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Items: 1 to 50 of 183

1.

True, True and Possibly Unrelated: Variability in Donor Heart Acceptance Practices across the United States.

Morris AA, David Vega J.

Am J Transplant. 2020 Mar 17. doi: 10.1111/ajt.15855. [Epub ahead of print]

PMID:
32185879
2.

Sex differences in eligibility for advanced heart failure therapies.

Steinberg RS, Nayak A, O'Connell C, Burford S, Pekarek A, Chesnut N, Cole RT, Gupta D, Laskar SR, Bhatt K, Burke M, Attia T, Smith A, Vega JD, Morris AA.

Clin Transplant. 2020 Feb 19:e13839. doi: 10.1111/ctr.13839. [Epub ahead of print]

PMID:
32073188
3.

2020 Focused Update of the 2017 ACC Expert Consensus Decision Pathway on the Management of Mitral Regurgitation.

Bonow RO, O'Gara PT, Adams DH, Badhwar V, Bavaria JE, Elmariah S, Hung JW, Lindenfeld J, Morris AA, Satpathy R, Whisenant B, Woo YJ.

J Am Coll Cardiol. 2020 Feb 10. pii: S0735-1097(20)30427-7. doi: 10.1016/j.jacc.2020.02.005. [Epub ahead of print]

PMID:
32068084
4.

Validating patient prioritization in the 2018 Revised United Network for Organ Sharing Heart Allocation System: A single-center experience.

Nayak A, Dong T, Ko YA, Chesnut N, Pekarek A, Cole RT, Bhatt K, Gupta D, Burke MA, Laskar SR, Attia T, Smith AL, Vega JD, Morris AA.

Clin Transplant. 2020 Mar;34(3):e13816. doi: 10.1111/ctr.13816. Epub 2020 Feb 28.

PMID:
32031719
5.

Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency.

van Rijt WJ, Jager EA, Allersma DP, Aktuğlu Zeybek AÇ, Bhattacharya K, Debray FG, Ellaway CJ, Gautschi M, Geraghty MT, Gil-Ortega D, Larson AA, Moore F, Morava E, Morris AA, Oishi K, Schiff M, Scholl-Bürgi S, Tchan MC, Vockley J, Witters P, Wortmann SB, van Spronsen F, Van Hove JLK, Derks TGJ.

Genet Med. 2020 Jan 6. doi: 10.1038/s41436-019-0739-z. [Epub ahead of print]

6.

Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients.

van Vliet K, van Ginkel WG, Jahja R, Daly A, MacDonald A, De Laet C, Vara R, Rahman Y, Cassiman D, Eyskens F, Timmer C, Mumford N, Bierau J, van Hasselt PM, Gissen P, Goyens PJ, McKiernan PJ, Wilcox G, Morris AAM, Jameson EA, Huijbregts SCJ, van Spronsen FJ.

Orphanet J Rare Dis. 2019 Dec 4;14(1):285. doi: 10.1186/s13023-019-1259-2.

7.

Different Lenses for the Same Story: Examining How Implicit Bias Can Lead Us to Different Clinical Decisions for the "Same" Patient.

Shirey TE, Morris AA.

J Am Heart Assoc. 2019 Nov 19;8(22):e014355. doi: 10.1161/JAHA.119.014355. Epub 2019 Nov 11.

8.

Serum ST2 and hospitalization rates in Caucasian and African American outpatients with heart failure.

Savvoulidis P, Snider JV, Rawal S, Morris AA, Butler J, Georgiopoulou VV, Kalogeropoulos AP.

Int J Cardiol. 2020 Apr 1;304:116-121. doi: 10.1016/j.ijcard.2019.11.002. Epub 2019 Nov 6.

PMID:
31706624
9.

Current management of children and young people with heterozygous familial hypercholesterolaemia - HEART UK statement of care.

Ramaswami U, Humphries SE, Priestley-Barnham L, Green P, Wald DS, Capps N, Anderson M, Dale P, Morris AA.

Atherosclerosis. 2019 Nov;290:1-8. doi: 10.1016/j.atherosclerosis.2019.09.005. Epub 2019 Sep 12. Review.

10.

Utilizing gene expression profiling to understand immunologic mechanisms that impact racial disparities after heart transplant.

Morris AA.

J Heart Lung Transplant. 2019 Aug;38(8):830-832. doi: 10.1016/j.healun.2019.06.020. Epub 2019 Jun 20. No abstract available.

PMID:
31352998
11.

Decisional regret in left ventricular assist device patient-caregiver dyads.

Stahl EP, Dickert NW, Cole RT, Laskar SR, Morris AA, Smith AL, Vega JD, Gupta D.

Heart Lung. 2019 Sep - Oct;48(5):400-404. doi: 10.1016/j.hrtlng.2019.05.003.

PMID:
31151756
12.

Leigh syndrome caused by mutations in MTFMT is associated with a better prognosis.

Hayhurst H, de Coo IFM, Piekutowska-Abramczuk D, Alston CL, Sharma S, Thompson K, Rius R, He L, Hopton S, Ploski R, Ciara E, Lake NJ, Compton AG, Delatycki MB, Verrips A, Bonnen PE, Jones SA, Morris AA, Shakespeare D, Christodoulou J, Wesol-Kucharska D, Rokicki D, Smeets HJM, Pronicka E, Thorburn DR, Gorman GS, McFarland R, Taylor RW, Ng YS.

Ann Clin Transl Neurol. 2019 Feb 17;6(3):515-524. doi: 10.1002/acn3.725. eCollection 2019 Mar. Erratum in: Ann Clin Transl Neurol. 2019 Apr 17;6(4):821.

13.

Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registry.

Huemer M, Diodato D, Martinelli D, Olivieri G, Blom H, Gleich F, Kölker S, Kožich V, Morris AA, Seifert B, Froese DS, Baumgartner MR, Dionisi-Vici C; EHOD consortium, Martin CA, Baethmann M, Ballhausen D, Blasco-Alonso J, Boy N, Bueno M, Burgos Peláez R, Cerone R, Chabrol B, Chapman KA, Couce ML, Crushell E, Dalmau Serra J, Diogo L, Ficicioglu C, García Jimenez MC, García Silva MT, Gaspar AM, Gautschi M, González-Lamuño D, Gouveia S, Grünewald S, Hendriksz C, Janssen MCH, Jesina P, Koch J, Konstantopoulou V, Lavigne C, Lund AM, Martins EG, Meavilla Olivas S, Mention K, Mochel F, Mundy H, Murphy E, Paquay S, Pedrón-Giner C, Ruiz Gómez MA, Santra S, Schiff M, Schwartz IV, Scholl-Bürgi S, Servais A, Skouma A, Tran C, Vives Piñera I, Walter J, Weisfeld-Adams J.

J Inherit Metab Dis. 2019 Mar;42(2):333-352. doi: 10.1002/jimd.12041. Epub 2019 Feb 17.

PMID:
30773687
14.

Newborn screening for homocystinurias: Recent recommendations versus current practice.

Keller R, Chrastina P, Pavlíková M, Gouveia S, Ribes A, Kölker S, Blom HJ, Baumgartner MR, Bártl J, Dionisi-Vici C, Gleich F, Morris AA, Kožich V, Huemer M; individual contributors of the European Network and Registry for Homocystinurias and Methylation Defects (E-HOD), Barić I, Ben-Omran T, Blasco-Alonso J, Bueno Delgado MA, Carducci C, Cassanello M, Cerone R, Couce ML, Crushell E, Delgado Pecellin C, Dulin E, Espada M, Ferino G, Fingerhut R, Garcia Jimenez I, Gonzalez Gallego I, González-Irazabal Y, Gramer G, Juan Fita MJ, Karg E, Klein J, Konstantopoulou V, la Marca G, Leão Teles E, Leuzzi V, Lilliu F, Lopez RM, Lund AM, Mayne P, Meavilla S, Moat SJ, Okun JG, Pasquini E, Pedron-Giner CC, Racz GZ, Ruiz Gomez MA, Vilarinho L, Yahyaoui R, Zerjav Tansek M, Zetterström RH, Zeyda M.

J Inherit Metab Dis. 2019 Jan;42(1):128-139. doi: 10.1002/jimd.12034.

PMID:
30740731
15.

Discussing Out-of-Pocket Costs With Patients: Shared Decision Making for Sacubitril-Valsartan in Heart Failure.

Smith GH, Shore S, Allen LA, Markham DW, Mitchell AR, Moore M, Morris AA, Speight CD, Dickert NW.

J Am Heart Assoc. 2019 Jan 8;8(1):e010635. doi: 10.1161/JAHA.118.010635.

16.

Mortality in status 2 patients listed for heart transplantation in the United States: Will understanding cause of death help justify implantation of left ventricular assist devices into less sick patients?

Morris AA, Chen C, Laskar SR, Smith AL, Vega JD.

Int J Cardiol. 2019 Feb 1;276:185-190. doi: 10.1016/j.ijcard.2018.11.015. Epub 2018 Nov 9.

PMID:
30482444
17.

Relation of Living in a "Food Desert" to Recurrent Hospitalizations in Patients With Heart Failure.

Morris AA, McAllister P, Grant A, Geng S, Kelli HM, Kalogeropoulos A, Quyyumi A, Butler J.

Am J Cardiol. 2019 Jan 15;123(2):291-296. doi: 10.1016/j.amjcard.2018.10.004. Epub 2018 Oct 18.

18.

Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy.

Sommerville EW, Zhou XL, Oláhová M, Jenkins J, Euro L, Konovalova S, Hilander T, Pyle A, He L, Habeebu S, Saunders C, Kelsey A, Morris AAM, McFarland R, Suomalainen A, Gorman GS, Wang ED, Thiffault I, Tyynismaa H, Taylor RW.

Hum Mol Genet. 2019 Jan 15;28(2):258-268. doi: 10.1093/hmg/ddy294.

19.

Definitions of Stage D heart failure and outcomes among outpatients with heart failure and reduced ejection fraction.

Hedley JS, Samman-Tahhan A, McCue AA, Bjork JB, Butler J, Georgiopoulou VV, Morris AA, Kalogeropoulos AP.

Int J Cardiol. 2018 Dec 1;272:250-254. doi: 10.1016/j.ijcard.2018.08.046. Epub 2018 Aug 15.

PMID:
30122504
20.

INTERMACS Profiles and Outcomes Among Non-Inotrope-Dependent Outpatients With Heart Failure and Reduced Ejection Fraction.

Samman-Tahhan A, Hedley JS, McCue AA, Bjork JB, Georgiopoulou VV, Morris AA, Butler J, Kalogeropoulos AP.

JACC Heart Fail. 2018 Sep;6(9):743-753. doi: 10.1016/j.jchf.2018.03.018. Epub 2018 Aug 8.

21.

Lathosterolosis: A Relatively Mild Case with Cataracts and Learning Difficulties.

Anderson R, Rust S, Ashworth J, Clayton-Smith J, Taylor RL, Clayton PT, Morris AAM.

JIMD Rep. 2019;44:79-84. doi: 10.1007/8904_2018_127. Epub 2018 Aug 11.

22.

Impact of insurance type on eligibility for advanced heart failure therapies and survival.

Hutcheson SS, Phillips V, Patzer R, Smith A, Vega JD, Morris AA.

Clin Transplant. 2018 Aug;32(8):e13328. doi: 10.1111/ctr.13328. Epub 2018 Jul 11.

23.

Race/Ethnic and Sex Differences in the Association of Atherosclerotic Cardiovascular Disease Risk and Healthy Lifestyle Behaviors.

Morris AA, Ko YA, Hutcheson SH, Quyyumi A.

J Am Heart Assoc. 2018 May 3;7(10). pii: e008250. doi: 10.1161/JAHA.117.008250.

24.

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.

Ng YS, Lax NZ, Maddison P, Alston CL, Blakely EL, Hepplewhite PD, Riordan G, Meldau S, Chinnery PF, Pierre G, Chronopoulou E, Du A, Hughes I, Morris AA, Kamakari S, Chrousos G, Rodenburg RJ, Saris CGJ, Feeney C, Hardy SA, Sakakibara T, Sudo A, Okazaki Y, Murayama K, Mundy H, Hanna MG, Ohtake A, Schaefer AM, Champion MP, Turnbull DM, Taylor RW, Pitceathly RDS, McFarland R, Gorman GS.

EBioMedicine. 2018 Apr;30:86-93. doi: 10.1016/j.ebiom.2018.02.010. Epub 2018 Feb 24.

25.

Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA).

Stivaros S, Garg S, Tziraki M, Cai Y, Thomas O, Mellor J, Morris AA, Jim C, Szumanska-Ryt K, Parkes LM, Haroon HA, Montaldi D, Webb N, Keane J, Castellanos FX, Silva AJ, Huson S, Williams S, Gareth Evans D, Emsley R, Green J; SANTA Consortium.

Mol Autism. 2018 Feb 22;9:12. doi: 10.1186/s13229-018-0190-z. eCollection 2018.

26.

Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.

Oláhová M, Yoon WH, Thompson K, Jangam S, Fernandez L, Davidson JM, Kyle JE, Grove ME, Fisk DG, Kohler JN, Holmes M, Dries AM, Huang Y, Zhao C, Contrepois K, Zappala Z, Frésard L, Waggott D, Zink EM, Kim YM, Heyman HM, Stratton KG, Webb-Robertson BM; Undiagnosed Diseases Network, Snyder M, Merker JD, Montgomery SB, Fisher PG, Feichtinger RG, Mayr JA, Hall J, Barbosa IA, Simpson MA, Deshpande C, Waters KM, Koeller DM, Metz TO, Morris AA, Schelley S, Cowan T, Friederich MW, McFarland R, Van Hove JLK, Enns GM, Yamamoto S, Ashley EA, Wangler MF, Taylor RW, Bellen HJ, Bernstein JA, Wheeler MT.

Am J Hum Genet. 2018 Mar 1;102(3):494-504. doi: 10.1016/j.ajhg.2018.01.020. Epub 2018 Feb 22.

27.

Comparisons of the Framingham and Pooled Cohort Equation Risk Scores for Detecting Subclinical Vascular Disease in Blacks Versus Whites.

Topel ML, Shen J, Morris AA, Al Mheid I, Sher S, Dunbar SB, Vaccarino V, Sperling LS, Gibbons GH, Martin GS, Quyyumi AA.

Am J Cardiol. 2018 Mar 1;121(5):564-569. doi: 10.1016/j.amjcard.2017.11.031. Epub 2017 Dec 12.

28.

The genotypic and phenotypic spectrum of MTO1 deficiency.

O'Byrne JJ, Tarailo-Graovac M, Ghani A, Champion M, Deshpande C, Dursun A, Ozgul RK, Freisinger P, Garber I, Haack TB, Horvath R, Barić I, Husain RA, Kluijtmans LAJ, Kotzaeridou U, Morris AA, Ross CJ, Santra S, Smeitink J, Tarnopolsky M, Wortmann SB, Mayr JA, Brunner-Krainz M, Prokisch H, Wasserman WW, Wevers RA, Engelke UF, Rodenburg RJ, Ting TW, McFarland R, Taylor RW, Salvarinova R, van Karnebeek CDM.

Mol Genet Metab. 2018 Jan;123(1):28-42. doi: 10.1016/j.ymgme.2017.11.003. Epub 2017 Nov 15.

29.

Racial differences in the development of de-novo donor-specific antibodies and treated antibody-mediated rejection after heart transplantation.

Cole RT, Gandhi J, Bray RA, Gebel HM, Yin M, Shekiladze N, Young A, Grant A, Mahoney I, Laskar SR, Gupta D, Bhatt K, Book W, Smith A, Nguyen D, Vega JD, Morris AA.

J Heart Lung Transplant. 2018 Apr;37(4):503-512. doi: 10.1016/j.healun.2017.11.003. Epub 2017 Nov 4.

PMID:
29198929
30.

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits.

Glasgow RIC, Thompson K, Barbosa IA, He L, Alston CL, Deshpande C, Simpson MA, Morris AAM, Neu A, Löbel U, Hall J, Prokisch H, Haack TB, Hempel M, McFarland R, Taylor RW.

Neurogenetics. 2017 Dec;18(4):227-235. doi: 10.1007/s10048-017-0526-4. Epub 2017 Oct 26.

31.

Quality and Equitable Health Care Gaps for Women: Attributions to Sex Differences in Cardiovascular Medicine.

Shaw LJ, Pepine CJ, Xie J, Mehta PK, Morris AA, Dickert NW, Ferdinand KC, Gulati M, Reynolds H, Hayes SN, Itchhaporia D, Mieres JH, Ofili E, Wenger NK, Bairey Merz CN.

J Am Coll Cardiol. 2017 Jul 18;70(3):373-388. doi: 10.1016/j.jacc.2017.05.051. Review.

32.

2017 ACC/AHA/HFSA/ISHLT/ACP Advanced Training Statement on Advanced Heart Failure and Transplant Cardiology (Revision of the ACCF/AHA/ACP/HFSA/ISHLT 2010 Clinical Competence Statement on Management of Patients With Advanced Heart Failure and Cardiac Transplant): A Report of the ACC Competency Management Committee.

Jessup M, Drazner MH, Book W, Cleveland JC Jr, Dauber I, Farkas S, Ginwalla M, Katz JN, Kirkwood P, Kittleson MM, Marine JE, Mather P, Morris AA, Polk DM, Sakr A, Schlendorf KH, Vorovich EE.

Circ Heart Fail. 2017 Jun;10(6). pii: e000021. doi: 10.1161/HHF.0000000000000021. Review. No abstract available. Erratum in: Circ Heart Fail. 2018 May;11(5):e000028.

PMID:
28607153
33.

Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing.

Ghosh A, Schlecht H, Heptinstall LE, Bassett JK, Cartwright E, Bhaskar SS, Urquhart J, Broomfield A, Morris AA, Jameson E, Schwahn BC, Walter JH, Douzgou S, Murphy H, Hendriksz C, Sharma R, Wilcox G, Crushell E, Monavari AA, Martin R, Doolan A, Senniappan S, Ramsden SC, Jones SA, Banka S.

Arch Dis Child. 2017 Nov;102(11):1019-1029. doi: 10.1136/archdischild-2017-312738. Epub 2017 May 3.

PMID:
28468868
34.

2017 ACC/AHA/HFSA/ISHLT/ACP Advanced Training Statement on Advanced Heart Failure and Transplant Cardiology (Revision of the ACCF/AHA/ACP/HFSA/ISHLT 2010 Clinical Competence Statement on Management of Patients With Advanced Heart Failure and Cardiac Transplant): A Report of the ACC Competency Management Committee.

Jessup M, Drazner MH, Book W, Cleveland JC Jr, Dauber I, Farkas S, Ginwalla M, Katz JN, Kirkwood P, Kittleson MM, Marine JE, Mather P, Morris AA, Polk DM, Sakr A, Schlendorf KH, Vorovich EE.

J Card Fail. 2017 Jun;23(6):492-511. doi: 10.1016/j.cardfail.2017.04.004. Epub 2017 Apr 25. No abstract available.

PMID:
28454730
35.

Phenotypic Heterogeneity in a Congenital Disorder of Glycosylation Caused by Mutations in STT3A.

Ghosh A, Urquhart J, Daly S, Ferguson A, Scotcher D, Morris AAM, Clayton-Smith J.

J Child Neurol. 2017 May;32(6):560-565. doi: 10.1177/0883073817696816. Epub 2017 Mar 16.

PMID:
28424003
36.

2017 ACC/AHA/HFSA/ISHLT/ACP Advanced Training Statement on Advanced Heart Failure and Transplant Cardiology (Revision of the ACCF/AHA/ACP/HFSA/ISHLT 2010 Clinical Competence Statement on Management of Patients With Advanced Heart Failure and Cardiac Transplant): A Report of the ACC Competency Management Committee.

Jessup M, Drazner MH, Book W, Cleveland JC Jr, Dauber I, Farkas S, Ginwalla M, Katz JN, Kirkwood P, Kittleson MM, Marine JE, Mather P, Morris AA, Polk DM, Sakr A, Schlendorf KH, Vorovich EE.

J Am Coll Cardiol. 2017 Jun 20;69(24):2977-3001. doi: 10.1016/j.jacc.2017.03.001. Epub 2017 Mar 8. No abstract available. Erratum in: J Am Coll Cardiol. 2018 Apr 24;71(16):1840.

37.

Expanding the phenotype in argininosuccinic aciduria: need for new therapies.

Baruteau J, Jameson E, Morris AA, Chakrapani A, Santra S, Vijay S, Kocadag H, Beesley CE, Grunewald S, Murphy E, Cleary M, Mundy H, Abulhoul L, Broomfield A, Lachmann R, Rahman Y, Robinson PH, MacPherson L, Foster K, Chong WK, Ridout DA, Bounford KM, Waddington SN, Mills PB, Gissen P, Davison JE.

J Inherit Metab Dis. 2017 May;40(3):357-368. doi: 10.1007/s10545-017-0022-x. Epub 2017 Mar 1.

38.

Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.

Morris AA, Kožich V, Santra S, Andria G, Ben-Omran TI, Chakrapani AB, Crushell E, Henderson MJ, Hochuli M, Huemer M, Janssen MC, Maillot F, Mayne PD, McNulty J, Morrison TM, Ogier H, O'Sullivan S, Pavlíková M, de Almeida IT, Terry A, Yap S, Blom HJ, Chapman KA.

J Inherit Metab Dis. 2017 Jan;40(1):49-74. doi: 10.1007/s10545-016-9979-0. Epub 2016 Oct 24. Review.

39.

Quetiapine Carboxylic Acid and Quetiapine Sulfoxide Prevalence in Patient Urine.

Strickland EC, Cummings OT, Morris AA, Clinkscales A, McIntire GL.

J Anal Toxicol. 2016 Oct;40(8):687-693. Epub 2016 Aug 25.

PMID:
27562964
40.

Thiocyanate Accumulation in Critically Ill Patients Receiving Nitroprusside Infusions.

Morris AA, Page RL 2nd, Baumgartner LJ, Mueller SW, MacLaren R, Fish DN, Kiser TH.

J Intensive Care Med. 2017 Oct;32(9):547-553. doi: 10.1177/0885066616657004. Epub 2016 Jul 19.

PMID:
27435907
41.

The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease.

Ng YS, Alston CL, Diodato D, Morris AA, Ulrick N, Kmoch S, Houštěk J, Martinelli D, Haghighi A, Atiq M, Gamero MA, Garcia-Martinez E, Kratochvílová H, Santra S, Brown RM, Brown GK, Ragge N, Monavari A, Pysden K, Ravn K, Casey JP, Khan A, Chakrapani A, Vassallo G, Simons C, McKeever K, O'Sullivan S, Childs AM, Østergaard E, Vanderver A, Goldstein A, Vogt J, Taylor RW, McFarland R.

J Med Genet. 2016 Nov;53(11):768-775. doi: 10.1136/jmedgenet-2016-103910. Epub 2016 Jul 13.

42.

Normalizing Oral Fluid Hydrocodone Data Using Calculated Blood Volume.

Cummings OT, Morris AA, Enders JR, McIntire GL.

J Anal Toxicol. 2016 Sep;40(7):486-91. doi: 10.1093/jat/bkw057. Epub 2016 Jul 11.

PMID:
27405365
43.

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.

Metodiev MD, Thompson K, Alston CL, Morris AA, He L, Assouline Z, Rio M, Bahi-Buisson N, Pyle A, Griffin H, Siira S, Filipovska A, Munnich A, Chinnery PF, McFarland R, Rötig A, Taylor RW.

Am J Hum Genet. 2016 Jul 7;99(1):246. doi: 10.1016/j.ajhg.2016.06.013. No abstract available.

45.

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.

Metodiev MD, Thompson K, Alston CL, Morris AAM, He L, Assouline Z, Rio M, Bahi-Buisson N, Pyle A, Griffin H, Siira S, Filipovska A, Munnich A, Chinnery PF, McFarland R, Rötig A, Taylor RW.

Am J Hum Genet. 2016 May 5;98(5):993-1000. doi: 10.1016/j.ajhg.2016.03.010. Epub 2016 Apr 28. Erratum in: Am J Hum Genet. 2016 Jul 7;99(1):246.

46.

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype.

Alston CL, Howard C, Oláhová M, Hardy SA, He L, Murray PG, O'Sullivan S, Doherty G, Shield JP, Hargreaves IP, Monavari AA, Knerr I, McCarthy P, Morris AA, Thorburn DR, Prokisch H, Clayton PE, McFarland R, Hughes J, Crushell E, Taylor RW.

J Med Genet. 2016 Sep;53(9):634-41. doi: 10.1136/jmedgenet-2015-103576. Epub 2016 Apr 18.

47.

Racial and ethnic disparities in outcomes after heart transplantation: A systematic review of contributing factors and future directions to close the outcomes gap.

Morris AA, Kransdorf EP, Coleman BL, Colvin M.

J Heart Lung Transplant. 2016 Aug;35(8):953-61. doi: 10.1016/j.healun.2016.01.1231. Epub 2016 Feb 12. Review.

48.

Sterols and oxysterols in plasma from Smith-Lemli-Opitz syndrome patients.

Griffiths WJ, Abdel-Khalik J, Crick PJ, Ogundare M, Shackleton CH, Tuschl K, Kwok MK, Bigger BW, Morris AA, Honda A, Xu L, Porter NA, Björkhem I, Clayton PT, Wang Y.

J Steroid Biochem Mol Biol. 2017 May;169:77-87. doi: 10.1016/j.jsbmb.2016.03.018. Epub 2016 Mar 11.

50.

When to Suspect and How to Diagnose Mitochondrial Disorders?

Korenev S, Morris AA.

Indian J Pediatr. 2016 Oct;83(10):1157-63. doi: 10.1007/s12098-015-1932-y. Epub 2016 Jan 13. Review.

PMID:
26759002

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