Keywords: Transient ischemic attack (TIA); emergency department; clinical prediction rule; ABCD2; survey;
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Keywords: ACAA1; 3-ketoacyl-CoA thiolase; ACOX1; Acyl-CoA oxidase 1; ACOX2; acyl-CoA oxidase 2; ABCD1; ABC transporter D1; ABCD2; ABC transporter D2; ABCD3; ABC transporter D3; AGPS; alkyl-dihydroxyacetonephosphate synthase; AGT; alanine-glyoxylate aminotransferase
d-Psicose, a sugar substitute, suppresses body fat deposition by altering networks of inflammatory response and lipid metabolism in C57BL/6J-ob/ob mice
Keywords: Abcd2; ATP-binding cassette, sub-family D, member 2; aP2; adipocyte protein 2; C/EBP-α; CCAAT/enhancer-binding protein-alpha; CPT-1; carnitine palmitoyltransferase-1; FAS; fatty acid synthase; FC; fold change; Fgf21; fibroblast growth factor 21; Fos; FBJ
The TriAGe+ Score for Vertigo or Dizziness: A Diagnostic Model for Stroke in the Emergency Department
Keywords: Vertigo; dizziness; stroke; diagnosis; emergency departments; ABCD2;
Disease specific therapies in leukodystrophies and leukoencephalopathies
Keywords: X-ALD; X-linked Adrenoleukodystrophy; AGS; Aicardi-Goutières Syndrome; CSF; cerebrospinal fluid; IFNα; α-interferon; RNA; ribonucleic acid; DNA; deoxyribonucleic acid; SLE; systemic lupus erythematosus; AxD; Alexander disease; GFAP; growth factor ass
Frequent inaccuracies in ABCD2 scoring in non-stroke specialists' referrals to a daily Rapid Access Stroke Prevention service
Keywords: TIA; Stroke; ABCD2; Prevention; Risk stratification; Inter-observer agreement;
Differential substrate specificities of human ABCD1 and ABCD2 in peroxisomal fatty acid β-oxidation
Keywords: Peroxisome; Beta-oxidation; ABC transporter; FA transport; ABCD1; ABCD2
X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype
Keywords: ABCD2; ALDR; X-linked adrenoleukodystrophy; X-ALD phenotypes; Modifier gene; Genotype phenotype; ABC-transporters; Peroxisomes; Peroxisomal disorders; Inflammation; Neurodegeneration; Modifier locus; Association study; Linkage analysis; Segregation analys