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Items: 1 to 50 of 145

1.

Synthetic CRISPR/Cas9 reagents facilitate genome editing and homology directed repair.

DiNapoli SE, Martinez-McFaline R, Gribbin CK, Wrighton PJ, Balgobin CA, Nelson I, Leonard A, Maskin CR, Shwartz A, Quenzer ED, Mailhiot D, Kao C, McConnell SC, de Jong JLO, Goessling W, Houvras Y.

Nucleic Acids Res. 2020 Feb 17. pii: gkaa085. doi: 10.1093/nar/gkaa085. [Epub ahead of print]

PMID:
32064511
2.

A Comparison of Emergency Preparedness Policies by Long-Term Care Setting Type in Ohio: Assisted Living Settings Lag Behind Nursing Homes in Key Areas.

Kennedy KA, Hua CL, Nelson I.

J Appl Gerontol. 2020 Feb 2:733464820902010. doi: 10.1177/0733464820902010. [Epub ahead of print]

PMID:
32008413
3.

Synthesis and characterization of novel calcium phosphate glass-derived cements for vital pulp therapy.

Howard J, Gardner L, Saifee Z, Geleil A, Nelson I, Colombo JS, Naleway SE, Carlson K.

J Mater Sci Mater Med. 2020 Jan 2;31(1):12. doi: 10.1007/s10856-019-6352-5.

PMID:
31897754
4.

Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES.

De Ridder W, Nelson I, Asselbergh B, De Paepe B, Beuvin M, Ben Yaou R, Masson C, Boland A, Deleuze JF, Maisonobe T, Eymard B, Symoens S, Schindler R, Brand T, Johnson K, Töpf A, Straub V, De Jonghe P, De Bleecker JL, Bonne G, Baets J.

Neurol Genet. 2019 Apr 1;5(2):e321. doi: 10.1212/NXG.0000000000000321. eCollection 2019 Apr.

5.

Is There a Woodwork Effect? Addressing a 200-Year Debate on the Impacts of Expanding Community-Based Services.

Berish D, Nelson I, Mehdizadeh S, Applebaum R.

J Aging Soc Policy. 2019 Jan-Feb;31(1):85-98. doi: 10.1080/08959420.2018.1528115. Epub 2018 Dec 1.

PMID:
30501484
6.

Prediction of Scoliosis Curve Correction Using Pedicle Screw Constructs in AIS: A Comparison of Fulcrum Bend Radiographs and Traction Radiographs Under General Anesthesia.

Tokala DP, Nelson IW, Mehta JS, Powell R, Grannum S, Hutchinson MJ.

Global Spine J. 2018 Oct;8(7):676-682. doi: 10.1177/2192568218763147. Epub 2018 Mar 26.

7.

Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies.

Ávila-Polo R, Malfatti E, Lornage X, Cheraud C, Nelson I, Nectoux J, Böhm J, Schneider R, Hedberg-Oldfors C, Eymard B, Monges S, Lubieniecki F, Brochier G, Thao Bui M, Madelaine A, Labasse C, Beuvin M, Lacène E, Boland A, Deleuze JF, Thompson J, Richard I, Taratuto AL, Udd B, Leturcq F, Bonne G, Oldfors A, Laporte J, Romero NB.

J Neuropathol Exp Neurol. 2018 Dec 1;77(12):1101-1114. doi: 10.1093/jnen/nly095.

PMID:
30365001
8.

A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1.

Ame van der Beek N, Nelson I, Froissart R, Levade T, Garcia V, Lacene E, Boland A, Masson C, Romero NB, Stojkovic T, Bonne G, Béhin A.

Eur J Hum Genet. 2019 Mar;27(3):337-339. doi: 10.1038/s41431-018-0250-z. Epub 2018 Oct 5. No abstract available.

PMID:
30291339
9.

Promoting resilience in individuals aging with multiple sclerosis: Results from a pilot randomized controlled trial.

Alschuler KN, Arewasikporn A, Nelson IK, Molton IR, Ehde DM.

Rehabil Psychol. 2018 Aug;63(3):338-348. doi: 10.1037/rep0000223. Epub 2018 Jul 19.

PMID:
30024203
10.

Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy.

Azibani F, Brull A, Arandel L, Beuvin M, Nelson I, Jollet A, Ziat E, Prudhon B, Benkhelifa-Ziyyat S, Bitoun M, Lorain S, Bonne G, Bertrand AT.

Mol Ther Nucleic Acids. 2018 Mar 2;10:376-386. doi: 10.1016/j.omtn.2017.12.012. Epub 2017 Dec 30.

11.

Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families.

Jonson PH, Palmio J, Johari M, Penttilä S, Evilä A, Nelson I, Bonne G, Wiart N, Meyer V, Boland A, Deleuze JF, Masson C, Stojkovic T, Chapon F, Romero NB, Solé G, Ferrer X, Ferreiro A, Hackman P, Richard I, Udd B.

Eur J Neurol. 2018 May;25(5):790-794. doi: 10.1111/ene.13598. Epub 2018 Mar 30.

PMID:
29437287
12.

Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency.

Ben Yaou R, Hubert A, Nelson I, Dahlqvist JR, Gaist D, Streichenberger N, Beuvin M, Krahn M, Petiot P, Parisot F, Michel F, Malfatti E, Romero N, Carlier RY, Eymard B, Labrune P, Duno M, Krag T, Cerino M, Bartoli M, Bonne G, Vissing J, Laforet P, Petit FM.

Neurol Genet. 2017 Dec 18;3(6):e208. doi: 10.1212/NXG.0000000000000208. eCollection 2017 Dec.

13.

Limb girdle muscular dystrophy due to mutations in POMT2.

Østergaard ST, Johnson K, Stojkovic T, Krag T, De Ridder W, De Jonghe P, Baets J, Claeys KG, Fernández-Torrón R, Phillips L, Topf A, Colomer J, Nafissi S, Jamal-Omidi S, Bouchet-Seraphin C, Leturcq F, MacArthur DG, Lek M, Xu L, Nelson I, Straub V, Vissing J.

J Neurol Neurosurg Psychiatry. 2018 May;89(5):506-512. doi: 10.1136/jnnp-2017-317018. Epub 2017 Nov 24.

PMID:
29175898
14.

Anti-HMGCR Antibody-Related Necrotizing Autoimmune Myopathy Mimicking Muscular Dystrophy.

Tard C, Tiffreau V, Jaillette E, Jouen F, Nelson I, Bonne G, Yaou RB, Romero N, Vallée L, Vermersch P, Nguyen S, Maurage CA, Cuisset JM.

Neuropediatrics. 2017 Dec;48(6):473-476. doi: 10.1055/s-0037-1604402. Epub 2017 Aug 4. No abstract available.

PMID:
28778101
15.

Instilling positive beliefs about disabilities: pilot testing a novel experiential learning activity for rehabilitation students.

Silverman AM, Pitonyak JS, Nelson IK, Matsuda PN, Kartin D, Molton IR.

Disabil Rehabil. 2018 May;40(9):1108-1113. doi: 10.1080/09638288.2017.1292321. Epub 2017 Feb 25.

PMID:
28637146
16.

Results of the Scoliosis Research Society Morbidity and Mortality Database 2009-2012: A Report From the Morbidity and Mortality Committee.

Burton DC, Carlson BB, Place HM, Fuller JE, Blanke K, Cho R, Fu KM, Ganju A, Heary R, Herrera-Soto JA, Larson AN, Lavelle WF, Nelson IW, Vernengo-Lezica A, Verska JM.

Spine Deform. 2016 Sep;4(5):338-343. doi: 10.1016/j.jspd.2016.05.003. Epub 2016 Aug 21.

PMID:
27927490
17.

FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.

Ziat E, Mamchaoui K, Beuvin M, Nelson I, Azibani F, Spuler S, Bonne G, Bertrand AT.

J Neuromuscul Dis. 2016 Nov 29;3(4):497-510.

PMID:
27911330
18.

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.

Avila-Smirnow D, Gueneau L, Batonnet-Pichon S, Delort F, Bécane HM, Claeys K, Beuvin M, Goudeau B, Jais JP, Nelson I, Richard P, Ben Yaou R, Romero NB, Wahbi K, Mathis S, Voit T, Furst D, van der Ven P, Gil R, Vicart P, Fardeau M, Bonne G, Behin A.

Rev Neurol (Paris). 2016 Oct;172(10):594-606. doi: 10.1016/j.neurol.2016.07.017. Epub 2016 Sep 12. Review.

PMID:
27633507
19.

Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea.

Bauché S, O'Regan S, Azuma Y, Laffargue F, McMacken G, Sternberg D, Brochier G, Buon C, Bouzidi N, Topf A, Lacène E, Remerand G, Beaufrere AM, Pebrel-Richard C, Thevenon J, El Chehadeh-Djebbar S, Faivre L, Duffourd Y, Ricci F, Mongini T, Fiorillo C, Astrea G, Burloiu CM, Butoianu N, Sandu C, Servais L, Bonne G, Nelson I, Desguerre I, Nougues MC, Bœuf B, Romero N, Laporte J, Boland A, Lechner D, Deleuze JF, Fontaine B, Strochlic L, Lochmuller H, Eymard B, Mayer M, Nicole S.

Am J Hum Genet. 2016 Sep 1;99(3):753-761. doi: 10.1016/j.ajhg.2016.06.033. Epub 2016 Aug 25.

20.

EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome.

Gargaun E, Seferian AM, Cardas R, Le Moing AG, Delanoe C, Nectoux J, Nelson I, Bonne G, Bihoreau MT, Deleuze JF, Boland A, Masson C, Servais L, Gidaro T.

J Neurol. 2016 Jul;263(7):1456-8. doi: 10.1007/s00415-016-8153-9. Epub 2016 May 9. No abstract available.

PMID:
27159987
21.

A comparison of revision and rerupture rates of ACL reconstruction between autografts and allografts in the skeletally immature.

Nelson IR, Chen J, Love R, Davis BR, Maletis GB, Funahashi TT.

Knee Surg Sports Traumatol Arthrosc. 2016 Mar;24(3):773-9. doi: 10.1007/s00167-016-4020-6. Epub 2016 Feb 9.

PMID:
26860097
22.

A new titinopathy: Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathy.

De Cid R, Ben Yaou R, Roudaut C, Charton K, Baulande S, Leturcq F, Romero NB, Malfatti E, Beuvin M, Vihola A, Criqui A, Nelson I, Nectoux J, Ben Aim L, Caloustian C, Olaso R, Udd B, Bonne G, Eymard B, Richard I.

Neurology. 2015 Dec 15;85(24):2126-35. doi: 10.1212/WNL.0000000000002200. Epub 2015 Nov 18.

23.

Myofibrillar myopathies: State of the art, present and future challenges.

Béhin A, Salort-Campana E, Wahbi K, Richard P, Carlier RY, Carlier P, Laforêt P, Stojkovic T, Maisonobe T, Verschueren A, Franques J, Attarian S, Maues de Paula A, Figarella-Branger D, Bécane HM, Nelson I, Duboc D, Bonne G, Vicart P, Udd B, Romero N, Pouget J, Eymard B.

Rev Neurol (Paris). 2015 Oct;171(10):715-29. doi: 10.1016/j.neurol.2015.06.002. Epub 2015 Sep 3. Review.

PMID:
26342832
24.

Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related Diseases.

Nelson I, Stojkovic T, Allamand V, Leturcq F, Bécane HM, Babuty D, Toutain A, Béroud C, Richard P, Romero NB, Eymard B, Ben Yaou R, Bonne G.

J Neuromuscul Dis. 2015 Sep 2;2(3):229-240.

25.

Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution.

Deconinck N, Richard P, Allamand V, Behin A, Lafôret P, Ferreiro A, de Becdelievre A, Ledeuil C, Gartioux C, Nelson I, Carlier RY, Carlier P, Wahbi K, Romero N, Zabot MT, Bouhour F, Tiffreau V, Lacour A, Eymard B, Stojkovic T.

J Neurol Neurosurg Psychiatry. 2015 Dec;86(12):1337-46. doi: 10.1136/jnnp-2013-307245. Epub 2014 Dec 22.

PMID:
25535305
26.

Detection of TRIM32 deletions in LGMD patients analyzed by a combined strategy of CGH array and massively parallel sequencing.

Nectoux J, de Cid R, Baulande S, Leturcq F, Urtizberea JA, Penisson-Besnier I, Nadaj-Pakleza A, Roudaut C, Criqui A, Orhant L, Peyroulan D, Ben Yaou R, Nelson I, Cobo AM, Arné-Bes MC, Uro-Coste E, Nitschke P, Claustres M, Bonne G, Lévy N, Chelly J, Richard I, Cossée M.

Eur J Hum Genet. 2015 Jul;23(7):929-34. doi: 10.1038/ejhg.2014.223. Epub 2014 Oct 29.

27.

The potential for indirect effects between co-flowering plants via shared pollinators depends on resource abundance, accessibility and relatedness.

Carvalheiro LG, Biesmeijer JC, Benadi G, Fründ J, Stang M, Bartomeus I, Kaiser-Bunbury CN, Baude M, Gomes SI, Merckx V, Baldock KC, Bennett AT, Boada R, Bommarco R, Cartar R, Chacoff N, Dänhardt J, Dicks LV, Dormann CF, Ekroos J, Henson KS, Holzschuh A, Junker RR, Lopezaraiza-Mikel M, Memmott J, Montero-Castaño A, Nelson IL, Petanidou T, Power EF, Rundlöf M, Smith HG, Stout JC, Temitope K, Tscharntke T, Tscheulin T, Vilà M, Kunin WE.

Ecol Lett. 2014 Nov;17(11):1389-99. doi: 10.1111/ele.12342. Epub 2014 Aug 28.

28.

Results of labral-level arthroscopic iliopsoas tenotomies for the treatment of labral impingement.

Nelson IR, Keene JS.

Arthroscopy. 2014 Jun;30(6):688-94. doi: 10.1016/j.arthro.2014.02.027. Epub 2014 Apr 3.

PMID:
24704071
29.

Phenotypic diversity associated with the MT-TV gene m.1644G>A mutation, a matter of quantity.

Fraidakis MJ, Jardel C, Allouche S, Nelson I, Auré K, Slama A, Lemière I, Thenint JP, Hamon JB, Zagnoli F, Heron D, Sedel F, Lombès A.

Mitochondrion. 2014 Mar;15:34-9. doi: 10.1016/j.mito.2014.03.010. Epub 2014 Mar 29.

30.

Association between components of body composition and scoliosis: a prospective cohort study reporting differences identifiable before the onset of scoliosis.

Clark EM, Taylor HJ, Harding I, Hutchinson J, Nelson I, Deanfield JE, Ness AR, Tobias JH.

J Bone Miner Res. 2014 Aug;29(8):1729-36. doi: 10.1002/jbmr.2207.

31.

Funnel plots and spine surgery: unit level and surgeon level outcome data.

Nelson IW.

Eur Spine J. 2014 Apr;23 Suppl 1:S4-5. doi: 10.1007/s00586-014-3228-8. Epub 2014 Feb 20. No abstract available.

32.

Admission inflammatory markers and isolation of a causative organism in patients with spontaneous spinal infection.

Torrie PA, Leonidou A, Harding IJ, Wynne Jones G, Hutchinson MJ, Nelson IW.

Ann R Coll Surg Engl. 2013 Nov;95(8):604-8. doi: 10.1308/003588413X13629960049351.

33.

Identifying scoliosis in population-based cohorts: development and validation of a novel method based on total-body dual-energy x-ray absorptiometric scans.

Taylor HJ, Harding I, Hutchinson J, Nelson I, Blom A, Tobias JH, Clark EM.

Calcif Tissue Int. 2013 Jun;92(6):539-47. doi: 10.1007/s00223-013-9713-y. Epub 2013 Feb 28.

PMID:
23456028
34.

Distinctive serum miRNA profile in mouse models of striated muscular pathologies.

Vignier N, Amor F, Fogel P, Duvallet A, Poupiot J, Charrier S, Arock M, Montus M, Nelson I, Richard I, Carrier L, Servais L, Voit T, Bonne G, Israeli D.

PLoS One. 2013;8(2):e55281. doi: 10.1371/journal.pone.0055281. Epub 2013 Feb 13.

35.

Fall risk factors in community-dwelling elderly who receive Medicaid-supported home- and community-based care services.

Yamashita T, Jeon H, Bailer AJ, Nelson IM, Mehdizadeh S.

J Aging Health. 2011 Jun;23(4):682-703. doi: 10.1177/0898264310390941. Epub 2010 Dec 23.

PMID:
21183726
36.

Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene.

Zsurka G, Hampel KG, Nelson I, Jardel C, Mirandola SR, Sassen R, Kornblum C, Marcorelles P, Lavoué S, Lombès A, Kunz WS.

Neurology. 2010 Feb 9;74(6):507-12. doi: 10.1212/WNL.0b013e3181cef7ab.

PMID:
20142618
37.

Street ball, swim team and the sour cream machine: a cluster analysis of out of school time participation portfolios.

Nelson IA, Gastic B.

J Youth Adolesc. 2009 Oct;38(9):1172-86. doi: 10.1007/s10964-008-9372-x. Epub 2008 Dec 20.

PMID:
19669898
38.

Clinical outcomes and fusion success associated with the use of BoneSave in spinal surgery.

Kapur RA, Amirfeyz R, Wylde V, Blom AW, Nelson IW, Hutchinson J.

Arch Orthop Trauma Surg. 2010 May;130(5):641-7. doi: 10.1007/s00402-009-0936-3. Epub 2009 Jul 23.

PMID:
19629506
39.

The value of radiographs obtained during forced traction under general anaesthesia in predicting flexibility in idiopathic scoliosis with Cobb angles exceeding 60 degree.

Ibrahim T, Gabbar OA, El-Abed K, Hutchinson MJ, Nelson IW.

J Bone Joint Surg Br. 2008 Nov;90(11):1473-6. doi: 10.1302/0301-620X.90B11.20690.

PMID:
18978268
40.

Serotonin (5-hydroxytryptamine) transporter inhibition causes bone loss in adult mice independently of estrogen deficiency.

Warden SJ, Nelson IR, Fuchs RK, Bliziotes MM, Turner CH.

Menopause. 2008 Nov-Dec;15(6):1176-83. doi: 10.1097/gme.0b013e318173566b.

PMID:
18725867
41.

Basic bookkeeping and avoiding theft.

Nelson IM.

Dent Clin North Am. 2008 Jul;52(3):529-34, viii. doi: 10.1016/j.cden.2008.02.004.

PMID:
18501732
42.

PTA testing, the Westmead post traumatic amnesia scale and opiate analgesia: a cautionary note.

McCarter RJ, Walton NH, Moore C, Ward A, Nelson I.

Brain Inj. 2007 Dec;21(13-14):1393-7.

PMID:
18066941
43.

Frequency-narrowed external-cavity diode-laser-array bar.

Chann B, Nelson I, Walker TG.

Opt Lett. 2000 Sep 15;25(18):1352-4.

PMID:
18066214
44.

Helical tomotherapy: image guidance and adaptive dose guidance.

Tomé WA, Jaradat HA, Nelson IA, Ritter MA, Mehta MP.

Front Radiat Ther Oncol. 2007;40:162-178. doi: 10.1159/000106034. Review.

PMID:
17641508
45.

A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.

Hanein S, Dürr A, Ribai P, Forlani S, Leutenegger AL, Nelson I, Babron MC, Elleuch N, Depienne C, Charon C, Brice A, Stevanin G.

Hum Genet. 2007 Nov;122(3-4):261-73. Epub 2007 Jun 28.

PMID:
17605047
46.

Exercise when young provides lifelong benefits to bone structure and strength.

Warden SJ, Fuchs RK, Castillo AB, Nelson IR, Turner CH.

J Bone Miner Res. 2007 Feb;22(2):251-9.

48.

A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene.

Namekawa M, Nelson I, Ribai P, Dürr A, Denis E, Stevanin G, Ruberg M, Brice A.

Neurogenetics. 2006 May;7(2):131-2. Epub 2006 Apr 13. No abstract available.

PMID:
16612642
49.

Quality assurance of treatment plans for interstitial and intracavitary high-dose-rate brachytherapy.

Das RK, Bradley KA, Nelson IA, Patel R, Thomadsen BR.

Brachytherapy. 2006 Jan-Mar;5(1):56-60.

PMID:
16563998
50.

A new phenotype linked to SPG27 and refinement of the critical region on chromosome.

Ribai P, Stevanin G, Bouslam N, Pontier B, Nelson I, Fontaine B, Dussert C, Charon C, Durr A, Brice A.

J Neurol. 2006 Jun;253(6):714-9. Epub 2006 Mar 6.

PMID:
16511635

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