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Items: 20

1.

Cytoplasmic "ciliary inclusions" in isolation are not sufficient for the diagnosis of primary ciliary dyskinesia.

Vece TJ, Sagel SD, Zariwala MA, Sullivan KM, Burns KA, Dutcher SK, Yusupov R, Leigh MW, Knowles MR.

Pediatr Pulmonol. 2020 Jan;55(1):130-135. doi: 10.1002/ppul.24528. Epub 2019 Sep 23.

PMID:
31549486
2.

Identifying Biomarkers in Pediatric Rare Lung Disease. chILD Grows Up.

Vece TJ, Esther CR.

Am J Respir Crit Care Med. 2019 Dec 15;200(12):1458-1459. doi: 10.1164/rccm.201908-1594ED. No abstract available.

3.

Evaluation of inter-observer variation for computed tomography identification of childhood interstitial lung disease.

Jacob J, Owens CM, Brody AS, Semple T, Watson TA, Calder A, Garcia-Peña P, Toma P, Devaraj A, Walton H, Moreno-Galdó A, Aurora P, Rice A, Vece TJ, Cunningham S, Altmann A, Wells AU, Nicholson AG, Bush A.

ERJ Open Res. 2019 Jul 29;5(3). pii: 00100-2019. doi: 10.1183/23120541.00100-2019. eCollection 2019 Jul.

4.

Diagnostic flexible versus rigid bronchoscopy for the assessment of tracheomalacia in children.

Choi J, Dharmarajan H, Yu J, Dunsky KA, Vece TJ, Chiou EH, Ongkasuwan J.

J Laryngol Otol. 2018 Dec 19:1-5. doi: 10.1017/S0022215118002050. [Epub ahead of print]

PMID:
30565533
5.

Continuous vancomycin in a pediatric cystic fibrosis patient.

McKinzie CJ, Esther CR, Vece TJ.

Pediatr Pulmonol. 2018 Jan;53(1):E4-E5. doi: 10.1002/ppul.23844. Epub 2017 Nov 29.

PMID:
29193836
6.

ATS Core Curriculum 2017: Part II. Pediatric Pulmonary Medicine.

Moore PE, Poston JT, Boyer D, Barsky E, Gaffin J, Boyne KB, Ross KR, Mann Dosier LB, Vece TJ, Casey AM, Welsh SK, Logan JW, Shepherd EG, Phinzy PA, Panitch HB, Papantonakis CM, Austin ED, Orandi AB, Kitcharoensakkul M, Abe MK, Horani A, Rettig JS, Pittman J.

Ann Am Thorac Soc. 2017 Aug;14(Suppl_2):S165-S181. doi: 10.1513/AnnalsATS.201702-143CME. Review. No abstract available.

7.

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.

Stray-Pedersen A, Sorte HS, Samarakoon P, Gambin T, Chinn IK, Coban Akdemir ZH, Erichsen HC, Forbes LR, Gu S, Yuan B, Jhangiani SN, Muzny DM, Rødningen OK, Sheng Y, Nicholas SK, Noroski LM, Seeborg FO, Davis CM, Canter DL, Mace EM, Vece TJ, Allen CE, Abhyankar HA, Boone PM, Beck CR, Wiszniewski W, Fevang B, Aukrust P, Tjønnfjord GE, Gedde-Dahl T, Hjorth-Hansen H, Dybedal I, Nordøy I, Jørgensen SF, Abrahamsen TG, Øverland T, Bechensteen AG, Skogen V, Osnes LTN, Kulseth MA, Prescott TE, Rustad CF, Heimdal KR, Belmont JW, Rider NL, Chinen J, Cao TN, Smith EA, Caldirola MS, Bezrodnik L, Lugo Reyes SO, Espinosa Rosales FJ, Guerrero-Cursaru ND, Pedroza LA, Poli CM, Franco JL, Trujillo Vargas CM, Aldave Becerra JC, Wright N, Issekutz TB, Issekutz AC, Abbott J, Caldwell JW, Bayer DK, Chan AY, Aiuti A, Cancrini C, Holmberg E, West C, Burstedt M, Karaca E, Yesil G, Artac H, Bayram Y, Atik MM, Eldomery MK, Ehlayel MS, Jolles S, Flatø B, Bertuch AA, Hanson IC, Zhang VW, Wong LJ, Hu J, Walkiewicz M, Yang Y, Eng CM, Boerwinkle E, Gibbs RA, Shearer WT, Lyle R, Orange JS, Lupski JR.

J Allergy Clin Immunol. 2017 Jan;139(1):232-245. doi: 10.1016/j.jaci.2016.05.042. Epub 2016 Jul 16. Erratum in: J Allergy Clin Immunol. 2018 Feb;141(2):832.

8.

Diffuse Alveolar Hemorrhage as a Manifestation of Childhood-Onset Systemic Lupus Erythematosus.

Singla S, Canter DL, Vece TJ, Muscal E, DeGuzman M.

Hosp Pediatr. 2016 Aug;6(8):496-500. doi: 10.1542/hpeds.2015-0281. Epub 2016 Jul 7.

9.

Response.

Young LR, Vece TJ, Guillerman RP.

Chest. 2016 Jun;149(6):1579-80. doi: 10.1016/j.chest.2016.03.020. No abstract available.

PMID:
27287578
10.

Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease.

Vece TJ, Watkin LB, Nicholas S, Canter D, Braun MC, Guillerman RP, Eldin KW, Bertolet G, McKinley S, de Guzman M, Forbes L, Chinn I, Orange JS.

J Clin Immunol. 2016 May;36(4):377-387. doi: 10.1007/s10875-016-0271-8. Epub 2016 Apr 5. Review.

11.

Childhood and adolescent tracheobronchial mucoepidermoid carcinoma (MEC): a case-series and review of the literature.

Jaramillo S, Rojas Y, Slater BJ, Baker ML, Hicks MJ, Muscal JA, Vece TJ, Wesson DE, Nuchtern JG.

Pediatr Surg Int. 2016 Apr;32(4):417-24. doi: 10.1007/s00383-015-3849-y. Epub 2016 Jan 20. Review.

PMID:
26790674
12.

Erratum to: A disorder of surfactant metabolism without identified genetic mutations.

Montella S, Vece TJ, Langston C, Carrera P, Nogee LM, Hamvas A, Manna A, Cervasio M, Santamaria F.

Ital J Pediatr. 2015 Dec 16;41:98. doi: 10.1186/s13052-015-0205-8. No abstract available.

13.

A disorder of surfactant metabolism without identified genetic mutations.

Montella S, Vece TJ, Langston C, Carrera P, Nogee LM, Hamvas A, Manna A, Cervasio M, Santamaria F.

Ital J Pediatr. 2015 Nov 25;41:93. doi: 10.1186/s13052-015-0198-3. Erratum in: Ital J Pediatr. 2015;41:98. Cervasio, Mara [corrected to Cervasio, Mariarosaria].

14.

Update on Diffuse Lung Disease in Children.

Vece TJ, Young LR.

Chest. 2016 Mar;149(3):836-45. doi: 10.1378/chest.15-1986. Epub 2016 Jan 12. Review.

15.

Idiopathic Pulmonary Hemosiderosis Presenting as Anemia, Failure to Thrive, and Jaundice in a Toddler.

Chen CC, McManemy JK, Vece TJ, Cruz AT.

Pediatr Emerg Care. 2016 Apr;32(4):237-9. doi: 10.1097/PEC.0000000000000501.

PMID:
26414632
16.

A 15-year-old boy with severe combined immunodeficiency, fungal infection, and weight gain.

Abul MH, Tuano K, Healy CM, Vece TJ, Quintanilla NM, Davis CM, Seeborg FO, Hanson IC.

Allergy Asthma Proc. 2015 Sep-Oct;36(5):407-11. doi: 10.2500/aap.2015.36.3876.

PMID:
26314823
17.

COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis.

Watkin LB, Jessen B, Wiszniewski W, Vece TJ, Jan M, Sha Y, Thamsen M, Santos-Cortez RL, Lee K, Gambin T, Forbes LR, Law CS, Stray-Pedersen A, Cheng MH, Mace EM, Anderson MS, Liu D, Tang LF, Nicholas SK, Nahmod K, Makedonas G, Canter DL, Kwok PY, Hicks J, Jones KD, Penney S, Jhangiani SN, Rosenblum MD, Dell SD, Waterfield MR, Papa FR, Muzny DM, Zaitlen N, Leal SM, Gonzaga-Jauregui C; Baylor-Hopkins Center for Mendelian Genomics, Boerwinkle E, Eissa NT, Gibbs RA, Lupski JR, Orange JS, Shum AK.

Nat Genet. 2015 Jun;47(6):654-60. doi: 10.1038/ng.3279. Epub 2015 Apr 20.

18.

Rapid and progressive pulmonary fibrosis in 2 families with DNA repair deficiencies of undetermined etiology.

Vece TJ, Schecter MG, Gatti RA, Tunuguntla R, Garcia CK, Langston C, Dishop MK, Moore RH, Fan LL.

J Pediatr. 2012 Apr;160(4):700-702.e3. doi: 10.1016/j.jpeds.2011.12.001. Epub 2012 Jan 10.

19.

Diagnosis and management of diffuse lung disease in children.

Vece TJ, Fan LL.

Paediatr Respir Rev. 2011 Dec;12(4):238-42. doi: 10.1016/j.prrv.2011.04.001. Epub 2011 May 6. Review.

PMID:
22018037
20.

Interstitial Lung Disease in Children Older Than 2 Years.

Vece TJ, Fan LL.

Pediatr Allergy Immunol Pulmonol. 2010 Mar;23(1):33-41.

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