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Results: 1 to 20 of 305

1.

Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28.

Gripp KW, Curry C, Olney AH, Sandoval C, Fisher J, Chong JX; UW Center for Mendelian Genomics, Pilchman L, Sahraoui R, Stabley DL, Sol-Church K.

Am J Med Genet A. 2014 Jun 18. doi: 10.1002/ajmg.a.36633. [Epub ahead of print]

PMID:
24942156
[PubMed - as supplied by publisher]
2.

Ethics and safety in home care: perspectives on home support workers.

Storch J, Curry CG, Stevenson L, Macdonald M, Lang A.

Nurs Leadersh (Tor Ont). 2014 Mar;27(1):76-96.

PMID:
24809426
[PubMed - in process]
3.

Nine patients with Xp22.31 microduplication, cognitive deficits, seizures, and talipes anomalies.

Esplin ED, Li B, Slavotinek A, Novelli A, Battaglia A, Clark R, Curry C, Hudgins L.

Am J Med Genet A. 2014 May 6. doi: 10.1002/ajmg.a.36598. [Epub ahead of print]

PMID:
24800990
[PubMed - as supplied by publisher]
4.

Reduction of plasma aldosterone and arterial stiffness in obese pre- and stage1 hypertensive subjects after aerobic exercise.

Collier SR, Sandberg K, Moody AM, Frechette V, Curry CD, Ji H, Gowdar R, Chaudhuri D, Meucci M.

J Hum Hypertens. 2014 May 1. doi: 10.1038/jhh.2014.33. [Epub ahead of print]

PMID:
24785976
[PubMed - as supplied by publisher]
5.

Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.

McMillin MJ, Beck AE, Chong JX, Shively KM, Buckingham KJ, Gildersleeve HI, Aracena MI, Aylsworth AS, Bitoun P, Carey JC, Clericuzio CL, Crow YJ, Curry CJ, Devriendt K, Everman DB, Fryer A, Gibson K, Giovannucci Uzielli ML, Graham JM Jr, Hall JG, Hecht JT, Heidenreich RA, Hurst JA, Irani S, Krapels IP, Leroy JG, Mowat D, Plant GT, Robertson SP, Schorry EK, Scott RH, Seaver LH, Sherr E, Splitt M, Stewart H, Stumpel C, Temel SG, Weaver DD, Whiteford M, Williams MS, Tabor HK, Smith JD, Shendure J, Nickerson DA; University of Washington Center for Mendelian Genomics, Bamshad MJ.

Am J Hum Genet. 2014 May 1;94(5):734-44. doi: 10.1016/j.ajhg.2014.03.015. Epub 2014 Apr 10.

PMID:
24726473
[PubMed - indexed for MEDLINE]
6.

Port-site metastases after robotic surgery for gynecologic malignancy.

Rindos N, Curry CL, Tabbarah R, Wright V.

JSLS. 2014 Jan-Mar;18(1):66-70. doi: 10.4293/108680813X13693422519271.

PMID:
24680146
[PubMed - in process]
Free PMC Article
7.

Cytogenetically cryptic and FISH-negative PML/RARA rearrangement in acute promyelocytic leukemia detected only by PCR: an exceedingly rare phenomenon.

Blanco EM, Curry CV, Lu XY, Sarabia SF, Redell MS, Lopez-Terrada DH, Roy A.

Cancer Genet. 2014 Jan-Feb;207(1-2):48-9. doi: 10.1016/j.cancergen.2014.01.001. Epub 2014 Jan 16. No abstract available.

PMID:
24561214
[PubMed - indexed for MEDLINE]
8.

Post cardiac transplantation T-cell lymphoproliferative disorder presenting as a solitary lung nodule.

Aqil B, Krishnan B, Curry CV, Elghetany MT, Szigeti R.

Int J Clin Exp Pathol. 2013 Nov 15;6(12):3009-13. eCollection 2013.

PMID:
24294392
[PubMed - in process]
Free PMC Article
9.

Expansion of the TARP syndrome phenotype associated with de novo mutations and mosaicism.

Johnston JJ, Sapp JC, Curry C, Horton M, Leon E, Cusmano-Ozog K, Dobyns WB, Hudgins L, Zackai E, Biesecker LG.

Am J Med Genet A. 2014 Jan;164A(1):120-8. doi: 10.1002/ajmg.a.36212. Epub 2013 Nov 20.

PMID:
24259342
[PubMed - in process]
10.

Effects of supervised exercise program on metabolic function in overweight adolescents.

Meucci M, Cook C, Curry CD, Guidetti L, Baldari C, Collier SR.

World J Pediatr. 2013 Nov;9(4):307-11. doi: 10.1007/s12519-013-0440-2. Epub 2013 Nov 14.

PMID:
24235064
[PubMed - in process]
11.

Quality management system in a private practice setting.

Allyn J, Curry C.

Int Anesthesiol Clin. 2013 Fall;51(4):37-52. doi: 10.1097/AIA.0b013e3182a70cb7. No abstract available.

PMID:
24088887
[PubMed - indexed for MEDLINE]
12.

Academic emergency medicine in India and international collaboration.

Arora P, Bhavnani A, Kole T, Curry C.

Emerg Med Australas. 2013 Aug;25(4):294-6. doi: 10.1111/1742-6723.12110. No abstract available.

PMID:
23911018
[PubMed - indexed for MEDLINE]
13.

Fine-needle aspiration cytology of T-lymphoblastic lymphoma associated FGFR1 rearrangement myeloproliferative neoplasm.

Patel RA, Sheehan AM, Finch CJ, Lopez-Terrada D, Hernandez VS, Curry CV.

Diagn Cytopathol. 2014 Jan;42(1):45-8. doi: 10.1002/dc.23030. Epub 2013 Aug 1.

PMID:
23904402
[PubMed - in process]
14.

Pediatric subcutaneous panniculitis-like T-cell lymphoma with features of hemophagocytic syndrome.

Merritt BY, Curry JL, Duvic M, Vega F, Sheehan AM, Curry CV.

Pediatr Blood Cancer. 2013 Nov;60(11):1916-7. doi: 10.1002/pbc.24638. Epub 2013 Jul 19. No abstract available.

PMID:
23868752
[PubMed - indexed for MEDLINE]
15.

The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.

Curry CJ, Rosenfeld JA, Grant E, Gripp KW, Anderson C, Aylsworth AS, Saad TB, Chizhikov VV, Dybose G, Fagerberg C, Falco M, Fels C, Fichera M, Graakjaer J, Greco D, Hair J, Hopkins E, Huggins M, Ladda R, Li C, Moeschler J, Nowaczyk MJ, Ozmore JR, Reitano S, Romano C, Roos L, Schnur RE, Sell S, Suwannarat P, Svaneby D, Szybowska M, Tarnopolsky M, Tervo R, Tsai AC, Tucker M, Vallee S, Wheeler FC, Zand DJ, Barkovich AJ, Aradhya S, Shaffer LG, Dobyns WB.

Am J Med Genet A. 2013 Aug;161A(8):1833-52. doi: 10.1002/ajmg.a.35996. Epub 2013 Jun 27.

PMID:
23813913
[PubMed - indexed for MEDLINE]
16.

Mutations in PIK3R1 cause SHORT syndrome.

Dyment DA, Smith AC, Alcantara D, Schwartzentruber JA, Basel-Vanagaite L, Curry CJ, Temple IK, Reardon W, Mansour S, Haq MR, Gilbert R, Lehmann OJ, Vanstone MR, Beaulieu CL; FORGE Canada Consortium, Majewski J, Bulman DE, O'Driscoll M, Boycott KM, Innes AM.

Am J Hum Genet. 2013 Jul 11;93(1):158-66. doi: 10.1016/j.ajhg.2013.06.005. Epub 2013 Jun 27.

PMID:
23810382
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Setting up an Emergency Medicine Training Program.

Curry C.

J Nepal Health Res Counc. 2013 Jan;11(23):76-9.

PMID:
23787532
[PubMed - indexed for MEDLINE]
18.

WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.

Laine CM, Joeng KS, Campeau PM, Kiviranta R, Tarkkonen K, Grover M, Lu JT, Pekkinen M, Wessman M, Heino TJ, Nieminen-Pihala V, Aronen M, Laine T, Kröger H, Cole WG, Lehesjoki AE, Nevarez L, Krakow D, Curry CJ, Cohn DH, Gibbs RA, Lee BH, Mäkitie O.

N Engl J Med. 2013 May 9;368(19):1809-16. doi: 10.1056/NEJMoa1215458.

PMID:
23656646
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Investigation of NRXN1 deletions: clinical and molecular characterization.

Dabell MP, Rosenfeld JA, Bader P, Escobar LF, El-Khechen D, Vallee SE, Dinulos MB, Curry C, Fisher J, Tervo R, Hannibal MC, Siefkas K, Wyatt PR, Hughes L, Smith R, Ellingwood S, Lacassie Y, Stroud T, Farrell SA, Sanchez-Lara PA, Randolph LM, Niyazov D, Stevens CA, Schoonveld C, Skidmore D, MacKay S, Miles JH, Moodley M, Huillet A, Neill NJ, Ellison JW, Ballif BC, Shaffer LG.

Am J Med Genet A. 2013 Apr;161A(4):717-31. doi: 10.1002/ajmg.a.35780. Epub 2013 Mar 12.

PMID:
23495017
[PubMed - indexed for MEDLINE]
20.

Specimen specific, 3D modeling of the elbow--prediction of strain in the medial collateral ligament.

Buford WL Jr, Snijders JW, Patel VV, Curry CM, Smith BA.

Conf Proc IEEE Eng Med Biol Soc. 2012;2012:3348-51. doi: 10.1109/EMBC.2012.6346682.

PMID:
23366643
[PubMed - indexed for MEDLINE]

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