, Flanigan KM, Manickam K, Zmuda E, Banks W, Gershoni-Baruch R, Mandel H, Dagan E, Raas-Rothschild A, Barash H, Filloux F, Creel D, Harris M, Hamosh A, Kölker S, Ebrahimi-Fakhari D, Hoffmann GF, Manchester D, Boyer PJ, Manzur AY, Lourenco CM, Pilz DT, Kamath A, Prabhakar P, Rao VK, Rogers RC, Ryan MM, Brown NJ, McLean CA, Said E, Schara U, Stein A, Sewry C, Travan L, Wijburg FA, Zenker M, Mohammed S, Fanto M, Gautel M, Jungbluth H.

Brain. 2016 Mar;139(Pt 3):765-81. doi: 10.1093/brain/awv393.

18.

Tubers are neither static nor discrete: Evidence from serial diffusion tensor imaging.

Peters JM, Prohl AK, Tomas-Fernandez XK, Taquet M, Scherrer B, Prabhu SP, Lidov HG, Singh JM, Jansen FE, Braun KP, Sahin M, Warfield SK, Stamm A.

Neurology. 2015 Nov 3;85(18):1536-45. doi: 10.1212/WNL.0000000000002055. Epub 2015 Oct 2.

19.

Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia.

Boisson B, Laplantine E, Dobbs K, Cobat A, Tarantino N, Hazen M, Lidov HG, Hopkins G, Du L, Belkadi A, Chrabieh M, Itan Y, Picard C, Fournet JC, Eibel H, Tsitsikov E, Pai SY, Abel L, Al-Herz W, Casanova JL, Israel A, Notarangelo LD.

J Exp Med. 2015 Jun 1;212(6):939-51. doi: 10.1084/jem.20141130. Epub 2015 May 25.

20.

Spatially heterogeneous choroid plexus transcriptomes encode positional identity and contribute to regional CSF production.

Lun MP, Johnson MB, Broadbelt KG, Watanabe M, Kang YJ, Chau KF, Springel MW, Malesz A, Sousa AM, Pletikos M, Adelita T, Calicchio ML, Zhang Y, Holtzman MJ, Lidov HG, Sestan N, Steen H, Monuki ES, Lehtinen MK.

J Neurosci. 2015 Mar 25;35(12):4903-16. doi: 10.1523/JNEUROSCI.3081-14.2015. Erratum in: J Neurosci. 2015 Jun 3;35(22):8686. Adelita, Tai [corrected to Adelita, Tais].

21.

Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas.

Brastianos PK, Taylor-Weiner A, Manley PE, Jones RT, Dias-Santagata D, Thorner AR, Lawrence MS, Rodriguez FJ, Bernardo LA, Schubert L, Sunkavalli A, Shillingford N, Calicchio ML, Lidov HG, Taha H, Martinez-Lage M, Santi M, Storm PB, Lee JY, Palmer JN, Adappa ND, Scott RM, Dunn IF, Laws ER Jr, Stewart C, Ligon KL, Hoang MP, Van Hummelen P, Hahn WC, Louis DN, Resnick AC, Kieran MW, Getz G, Santagata S.

Nat Genet. 2014 Feb;46(2):161-5. doi: 10.1038/ng.2868. Epub 2014 Jan 12.

22.

The lost art of localization: Franc Ingraham's legacy in pediatric neurosurgery.

Cohen AR, Vogel TW, Lidov HG.

J Neurosurg Pediatr. 2013 Dec;12(6):642-54. doi: 10.3171/2013.8.PEDS1377. Epub 2013 Sep 27.

PMID:
24073750
23.

Intrasacral meningocele in the pediatric population.

Lohani S, Rodriguez DP, Lidov HG, Scott RM, Proctor MR.

J Neurosurg Pediatr. 2013 Jun;11(6):615-22. doi: 10.3171/2013.3.PEDS12519. Epub 2013 Apr 19.

PMID:
23601014
24.

OTX2 represses myogenic and neuronal differentiation in medulloblastoma cells.

Bai RY, Staedtke V, Lidov HG, Eberhart CG, Riggins GJ.

Cancer Res. 2012 Nov 15;72(22):5988-6001. doi: 10.1158/0008-5472.CAN-12-0614. Epub 2012 Sep 17.

25.

Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores.

Boyden SE, Mahoney LJ, Kawahara G, Myers JA, Mitsuhashi S, Estrella EA, Duncan AR, Dey F, DeChene ET, Blasko-Goehringer JM, Bönnemann CG, Darras BT, Mendell JR, Lidov HG, Nishino I, Beggs AH, Kunkel LM, Kang PB.

Neurogenetics. 2012 May;13(2):115-24. doi: 10.1007/s10048-012-0315-z. Epub 2012 Feb 28.

26.

Rapid reversal of uremic neuropathy following renal transplantation in an adolescent.

Ho DT, Rodig NM, Kim HB, Lidov HG, Shapiro FD, Raju GP, Kang PB.

Pediatr Transplant. 2012 Nov;16(7):E296-300. doi: 10.1111/j.1399-3046.2011.01630.x. Epub 2011 Dec 21.

27.

Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE.

Boyden SE, Duncan AR, Estrella EA, Lidov HG, Mahoney LJ, Katz JS, Kunkel LM, Kang PB.

BMC Med Genet. 2011 Jun 28;12:87. doi: 10.1186/1471-2350-12-87.

28.

Pediatric sciatic neuropathy associated with neoplasms.

McMillan HJ, Srinivasan J, Darras BT, Ryan MM, Davis J, Lidov HG, Gill D, Jones HR.

Muscle Nerve. 2011 Feb;43(2):183-8. doi: 10.1002/mus.21867.

PMID:
21254082
29.

Hypothermic circulatory arrest increases permeability of the blood brain barrier in watershed areas.

Okamura T, Ishibashi N, Kumar TS, Zurakowski D, Iwata Y, Lidov HG, Jonas RA.

Ann Thorac Surg. 2010 Dec;90(6):2001-8. doi: 10.1016/j.athoracsur.2010.06.118.

30.

Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies.

Chan YM, Keramaris-Vrantsis E, Lidov HG, Norton JH, Zinchenko N, Gruber HE, Thresher R, Blake DJ, Ashar J, Rosenfeld J, Lu QL.

Hum Mol Genet. 2010 Oct 15;19(20):3995-4006. doi: 10.1093/hmg/ddq314. Epub 2010 Jul 30.

PMID:
20675713
31.

Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene.

Zhou Y, Cheunsuchon P, Nakayama Y, Lawlor MW, Zhong Y, Rice KA, Zhang L, Zhang X, Gordon FE, Lidov HG, Bronson RT, Klibanski A.

Development. 2010 Aug;137(16):2643-52. doi: 10.1242/dev.045724. Epub 2010 Jul 7.

32.

Inefficient dystrophin expression after cord blood transplantation in Duchenne muscular dystrophy.

Kang PB, Lidov HG, White AJ, Mitchell M, Balasubramanian A, Estrella E, Bennett RR, Darras BT, Shapiro FD, Bambach BJ, Kurtzberg J, Gussoni E, Kunkel LM.

Muscle Nerve. 2010 Jun;41(6):746-50. doi: 10.1002/mus.21702.

33.

Differential neuronal vulnerability varies according to specific cardiopulmonary bypass insult in a porcine survival model.

Ishibashi N, Iwata Y, Okamura T, Zurakowski D, Lidov HG, Jonas RA.

J Thorac Cardiovasc Surg. 2010 Dec;140(6):1408-15.e1-3. doi: 10.1016/j.jtcvs.2010.03.008.

34.

Aprotinin protects the cerebral microcirculation during cardiopulmonary bypass.

Ishibashi N, Iwata Y, Zurakowski D, Lidov HG, Jonas RA.

Perfusion. 2009 Mar;24(2):99-105. doi: 10.1177/0267659109106701.

35.

Optimal dose of aprotinin for neuroprotection and renal function in a piglet survival model.

Iwata Y, Okamura T, Ishibashi N, Zurakowski D, Lidov HG, Jonas RA.

J Thorac Cardiovasc Surg. 2009 Jun;137(6):1521-9; discussion 1529. doi: 10.1016/j.jtcvs.2008.06.049. Epub 2009 Apr 21.

36.

A case of congenital glycogen storage disease type IV with a novel GBE1 mutation.

Raju GP, Li HC, Bali DS, Chen YT, Urion DK, Lidov HG, Kang PB.

J Child Neurol. 2008 Mar;23(3):349-52. doi: 10.1177/0883073807309248. Epub 2008 Jan 29.

PMID:
18230843
37.

Distinctive patterns of microRNA expression in primary muscular disorders.

Eisenberg I, Eran A, Nishino I, Moggio M, Lamperti C, Amato AA, Lidov HG, Kang PB, North KN, Mitrani-Rosenbaum S, Flanigan KM, Neely LA, Whitney D, Beggs AH, Kohane IS, Kunkel LM.

Proc Natl Acad Sci U S A. 2007 Oct 23;104(43):17016-21. Epub 2007 Oct 17. Erratum in: Proc Natl Acad Sci U S A. 2008 Jan 8;105(1):399.

38.

Aprotinin improves cerebral protection: evidence from a survival porcine model.

Anttila V, Hagino I, Iwata Y, Mettler BA, Lidov HG, Zurakowski D, Jonas RA.

J Thorac Cardiovasc Surg. 2006 Oct;132(4):948-53.

39.

A novel mutation in two families with limb-girdle muscular dystrophy type 2C.

Duncan DR, Kang PB, Rabbat JC, Briggs CE, Lidov HG, Darras BT, Kunkel LM.

Neurology. 2006 Jul 11;67(1):167-9.

PMID:
16832103
40.

Specific bypass conditions determine safe minimum flow rate.

Anttila V, Hagino I, Zurakowski D, Iwata Y, Duebener L, Lidov HG, Jonas RA.

Ann Thorac Surg. 2005 Oct;80(4):1460-7.

PMID:
16181887
41.

Tissue oxygenation index is a useful monitor of histologic and neurologic outcome after cardiopulmonary bypass in piglets.

Hagino I, Anttila V, Zurakowski D, Duebener LF, Lidov HG, Jonas RA.

J Thorac Cardiovasc Surg. 2005 Aug;130(2):384-92.

42.

Variations in gene expression among different types of human skeletal muscle.

Kang PB, Kho AT, Sanoudou D, Haslett JN, Dow CP, Han M, Blasko JM, Lidov HG, Beggs AH, Kunkel LM.

Muscle Nerve. 2005 Oct;32(4):483-91.

PMID:
15962335
43.

IKKbeta/NF-kappaB activation causes severe muscle wasting in mice.

Cai D, Frantz JD, Tawa NE Jr, Melendez PA, Oh BC, Lidov HG, Hasselgren PO, Frontera WR, Lee J, Glass DJ, Shoelson SE.

Cell. 2004 Oct 15;119(2):285-98.

44.

Interaction of temperature with hematocrit level and pH determines safe duration of hypothermic circulatory arrest.

Sakamoto T, Zurakowski D, Duebener LF, Lidov HG, Holmes GL, Hurley RJ, Laussen PC, Jonas RA.

J Thorac Cardiovasc Surg. 2004 Aug;128(2):220-32.

45.

Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.

Ho M, Post CM, Donahue LR, Lidov HG, Bronson RT, Goolsby H, Watkins SC, Cox GA, Brown RH Jr.

Hum Mol Genet. 2004 Sep 15;13(18):1999-2010. Epub 2004 Jul 14.

PMID:
15254015
46.

Higher bypass temperature correlates with increased white cell activation in the cerebral microcirculation.

Anttila V, Hagino I, Zurakowski D, Lidov HG, Jonas RA.

J Thorac Cardiovasc Surg. 2004 Jun;127(6):1781-8.

47.

Diagnostic value of electromyography and muscle biopsy in arthrogryposis multiplex congenita.

Kang PB, Lidov HG, David WS, Torres A, Anthony DC, Jones HR, Darras BT.

Ann Neurol. 2003 Dec;54(6):790-5.

PMID:
14681888
48.

Cerebral amyloid angiopathy associated with primary angiitis of the central nervous system: report of 2 cases and review of the literature.

Schwab P, Lidov HG, Schwartz RB, Anderson RJ.

Arthritis Rheum. 2003 Jun 15;49(3):421-7. Review. No abstract available.

49.

Expression profiling reveals altered satellite cell numbers and glycolytic enzyme transcription in nemaline myopathy muscle.

Sanoudou D, Haslett JN, Kho AT, Guo S, Gazda HT, Greenberg SA, Lidov HG, Kohane IS, Kunkel LM, Beggs AH.

Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4666-71. Epub 2003 Apr 3.

50.

Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation.

Gussoni E, Bennett RR, Muskiewicz KR, Meyerrose T, Nolta JA, Gilgoff I, Stein J, Chan YM, Lidov HG, Bönnemann CG, Von Moers A, Morris GE, Den Dunnen JT, Chamberlain JS, Kunkel LM, Weinberg K.

J Clin Invest. 2002 Sep;110(6):807-14.

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