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Items: 1 to 50 of 107

1.

2D and 3D radiographic outcome assessment of the effect of guided tissue regeneration using resorbable collagen membrane in the healing of through-and-through periapical lesions - A randomized controlled trial.

Parmar PD, Dhamija R, Tewari S, Sangwan P, Gupta A, Duhan J, Mittal S.

Int Endod J. 2019 Feb 13. doi: 10.1111/iej.13098. [Epub ahead of print]

PMID:
30758848
2.

Spectrum of neurological complications in chikungunya fever: experience at a tertiary care centre and review of literature.

Anand KS, Agrawal AK, Garg J, Dhamija RK, Mahajan RK.

Trop Doct. 2019 Jan 24:49475518825219. doi: 10.1177/0049475518825219. [Epub ahead of print]

PMID:
30678544
3.

Teaching Video NeuroImages: MT-TL1 mutation presenting as chronic progressive external ophthalmoplegia.

Parsons AM, Mehta SH, Acierno MD, Dhamija R.

Neurology. 2019 Jan 22;92(4):e394. doi: 10.1212/WNL.0000000000006817. No abstract available.

PMID:
30665919
4.

A double-blind randomized controlled trial to assess efficacy of bromocriptine in cirrhotic patients with hepatic parkinsonism.

Sahney A, Sharma BC, Jindal A, Anand L, Arora V, Vijayaraghavan R, Dhamija RM, Kumar G, Bhardwaj A, Sarin SK.

Liver Int. 2018 Dec 16. doi: 10.1111/liv.14024. [Epub ahead of print]

PMID:
30554466
5.

A case of YY1-associated syndromic learning disability or Gabriele-de Vries syndrome with myasthenia gravis.

Morales-Rosado JA, Kaiwar C, Smith BE, Klee EW, Dhamija R.

Am J Med Genet A. 2018 Dec;176(12):2846-2849. doi: 10.1002/ajmg.a.40626. Epub 2018 Dec 14.

PMID:
30549423
6.

Ictal onset patterns of subdural intracranial electroencephalogram in children: How helpful for predicting epilepsy surgery outcome?

Alter AS, Dhamija R, McDonough TL, Shen S, McBrian DK, Mandel AM, McKhann GM, Feldstein NA, Akman CI.

Epilepsy Res. 2019 Jan;149:44-52. doi: 10.1016/j.eplepsyres.2018.10.008. Epub 2018 Oct 28.

PMID:
30476812
7.

Updated Imaging Features of Dysplastic Cerebellar Gangliocytoma.

Dhamija R, Wood CP, Porter AB, Hu LS, Weindling SM, Hoxworth JM.

J Comput Assist Tomogr. 2018 Nov 6. doi: 10.1097/RCT.0000000000000814. [Epub ahead of print]

PMID:
30407243
8.

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond.

Marini C, Porro A, Rastetter A, Dalle C, Rivolta I, Bauer D, Oegema R, Nava C, Parrini E, Mei D, Mercer C, Dhamija R, Chambers C, Coubes C, Thévenon J, Kuentz P, Julia S, Pasquier L, Dubourg C, Carré W, Rosati A, Melani F, Pisano T, Giardino M, Innes AM, Alembik Y, Scheidecker S, Santos M, Figueiroa S, Garrido C, Fusco C, Frattini D, Spagnoli C, Binda A, Granata T, Ragona F, Freri E, Franceschetti S, Canafoglia L, Castellotti B, Gellera C, Milanesi R, Mancardi MM, Clark DR, Kok F, Helbig KL, Ichikawa S, Sadler L, Neupauerová J, Laššuthova P, Šterbová K, Laridon A, Brilstra E, Koeleman B, Lemke JR, Zara F, Striano P, Soblet J, Smits G, Deconinck N, Barbuti A, DiFrancesco D, LeGuern E, Guerrini R, Santoro B, Hamacher K, Thiel G, Moroni A, DiFrancesco JC, Depienne C.

Brain. 2018 Nov 1;141(11):3160-3178. doi: 10.1093/brain/awy263.

PMID:
30351409
9.

Neuroimaging abnormalities in patients with Cowden syndrome: Retrospective single-center study.

Dhamija R, Weindling SM, Porter AB, Hu LS, Wood CP, Hoxworth JM.

Neurol Clin Pract. 2018 Jun;8(3):207-213. doi: 10.1212/CPJ.0000000000000463.

PMID:
30105160
10.

Phase determination using chromosomal microarray and fluorescence in situ hybridization in a patient with early onset Parkinson disease and two deletions in PRKN.

Williams ES, Barrett MJ, Dhamija R, Toran L, Chambers C, Mahadevan MS, Golden WL.

Mol Genet Genomic Med. 2018 May;6(3):457-462. doi: 10.1002/mgg3.386. Epub 2018 Mar 25.

11.

Schwannomatosis.

Dhamija R, Plotkin S, Asthagiri A, Messiaen L, Babovic-Vuksanovic D.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2018 Mar 8.

12.

Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.

Koczkowska M, Chen Y, Callens T, Gomes A, Sharp A, Johnson S, Hsiao MC, Chen Z, Balasubramanian M, Barnett CP, Becker TA, Ben-Shachar S, Bertola DR, Blakeley JO, Burkitt-Wright EMM, Callaway A, Crenshaw M, Cunha KS, Cunningham M, D'Agostino MD, Dahan K, De Luca A, Destrée A, Dhamija R, Eoli M, Evans DGR, Galvin-Parton P, George-Abraham JK, Gripp KW, Guevara-Campos J, Hanchard NA, Hernández-Chico C, Immken L, Janssens S, Jones KJ, Keena BA, Kochhar A, Liebelt J, Martir-Negron A, Mahoney MJ, Maystadt I, McDougall C, McEntagart M, Mendelsohn N, Miller DT, Mortier G, Morton J, Pappas J, Plotkin SR, Pond D, Rosenbaum K, Rubin K, Russell L, Rutledge LS, Saletti V, Schonberg R, Schreiber A, Seidel M, Siqveland E, Stockton DW, Trevisson E, Ullrich NJ, Upadhyaya M, van Minkelen R, Verhelst H, Wallace MR, Yap YS, Zackai E, Zonana J, Zurcher V, Claes K, Martin Y, Korf BR, Legius E, Messiaen LM.

Am J Hum Genet. 2018 Jan 4;102(1):69-87. doi: 10.1016/j.ajhg.2017.12.001. Epub 2017 Dec 28.

13.

A Case of KCNQ2-Associated Movement Disorder Triggered by Fever.

Dhamija R, Goodkin HP, Bailey R, Chambers C, Brenton JN.

J Child Neurol. 2017 Dec;32(14):1123-1124. doi: 10.1177/0883073817736702.

PMID:
29129156
14.

Autosomal recessive inheritance of ADCY5-related generalized dystonia and myoclonus.

Barrett MJ, Williams ES, Chambers C, Dhamija R.

Neurol Genet. 2017 Sep 25;3(5):193. doi: 10.1212/NXG.0000000000000193. eCollection 2017 Oct. No abstract available.

15.

Transient Neonatal Diabetes due to a Mutation in KCNJ11 in a Child with Klinefelter Syndrome.

Dahl AR, Dhamija R, Al Nofal A, Pittock ST, Schwenk WF, Kumar S.

J Clin Res Pediatr Endocrinol. 2018 Mar 1;10(1):79-82. doi: 10.4274/jcrpe.4807. Epub 2017 Aug 2.

16.

Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation.

Conboy E, Vairo F, Waggoner D, Ober C, Das S, Dhamija R, Klee EW, Pichurin P.

Case Rep Genet. 2017;2017:9184265. doi: 10.1155/2017/9184265. Epub 2017 Apr 12.

17.

Clinical Reasoning: A 13-year-old boy with chronic ataxia and developmental delay.

Abu Libdeh A, Talman L, Chambers C, Dhamija R.

Neurology. 2017 Mar 28;88(13):e116-e121. doi: 10.1212/WNL.0000000000003768. No abstract available.

PMID:
28348125
18.

Congenital Toxoplasmosis.

Guha R, Miley L, Aspiri M, Dhamija R.

Pediatr Neurol. 2017 May;70:81-82. doi: 10.1016/j.pediatrneurol.2017.01.012. Epub 2017 Jan 20. No abstract available.

PMID:
28254246
19.
20.

Axenfeld-Rieger Syndrome and Leukoencephalopathy Caused by a Mutation in FOXC1.

Kumar M, Chambers C, Dhamija R.

Pediatr Neurol. 2017 Jan;66:113-114. doi: 10.1016/j.pediatrneurol.2016.08.020. Epub 2016 Sep 9. No abstract available.

PMID:
27697311
21.

Detection of gonadal mosaicism in Hartsfield syndrome by next generation sequencing.

Shi Y, Dhamija R, Wren C, Wang X, Babovic-Vuksanovic D, Spector E.

Am J Med Genet A. 2016 Dec;170(12):3359. doi: 10.1002/ajmg.a.37869. Epub 2016 Sep 8. No abstract available.

PMID:
27604603
22.

Teaching NeuroImages: Intracranial hypotension in a patient with Marfan syndrome.

Abu Libdeh A, Matsumoto JA, Dhamija R.

Neurology. 2016 Jul 26;87(4):e40-1. doi: 10.1212/WNL.0000000000002896. No abstract available.

PMID:
27462045
23.

Clinical and Molecular Characterization of ALG1-CDG.

Dhamija R, Chambers C.

Pediatr Neurol Briefs. 2016 Feb;30(2):14. doi: 10.15844/pedneurbriefs-30-2-5.

24.

Author Response.

Kumar M, Dhamija R.

Neurology. 2015 Dec 15;85(24):2181. No abstract available.

PMID:
27030849
25.

Diagnostic NGS for Severe Neuromuscular Disorders.

Dhamija R, Chambers C.

Pediatr Neurol Briefs. 2015 Nov;29(11):82. doi: 10.15844/pedneurbriefs-29-11-1.

26.

Hartsfield Syndrome.

Dhamija R, Babovic-Vuksanovic D.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2016 Mar 3.

27.

A Patient With DNMT1 Gene Mutation Presenting With Polyneuropathy, Hearing Loss, and Personality Changes.

Kinariwala D, Yu J, Dhamija R.

JAMA Otolaryngol Head Neck Surg. 2016 Feb;142(2):193-4. doi: 10.1001/jamaoto.2015.3137. No abstract available.

PMID:
26747177
28.

Review of Commercially Available Epilepsy Genetic Panels.

Chambers C, Jansen LA, Dhamija R.

J Genet Couns. 2016 Apr;25(2):213-7. doi: 10.1007/s10897-015-9906-9. Epub 2015 Nov 5.

PMID:
26536886
29.

Evolution of brain lesions in a patient with TREX1 cerebroretinal vasculopathy.

Dhamija R, Schiff D, Lopes MB, Jen JC, Lin DD, Worrall BB.

Neurology. 2015 Nov 3;85(18):1633-4. doi: 10.1212/WNL.0000000000002092. No abstract available.

PMID:
26527794
30.

Paraspinal neurofibromas and hypertrophic neuropathy in Noonan syndrome with multiple lentigines.

Conboy E, Dhamija R, Wang M, Xie J, Dyck PJ, Bridges AG, Spinner RJ, Clayton AC, Watson RE, Messiaen L, Babovic-Vuksanovic D.

J Med Genet. 2016 Feb;53(2):123-6. doi: 10.1136/jmedgenet-2015-103177. Epub 2015 Sep 2.

PMID:
26337637
31.

22q11.2 deletion syndrome presenting with early-onset Parkinson's disease.

Rehman AF, Dhamija R, Williams ES, Barrett MJ.

Mov Disord. 2015 Aug;30(9):1289-90. doi: 10.1002/mds.26305. Epub 2015 Jul 21. No abstract available.

PMID:
26195290
32.

Teaching NeuroImages: Neurocutaneous melanosis.

Kumar M, Dhamija R.

Neurology. 2015 Jun 16;84(24):e207. doi: 10.1212/WNL.0000000000001689. No abstract available.

PMID:
26078408
33.

Subcutaneous implantable cardioverter defibrillator for dialysis patients: a strategy to reduce central vein stenoses and infections.

Dhamija RK, Tan H, Philbin E, Mathew RO, Sidhu MS, Wang J, Saour B, Haqqie SS, Beathard G, Yevzlin AS, Salman L, Boden WE, Siskin G, Asif A.

Am J Kidney Dis. 2015 Jul;66(1):154-8. doi: 10.1053/j.ajkd.2015.01.028. Epub 2015 Apr 22.

PMID:
25911316
34.

Monitoring and Surveillance of Hemodialysis Vascular Access Using StenTec and Physical Exam.

Dhamija R, Nash SK, Nguyen SV, Slack K, Tadeo J.

Semin Dial. 2015 May-Jun;28(3):299-304. doi: 10.1111/sdi.12311. Epub 2014 Oct 23.

PMID:
25346002
35.

Recurrent episodes of weak spells in a 15-year-old boy.

Dhamija R, Bodensteiner JB.

Semin Pediatr Neurol. 2014 Jun;21(2):91-4. doi: 10.1016/j.spen.2014.04.009. Epub 2014 Apr 13. No abstract available.

PMID:
25149934
36.

A 7-year-old girl with hypertrophic cardiomyopathy and progressive scoliosis.

Dhamija R, Kirmani S.

Semin Pediatr Neurol. 2014 Jun;21(2):67-71. doi: 10.1016/j.spen.2014.04.003. Epub 2014 Apr 3. Review.

PMID:
25149925
37.

Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.

Dhamija R, Kirmani S, Wang X, Ferber MJ, Wieben ED, Lazaridis KN, Babovic-Vuksanovic D.

Am J Med Genet A. 2014 Sep;164A(9):2356-9. doi: 10.1002/ajmg.a.36621. Epub 2014 May 28.

PMID:
24888332
38.

Sleep abnormalities in children with Dravet syndrome.

Dhamija R, Erickson MK, St Louis EK, Wirrell E, Kotagal S.

Pediatr Neurol. 2014 May;50(5):474-8. doi: 10.1016/j.pediatrneurol.2014.01.017. Epub 2014 Jan 7.

PMID:
24656210
39.

Novel de novo SPOCK1 mutation in a proband with developmental delay, microcephaly and agenesis of corpus callosum.

Dhamija R, Graham JM Jr, Smaoui N, Thorland E, Kirmani S.

Eur J Med Genet. 2014 Mar;57(4):181-4. doi: 10.1016/j.ejmg.2014.02.009. Epub 2014 Feb 27.

PMID:
24583203
40.

Novel de novo SCN2A mutation in a child with migrating focal seizures of infancy.

Dhamija R, Wirrell E, Falcao G, Kirmani S, Wong-Kisiel LC.

Pediatr Neurol. 2013 Dec;49(6):486-8. doi: 10.1016/j.pediatrneurol.2013.07.004. Epub 2013 Aug 26.

PMID:
23988467
41.

Septo-optic dysplasia in a patient with an unbalanced 5;12 translocation.

Dhamija R, Waltman L, Hoppman N, Kirmani S.

Pediatr Neurol. 2013 Jul;49(1):e2-3. doi: 10.1016/j.pediatrneurol.2013.04.019. No abstract available.

PMID:
23827435
42.

The role of nocturnal polysomnography in assessing children with Chiari type I malformation.

Dhamija R, Wetjen NM, Slocumb NL, Mandrekar J, Kotagal S.

Clin Neurol Neurosurg. 2013 Sep;115(9):1837-41. doi: 10.1016/j.clineuro.2013.05.025. Epub 2013 Jun 18.

PMID:
23791431
43.

Posttransplant lymphoproliferative disorder in an 11-year-old immunosuppressed boy.

Nelson A, Dhamija R, Nickels K.

Pediatr Neurol. 2013 May;48(5):397-9. doi: 10.1016/j.pediatrneurol.2012.12.018.

PMID:
23583059
44.

Clinical reasoning: a 56-year-old man with progressive spasticity.

Dhamija R, Raymond GV, Gavrilova R.

Neurology. 2013 Feb 26;80(9):e84-8. doi: 10.1212/WNL.0b013e3182840729. No abstract available.

45.

Ketogenic diet.

Dhamija R, Eckert S, Wirrell E.

Can J Neurol Sci. 2013 Mar;40(2):158-67. Review.

PMID:
23419562
46.

Association of PDE4D gene with ischaemic stroke.

Dhamija RK, Ranjan P, Kumar B, Mishra SK, Kallur SN.

Int J Stroke. 2012 Oct;7(7):E8. doi: 10.1111/j.1747-4949.2012.00874.x. No abstract available.

PMID:
22989401
47.

Biological grafts for hemodialysis access: historical lessons, state-of-the-art and future directions.

Dukkipati R, Peck M, Dhamija R, Hentschel DM, Reynolds T, Tammewar G, McAllister T.

Semin Dial. 2013 Mar-Apr;26(2):233-9. doi: 10.1111/j.1525-139X.2012.01106.x. Epub 2012 Aug 22. Review.

PMID:
22909001
48.

Standardized sign-out improves completeness and perceived accuracy of inpatient neurology handoffs.

Moseley BD, Smith JH, Diaz-Medina GE, Paz Soldan MM, Wicklund M, Dhamija R, Reda H, Presti MF, Britton JW.

Neurology. 2012 Sep 4;79(10):1060-4. doi: 10.1212/WNL.0b013e318265a698. Epub 2012 Aug 8.

PMID:
22875095
49.

Epilepsy in children--when should we think neurometabolic disease?

Dhamija R, Patterson MC, Wirrell EC.

J Child Neurol. 2012 May;27(5):663-71. doi: 10.1177/0883073811435829. Epub 2012 Feb 28. Review.

PMID:
22378665
50.

The StenTec gauge for measuring static intra-access pressure ratio (P(Ia Ratio) ) of fistulas and grafts.

Ash SR, Dhamija R, Zaroura MY, Hentschel DM.

Semin Dial. 2012 Jul;25(4):474-81. doi: 10.1111/j.1525-139X.2011.01037.x. Epub 2012 Feb 23.

PMID:
22356546

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