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 *

175 related articles for article (PubMed ID: 2234436)

  • 121. Electron-transferring flavoprotein deficiency in the multiple acyl-CoA dehydrogenation disorders, glutaric aciduria type II and ethylmalonic--adipic aciduria.
    Rhead WJ; Amendt BA
    J Inherit Metab Dis; 1984; 7 Suppl 2():99-100. PubMed ID: 6434879
    [No Abstract]   [Full Text] [Related]  

  • 122. Morphologic studies of the placenta and autopsy findings in neonatal-onset glutaric acidemia type II.
    Slukvin II; Salamat MS; Chandra S
    Pediatr Dev Pathol; 2002; 5(3):315-21. PubMed ID: 12007026
    [TBL] [Abstract][Full Text] [Related]  

  • 123. Acylcarnitine analysis in the investigation of myopathy.
    Moore SJ; Haites NE; Broom I; White I; Coleman RJ; Pourfarzam M; Morris AA
    J Inherit Metab Dis; 1998 Jun; 21(4):427-8. PubMed ID: 9700602
    [No Abstract]   [Full Text] [Related]  

  • 124. Molecular Oxygen Binding in the Mitochondrial Electron Transfer Flavoprotein.
    Husen P; Nielsen C; Martino CF; Solov'yov IA
    J Chem Inf Model; 2019 Nov; 59(11):4868-4879. PubMed ID: 31665600
    [TBL] [Abstract][Full Text] [Related]  

  • 125. Hypoketotic hypoglycemic coma in a 21-month-old child.
    Hostetler MA; Arnold GL; Mooney R; Bennett MJ; Rinaldo P; Roe CR
    Ann Emerg Med; 1999 Sep; 34(3):394-8. PubMed ID: 10459098
    [TBL] [Abstract][Full Text] [Related]  

  • 126. Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitine.
    Bernsen PL; Gabreëls FJ; Ruitenbeek W; Sengers RC; Stadhouders AM; Renier WO
    Arch Neurol; 1991 Mar; 48(3):334-8. PubMed ID: 1900413
    [TBL] [Abstract][Full Text] [Related]  

  • 127. Stroke, hemiparesis and deficient mitochondrial beta-oxidation.
    Vallée L; Fontaine M; Nuyts JP; Ricart G; Krivosic I; Divry P; Vianey-Saban C; Lhermitte M; Vamecq J
    Eur J Pediatr; 1994 Aug; 153(8):598-603. PubMed ID: 7957409
    [TBL] [Abstract][Full Text] [Related]  

  • 128. Hepatitis-associated lipid storage myopathy.
    Patten BM; Shabot JM; Alperin J; Dodson RF
    Ann Intern Med; 1977 Oct; 87(4):417-21. PubMed ID: 907240
    [TBL] [Abstract][Full Text] [Related]  

  • 129. Riboflavin-responsive multiple acyl coenzyme A dehydrogenase deficiency presenting as a proximal myopathy in a young adult.
    Gilkeson GS; Caldwell DS
    Arthritis Rheum; 1988 May; 31(5):695-6. PubMed ID: 3377873
    [No Abstract]   [Full Text] [Related]  

  • 130. [Analysis of ETFDH gene variation in a Chinese family affected with lipid storage myopathy].
    Xia Y; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):1002-1005. PubMed ID: 31598946
    [TBL] [Abstract][Full Text] [Related]  

  • 131. Ethylmalonic adipic aciduria--a treatable hepatomuscular disorder in two adult brothers.
    Elias E; Gray RG; Poulton K; Green A
    J Hepatol; 1997 Feb; 26(2):433-6. PubMed ID: 9059968
    [TBL] [Abstract][Full Text] [Related]  

  • 132. Glutaric acidemia type II: clinical, biochemical, and morphologic considerations.
    Goodman SI; Stene DO; McCabe ER; Norenberg MD; Shikes RH; Stumpf DA; Blackburn GK
    J Pediatr; 1982 Jun; 100(6):946-50. PubMed ID: 7086597
    [No Abstract]   [Full Text] [Related]  

  • 133. Successful carnitine treatment in a non-carnitine-deficient lipid storage myopathy.
    Sengers RC; Bakkeren JA; Trijbels JM; Stadhouders AM; Egberink GJ; ter Laak HJ; Jaspar HJ
    Eur J Pediatr; 1980 Dec; 135(2):205-9. PubMed ID: 7449803
    [TBL] [Abstract][Full Text] [Related]  

  • 134. Riboflavin responsive multiple acyl-CoA dehydrogenation deficiency. Assessment of 3 years of riboflavin treatment.
    Gregersen N; Christensen MF; Christensen E; Kølvraa S
    Acta Paediatr Scand; 1986 Jul; 75(4):676-81. PubMed ID: 3751563
    [TBL] [Abstract][Full Text] [Related]  

  • 135. Phylogenetic characterization of the ubiquitous electron transfer flavoprotein families ETF-alpha and ETF-beta.
    Tsai MH; Saier MH
    Res Microbiol; 1995 Jun; 146(5):397-404. PubMed ID: 8525056
    [TBL] [Abstract][Full Text] [Related]  

  • 136. Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism.
    Scaglia F; Scheuerle AE; Towbin JA; Armstrong DL; Sweetman L; Wong LJ
    BMC Pediatr; 2002 Dec; 2():12. PubMed ID: 12507404
    [TBL] [Abstract][Full Text] [Related]  

  • 137. Lipid storage myopathy associated with recurrent Reye syndrome-like attacks, but with a normal carnitine level.
    Matsuishi T; Yuge K; Aramaki S; Yoshino M; Yoshida I; Yamashita F
    Brain Dev; 1988; 10(2):125-9. PubMed ID: 3389475
    [TBL] [Abstract][Full Text] [Related]  

  • 138. Carnitine prevents Reye-like syndrome in atypical carnitine deficiency.
    Matsubasa T; Ohtani Y; Miike T; Kitano A; Endo F; Matsuda I
    Pediatr Neurol; 1986; 2(2):80-4. PubMed ID: 3508683
    [TBL] [Abstract][Full Text] [Related]  

  • 139. Adult onset systemic carnitine deficiency: favorable response to L-carnitine supplementation.
    Levitan MD; Murphy JT; Sherwood WG; Deck J; Sawa GM
    Can J Neurol Sci; 1987 Feb; 14(1):50-4. PubMed ID: 3815165
    [TBL] [Abstract][Full Text] [Related]  

  • 140. Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency.
    Dawson DB; Waber L; Hale DE; Bennett MJ
    J Pediatr; 1995 Jan; 126(1):69-71. PubMed ID: 7815229
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.