These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 30128629)

  • 21. Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency.
    Wang Z; Hong D; Zhang W; Li W; Shi X; Zhao D; Yang X; Lv H; Yuan Y
    Neuromuscul Disord; 2016 Feb; 26(2):170-5. PubMed ID: 26821934
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy.
    Auranen M; Paetau A; Piirilä P; Pohju A; Salmi T; Lamminen A; Löfberg M; Mosegaard S; Olsen RK; Tyni T
    Neuromuscul Disord; 2017 Jun; 27(6):581-584. PubMed ID: 28433476
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Multiple acyl-CoA dehydrogenase deficiency/glutaric aciduria type 2: difficult diagnosis, easy to treat].
    Rabenstein M; Weis J; Abicht A; Fink GR; Lehmann HC; Wunderlich G
    Nervenarzt; 2020 Apr; 91(4):349-352. PubMed ID: 32076759
    [No Abstract]   [Full Text] [Related]  

  • 24. Encephalopathy associated with a reversible splenial lesion in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Touat M; Michaud M; Alamowitch S; Maisonobe T; Acquaviva-Bourdain C; Laforêt P
    Rev Neurol (Paris); 2018 Dec; 174(10):747-750. PubMed ID: 30072122
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. [Multiple acyl-CoA dehydrogenase deficiency in a neonate].
    Chen JC; Chen PY
    Zhongguo Dang Dai Er Ke Za Zhi; 2013 Dec; 15(12):1098-9. PubMed ID: 24342206
    [No Abstract]   [Full Text] [Related]  

  • 27. A Term Newborn with Respiratory Distress, Acidosis, and Hypoglycemia.
    Peake RW; Kozakewich HP
    Clin Chem; 2017 Feb; 63(2):613-615. PubMed ID: 28130481
    [No Abstract]   [Full Text] [Related]  

  • 28. [Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in the horse].
    Van Der Kolk H
    Tijdschr Diergeneeskd; 2013 Jun; 138(6):38-9. PubMed ID: 23847852
    [No Abstract]   [Full Text] [Related]  

  • 29. High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Er TK; Liang WC; Chang JG; Jong YJ
    Clin Chim Acta; 2010 May; 411(9-10):690-9. PubMed ID: 20138856
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiency.
    Henriques BJ; Bross P; Gomes CM
    Biochim Biophys Acta; 2010 Nov; 1802(11):1070-7. PubMed ID: 20674745
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The ETFDH c.158A>G variation disrupts the balanced interplay of ESE- and ESS-binding proteins thereby causing missplicing and multiple Acyl-CoA dehydrogenation deficiency.
    Olsen RK; Brøner S; Sabaratnam R; Doktor TK; Andersen HS; Bruun GH; Gahrn B; Stenbroen V; Olpin SE; Dobbie A; Gregersen N; Andresen BS
    Hum Mutat; 2014 Jan; 35(1):86-95. PubMed ID: 24123825
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Amelioration of acylcarnitine profile using bezafibrate and riboflavin in a case of adult-onset glutaric acidemia type 2 with novel mutations of the electron transfer flavoprotein dehydrogenase (ETFDH) gene.
    Shioya A; Takuma H; Yamaguchi S; Ishii A; Hiroki M; Fukuda T; Sugie H; Shigematsu Y; Tamaoka A
    J Neurol Sci; 2014 Nov; 346(1-2):350-2. PubMed ID: 25216552
    [No Abstract]   [Full Text] [Related]  

  • 34. Acquired multiple acyl-CoA dehydrogenase deficiency and marked selenium deficiency causing severe rhabdomyolysis in a horse.
    Gomez DE; Valberg SJ; Magdesian KG; Hanna PE; Lofstedt J
    Can Vet J; 2015 Nov; 56(11):1166-71. PubMed ID: 26538673
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene.
    Andresen BS; Bross P; Vianey-Saban C; Divry P; Zabot MT; Roe CR; Nada MA; Byskov A; Kruse TA; Neve S; Kristiansen K; Knudsen I; Corydon MJ; Gregersen N
    Hum Mol Genet; 1996 Apr; 5(4):461-72. PubMed ID: 8845838
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Glutaric aciduria type 2 and newborn screening: commentary.
    Vockley J
    Mol Genet Metab; 2008 Jan; 93(1):5-6. PubMed ID: 17988913
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysis.
    Penzien JM; Molz G; Wiesmann UN; Colombo JP; Bühlmann R; Wermuth B
    Eur J Pediatr; 1994 May; 153(5):352-7. PubMed ID: 8033926
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Adult-onset multiple acyl CoA dehydrogenation deficiency associated with an abnormal isoenzyme pattern of serum lactate dehydrogenase.
    Sugai F; Baba K; Toyooka K; Liang WC; Nishino I; Yamadera M; Sumi H; Fujimura H; Nishikawa Y
    Neuromuscul Disord; 2012 Feb; 22(2):159-61. PubMed ID: 21907580
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 5.