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Items: 1 to 50 of 71

1.

Extensor Tendon Transfers for Treatment of Foot Drop in Charcot-Marie-Tooth Disease: A Biomechanical Evaluation.

Pfeffer GB, Michalski M, Nelson T, An TW, Metzger M.

Foot Ankle Int. 2020 Jan 15:1071100719901119. doi: 10.1177/1071100719901119. [Epub ahead of print]

PMID:
31941350
2.

Systematic review of the clinical spectrum of CASPR2 antibody syndrome.

Boyko M, Au KLK, Casault C, de Robles P, Pfeffer G.

J Neurol. 2020 Jan 7. doi: 10.1007/s00415-019-09686-2. [Epub ahead of print]

PMID:
31912210
3.

Dexamethasone Addition to Popliteal Nerve Blocks: Effects on Duration of Analgesia and Incidence of Postoperative Nerve Complication.

Noori N, Anand K, Pfeffer G, Thordarson D.

Foot Ankle Spec. 2020 Jan 6:1938640019897224. doi: 10.1177/1938640019897224. [Epub ahead of print]

PMID:
31904292
4.

Superiority Versus Noninferiority.

Pfeffer G, Pinzur MS, Adams W.

Foot Ankle Int. 2019 Nov 11:1071100719886571. doi: 10.1177/1071100719886571. [Epub ahead of print] No abstract available.

PMID:
31707859
5.

Neuropathy due to impaired axonal transport of non-fragmented mitochondria in MYH14 mutation carriers-Authors' reply.

Pfeffer G, Innes AM, Shutt TE.

EBioMedicine. 2019 Nov;49:25. doi: 10.1016/j.ebiom.2019.09.047. Epub 2019 Oct 17. No abstract available.

6.

Long noncoding RNAs associated with phenotypic severity in multiple sclerosis.

Gupta M, Martens K, Metz LM, de Koning AJ, Pfeffer G.

Mult Scler Relat Disord. 2019 Nov;36:101407. doi: 10.1016/j.msard.2019.101407. Epub 2019 Sep 19.

7.

Radiographic and Magnetic Resonance Imaging of the Symptomatic Synthetic Cartilage Implant.

An TW, Cassinelli S, Charlton TP, Pfeffer GB, Thordarson DB.

Foot Ankle Int. 2020 Jan;41(1):25-30. doi: 10.1177/1071100719877147. Epub 2019 Sep 20.

PMID:
31538827
8.

Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy.

Quadir A, Pontifex CS, Lee Robertson H, Labos C, Pfeffer G.

Neurol Genet. 2019 Jun 12;5(4):e339. doi: 10.1212/NXG.0000000000000339. eCollection 2019 Aug.

9.

The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy.

Almutawa W, Smith C, Sabouny R, Smit RB, Zhao T, Wong R, Lee-Glover L, Desrochers-Goyette J, Ilamathi HS; Care4Rare Canada Consortium, Suchowersky O, Germain M, Mains PE, Parboosingh JS, Pfeffer G, Innes AM, Shutt TE.

EBioMedicine. 2019 Jul;45:379-392. doi: 10.1016/j.ebiom.2019.06.018. Epub 2019 Jun 21.

10.

Biomechanical Comparison of Achilles Tendon Pullout Strength Following Midline Tendon-Splitting and Endoscopic Approaches for Calcaneoplasty.

Michalski MP, Gonzalez TA, Metzger MF, Nelson TJ, Eberlein S, Pfeffer GB.

Foot Ankle Int. 2019 Oct;40(10):1219-1225. doi: 10.1177/1071100719856939. Epub 2019 Jun 17.

PMID:
31203670
11.

Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data.

Gupta M, Nikolic A, Ng D, Martens K, Ebadi H, Chhibber S, Pfeffer G.

Front Neurol. 2019 May 24;10:553. doi: 10.3389/fneur.2019.00553. eCollection 2019.

12.

High diagnostic yield and novel variants in very late-onset spasticity.

Almomen M, Martens K, Quadir A, Pontifex CS, Hanson A, Korngut L, Pfeffer G.

J Neurogenet. 2019 Mar;33(1):27-32. doi: 10.1080/01677063.2019.1566326. Epub 2019 Feb 12.

PMID:
30747022
13.

GNE Myopathy With Novel Mutations and Pronounced Paraspinal Muscle Atrophy.

Soule T, Phan C, White C, Resch L, Lacson A, Martens K, Pfeffer G.

Front Neurol. 2018 Nov 8;9:942. doi: 10.3389/fneur.2018.00942. eCollection 2018.

14.

Comparison of Lateralizing Calcaneal Osteotomies for Varus Hindfoot Correction.

An TW, Michalski M, Jansson K, Pfeffer G.

Foot Ankle Int. 2018 Oct;39(10):1229-1236. doi: 10.1177/1071100718781572. Epub 2018 Jul 16.

PMID:
30011380
15.

Achilles Pullout Strength After Open Calcaneoplasty for Haglund's Syndrome.

Pfeffer G, Gonzalez T, Zapf M, Nelson TJ, Metzger MF.

Foot Ankle Int. 2018 Aug;39(8):966-969. doi: 10.1177/1071100718770391. Epub 2018 Apr 13.

PMID:
29652192
16.

Myopathy With SQSTM1 and TIA1 Variants: Clinical and Pathological Features.

Niu Z, Pontifex CS, Berini S, Hamilton LE, Naddaf E, Wieben E, Aleff RA, Martens K, Gruber A, Engel AG, Pfeffer G, Milone M.

Front Neurol. 2018 Mar 19;9:147. doi: 10.3389/fneur.2018.00147. eCollection 2018.

17.

Online Reputation Management and Patient Satisfaction.

Pfeffer GB, Besh B, Lee TH, Pearson A.

Instr Course Lect. 2018 Feb 15;67:659-666.

PMID:
31411447
18.

Use of 3D Prints to Compare the Efficacy of Three Different Calcaneal Osteotomies for the Correction of Heel Varus.

Pfeffer GB, Michalski MP, Basak T, Giaconi JC.

Foot Ankle Int. 2018 May;39(5):591-597. doi: 10.1177/1071100717753622. Epub 2018 Jan 24.

PMID:
29366341
19.

Prevalence and orthopedic management of foot and ankle deformities in Charcot-Marie-Tooth disease.

Laurá M, Singh D, Ramdharry G, Morrow J, Skorupinska M, Pareyson D, Burns J, Lewis RA, Scherer SS, Herrmann DN, Cullen N, Bradish C, Gaiani L, Martinelli N, Gibbons P, Pfeffer G, Phisitkul P, Wapner K, Sanders J, Flemister S, Shy ME, Reilly MM; Inherited Neuropathies Consortium.

Muscle Nerve. 2018 Feb;57(2):255-259. doi: 10.1002/mus.25724. Epub 2017 Jul 7.

20.

Respiratory management of patients with neuromuscular disease: current perspectives.

Pfeffer G, Povitz M.

Degener Neurol Neuromuscul Dis. 2016 Nov 18;6:111-118. doi: 10.2147/DNND.S87323. eCollection 2016. Review.

21.

Emerging therapies for mitochondrial disorders.

Nightingale H, Pfeffer G, Bargiela D, Horvath R, Chinnery PF.

Brain. 2016 Jun;139(Pt 6):1633-48. doi: 10.1093/brain/aww081. Epub 2016 May 3. Review.

22.

Erratum to: The neurological and ophthalmological manifestations of SPG4-related hereditary spastic paraplegia.

Guthrie G, Pfeffer G, Bailie M, Bradshaw K, Browning AC, Horvath R, Chinnery PF, Yu-Wai-Man P.

J Neurol. 2016 Feb;263(2):419-420. doi: 10.1007/s00415-015-8008-9. No abstract available.

23.

SPG7 mutations are a common cause of undiagnosed ataxia.

Pfeffer G, Pyle A, Griffin H, Miller J, Wilson V, Turnbull L, Fawcett K, Sims D, Eglon G, Hadjivassiliou M, Horvath R, Németh A, Chinnery PF.

Neurology. 2015 Mar 17;84(11):1174-6. doi: 10.1212/WNL.0000000000001369. Epub 2015 Feb 13. No abstract available. Erratum in: Neurology. 2015 May 5;84(18):1911.

24.

Raising the bar for online physician review sites.

Pfeffer GB.

Am J Orthop (Belle Mead NJ). 2015 Jan;44(1):11-2. No abstract available.

PMID:
25566550
25.

Exome sequencing in undiagnosed inherited and sporadic ataxias.

Pyle A, Smertenko T, Bargiela D, Griffin H, Duff J, Appleton M, Douroudis K, Pfeffer G, Santibanez-Koref M, Eglon G, Yu-Wai-Man P, Ramesh V, Horvath R, Chinnery PF.

Brain. 2015 Feb;138(Pt 2):276-83. doi: 10.1093/brain/awu348. Epub 2014 Dec 12.

26.

Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28.

Gorman GS, Pfeffer G, Griffin H, Blakely EL, Kurzawa-Akanbi M, Gabriel J, Sitarz K, Roberts M, Schoser B, Pyle A, Schaefer AM, McFarland R, Turnbull DM, Horvath R, Chinnery PF, Taylor RW.

JAMA Neurol. 2015 Jan;72(1):106-11. doi: 10.1001/jamaneurol.2014.1753.

PMID:
25420100
27.

Diagnosis of muscle diseases presenting with early respiratory failure.

Pfeffer G, Povitz M, Gibson GJ, Chinnery PF.

J Neurol. 2015 May;262(5):1101-14. doi: 10.1007/s00415-014-7526-1. Epub 2014 Nov 7. Review.

PMID:
25377282
28.

Commentary to "5 points on total ankle arthroplasty".

Pfeffer GB.

Am J Orthop (Belle Mead NJ). 2014 Oct;43(10):457. No abstract available.

PMID:
25303443
29.

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.

Pfeffer G, Gorman GS, Griffin H, Kurzawa-Akanbi M, Blakely EL, Wilson I, Sitarz K, Moore D, Murphy JL, Alston CL, Pyle A, Coxhead J, Payne B, Gorrie GH, Longman C, Hadjivassiliou M, McConville J, Dick D, Imam I, Hilton D, Norwood F, Baker MR, Jaiser SR, Yu-Wai-Man P, Farrell M, McCarthy A, Lynch T, McFarland R, Schaefer AM, Turnbull DM, Horvath R, Taylor RW, Chinnery PF.

Brain. 2014 May;137(Pt 5):1323-36. doi: 10.1093/brain/awu060. Epub 2014 Apr 10.

30.

Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain.

Pfeffer G, Chinnery PF.

Brain. 2014 Jun;137(Pt 6):e280. doi: 10.1093/brain/awu034. Epub 2014 Feb 27. No abstract available.

31.

Hereditary Myopathy with Early Respiratory Failure.

Pfeffer G, Chinnery PF.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020.
2014 Feb 27.

32.

Chronic and slowly progressive weakness of the legs and hands.

Nightingale H, Pfeffer G, Horvath R.

BMJ. 2014 Jan 28;348:g459. doi: 10.1136/bmj.g459. Review. No abstract available.

PMID:
24473995
33.

A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failure.

Pfeffer G, Sambuughin N, Olivé M, Tyndel F, Toro C, Goldfarb LG, Chinnery PF.

Neuromuscul Disord. 2014 Mar;24(3):241-4. doi: 10.1016/j.nmd.2013.12.001. Epub 2013 Dec 11.

34.

Titinopathy in a Canadian family sharing the British founder haplotype.

Pfeffer G, Joseph JT, Innes AM, Frizzell JB, Wilson IJ, Brownell AK, Chinnery PF.

Can J Neurol Sci. 2014 Jan;41(1):90-4. No abstract available.

35.

Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain.

Pfeffer G, Griffin H, Pyle A, Horvath R, Chinnery PF.

Brain. 2014 Apr;137(Pt 4):e271. doi: 10.1093/brain/awt306. Epub 2013 Nov 21. No abstract available.

36.

Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations.

Pfeffer G, Burke A, Yu-Wai-Man P, Compston DA, Chinnery PF.

Neurology. 2013 Dec 10;81(24):2073-81. doi: 10.1212/01.wnl.0000437308.22603.43. Epub 2013 Nov 6. Review.

37.

New treatments for mitochondrial disease-no time to drop our standards.

Pfeffer G, Horvath R, Klopstock T, Mootha VK, Suomalainen A, Koene S, Hirano M, Zeviani M, Bindoff LA, Yu-Wai-Man P, Hanna M, Carelli V, McFarland R, Majamaa K, Turnbull DM, Smeitink J, Chinnery PF.

Nat Rev Neurol. 2013 Aug;9(8):474-81. doi: 10.1038/nrneurol.2013.129. Epub 2013 Jul 2. Review.

38.

Podiatric "physicians and surgeons".

Pfeffer GB.

Am J Orthop (Belle Mead NJ). 2013 Mar;42(3):112. No abstract available.

PMID:
23527326
39.

Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure.

Pfeffer G, Barresi R, Wilson IJ, Hardy SA, Griffin H, Hudson J, Elliott HR, Ramesh AV, Radunovic A, Winer JB, Vaidya S, Raman A, Busby M, Farrugia ME, Ming A, Everett C, Emsley HC, Horvath R, Straub V, Bushby K, Lochmüller H, Chinnery PF, Sarkozy A.

J Neurol Neurosurg Psychiatry. 2014 Mar;85(3):331-8. doi: 10.1136/jnnp-2012-304728. Epub 2013 Mar 13.

40.

The neurological and ophthalmological manifestations of SPG4-related hereditary spastic paraplegia.

Guthrie G, Pfeffer G, Bailie M, Bradshaw K, Browning AC, Horvath R, Chinnery PF, Yu-Wai-Man P.

J Neurol. 2013 Mar;260(3):906-9. doi: 10.1007/s00415-012-6780-3. Epub 2012 Dec 13. No abstract available. Erratum in: J Neurol. 2016 Feb;263(2):419-20.

41.

Cardiac screening investigations in adult-onset progressive external ophthalmoplegia patients.

Pfeffer G, Mezei MM.

Muscle Nerve. 2012 Oct;46(4):593-6. doi: 10.1002/mus.23538. Review.

PMID:
22987704
42.

Levator palpebrae biopsy and diagnosis of progressive external ophthalmoplegia.

Pfeffer G, Waters PJ, Maguire J, Vallance HD, Wong VA, Mezei MM.

Can J Neurol Sci. 2012 Jul;39(4):520-4.

PMID:
22728862
43.

Adult-onset spinocerebellar ataxia syndromes due to MTATP6 mutations.

Pfeffer G, Blakely EL, Alston CL, Hassani A, Boggild M, Horvath R, Samuels DC, Taylor RW, Chinnery PF.

J Neurol Neurosurg Psychiatry. 2012 Sep;83(9):883-6. doi: 10.1136/jnnp-2012-302568. Epub 2012 May 10.

44.

Titin mutation segregates with hereditary myopathy with early respiratory failure.

Pfeffer G, Elliott HR, Griffin H, Barresi R, Miller J, Marsh J, Evilä A, Vihola A, Hackman P, Straub V, Dick DJ, Horvath R, Santibanez-Koref M, Udd B, Chinnery PF.

Brain. 2012 Jun;135(Pt 6):1695-713. doi: 10.1093/brain/aws102. Epub 2012 May 9.

45.

Treatment for mitochondrial disorders.

Pfeffer G, Majamaa K, Turnbull DM, Thorburn D, Chinnery PF.

Cochrane Database Syst Rev. 2012 Apr 18;(4):CD004426. doi: 10.1002/14651858.CD004426.pub3. Review.

PMID:
22513923
46.

Diagnosis and treatment of mitochondrial myopathies.

Pfeffer G, Chinnery PF.

Ann Med. 2013 Feb;45(1):4-16. doi: 10.3109/07853890.2011.605389. Epub 2011 Aug 25. Review.

47.

Cosmetic foot surgery: a step in the wrong direction.

Pfeffer GB.

Am J Orthop (Belle Mead NJ). 2011 Apr;40(4):174. No abstract available.

PMID:
21731924
48.

Stroke in young women.

Salisbury M, Pfeffer G, Yip S.

Can J Neurol Sci. 2011 May;38(3):404-10. Review.

PMID:
21515497
49.

The ocular motor features of adult-onset alexander disease: a case and review of the literature.

Pfeffer G, Abegg M, Vertinsky AT, Ceccherini I, Caroli F, Barton JJ.

J Neuroophthalmol. 2011 Jun;31(2):155-9. doi: 10.1097/WNO.0b013e31820ecb28. Review.

PMID:
21403579
50.

Multisystem disorder in late-onset chronic progressive external ophthalmoplegia.

Pfeffer G, Sirrs S, Wade NK, Mezei MM.

Can J Neurol Sci. 2011 Jan;38(1):119-23.

PMID:
21156440

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