Bela Turk - Publications

Affiliations: 
2016- Neurogenetics Kennedy Krieger Institute, Baltimore, MD, United States 

10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Yska HAF, Turk BR, Fatemi A, Goodman J, Voermans M, Amos D, Amanat M, van de Stadt S, Engelen M, Smith-Fine A, Keller J. International validation of meaningfulness of postural sway and gait to assess myeloneuropathy in adults with adrenoleukodystrophy. Journal of Inherited Metabolic Disease. PMID 38795020 DOI: 10.1002/jimd.12753  0.461
2022 Turk BR, Poisson LM, Nemeth CL, Goodman J, Moser AB, Jones RO, Fatemi A, Singh J. MicroRNA and metabolomics signatures for adrenomyeloneuropathy disease severity. Jimd Reports. 63: 593-603. PMID 36341174 DOI: 10.1002/jmd2.12323  0.456
2022 Engelen M, van Ballegoij WJC, Mallack EJ, Van Haren KP, Köhler W, Salsano E, van Trotsenburg ASP, Mochel F, Sevin C, Regelman MO, Tritos NA, Halper A, Lachmann RH, Davison J, Raymond GV, ... ... Turk BR, et al. International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach. Neurology. PMID 36175155 DOI: 10.1212/WNL.0000000000201374  0.491
2022 Smith Fine A, Kaufman M, Goodman J, Turk B, Bastian A, Lin D, Fatemi A, Keller J. Wearable sensors detect impaired gait and coordination in LBSL during remote assessments. Annals of Clinical and Translational Neurology. 9: 468-477. PMID 35257509 DOI: 10.1002/acn3.51509  0.411
2020 Mallack EJ, Turk BR, Yan H, Price C, Mlis MD, Moser AB, Becker C, Hollandsworth K, Adang L, Vanderver A, Van Haren K, Ruzhnikov M, Kurtzberg J, Maegawa G, Orchard PJ, et al. MRI Surveillance of Boys with X-linked Adrenoleukodystrophy Identified by Newborn Screening: Meta-analysis and Consensus Guidelines. Journal of Inherited Metabolic Disease. PMID 33373467 DOI: 10.1002/jimd.12356  0.472
2020 Turk BR, Theda C, Fatemi A, Moser AB. X-linked adrenoleukodystrophy: Pathology, pathophysiology, diagnostic testing, newborn screening and therapies. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 80: 52-72. PMID 31909500 DOI: 10.1002/Jdn.10003  0.541
2019 Turk BR, Theda C, Fatemi A, Moser AB. X-linked Adrenoleukodystrophy: Pathology, Pathophysiology, Diagnostic Testing, Newborn Screening, and Therapies. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. PMID 31778737 DOI: 10.1016/j.ijdevneu.2019.11.002  0.541
2018 Turk BR, Nemeth CL, Marx JS, Tiffany C, Jones RO, Theisen BE, Murray CF, Kambhampati SP, Ramireddy R, Singh S, Rosen MR, Kaufman M, Watkins PA, Kannan S, Kannan RM, et al. Dendrimer N-acetylcysteine modulates monophagocytic response in adrenoleukodystrophy. Annals of Neurology. PMID 30069915 DOI: 10.1002/Ana.25303  0.469
2017 Turk BR, Moser AB, Fatemi A. Therapeutic strategies in adrenoleukodystrophy. Wiener Medizinische Wochenschrift (1946). 167: 219-226. PMID 28493141 DOI: 10.1007/S10354-016-0534-2  0.541
2017 Turk BR, Theisen BE, Nemeth CL, Marx JS, Shi X, Rosen M, Jones RO, Moser AB, Watkins PA, Raymond GV, Tiffany C, Fatemi A. Antioxidant Capacity and Superoxide Dismutase Activity in Adrenoleukodystrophy. Jama Neurology. PMID 28288261 DOI: 10.1001/jamaneurol.2016.5715  0.476
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