BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 22041377)

  • 1. A case of late onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting as recurrent rhabdomyolysis and acute renal failure.
    Izumi R; Suzuki N; Nagata M; Hasegawa T; Abe Y; Saito Y; Mochizuki H; Tateyama M; Aoki M
    Intern Med; 2011; 50(21):2663-8. PubMed ID: 22041377
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Missaglia S; Tavian D; Moro L; Angelini C
    Lipids Health Dis; 2018 Nov; 17(1):254. PubMed ID: 30424791
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency.
    Yıldız Y; Talim B; Haliloglu G; Topaloglu H; Akçören Z; Dursun A; Sivri HS; Coşkun T; Tokatlı A
    Pediatr Neurol; 2019 Oct; 99():69-75. PubMed ID: 31331668
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene.
    Zhuo Z; Jin P; Li F; Li H; Chen X; Wang H
    J Neurol Sci; 2015; 353(1-2):84-6. PubMed ID: 25913573
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple acyl-CoA dehydrogenation deficiency as decreased acyl-carnitine profile in serum.
    Wen B; Li D; Li W; Zhao Y; Yan C
    Neurol Sci; 2015 Jun; 36(6):853-9. PubMed ID: 25827849
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Law LK; Tang NL; Hui J; Fung SL; Ruiter J; Wanders RJ; Fok TF; Lam CW
    Clin Chim Acta; 2009 Jun; 404(2):95-9. PubMed ID: 19265687
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report.
    Goh LL; Lee Y; Tan ES; Lim JSC; Lim CW; Dalan R
    BMC Med Genomics; 2018 Apr; 11(1):37. PubMed ID: 29615056
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Ishii K; Komaki H; Ohkuma A; Nishino I; Nonaka I; Sasaki M
    Brain Dev; 2010 Sep; 32(8):669-72. PubMed ID: 19783111
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report.
    Yamada K; Ito M; Kobayashi H; Hasegawa Y; Fukuda S; Yamaguchi S; Taketani T
    Brain Dev; 2019 Aug; 41(7):638-642. PubMed ID: 30982706
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases report.
    Hong D; Yu Y; Wang Y; Xu Y; Zhang J
    BMC Neurol; 2018 Dec; 18(1):219. PubMed ID: 30587156
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations.
    Chen W; Zhang Y; Ni Y; Cai S; Zheng X; Mastaglia FL; Wu J
    BMC Neurol; 2019 Dec; 19(1):330. PubMed ID: 31852447
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease.
    Béhin A; Acquaviva-Bourdain C; Souvannanorath S; Streichenberger N; Attarian S; Bassez G; Brivet M; Fouilhoux A; Labarre-Villa A; Laquerrière A; Pérard L; Kaminsky P; Pouget J; Rigal O; Vanhulle C; Eymard B; Vianey-Saban C; Laforêt P
    Rev Neurol (Paris); 2016 Mar; 172(3):231-41. PubMed ID: 27038534
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sensory neuropathy as a manifestation of multiple acyl-coenzyme A dehydrogenase deficiency.
    Harding JN; Mohannak N; Georgieva Z; Cunniffe NG
    BMJ Case Rep; 2024 Mar; 17(3):. PubMed ID: 38490702
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Late-onset multiple acyl-CoA dehydrogenase deficiency mimicking myositis in an elderly patient: a case report.
    Zheng Y; Zhao Y; Zhang W; Wang Z; Yuan Y
    BMC Neurol; 2020 Dec; 20(1):436. PubMed ID: 33267805
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Skin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin.
    Xu H; Chen X; Lian Y; Wang S; Ji T; Zhang L; Li S
    Int J Neurosci; 2020 Dec; 130(12):1192-1198. PubMed ID: 32064983
    [No Abstract]   [Full Text] [Related]  

  • 16. Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
    Fu HX; Liu XY; Wang ZQ; Jin M; Wang DN; He JJ; Lin MT; Wang N
    Neurol Sci; 2016 Jul; 37(7):1099-105. PubMed ID: 27000805
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A.
    Wang ZQ; Chen XJ; Murong SX; Wang N; Wu ZY
    J Mol Med (Berl); 2011 Jun; 89(6):569-76. PubMed ID: 21347544
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency.
    Zhang J; Han J; Wang Y; Wu Y; Ma L; Song X; Ji G
    Balkan Med J; 2022 Jul; 39(4):290-296. PubMed ID: 35734957
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect.
    Cotelli MS; Vielmi V; Rimoldi M; Rizzetto M; Castellotti B; Bertasi V; Todeschini A; Gregorelli V; Baronchelli C; Gellera C; Padovani A; Filosto M
    Neurol Sci; 2012 Dec; 33(6):1383-7. PubMed ID: 22190129
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.