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Items: 1 to 20 of 22

1.

TNF-α-driven inflammation and mitochondrial dysfunction define the platelet hyperreactivity of aging.

Davizon-Castillo P, McMahon B, Aguila S, Bark D, Ashworth K, Allawzi A, Campbell RA, Montenont E, Nemkov T, D'Alessandro A, Clendenen N, Shih L, Sanders NA, Higa K, Cox A, Padilla-Romo Z, Hernandez G, Wartchow E, Trahan GD, Nozik-Grayck E, Jones K, Pietras EM, DeGregori J, Rondina MT, Di Paola J.

Blood. 2019 Aug 29;134(9):727-740. doi: 10.1182/blood.2019000200. Epub 2019 Jul 16.

2.

Marijuana medusa: The many pulmonary faces of marijuana inhalation in adolescent males.

McGraw MD, Houser GH, Galambos C, Wartchow EP, Stillwell PC, Weinman JP.

Pediatr Pulmonol. 2018 Dec;53(12):1619-1626. doi: 10.1002/ppul.24171. Epub 2018 Oct 23.

PMID:
30353708
3.

Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder.

Friederich MW, Timal S, Powell CA, Dallabona C, Kurolap A, Palacios-Zambrano S, Bratkovic D, Derks TGJ, Bick D, Bouman K, Chatfield KC, Damouny-Naoum N, Dishop MK, Falik-Zaccai TC, Fares F, Fedida A, Ferrero I, Gallagher RC, Garesse R, Gilberti M, González C, Gowan K, Habib C, Halligan RK, Kalfon L, Knight K, Lefeber D, Mamblona L, Mandel H, Mory A, Ottoson J, Paperna T, Pruijn GJM, Rebelo-Guiomar PF, Saada A, Sainz B Jr, Salvemini H, Schoots MH, Smeitink JA, Szukszto MJ, Ter Horst HJ, van den Brandt F, van Spronsen FJ, Veltman JA, Wartchow E, Wintjes LT, Zohar Y, Fernández-Moreno MA, Baris HN, Donnini C, Minczuk M, Rodenburg RJ, Van Hove JLK.

Nat Commun. 2018 Oct 3;9(1):4065. doi: 10.1038/s41467-018-06250-w.

4.

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures.

Begay RL, Graw SL, Sinagra G, Asimaki A, Rowland TJ, Slavov DB, Gowan K, Jones KL, Brun F, Merlo M, Miani D, Sweet M, Devaraj K, Wartchow EP, Gigli M, Puggia I, Salcedo EE, Garrity DM, Ambardekar AV, Buttrick P, Reece TB, Bristow MR, Saffitz JE, Mestroni L, Taylor MRG.

JACC Clin Electrophysiol. 2018 Apr;4(4):504-514. doi: 10.1016/j.jacep.2017.12.003. Epub 2018 Feb 2.

5.

Neonatal Onset Interstitial Lung Disease as a Primary Presenting Manifestation of Mucopolysaccharidosis Type I.

Bush D, Sremba L, Lomax K, Lipsett J, Ketteridge D, Bratkovic D, Enchautegui-Colon Y, Weisfeld-Adams J, Galambos C, Lummus S, Wartchow E, Weinman J, Liptzin DR, Baker P 2nd.

JIMD Rep. 2019;43:71-77. doi: 10.1007/8904_2018_101. Epub 2018 Apr 14.

6.

Histologic and ultrastructural features in early and advanced phases of Zellweger spectrum disorder (infantile Refsum disease).

Warren M, Mierau G, Wartchow EP, Shimada H, Yano S.

Ultrastruct Pathol. 2018 May-Jun;42(3):220-227. doi: 10.1080/01913123.2018.1440272. Epub 2018 Feb 26.

PMID:
29482424
7.

Mutations in the accessory subunit NDUFB10 result in isolated complex I deficiency and illustrate the critical role of intermembrane space import for complex I holoenzyme assembly.

Friederich MW, Erdogan AJ, Coughlin CR 2nd, Elos MT, Jiang H, O'Rourke CP, Lovell MA, Wartchow E, Gowan K, Chatfield KC, Chick WS, Spector EB, Van Hove JLK, Riemer J.

Hum Mol Genet. 2017 Feb 15;26(4):702-716. doi: 10.1093/hmg/ddw431.

8.

Atypical presentation of neuronal ceroid lipofuscinosis type 8 in a sibling pair and review of the eye findings and neurological features.

Sanchez RL, Yan J, Richards S, Mierau G, Wartchow EP, Collins CD, Shankar SP.

Am J Ophthalmol Case Rep. 2016 Aug 27;4:50-53. doi: 10.1016/j.ajoc.2016.07.005. eCollection 2016 Dec.

9.

TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype.

Donkervoort S, Papadaki M, de Winter JM, Neu MB, Kirschner J, Bolduc V, Yang ML, Gibbons MA, Hu Y, Dastgir J, Leach ME, Rutkowski A, Foley AR, Krüger M, Wartchow EP, McNamara E, Ong R, Nowak KJ, Laing NG, Clarke NF, Ottenheijm C, Marston SB, Bönnemann CG.

Ann Neurol. 2015 Dec;78(6):982-994. doi: 10.1002/ana.24535. Epub 2015 Nov 13.

10.

Primary intracranial Ewing's sarcoma with unusual features.

VandenHeuvel KA, Al-Rohil RN, Stevenson ME, Qian J, Gross NL, McNall-Knapp R, Li S, Wartchow EP, Mierau GW, Fung KM.

Int J Clin Exp Pathol. 2015 Jan 1;8(1):260-74. eCollection 2015.

11.

Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing.

Chatfield KC, Coughlin CR 2nd, Friederich MW, Gallagher RC, Hesselberth JR, Lovell MA, Ofman R, Swanson MA, Thomas JA, Wanders RJ, Wartchow EP, Van Hove JL.

Mitochondrion. 2015 Mar;21:1-10. doi: 10.1016/j.mito.2014.12.005. Epub 2015 Jan 6.

12.

Ultrastructural features of eosinophilic oesophagitis: impact of treatment on desmosomes.

Capocelli KE, Fernando SD, Menard-Katcher C, Furuta GT, Masterson JC, Wartchow EP.

J Clin Pathol. 2015 Jan;68(1):51-6. doi: 10.1136/jclinpath-2014-202586. Epub 2014 Oct 30.

13.

Ciliary inclusion disease: report of a new primary ciliary dyskinesia variant.

Wartchow EP, Jaffe R, Mierau GW.

Pediatr Dev Pathol. 2014 Nov-Dec;17(6):465-9. doi: 10.2350/14-06-1504-OA.1. Epub 2014 Oct 9.

PMID:
25299134
14.

Features of intraventricular tanycytic ependymoma: report of a case and review of literature.

Agarwal S, Stevenson ME, Sughrue ME, Wartchow EP, Mierau GW, Fung KM.

Int J Clin Exp Pathol. 2014 May 15;7(6):3399-407. eCollection 2014. Review.

15.

Ultrastructural features of NUT midline carcinoma.

Wartchow EP, Moore TS, French CA, Mierau GW.

Ultrastruct Pathol. 2012 Aug;36(4):280-4. doi: 10.3109/01913123.2012.664613.

PMID:
22849529
16.

Papillary tumor of the pineal region: ultrastructural study of a case.

Cykowski MD, Wartchow EP, Mierau GW, Stolzenberg ED, Gumerlock MK, Fung KM.

Ultrastruct Pathol. 2012 Feb;36(1):68-77. doi: 10.3109/01913123.2011.620222.

PMID:
22292738
17.

Renal diseases associated with hematuria in children and adolescents: a brief tutorial.

Hicks J, Mierau G, Wartchow E, Eldin K.

Ultrastruct Pathol. 2012 Feb;36(1):1-18. doi: 10.3109/01913123.2011.620731. Review.

PMID:
22292732
18.

Primary Ciliary Dyskinesia in Children: A Review for Pediatricians, Allergists, and Pediatric Pulmonologists.

Stillwell PC, Wartchow EP, Sagel SD.

Pediatr Allergy Immunol Pulmonol. 2011 Dec;24(4):191-196.

19.

Glycogen storage diseases: a brief review and update on clinical features, genetic abnormalities, pathologic features, and treatment.

Hicks J, Wartchow E, Mierau G.

Ultrastruct Pathol. 2011 Oct;35(5):183-96. doi: 10.3109/01913123.2011.601404. Review.

PMID:
21910565
20.

Plexiform fibrohistiocytic tumor: ultrastructural studies may aid in discrimination from cellular neurothekeoma.

Wartchow EP, Goin L, Schreiber J, Mierau GW, Terella A, Allen GC.

Ultrastruct Pathol. 2009 Dec;33(6):286-92. doi: 10.3109/01913120903348860.

PMID:
19929176

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