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Items: 1 to 50 of 68

1.

Severity Adjusted Risk of Long-Term Adverse Sequelae Among Children with Osteomyelitis.

Vorhies JS, Lindsay EA, Tareen NG, Kellum RJ, Jo CH, Copley LAB.

Pediatr Infect Dis J. 2018 May 4. doi: 10.1097/INF.0000000000002044. [Epub ahead of print]

PMID:
29742649
2.

Seasonal Variation and Weather Changes Related to the Occurrence and Severity of Acute Hematogenous Osteomyelitis in Children.

Lindsay EA, Tareen N, Jo CH, Copley LA.

J Pediatric Infect Dis Soc. 2018 May 15;7(2):e16-e23. doi: 10.1093/jpids/pix085.

PMID:
29045692
3.

Validation and Modification of a Severity of Illness Score for Children With Acute Hematogenous Osteomyelitis.

Athey AG, Mignemi ME, Gheen WT, Lindsay EA, Jo CH, Copley LA.

J Pediatr Orthop. 2016 Oct 12. [Epub ahead of print]

PMID:
27741035
4.

Sequential Parenteral to Oral Clindamycin Dosing in Pediatric Musculoskeletal Infection: A Retrospective Review of 30 mg/kg/d Versus 40 mg/kg/d.

Erickson CM, Sue PK, Stewart K, Thomas MI, Lindsay EA, Jo C, Copley LA.

Pediatr Infect Dis J. 2016 Oct;35(10):1092-6. doi: 10.1097/INF.0000000000001272.

PMID:
27286561
5.

Improved Magnetic Resonance Imaging Utilization for Children with Musculoskeletal Infection.

Mueller AJ, Kwon JK, Steiner JW, Mittal VS, Fernandes NJ, Jo CH, Lindsay EA, Copley LA.

J Bone Joint Surg Am. 2015 Nov 18;97(22):1869-76. doi: 10.2106/JBJS.O.00403.

PMID:
26582617
6.

Bioactive dietary polyphenols inhibit heme iron absorption in a dose-dependent manner in human intestinal Caco-2 cells.

Ma Q, Kim EY, Lindsay EA, Han O.

J Food Sci. 2011 Jun-Jul;76(5):H143-50. doi: 10.1111/j.1750-3841.2011.02184.x. Epub 2011 May 4.

7.

The abundance of microbial functional genes in grassy woodlands is influenced more by soil nutrient enrichment than by recent weed invasion or livestock exclusion.

Lindsay EA, Colloff MJ, Gibb NL, Wakelin SA.

Appl Environ Microbiol. 2010 Aug;76(16):5547-55. doi: 10.1128/AEM.03054-09. Epub 2010 Jul 2.

9.

Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.

Xu H, Morishima M, Wylie JN, Schwartz RJ, Bruneau BG, Lindsay EA, Baldini A.

Development. 2004 Jul;131(13):3217-27. Epub 2004 Jun 2.

10.

Genetic dissection of the DiGeorge syndrome phenotype.

Vitelli F, Lindsay EA, Baldini A.

Cold Spring Harb Symp Quant Biol. 2002;67:327-32. No abstract available.

PMID:
12858556
11.

Investigation of the genetic diversity among isolates of Salmonella enterica serovar Dublin from animals and humans from England, Wales and Ireland.

Liebana E, Garcia-Migura L, Clouting C, Cassar CA, Clifton-Hadley FA, Lindsay EA, Threlfall EJ, Chappell SA, Davies RH.

J Appl Microbiol. 2002;93(5):732-44.

12.

A genetic link between Tbx1 and fibroblast growth factor signaling.

Vitelli F, Taddei I, Morishima M, Meyers EN, Lindsay EA, Baldini A.

Development. 2002 Oct;129(19):4605-11.

13.

Role of electronic data exchange in an international outbreak caused by Salmonella enterica serotype Typhimurium DT204b.

Lindsay EA, Lawson AJ, Walker RA, Ward LR, Smith HR, Scott FW, O'Brien SJ, Fisher IS, Crook PD, Wilson D, Brown DJ, Hardardottir H, Wannet WJ, Tschäpe H, Threlfall EJ.

Emerg Infect Dis. 2002 Jul;8(7):732-4.

14.

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.

Vitelli F, Morishima M, Taddei I, Lindsay EA, Baldini A.

Hum Mol Genet. 2002 Apr 15;11(8):915-22.

PMID:
11971873
15.

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

Paylor R, McIlwain KL, McAninch R, Nellis A, Yuva-Paylor LA, Baldini A, Lindsay EA.

Hum Mol Genet. 2001 Nov 1;10(23):2645-50.

PMID:
11726551
16.

Chromosomal microdeletions: dissecting del22q11 syndrome.

Lindsay EA.

Nat Rev Genet. 2001 Nov;2(11):858-68. Review.

PMID:
11715041
17.

Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes.

Taddei I, Morishima M, Huynh T, Lindsay EA.

Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11428-31. Epub 2001 Sep 18.

18.
19.

Use of a LightCycler gyrA mutation assay for rapid identification of mutations conferring decreased susceptibility to ciprofloxacin in multiresistant Salmonella enterica serotype Typhimurium DT104 isolates.

Walker RA, Saunders N, Lawson AJ, Lindsay EA, Dassama M, Ward LR, Woodward MJ, Davies RH, Liebana E, Threlfall EJ.

J Clin Microbiol. 2001 Apr;39(4):1443-8.

20.

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.

Lindsay EA, Vitelli F, Su H, Morishima M, Huynh T, Pramparo T, Jurecic V, Ogunrinu G, Sutherland HF, Scambler PJ, Bradley A, Baldini A.

Nature. 2001 Mar 1;410(6824):97-101.

PMID:
11242049
21.

Antibacterial compounds from Carissa lanceolata R.Br.

Lindsay EA, Berry Y, Jamie JF, Bremner JB.

Phytochemistry. 2000 Nov;55(5):403-6.

PMID:
11140600
22.

Decreased susceptibility to ciprofloxacin in outbreak-associated multiresistant Salmonella typhimurium DT104.

Walker RA, Lawson AJ, Lindsay EA, Ward LR, Wright PA, Bolton FJ, Wareing DR, Corkish JD, Davies RH, Threlfall EJ.

Vet Rec. 2000 Sep 30;147(14):395-6. No abstract available.

PMID:
11073003
23.

Congenital heart disease in mice deficient for the DiGeorge syndrome region.

Lindsay EA, Botta A, Jurecic V, Carattini-Rivera S, Cheah YC, Rosenblatt HM, Bradley A, Baldini A.

Nature. 1999 Sep 23;401(6751):379-83.

PMID:
10517636
24.

Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes.

Wakamiya M, Lindsay EA, Rivera-Pérez JA, Baldini A, Behringer RR.

Hum Mol Genet. 1998 Nov;7(12):1835-40.

PMID:
9811926
25.

A critical review of research related to family physician-assisted smoking cessation interventions.

Ritvo PG, Irvine MJ, Lindsay EA, Kraetschmer N, Blair N, Shnek ZM.

Cancer Prev Control. 1997 Oct;1(4):289-303. Review.

PMID:
9765753
26.

Congenital heart defects and 22q11 deletions: which genes count?

Lindsay EA, Baldini A.

Mol Med Today. 1998 Aug;4(8):350-7. Review.

PMID:
9755454
28.

Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.

Botta A, Lindsay EA, Jurecic V, Baldini A.

Mamm Genome. 1997 Dec;8(12):890-5. Erratum in: Mamm Genome 1998 Apr;9(4):344.

PMID:
9383280
29.

Deletion of chromosome 22q11 and pseudohypoparathyroidism.

Craigen WJ, Lindsay EA, Bricker JT, Hawkins EP, Baldini A.

Am J Med Genet. 1997 Oct 3;72(1):63-5.

PMID:
9295077
30.

A genetic etiology for interruption of the aortic arch type B.

Lewin MB, Lindsay EA, Jurecic V, Goytia V, Towbin JA, Baldini A.

Am J Cardiol. 1997 Aug 15;80(4):493-7.

PMID:
9285664
31.

Increasing physician involvement In cholesterol-lowering practices: The role of knowledge, attitudes and perceptions.

Mann KV, Lindsay EA, Putnam RW, Davis DA.

Adv Health Sci Educ Theory Pract. 1997;2(3):237-253.

PMID:
12386401
33.

Tobacco control activities of primary-care physicians in the Community Intervention Trial for Smoking Cessation. COMMIT Research Group.

Ockene JK, Lindsay EA, Hymowitz N, Giffen C, Purcell T, Pomrehn P, Pechacek T.

Tob Control. 1997;6 Suppl 2:S49-56.

34.

Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans.

Rizzu P, Lindsay EA, Taylor C, O'Donnell H, Levy A, Scambler P, Baldini A.

Mamm Genome. 1996 Sep;7(9):639-43.

PMID:
8703114
35.

A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.

Lindsay EA, Rizzu P, Antonacci R, Jurecic V, Delmas-Mata J, Lee CC, Kim UJ, Scambler PJ, Baldini A.

Genomics. 1996 Feb 15;32(1):104-12.

PMID:
8786095
36.

LIS2, gene and pseudogene, homologous to LIS1 (lissencephaly 1), located on the short and long arms of chromosome 2.

Reiner O, Bar-Am I, Sapir T, Shmueli O, Carrozzo R, Lindsay EA, Baldini A, Ledbetter DH, Cahana A.

Genomics. 1995 Nov 20;30(2):251-6.

PMID:
8586424
37.

Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization.

Juyal RC, Greenberg F, Mengden GA, Lupski JR, Trask BJ, van den Engh G, Lindsay EA, Christy H, Chen KS, Baldini A, et al.

Am J Med Genet. 1995 Sep 11;58(3):286-91.

PMID:
8533833
38.

Isolation of chromosome-specific genes by reciprocal probing of arrayed cDNA and cosmid libraries.

Lee CC, Yazdani A, Wehnert M, Zhao ZY, Lindsay EA, Bailey J, Coolbaugh MI, Couch L, Xiong M, Chinault AC, et al.

Hum Mol Genet. 1995 Aug;4(8):1373-80.

PMID:
7581376
39.

Diagnosis of X-linked adrenal hypoplasia congenita by mutation analysis of the DAX1 gene.

Guo W, Mason JS, Stone CG Jr, Morgan SA, Madu SI, Baldini A, Lindsay EA, Biesecker LG, Copeland KC, Horlick MN, et al.

JAMA. 1995 Jul 26;274(4):324-30.

PMID:
7609262
40.

Rapid molecular cytogenetic analysis of X-chromosomal microdeletions: fluorescence in situ hybridization (FISH) for complex glycerol kinase deficiency.

Worley KC, Lindsay EA, Bailey W, Wise J, McCabe ER, Baldini A.

Am J Med Genet. 1995 Jul 17;57(4):615-9.

PMID:
7573140
41.

Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.

Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A.

Am J Med Genet. 1995 Jul 3;57(3):514-22.

PMID:
7677167
42.

Schizophrenia and chromosomal deletions within 22q11.2.

Lindsay EA, Morris MA, Gos A, Nestadt G, Wolyniec PS, Lasseter VK, Shprintzen R, Antonarakis SE, Baldini A, Pulver AE.

Am J Hum Genet. 1995 Jun;56(6):1502-3. No abstract available.

43.

De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.

Lindsay EA, Shaffer LG, Carrozzo R, Greenberg F, Baldini A.

Am J Med Genet. 1995 Apr 10;56(3):296-9.

PMID:
7778594
44.

Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.

Lindsay EA, Greenberg F, Shaffer LG, Shapira SK, Scambler PJ, Baldini A.

Am J Med Genet. 1995 Mar 27;56(2):191-7.

PMID:
7625444
45.

Duplication 3q syndrome: molecular delineation of the critical region.

Aqua MS, Rizzu P, Lindsay EA, Shaffer LG, Zackai EH, Overhauser J, Baldini A.

Am J Med Genet. 1995 Jan 2;55(1):33-7.

PMID:
7702094
46.

Mapping segmental imbalances using comparative genomic hybridization and eigenanalysis.

Haddad B, Antonacci R, Rizzu P, Lindsay EA, Hughes MR, Smith LC, Knapp RD, Baldini A.

Cytogenet Cell Genet. 1995;71(3):276-9.

PMID:
7587393
47.

Screening in the office for elevated cholesterol levels: still a dilemma.

Morgan PP, Lindsay EA.

CMAJ. 1994 Jul 1;151(1):25-7. No abstract available.

48.

Medicine and health care: a marriage of necessity.

Lindsay EA, Herbert C.

CMAJ. 1994 Jun 1;150(11):1765-8. No abstract available.

49.

Physicians and smoking cessation. A survey of office procedures and practices in the Community Intervention Trial for Smoking Cessation.

Lindsay EA, Ockene JK, Hymowitz N, Giffen C, Berger L, Pomrehn P.

Arch Fam Med. 1994 Apr;3(4):341-8.

PMID:
8012622
50.

Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.

Lindsay EA, Grillo A, Ferrero GB, Roth EJ, Magenis E, Grompe M, Hultén M, Gould C, Baldini A, Zoghbi HY, et al.

Am J Med Genet. 1994 Jan 15;49(2):229-34.

PMID:
8116674

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