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Items: 1 to 20 of 31


Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1.

Blackburn PR, Selcen D, Gass JM, Jackson JL, Macklin S, Cousin MA, Boczek NJ, Klee EW, Dimberg EL, Kennelly KD, Atwal PS.

Mol Genet Genomic Med. 2017 Mar 30;5(3):295-302. doi: 10.1002/mgg3.280. eCollection 2017 May.


Occurrence of Crohn's disease with Parkinson's disease.

Fujioka S, Curry SE, Kennelly KD, Tacik P, Heckman MG, Tsuboi Y, Strongosky AJ, van Gerpen JA, Uitti RJ, Ross OA, Ikezu T, Wszolek ZK.

Parkinsonism Relat Disord. 2017 Apr;37:116-117. doi: 10.1016/j.parkreldis.2017.01.013. Epub 2017 Feb 10.


Early Subretinal Allograft Rejection Is Characterized by Innate Immune Activity.

Kennelly KP, Holmes TM, Wallace DM, O'Farrelly C, Keegan DJ.

Cell Transplant. 2017 Jun 9;26(6):983-1000. doi: 10.3727/096368917X694697. Epub 2017 Jan 20.


Angiographic features and disease outcomes of symptomatic retinal arterial macroaneurysms.

Hughes EL, Dooley IJ, Kennelly KP, Doyle F, Siah WF, Connell P.

Graefes Arch Clin Exp Ophthalmol. 2016 Nov;254(11):2203-2207. Epub 2016 May 25.


Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine.

Burns TM, Smith GA, Allen JA, Amato AA, Arnold WD, Barohn R, Benatar M, Bird SJ, Bromberg M, Chahin N, Ciafaloni E, Cohen JA, Corse A, Crum BA, David WS, Dimberg E, Sousa EA, Donofrio PD, Dyck PJ, Engel AG, Ensrud ER, Ferrante M, Freimer M, Gable KL, Gibson S, Gilchrist JM, Goldstein JM, Gooch CL, Goodman BP, Gorelov D, Gospe SM Jr, Goyal NA, Guidon AC, Guptill JT, Gutmann L, Gutmann L, Gwathmey K, Harati Y, Harper CM Jr, Hehir MK, Hobson-Webb LD, Howard JF Jr, Jackson CE, Johnson N, Jones SM, Juel VC, Kaminski HJ, Karam C, Kennelly KD, Khella S, Khoury J, Kincaid JC, Kissel JT, Kolb N, Lacomis D, Ladha S, Larriviere D, Lewis RA, Li Y, Litchy WJ, Logigian E, Lou JS, MacGowen DJ, Maselli R, Massey JM, Mauermann ML, Mathews KD, Meriggioli MN, Miller RG, Moon JS, Mozaffar T, Nations SP, Nowak RJ, Ostrow LW, Pascuzzi RM, Peltier A, Ruzhansky K, Richman DP, Ross MA, Rubin DI, Russell JA, Sachs GM, Salajegheh MK, Saperstein DS, Scelsa S, Selcen D, Shaibani A, Shieh PB, Silvestri NJ, Singleton JR, Smith BE, So YT, Solorzano G, Sorenson EJ, Srinivasen J, Tavee J, Tawil R, Thaisetthawatkul P, Thornton C, Trivedi J, Vernino S, Wang AK, Webb TA, Weiss MD, Windebank AJ, Wolfe GI.

Muscle Nerve. 2016 Feb;53(2):165-8. doi: 10.1002/mus.25009. Epub 2015 Dec 21. No abstract available.


Objective assessment of symptomatic vitreous floaters using optical coherence tomography: a case report.

Kennelly KP, Morgan JP, Keegan DJ, Connell PP.

BMC Ophthalmol. 2015 Mar 8;15:22. doi: 10.1186/s12886-015-0003-5.


Randomized phase 2 trial of NP001-a novel immune regulator: Safety and early efficacy in ALS.

Miller RG, Block G, Katz JS, Barohn RJ, Gopalakrishnan V, Cudkowicz M, Zhang JR, McGrath MS, Ludington E, Appel SH, Azhir A; Phase 2 Trial NP001 Investigators.

Neurol Neuroimmunol Neuroinflamm. 2015 Apr 9;2(3):e100. doi: 10.1212/NXI.0000000000000100. eCollection 2015 Jun.


Three new families with recurrent male miscarriages and hypercoiled umbilical cord.

Hoffman JD, Kleeman L, Kennelly K, Honey E, Reardon W.

Clin Dysmorphol. 2015 Jul;24(3):128-31. doi: 10.1097/MCD.0000000000000084. No abstract available.


Cryoglobulinemic vasculitis in a patient with CREST syndrome.

Hurst RL, Berianu F, Ginsburg WW, Klein CJ, Englestad JK, Kennelly KD.

J Clin Neurosci. 2014 Oct;21(10):1821-3. doi: 10.1016/j.jocn.2014.01.015. Epub 2014 May 19.


Reply: To PMID 24122745.

Mauricio EA, Dimberg EL, Kennelly KD, Rubin DI.

Muscle Nerve. 2014 May;49(5):772. doi: 10.1002/mus.24206. Epub 2014 Mar 17. No abstract available.


Popliteus muscle hemorrhage as a rare cause of a proximal tibial neuropathy.

Dimberg EL, Rubin DI, Ortiguera CJ, Kennelly KD.

J Clin Neurosci. 2014 Mar;21(3):520-1. doi: 10.1016/j.jocn.2013.05.008. Epub 2013 Oct 11.


Electrodiagnostic approach to cranial neuropathies.

Kennelly KD.

Neurol Clin. 2012 May;30(2):661-84. doi: 10.1016/j.ncl.2011.12.014. Epub 2012 Jan 17. Review.


Preparation of pre-confluent retinal cells increases graft viability in vitro and in vivo: a mouse model.

Kennelly KP, Wallace DM, Holmes TM, Hankey DJ, Grant TS, O'Farrelly C, Keegan DJ.

PLoS One. 2011;6(6):e21365. doi: 10.1371/journal.pone.0021365. Epub 2011 Jun 29.


Phrenic nerve palsy and Parsonage-Turner syndrome.

Odell JA, Kennelly K, Stauffer J.

Ann Thorac Surg. 2011 Jul;92(1):349-51. doi: 10.1016/j.athoracsur.2010.12.067.


The effect of paired stimuli on blink reflex latencies in normal subjects.

Rubin DI, Dimberg EL, Kennelly KD.

Muscle Nerve. 2011 Aug;44(2):235-40. doi: 10.1002/mus.22034. Epub 2011 Jun 9.


Histological characterisation of the ethanol-induced microphthalmia phenotype in a chick embryo model system.

Kennelly K, Brennan D, Chummun K, Giles S.

Reprod Toxicol. 2011 Sep;32(2):227-34. doi: 10.1016/j.reprotox.2011.05.021. Epub 2011 May 30.


Safety and efficacy of lithium in combination with riluzole for treatment of amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial.

Aggarwal SP, Zinman L, Simpson E, McKinley J, Jackson KE, Pinto H, Kaufman P, Conwit RA, Schoenfeld D, Shefner J, Cudkowicz M; Northeast and Canadian Amyotrophic Lateral Sclerosis consortia.

Lancet Neurol. 2010 May;9(5):481-8. doi: 10.1016/S1474-4422(10)70068-5. Epub 2010 Apr 1.


De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.

DeJesus-Hernandez M, Kocerha J, Finch N, Crook R, Baker M, Desaro P, Johnston A, Rutherford N, Wojtas A, Kennelly K, Wszolek ZK, Graff-Radford N, Boylan K, Rademakers R.

Hum Mutat. 2010 May;31(5):E1377-89. doi: 10.1002/humu.21241.


Total laryngectomy in patients with advanced bulbar symptoms of amyotrophic lateral sclerosis.

Garvey CM, Boylan KB, Salassa JR, Kennelly KD.

Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):470-5. doi: 10.3109/17482960802578373.


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