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Items: 1 to 50 of 370

1.

AQURE PASSPORT Intracranial Catheter for Mechanical Thrombectomy in Acute Ischemic Stroke Patients.

Qureshi AI, Zhiyong Z, Singh B, Liaqat J, Suri MFK.

J Vasc Interv Neurol. 2019 May;10(3):46-52.

2.

Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.

Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, McBride KL, Komara M, Al-Gazali L, Al Shamsi A, Fanning EA, Wierenga KJ, Scott DA, Ben-Neriah Z, Meiner V, Cassuto H, Elpeleg O, Lloyd Holder J Jr, Burrage LC, Seaver LH, Van Maldergem L, Mahida S, Soul JS, Marlatt M, Matyakhina L, Vogt J, Gold JA, Park SM, Varghese V, Lampe AK, Kumar A, Lees M, Holder-Espinasse M, McConnell V, Bernhard B, Blair E, Harrison V; DDD study, Muzny DM, Gibbs RA, Elsea SH, Posey JE, Bi W, Lalani S, Xia F, Yang Y, Eng CM, Lupski JR, Liu P.

Genome Med. 2019 Mar 25;11(1):16. doi: 10.1186/s13073-019-0630-1.

3.

CDK13-related disorder.

Hamilton MJ, Suri M.

Adv Genet. 2019;103:163-182. doi: 10.1016/bs.adgen.2018.11.001. Epub 2018 Dec 11.

PMID:
30904094
4.

U.S. farmers' opinions on the use of nontraditional water sources for agricultural activities.

Suri MR, Dery JL, Pérodin J, Brassill N, He X, Ammons S, Gerdes ME, Rock C, Goldstein RER.

Environ Res. 2019 May;172:345-357. doi: 10.1016/j.envres.2019.02.035. Epub 2019 Feb 22.

PMID:
30825685
5.

De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.

Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, McBride KL, Komara M, Al-Gazali L, Al Shamsi A, Fanning EA, Wierenga KJ, Scott DA, Ben-Neriah Z, Meiner V, Cassuto H, Elpeleg O, Holder JL Jr, Burrage LC, Seaver LH, Van Maldergem L, Mahida S, Soul JS, Marlatt M, Matyakhina L, Vogt J, Gold JA, Park SM, Varghese V, Lampe AK, Kumar A, Lees M, Holder-Espinasse M, McConnell V, Bernhard B, Blair E, Harrison V; DDD study, Muzny DM, Gibbs RA, Elsea SH, Posey JE, Bi W, Lalani S, Xia F, Yang Y, Eng CM, Lupski JR, Liu P.

Genome Med. 2019 Feb 28;11(1):12. doi: 10.1186/s13073-019-0623-0. Erratum in: Genome Med. 2019 Mar 25;11(1):16.

6.

Understanding grower perceptions and attitudes on the use of nontraditional water sources, including reclaimed or recycled water, in the semi-arid Southwest United States.

Dery JL, Rock CM, Goldstein RR, Onumajuru C, Brassill N, Zozaya S, Suri MR.

Environ Res. 2019 Mar;170:500-509. doi: 10.1016/j.envres.2018.12.039. Epub 2018 Dec 18.

PMID:
30703624
7.

A Bayesian hierarchical model estimating CACE in meta-analysis of randomized clinical trials with noncompliance.

Zhou J, Hodges JS, Suri MFK, Chu H.

Biometrics. 2019 Sep;75(3):978-987. doi: 10.1111/biom.13028. Epub 2019 Apr 4.

PMID:
30690716
8.

Groundwater level changes with a focus on agricultural areas in the Mid-Atlantic region of the United States, 2002-2016.

Dong Y, Jiang C, Suri MR, Pee D, Meng L, Rosenberg Goldstein RE.

Environ Res. 2019 Apr;171:193-203. doi: 10.1016/j.envres.2019.01.004. Epub 2019 Jan 4.

PMID:
30665121
9.

Deliquescent Chromism of Nickel(II) Iodide Thin Films.

Siegler TD, Reimnitz LC, Suri M, Cho SH, Bergerud AJ, Abney MK, Milliron DJ, Korgel BA.

Langmuir. 2019 Feb 12;35(6):2146-2152. doi: 10.1021/acs.langmuir.8b03979. Epub 2019 Jan 23.

PMID:
30616351
10.

Genotype, extrapyramidal features, and severity of variant ataxia-telangiectasia.

Schon K, van Os NJH, Oscroft N, Baxendale H, Scoffings D, Ray J, Suri M, Whitehouse WP, Mehta PR, Everett N, Bottolo L, van de Warrenburg BP, Byrd PJ, Weemaes C, Willemsen MA, Tischkowitz M, Taylor AM, Hensiek AE.

Ann Neurol. 2019 Feb;85(2):170-180. doi: 10.1002/ana.25394.

11.

Reliability and validity of clinical tests to assess posture, pain location, and cervical spine mobility in adults with neck pain and its associated disorders: Part 4. A systematic review from the cervical assessment and diagnosis research evaluation (CADRE) collaboration.

Lemeunier N, Jeoun EB, Suri M, Tuff T, Shearer H, Mior S, Wong JJ, da Silva-Oolup S, Torres P, D'Silva C, Stern P, Yu H, Millan M, Sutton D, Murnaghan K, Cȏté P.

Musculoskelet Sci Pract. 2018 Dec;38:128-147. doi: 10.1016/j.msksp.2018.09.013. Epub 2018 Oct 5.

PMID:
30455032
12.

PEHO syndrome: the endpoint of different genetic epilepsies.

Chitre M, Nahorski MS, Stouffer K, Dunning-Davies B, Houston H, Wakeling EL, Brady AF, Zuberi SM, Suri M, Parker APJ, Woods CG.

J Med Genet. 2018 Dec;55(12):803-813. doi: 10.1136/jmedgenet-2018-105288. Epub 2018 Oct 4.

PMID:
30287594
13.

SLC35A2-related congenital disorder of glycosylation: Defining the phenotype.

Yates TM, Suri M, Desurkar A, Lesca G, Wallgren-Pettersson C, Hammer TB, Raghavan A, Poulat AL, Møller RS, Thuresson AC, Balasubramanian M.

Eur J Paediatr Neurol. 2018 Nov;22(6):1095-1102. doi: 10.1016/j.ejpn.2018.08.002. Epub 2018 Aug 27.

14.

Targeted Ligand-Exchange Chemistry on Cesium Lead Halide Perovskite Quantum Dots for High-Efficiency Photovoltaics.

Wheeler LM, Sanehira EM, Marshall AR, Schulz P, Suri M, Anderson NC, Christians JA, Nordlund D, Sokaras D, Kroll T, Harvey SP, Berry JJ, Lin LY, Luther JM.

J Am Chem Soc. 2018 Aug 22;140(33):10504-10513. doi: 10.1021/jacs.8b04984. Epub 2018 Aug 9.

PMID:
30044630
15.

The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants.

Tatton-Brown K, Zachariou A, Loveday C, Renwick A, Mahamdallie S, Aksglaede L, Baralle D, Barge-Schaapveld D, Blyth M, Bouma M, Breckpot J, Crabb B, Dabir T, Cormier-Daire V, Fauth C, Fisher R, Gener B, Goudie D, Homfray T, Hunter M, Jorgensen A, Kant SG, Kirally-Borri C, Koolen D, Kumar A, Labilloy A, Lees M, Marcelis C, Mercer C, Mignot C, Miller K, Neas K, Newbury-Ecob R, Pilz DT, Posmyk R, Prada C, Ramsey K, Randolph LM, Selicorni A, Shears D, Suri M, Temple IK, Turnpenny P, Val Maldergem L, Varghese V, Veenstra-Knol HE, Yachelevich N, Yates L; Clinical Assessment of the Utility of Sequencing and Evaluation as a Service (CAUSES) Research Study; Deciphering Developmental Disorders (DDD) Study, Rahman N.

Wellcome Open Res. 2018 Apr 23;3:46. doi: 10.12688/wellcomeopenres.14430.1. eCollection 2018.

16.

Further delineation of Malan syndrome.

Priolo M, Schanze D, Tatton-Brown K, Mulder PA, Tenorio J, Kooblall K, Acero IH, Alkuraya FS, Arias P, Bernardini L, Bijlsma EK, Cole T, Coubes C, Dapia I, Davies S, Di Donato N, Elcioglu NH, Fahrner JA, Foster A, González NG, Huber I, Iascone M, Kaiser AS, Kamath A, Liebelt J, Lynch SA, Maas SM, Mammì C, Mathijssen IB, McKee S, Menke LA, Mirzaa GM, Montgomery T, Neubauer D, Neumann TE, Pintomalli L, Pisanti MA, Plomp AS, Price S, Salter C, Santos-Simarro F, Sarda P, Segovia M, Shaw-Smith C, Smithson S, Suri M, Valdez RM, Van Haeringen A, Van Hagen JM, Zollino M, Lapunzina P, Thakker RV, Zenker M, Hennekam RC.

Hum Mutat. 2018 Sep;39(9):1226-1237. doi: 10.1002/humu.23563. Epub 2018 Jun 25.

17.

Response.

Vasudevan PC, Suri M.

Clin Med (Lond). 2018 Mar;18(2):192. doi: 10.7861/clinmedicine.18-2-192. No abstract available.

18.

Cognitive impairment and intracranial atherosclerotic stenosis in general population.

Suri MFK, Zhou J, Qiao Y, Chu H, Qureshi AI, Mosley T, Gottesman RF, Wruck L, Sharrett AR, Alonso A, Wasserman BA.

Neurology. 2018 Apr 3;90(14):e1240-e1247. doi: 10.1212/WNL.0000000000005250. Epub 2018 Mar 9.

19.

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

Mikropoulos C, Hutten Selkirk CG, Saya S, Bancroft E, Vertosick E, Dadaev T, Brendler C, Page E, Dias A, Evans DG, Rothwell J, Maehle L, Axcrona K, Richardson K, Eccles D, Jensen T, Osther PJ, van Asperen CJ, Vasen H, Kiemeney LA, Ringelberg J, Cybulski C, Wokolorczyk D, Hart R, Glover W, Lam J, Taylor L, Salinas M, Feliubadaló L, Oldenburg R, Cremers R, Verhaegh G, van Zelst-Stams WA, Oosterwijk JC, Cook J, Rosario DJ, Buys SS, Conner T, Domchek S, Powers J, Ausems MGEM, Teixeira MR, Maia S, Izatt L, Schmutzler R, Rhiem K, Foulkes WD, Boshari T, Davidson R, Ruijs M, Helderman-van den Enden ATJM, Andrews L, Walker L, Snape K, Henderson A, Jobson I, Lindeman GJ, Liljegren A, Harris M, Adank MA, Kirk J, Taylor A, Susman R, Chen-Shtoyerman R, Pachter N, Spigelman A, Side L, Zgajnar J, Mora J, Brewer C, Gadea N, Brady AF, Gallagher D, van Os T, Donaldson A, Stefansdottir V, Barwell J, James PA, Murphy D, Friedman E, Nicolai N, Greenhalgh L, Obeid E, Murthy V, Copakova L, McGrath J, Teo SH, Strom S, Kast K, Leongamornlert DA, Chamberlain A, Pope J, Newlin AC, Aaronson N, Ardern-Jones A, Bangma C, Castro E, Dearnaley D, Eyfjord J, Falconer A, Foster CS, Gronberg H, Hamdy FC, Johannsson O, Khoo V, Lubinski J, Grindedal EM, McKinley J, Shackleton K, Mitra AV, Moynihan C, Rennert G, Suri M, Tricker K; IMPACT study collaborators, Moss S, Kote-Jarai Z, Vickers A, Lilja H, Helfand BT, Eeles RA.

Br J Cancer. 2018 Mar 20;118(6):e17. doi: 10.1038/bjc.2018.11. Epub 2018 Mar 6.

20.

Prolonged Microcatheter-Based Local Thrombolytic Infusion as a Salvage Treatment After Failed Endovascular Treatment for Cerebral Venous Thrombosis: A Multicenter Experience.

Qureshi AI, Grigoryan M, Saleem MA, Aytac E, Wallery SS, Rodriguez GJ, Suri MFK.

Neurocrit Care. 2018 Aug;29(1):54-61. doi: 10.1007/s12028-018-0502-3.

PMID:
29484582
21.

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

Mikropoulos C, Selkirk CGH, Saya S, Bancroft E, Vertosick E, Dadaev T, Brendler C, Page E, Dias A, Evans DG, Rothwell J, Maehle L, Axcrona K, Richardson K, Eccles D, Jensen T, Osther PJ, van Asperen CJ, Vasen H, Kiemeney LA, Ringelberg J, Cybulski C, Wokolorczyk D, Hart R, Glover W, Lam J, Taylor L, Salinas M, Feliubadaló L, Oldenburg R, Cremers R, Verhaegh G, van Zelst-Stams WA, Oosterwijk JC, Cook J, Rosario DJ, Buys SS, Conner T, Domchek S, Powers J, Ausems MG, Teixeira MR, Maia S, Izatt L, Schmutzler R, Rhiem K, Foulkes WD, Boshari T, Davidson R, Ruijs M, Helderman-van den Enden AT, Andrews L, Walker L, Snape K, Henderson A, Jobson I, Lindeman GJ, Liljegren A, Harris M, Adank MA, Kirk J, Taylor A, Susman R, Chen-Shtoyerman R, Pachter N, Spigelman A, Side L, Zgajnar J, Mora J, Brewer C, Gadea N, Brady AF, Gallagher D, van Os T, Donaldson A, Stefansdottir V, Barwell J, James PA, Murphy D, Friedman E, Nicolai N, Greenhalgh L, Obeid E, Murthy V, Copakova L, McGrath J, Teo SH, Strom S, Kast K, Leongamornlert DA, Chamberlain A, Pope J, Newlin AC, Aaronson N, Ardern-Jones A, Bangma C, Castro E, Dearnaley D, Eyfjord J, Falconer A, Foster CS, Gronberg H, Hamdy FC, Johannsson O, Khoo V, Lubinski J, Grindedal EM, McKinley J, Shackleton K, Mitra AV, Moynihan C, Rennert G, Suri M, Tricker K; IMPACT study collaborators, Moss S, Kote-Jarai Z, Vickers A, Lilja H, Helfand BT, Eeles RA.

Br J Cancer. 2018 Jan;118(2):266-276. doi: 10.1038/bjc.2017.429. Epub 2018 Jan 4. Erratum in: Br J Cancer. 2018 Mar 06;:.

22.

A clinical approach to developmental delay and intellectual disability.

Vasudevan P, Suri M.

Clin Med (Lond). 2017 Dec;17(6):558-561. doi: 10.7861/clinmedicine.17-6-558. Review.

23.

Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.

Hamilton MJ, Caswell RC, Canham N, Cole T, Firth HV, Foulds N, Heimdal K, Hobson E, Houge G, Joss S, Kumar D, Lampe AK, Maystadt I, McKay V, Metcalfe K, Newbury-Ecob R, Park SM, Robert L, Rustad CF, Wakeling E, Wilkie AOM, Study TDDD, Twigg SRF, Suri M.

J Med Genet. 2018 Jan;55(1):28-38. doi: 10.1136/jmedgenet-2017-104620. Epub 2017 Oct 11.

24.

Protein structure and phenotypic analysis of pathogenic and population missense variants in STXBP1.

Suri M, Evers JMG, Laskowski RA, O'Brien S, Baker K, Clayton-Smith J, Dabir T, Josifova D, Joss S, Kerr B, Kraus A, McEntagart M, Morton J, Smith A, Splitt M, Thornton JM; DDD Study, Wright CF.

Mol Genet Genomic Med. 2017 Jun 20;5(5):495-507. doi: 10.1002/mgg3.304. eCollection 2017 Sep.

25.

De Novo Mutations in YWHAG Cause Early-Onset Epilepsy.

Guella I, McKenzie MB, Evans DM, Buerki SE, Toyota EB, Van Allen MI; Epilepsy Genomics Study, Suri M, Elmslie F; Deciphering Developmental Disorders Study, Simon MEH, van Gassen KLI, Héron D, Keren B, Nava C, Connolly MB, Demos M, Farrer MJ.

Am J Hum Genet. 2017 Aug 3;101(2):300-310. doi: 10.1016/j.ajhg.2017.07.004.

26.

Phantom-based standardization of CT angiography images for spot sign detection.

Morotti A, Romero JM, Jessel MJ, Hernandez AM, Vashkevich A, Schwab K, Burns JD, Shah QA, Bergman TA, Suri MFK, Ezzeddine M, Kirmani JF, Agarwal S, Shapshak AH, Messe SR, Venkatasubramanian C, Palmieri K, Lewandowski C, Chang TR, Chang I, Rose DZ, Smith W, Hsu CY, Liu CL, Lien LM, Hsiao CY, Iwama T, Afzal MR, Cassarly C, Greenberg SM, Martin RH, Qureshi AI, Rosand J, Boone JM, Goldstein JN; ATACH-II and NETT Investigators.

Neuroradiology. 2017 Sep;59(9):839-844. doi: 10.1007/s00234-017-1857-4. Epub 2017 Jul 20.

27.

A Population-Based Study of the Incidence of Acute Spinal Cord Infarction.

Qureshi AI, Afzal MR, Suri MFK.

J Vasc Interv Neurol. 2017 Jun;9(4):44-48.

28.

Open-Label Phase I Clinical Study to Assess the Safety and Efficacy of Cilostazol in Patients Undergoing Internal Carotid Artery Stent Placement.

Hassan AE, Zacharatos H, Grigoryan M, Tekle WG, Khan A, Siddiq F, Rodriguez GJ, Tummala R, Jagadeesan B, Suri MFK, Qureshi AI.

Interv Neurol. 2017 Mar;6(1-2):42-48. doi: 10.1159/000452308. Epub 2016 Dec 8.

29.

Intracranial atherosclerosis and dementia: The Atherosclerosis Risk in Communities (ARIC) Study.

Dearborn JL, Zhang Y, Qiao Y, Suri MFK, Liu L, Gottesman RF, Rawlings AM, Mosley TH, Alonso A, Knopman DS, Guallar E, Wasserman BA.

Neurology. 2017 Apr 18;88(16):1556-1563. doi: 10.1212/WNL.0000000000003837. Epub 2017 Mar 22.

30.

Precision and Accuracy of Identification of Anatomical Surface Landmarks by 30 Expert Hip Arthroscopists.

Christoforetti JJ, Delong J, Hanypsiak BT, Suri M, Domb BG, Snibbe JC, Gerhardt MB.

Am J Orthop (Belle Mead NJ). 2017 Jan/Feb;46(1):E65-E70.

PMID:
28235126
31.

Study of kite string injuries in Western India.

Prajapati C, Agrawal A, Atha R, Suri MP, Sachde JP, Shaikh MF.

Int J Inj Contr Saf Promot. 2017 Mar;24(1):136-139. doi: 10.1080/17457300.2015.1076850. Epub 2015 Oct 8.

PMID:
28067128
32.

Osteochondral Allograft Transplantation for Femoral Trochlear Dysplasia.

Vansadia DV, Heltsley JR, Montgomery S, Suri M, Jones DG.

Ochsner J. 2016 Winter;16(4):475-480.

33.

Factors Affecting the Union of Opening Wedge High Tibial Osteotomy Using a Titanium Wedge Plate.

Nawas HT, Vansadia DV, Heltsley JR, Suri M, Montgomery S, Jones DG.

Ochsner J. 2016 Winter;16(4):464-470.

34.

Pregnancy in advanced age and the risk of stroke in postmenopausal women: analysis of Women's Health Initiative Study.

Qureshi AI, Saeed O, Malik AA, Suri MF.

Am J Obstet Gynecol. 2017 Apr;216(4):409.e1-409.e6. doi: 10.1016/j.ajog.2016.12.004. Epub 2016 Dec 9.

PMID:
27956201
35.

Anthelmintic potential of Calotropis procera, Azadirachta indica and Punica granatum against Gastrothylax indicus.

Aggarwal R, Kaur K, Suri M, Bagai U.

J Parasit Dis. 2016 Dec;40(4):1230-1238. Epub 2015 Feb 15.

36.

De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations.

Dennert N, Engels H, Cremer K, Becker J, Wohlleber E, Albrecht B, Ehret JK, Lüdecke HJ, Suri M, Carignani G, Renieri A, Kukuk GM, Wieland T, Andrieux J, Strom TM, Wieczorek D, Dieux-Coëslier A, Zink AM.

Am J Med Genet A. 2017 Feb;173(2):435-443. doi: 10.1002/ajmg.a.38034. Epub 2016 Nov 14. Review.

PMID:
27862890
37.
38.

Ataxia telangiectasia: presentation and diagnostic delay.

Devaney R, Pasalodos S, Suri M, Bush A, Bhatt JM.

Arch Dis Child. 2017 Apr;102(4):328-330. doi: 10.1136/archdischild-2016-310477. Epub 2016 Oct 31.

PMID:
27799156
39.

Functional Characterization and Rescue of a Deep Intronic Mutation in OCRL Gene Responsible for Lowe Syndrome.

Rendu J, Montjean R, Coutton C, Suri M, Chicanne G, Petiot A, Brocard J, Grunwald D, Pietri Rouxel F, Payrastre B, Lunardi J, Dorseuil O, Marty I, Fauré J.

Hum Mutat. 2017 Feb;38(2):152-159. doi: 10.1002/humu.23139. Epub 2016 Nov 21.

PMID:
27790796
40.

Growth and nutrition in children with ataxia telangiectasia.

Stewart E, Prayle AP, Tooke A, Pasalodos S, Suri M, Bush A, Bhatt JM.

Arch Dis Child. 2016 Dec;101(12):1137-1141. doi: 10.1136/archdischild-2015-310373. Epub 2016 Aug 29.

41.

Rubinstein-Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrum.

Hamilton MJ, Newbury-Ecob R, Holder-Espinasse M, Yau S, Lillis S, Hurst JA, Clement E, Reardon W, Joss S, Hobson E, Blyth M, Al-Shehhi M, Lynch SA, Suri M; DDD Study.

Clin Dysmorphol. 2016 Oct;25(4):135-45. doi: 10.1097/MCD.0000000000000143.

PMID:
27465822
42.

Syncope in Patient with Bilateral Severe Internal Carotid Arteries Stenosis/Near Occlusion: A Case Report and Literature Review.

Miran MS, Suri MF, Qureshi MH, Ahmad A, Suri MK, Basreen R, Qureshi AI.

J Vasc Interv Neurol. 2016 Jun;9(1):42-5.

43.

Risk of Ischemic Stroke in High Risk Atrial Fibrillation Patients during Periods of Warfarin Discontinuation for Surgical Procedures.

Qureshi AI, Jahangir N, Malik AA, Afzal MR, Orfi F, Suri MF.

Cerebrovasc Dis. 2016;42(5-6):346-351. Epub 2016 Jun 21.

PMID:
27322535
44.

3p14p12 deletion syndrome: report of a new case providing further evidence of a clinically recognizable syndrome.

Johnson K, Yates K, Martin K, Suri M.

Clin Dysmorphol. 2016 Oct;25(4):163-6. doi: 10.1097/MCD.0000000000000135. No abstract available.

PMID:
27253321
45.

Rothmund-Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene.

Suter AA, Itin P, Heinimann K, Ahmed M, Ashraf T, Fryssira H, Kini U, Lapunzina P, Miny P, Sommerlund M, Suri M, Vaeth S, Vasudevan P, Gallati S.

Mol Genet Genomic Med. 2016 Feb 24;4(3):359-66. doi: 10.1002/mgg3.209. eCollection 2016 May.

46.

Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.

Armour CM, Smith A, Hartley T, Chardon JW, Sawyer S, Schwartzentruber J, Hennekam R, Majewski J, Bulman DE; FORGE Canada Consortium, Suri M, Boycott KM.

Am J Med Genet A. 2016 Jul;170(7):1820-5. doi: 10.1002/ajmg.a.37684. Epub 2016 May 2.

PMID:
27133561
47.

Prevalence of Intracranial Atherosclerotic Stenosis Using High-Resolution Magnetic Resonance Angiography in the General Population: The Atherosclerosis Risk in Communities Study.

Suri MF, Qiao Y, Ma X, Guallar E, Zhou J, Zhang Y, Liu L, Chu H, Qureshi AI, Alonso A, Folsom AR, Wasserman BA.

Stroke. 2016 May;47(5):1187-93. doi: 10.1161/STROKEAHA.115.011292. Epub 2016 Apr 7.

48.

Lumbar Catheter Placement Using Paramedian Approach Under Fluoroscopic Guidance.

Qureshi AI, Khan AA, Malik AA, Afzal MR, Herial NA, Qureshi MH, Suri MF.

J Vasc Interv Neurol. 2016 Jan;8(5):55-62.

49.

Histopathological Characteristics of IV Recombinant Tissue Plasminogen -Resistant Thrombi in Patients with Acute Ischemic Stroke.

Qureshi AI, Qureshi MH, Lobanova I, Bashir A, Khan AA, Bologna SM, Peterson M, Suri MF.

J Vasc Interv Neurol. 2016 Jan;8(5):38-45. No abstract available.

50.

Stent-Assisted Clip Placement for Complex Internal Carotid Artery Intracranial Aneurysms.

Qureshi AI, Chughtai M, Khan AA, Suri MF, Sherr GT.

J Vasc Interv Neurol. 2016 Jan;8(5):23-9.

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