Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 52

1.

Usefulness of testing for hereditary alpha tryptasemia in symptomatic patients with elevated tryptase.

Carrigan C, Milner JD, Lyons JJ, Vadas P.

J Allergy Clin Immunol Pract. 2020 Jan 23. pii: S2213-2198(20)30051-9. doi: 10.1016/j.jaip.2020.01.012. [Epub ahead of print] No abstract available.

PMID:
31981732
2.

Cyclic lava effusion during the 2018 eruption of Kīlauea Volcano.

Patrick MR, Dietterich HR, Lyons JJ, Diefenbach AK, Parcheta C, Anderson KR, Namiki A, Sumita I, Shiro B, Kauahikaua JP.

Science. 2019 Dec 6;366(6470). pii: eaay9070. doi: 10.1126/science.aay9070. Epub 2019 Dec 5.

PMID:
31806788
3.

Mast cell activation in the context of elevated basal serum tryptase: genetics and presentations.

Khoury P, Lyons JJ.

Curr Allergy Asthma Rep. 2019 Nov 27;19(12):55. doi: 10.1007/s11882-019-0887-x. Review.

PMID:
31776770
4.

Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions.

Ittiwut C, Manuyakorn W, Tongkobpetch S, Benjaponpitak S, Fisher MR, Milner JD, Lyons JJ, Suphapeetiporn K, Shotelersuk V.

J Clin Immunol. 2020 Jan;40(1):227-231. doi: 10.1007/s10875-019-00693-6. Epub 2019 Nov 9. No abstract available.

PMID:
31707513
5.

Clinical response to omalizumab in patients with hereditary α-tryptasemia.

Mendoza Alvarez LB, Barker R, Nelson C, DiMaggio T, Stone KD, Milner JD, Rosenthal JA, Petroni DH, Glover SC, Lyons JJ.

Ann Allergy Asthma Immunol. 2020 Jan;124(1):99-100.e1. doi: 10.1016/j.anai.2019.09.026. Epub 2019 Oct 9. No abstract available.

PMID:
31605754
6.

Impact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia.

Le QT, Lyons JJ, Naranjo AN, Olivera A, Lazarus RA, Metcalfe DD, Milner JD, Schwartz LB.

J Exp Med. 2019 Oct 7;216(10):2348-2361. doi: 10.1084/jem.20190701. Epub 2019 Jul 23.

PMID:
31337736
7.

Skewed Lymphocyte Subpopulations and Associated Phenotypes in Patients with Mastocytosis.

Kulinski JM, Eisch R, Young ML, Rampertaap S, Stoddard J, Monsale J, Romito K, Lyons JJ, Rosenzweig SD, Metcalfe DD, Komarow HD.

J Allergy Clin Immunol Pract. 2020 Jan;8(1):292-301.e2. doi: 10.1016/j.jaip.2019.07.004. Epub 2019 Jul 15.

PMID:
31319217
8.

Why the 20% + 2 Tryptase Formula Is a Diagnostic Gold Standard for Severe Systemic Mast Cell Activation and Mast Cell Activation Syndrome.

Valent P, Bonadonna P, Hartmann K, Broesby-Olsen S, Brockow K, Butterfield JH, Triggiani M, Lyons JJ, Oude Elberink JNG, Arock M, Metcalfe DD, Akin C.

Int Arch Allergy Immunol. 2019;180(1):44-51. doi: 10.1159/000501079. Epub 2019 Jun 28. Review.

9.

GATA-2-deficient mast cells limit IgE-mediated immediate hypersensitivity reactions in human subjects.

Desai A, Sowerwine K, Liu Y, Lawrence MG, Chovanec J, Hsu AP, O'Connell MP, Kim J, Boris L, Jones N, Wisch L, Eisch RR, Carter MC, Komarow HD, Zerbe C, Milner JD, Maric I, Sun X, Lee CR, Tunc I, Pirooznia M, Stone KD, Holland SM, Metcalfe DD, Lyons JJ.

J Allergy Clin Immunol. 2019 Aug;144(2):613-617.e14. doi: 10.1016/j.jaci.2019.05.007. Epub 2019 May 15. No abstract available.

PMID:
31102699
10.

The clinical and mechanistic intersection of primary atopic disorders and inborn errors of growth and metabolism.

Lyons JJ, Milner JD.

Immunol Rev. 2019 Jan;287(1):135-144. doi: 10.1111/imr.12727. Review.

PMID:
30565252
11.

Hereditary Alpha Tryptasemia: Genotyping and Associated Clinical Features.

Lyons JJ.

Immunol Allergy Clin North Am. 2018 Aug;38(3):483-495. doi: 10.1016/j.iac.2018.04.003. Epub 2018 Jun 9. Review.

12.

First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease.

Sabato V, Chovanec J, Faber M, Milner JD, Ebo D, Lyons JJ.

J Clin Immunol. 2018 May;38(4):457-459. doi: 10.1007/s10875-018-0506-y. Epub 2018 May 11. No abstract available.

PMID:
29748908
13.

Primary atopic disorders.

Lyons JJ, Milner JD.

J Exp Med. 2018 Apr 2;215(4):1009-1022. doi: 10.1084/jem.20172306. Epub 2018 Mar 16. Review.

14.

Editorial: Stressing out mast cells via CRF1.

Lyons JJ, Rosenberg HF, Druey KM.

J Leukoc Biol. 2017 Dec;102(6):1284-1285. doi: 10.1189/jlb.2CE0617-248RR. No abstract available.

PMID:
29191866
15.

Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease.

Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg ND, Meffre E, Gelfand EW, Snow AL, Milner JD.

Nat Genet. 2017 Oct 27;49(11):1661. doi: 10.1038/ng1117-1661b.

PMID:
29074947
16.

Persistent tryptase elevation in a patient with Gaucher disease.

Schussler E, Yang A, Lyons JJ, Milner JD, Wang J.

J Allergy Clin Immunol Pract. 2018 Mar - Apr;6(2):697-699. doi: 10.1016/j.jaip.2017.08.039. Epub 2017 Oct 13. No abstract available.

PMID:
29033258
17.

A common haplotype containing functional CACNA1H variants is frequently coinherited with increased TPSAB1 copy number.

Lyons JJ, Stotz SC, Chovanec J, Liu Y, Lewis KL, Nelson C, DiMaggio T, Jones N, Stone KD, Sung H, Biesecker LG, Colicos MA, Milner JD.

Genet Med. 2018 Apr;20(5):503-512. doi: 10.1038/gim.2017.136. Epub 2017 Sep 21.

PMID:
28933792
18.

PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients.

Zhang Y, Ma CA, Lawrence MG, Break TJ, O'Connell MP, Lyons JJ, López DB, Barber JS, Zhao Y, Barber DL, Freeman AF, Holland SM, Lionakis MS, Milner JD.

J Exp Med. 2017 Sep 4;214(9):2523-2533. doi: 10.1084/jem.20161427. Epub 2017 Jul 14.

19.

Germline hypomorphic CARD11 mutations in severe atopic disease.

Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg N, Meffre E, Gelfand EW, Snow AL, Milner JD.

Nat Genet. 2017 Aug;49(8):1192-1201. doi: 10.1038/ng.3898. Epub 2017 Jun 19. Erratum in: Nat Genet. 2017 Oct 27;49(11):1661.

20.

Correction: ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans.

Lyons JJ, Liu Y, Ma CA, Yu X, O'Connell MP, Lawrence MG, Zhang Y, Karpe K, Zhao M, Siegel AM, Stone KD, Nelson C, Jones N, DiMaggio T, Darnell DN, Mendoza-Caamal E, Orozco L, Hughes JD, McElwee J, Hohman RJ, Frischmeyer-Guerrerio PA, Rothenberg ME, Freeman AF, Holland SM, Milner JD.

J Exp Med. 2017 Apr 3;214(4):1201. doi: 10.1084/jem.2016143503082017c. Epub 2017 Mar 13. No abstract available.

21.

ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans.

Lyons JJ, Liu Y, Ma CA, Yu X, O'Connell MP, Lawrence MG, Zhang Y, Karpe K, Zhao M, Siegel AM, Stone KD, Nelson C, Jones N, DiMaggio T, Darnell DN, Mendoza-Caamal E, Orozco L, Hughes JD, McElwee J, Hohman RJ, Frischmeyer-Guerrerio PA, Rothenberg ME, Freeman AF, Holland SM, Milner JD.

J Exp Med. 2017 Mar 6;214(3):669-680. doi: 10.1084/jem.20161435. Epub 2017 Jan 26. Erratum in: J Exp Med. 2017 Apr 3;214(4):1201.

22.

Detection of phosphoglucomutase-3 deficiency by lectin-based flow cytometry.

Carlson RJ, Bond MR, Hutchins S, Brown Y, Wolfe LA, Lam C, Nelson C, DiMaggio T, Jones N, Rosenzweig SD, Stone KD, Freeman AF, Holland SM, Hanover JA, Milner JD, Lyons JJ.

J Allergy Clin Immunol. 2017 Jul;140(1):291-294.e4. doi: 10.1016/j.jaci.2016.12.951. Epub 2017 Jan 4. No abstract available.

23.
24.

Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.

Lyons JJ, Yu X, Hughes JD, Le QT, Jamil A, Bai Y, Ho N, Zhao M, Liu Y, O'Connell MP, Trivedi NN, Nelson C, DiMaggio T, Jones N, Matthews H, Lewis KL, Oler AJ, Carlson RJ, Arkwright PD, Hong C, Agama S, Wilson TM, Tucker S, Zhang Y, McElwee JJ, Pao M, Glover SC, Rothenberg ME, Hohman RJ, Stone KD, Caughey GH, Heller T, Metcalfe DD, Biesecker LG, Schwartz LB, Milner JD.

Nat Genet. 2016 Dec;48(12):1564-1569. doi: 10.1038/ng.3696. Epub 2016 Oct 17.

25.

FOXP3+ Tregs require WASP to restrain Th2-mediated food allergy.

Lexmond WS, Goettel JA, Lyons JJ, Jacobse J, Deken MM, Lawrence MG, DiMaggio TH, Kotlarz D, Garabedian E, Sackstein P, Nelson CC, Jones N, Stone KD, Candotti F, Rings EH, Thrasher AJ, Milner JD, Snapper SB, Fiebiger E.

J Clin Invest. 2016 Oct 3;126(10):4030-4044. doi: 10.1172/JCI85129. Epub 2016 Sep 19.

26.

Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation.

Lam C, Ferreira C, Krasnewich D, Toro C, Latham L, Zein WM, Lehky T, Brewer C, Baker EH, Thurm A, Farmer CA, Rosenzweig SD, Lyons JJ, Schreiber JM, Gropman A, Lingala S, Ghany MG, Solomon B, Macnamara E, Davids M, Stratakis CA, Kimonis V, Gahl WA, Wolfe L.

Genet Med. 2017 Feb;19(2):160-168. doi: 10.1038/gim.2016.75. Epub 2016 Jul 7.

PMID:
27388694
27.

Diminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxis.

Hox V, O'Connell MP, Lyons JJ, Sackstein P, Dimaggio T, Jones N, Nelson C, Boehm M, Holland SM, Freeman AF, Tweardy DJ, Olivera A, Metcalfe DD, Milner JD.

J Allergy Clin Immunol. 2016 Jul;138(1):187-199. doi: 10.1016/j.jaci.2015.11.024. Epub 2016 Mar 2. Erratum in: J Allergy Clin Immunol. 2017 Jul;140(1):320.

28.

Food allergies can persist after myeloablative hematopoietic stem cell transplantation in dedicator of cytokinesis 8-deficient patients.

Happel CS, Stone KD, Freeman AF, Shah NN, Wang A, Lyons JJ, Guerrerio PA, Hickstein DD, Su HC.

J Allergy Clin Immunol. 2016 Jun;137(6):1895-1898.e5. doi: 10.1016/j.jaci.2015.11.017. Epub 2016 Jan 28. No abstract available.

29.

A two-stage clinical decision support system for early recognition and stratification of patients with sepsis: an observational cohort study.

Amland RC, Lyons JJ, Greene TL, Haley JM.

JRSM Open. 2015 Oct 8;6(10):2054270415609004. doi: 10.1177/2054270415609004. eCollection 2015 Oct.

30.

Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease.

Zhou Q, Wang H, Schwartz DM, Stoffels M, Park YH, Zhang Y, Yang D, Demirkaya E, Takeuchi M, Tsai WL, Lyons JJ, Yu X, Ouyang C, Chen C, Chin DT, Zaal K, Chandrasekharappa SC, Hanson EP, Yu Z, Mullikin JC, Hasni SA, Wertz IE, Ombrello AK, Stone DL, Hoffmann P, Jones A, Barham BK, Leavis HL, van Royen-Kerkof A, Sibley C, Batu ED, Gül A, Siegel RM, Boehm M, Milner JD, Ozen S, Gadina M, Chae J, Laxer RM, Kastner DL, Aksentijevich I.

Nat Genet. 2016 Jan;48(1):67-73. doi: 10.1038/ng.3459. Epub 2015 Dec 7.

31.

GATA3 haploinsufficiency does not block allergic sensitization or atopic disease.

Lawrence MG, Leiding JW, Lyons JJ, Hsu AP, Nelson CC, Jones N, Fitzgerald A, Chien WW, Workman L, Platts-Mills TA, Brewer C, Gafni RI, Stone KD, Milner JD, Holland SM.

J Allergy Clin Immunol. 2016 Feb;137(2):627-629.e2. doi: 10.1016/j.jaci.2015.06.041. Epub 2015 Aug 15. No abstract available.

32.

Glycans Instructing Immunity: The Emerging Role of Altered Glycosylation in Clinical Immunology.

Lyons JJ, Milner JD, Rosenzweig SD.

Front Pediatr. 2015 Jun 11;3:54. doi: 10.3389/fped.2015.00054. eCollection 2015. Review.

33.

Sharing the care of mechanical circulatory support: collaborative efforts of patients/caregivers, shared-care sites, and left ventricular assist device implanting centers.

Kiernan MS, Joseph SM, Katz JN, Kilic A, Rich JD, Tallman MP, Van Buren P, Lyons JJ, Bethea B, Eckman P, Gosev I, Lee SS, Soleimani B, Takayama H, Patel CB, Uriel N; Evolving Mechanical Support Research Group (EMERG) Investigators.

Circ Heart Fail. 2015 May;8(3):629-35. doi: 10.1161/CIRCHEARTFAILURE.114.001767. No abstract available.

PMID:
25991805
34.

A cold taken to heart.

Mody KP, Lyons JJ, Jorde UP, Uriel N.

Circulation. 2015 May 12;131(19):1703-11. doi: 10.1161/CIRCULATIONAHA.114.013355. No abstract available.

PMID:
25964280
35.

Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations.

Aderibigbe OM, Priel DL, Lee CC, Ombrello MJ, Prajapati VH, Liang MG, Lyons JJ, Kuhns DB, Cowen EW, Milner JD.

JAMA Dermatol. 2015 Jun;151(6):627-34. doi: 10.1001/jamadermatol.2014.5641.

36.

Atopic dermatitis in children: clinical features, pathophysiology, and treatment.

Lyons JJ, Milner JD, Stone KD.

Immunol Allergy Clin North Am. 2015 Feb;35(1):161-83. doi: 10.1016/j.iac.2014.09.008. Epub 2014 Nov 21. Review.

37.

Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations.

Milner JD, Vogel TP, Forbes L, Ma CA, Stray-Pedersen A, Niemela JE, Lyons JJ, Engelhardt KR, Zhang Y, Topcagic N, Roberson ED, Matthews H, Verbsky JW, Dasu T, Vargas-Hernandez A, Varghese N, McClain KL, Karam LB, Nahmod K, Makedonas G, Mace EM, Sorte HS, Perminow G, Rao VK, O'Connell MP, Price S, Su HC, Butrick M, McElwee J, Hughes JD, Willet J, Swan D, Xu Y, Santibanez-Koref M, Slowik V, Dinwiddie DL, Ciaccio CE, Saunders CJ, Septer S, Kingsmore SF, White AJ, Cant AJ, Hambleton S, Cooper MA.

Blood. 2015 Jan 22;125(4):591-9. doi: 10.1182/blood-2014-09-602763. Epub 2014 Oct 30.

38.

Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment.

Zhang Y, Yu X, Ichikawa M, Lyons JJ, Datta S, Lamborn IT, Jing H, Kim ES, Biancalana M, Wolfe LA, DiMaggio T, Matthews HF, Kranick SM, Stone KD, Holland SM, Reich DS, Hughes JD, Mehmet H, McElwee J, Freeman AF, Freeze HH, Su HC, Milner JD.

J Allergy Clin Immunol. 2014 May;133(5):1400-9, 1409.e1-5. doi: 10.1016/j.jaci.2014.02.013. Epub 2014 Feb 28.

39.

Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities.

Lyons JJ, Sun G, Stone KD, Nelson C, Wisch L, O'Brien M, Jones N, Lindsley A, Komarow HD, Bai Y, Scott LM, Cantave D, Maric I, Abonia JP, Rothenberg ME, Schwartz LB, Milner JD, Wilson TM.

J Allergy Clin Immunol. 2014 May;133(5):1471-4. doi: 10.1016/j.jaci.2013.11.039. Epub 2014 Jan 25. No abstract available.

40.

Systemic hypersensitivity reaction mimicking anaphylaxis after first filgrastim administration in a healthy donor.

Tholpady A, Chiosea I, Lyons JJ, Baird K, Leitman SF.

Transfusion. 2013 May;53(5):1146-7. doi: 10.1111/trf.12149. No abstract available.

41.

Dates and date pits as ingredients in broiler starting and coturnix quail breeder diets.

Vandepopuliere JM, al-Yousef Y, Lyons JJ.

Poult Sci. 1995 Jul;74(7):1134-42.

42.
43.

Influence of wet and dry feed on laying hens under heat stress.

Tadtiyanant C, Lyons JJ, Vandepopuliere JM.

Poult Sci. 1991 Jan;70(1):44-52.

44.

A new in-cage treatment system for control of northern fowl mites on laying hens.

Hall RD, Vandepopuliere JM, Fischer FJ, Lyons JJ, Van Horn JD.

Poult Sci. 1984 Apr;63(4):628-32.

45.
46.

Comparative evaluation of four registered acaricides for field control of northern fowl mites on caged laying hens.

Hall RD, Vandepopuliere JM, English LM, Jaynes W, Lyons JJ, Doisy KE, Foehse MC.

Poult Sci. 1980 Nov;59(11):2424-30.

PMID:
6780991
47.

The encoding of ignored information.

Lyons JJ.

Mem Cognit. 1974 Jan;2(1):161-8. doi: 10.3758/BF03197509.

PMID:
24214716
48.

Speed-accuracy trade-off with different types of stimuli.

Lyons JJ, Briggs GE.

J Exp Psychol. 1971 Nov;91(1):115-9. No abstract available.

PMID:
5126643
49.

Medicaid at county level.

Lyons JJ.

N Y State J Med. 1970 Aug 1;70(15):2032-3. No abstract available.

PMID:
5270544
50.

Selection of antibiotics and the problems of resistance.

COVERT SV, LYONS JJ.

Med Sci. 1963 Feb 25;13:261-76. No abstract available.

PMID:
14023507

Supplemental Content

Loading ...
Support Center