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Items: 1 to 20 of 92

1.

Adult-Onset Presentation of Glutaric Acidemia Type II With Myopathy.

Mareska MC, Adams KK, Muenzer J, Frerman F, Braun TG, Howard JF Jr.

J Clin Neuromuscul Dis. 2003 Mar;4(3):124-8.

PMID:
19078703
2.

Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult.

Bell RB, Brownell AK, Roe CR, Engel AG, Goodman SI, Frerman FE, Seccombe DW, Snyder FF.

Neurology. 1990 Nov;40(11):1779-82.

PMID:
2234436
3.

A riboflavin-responsive lipid storage myopathy due to multiple acyl-CoA dehydrogenase deficiency: an adult case.

Araki E, Kobayashi T, Kohtake N, Goto I, Hashimoto T.

J Neurol Sci. 1994 Nov;126(2):202-5.

PMID:
7853027
4.

Glutaric aciduria type II presenting as myopathy and rhabdomyolysis in a teenager.

Prasad M, Hussain S.

J Child Neurol. 2015 Jan;30(1):96-9. doi: 10.1177/0883073813516676.

PMID:
24453145
5.

[Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)].

Liang Y, Liu L, Wei H, Luo XP, Wang MT.

Zhonghua Er Ke Za Zhi. 2003 Dec;41(12):916-20. Chinese.

PMID:
14723814
6.

[A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)].

Tojo M, Gunji T, Yamaguchi S, Shimizu N, Koga Y, Nonaka I.

No To Hattatsu. 2000 Mar;32(2):163-8. Japanese.

PMID:
10723193
7.

Glutaric aciduria type 2, late onset type in Thai siblings with myopathy.

Wasant P, Kuptanon C, Vattanavicharn N, Liammongkolkul S, Ratanarak P, Sangruchi T, Yamaguchi S.

Pediatr Neurol. 2010 Oct;43(4):279-82. doi: 10.1016/j.pediatrneurol.2010.05.018.

PMID:
20837308
10.

Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency.

Pollard LM, Williams NR, Espinoza L, Wood TC, Spector EB, Schroer RJ, Holden KR.

J Child Neurol. 2010 Aug;25(8):954-60. doi: 10.1177/0883073809351984.

PMID:
20023066
11.

Riboflavin-responsive glutaric aciduria type II with recurrent pancreatitis.

Liang WC, Tsai KB, Lai CL, Chen LH, Jong YJ.

Pediatr Neurol. 2004 Sep;31(3):218-21.

PMID:
15351024
12.

Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.

Westermann CM, Dorland L, Votion DM, de Sain-van der Velden MG, Wijnberg ID, Wanders RJ, Spliet WG, Testerink N, Berger R, Ruiter JP, van der Kolk JH.

Neuromuscul Disord. 2008 May;18(5):355-64. doi: 10.1016/j.nmd.2008.02.007.

PMID:
18406615
13.

Recurrent hypoglycemia associated with glutaric aciduria type II in an adult.

Dusheiko G, Kew MC, Joffe BI, Lewin JR, Mantagos S, Tanaka K.

N Engl J Med. 1979 Dec 27;301(26):1405-9.

PMID:
514320
14.

Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiency.

Whitaker CH, Felice KJ, Silvers D, Wu Q.

Muscle Nerve. 2015 Aug;52(2):289-93. doi: 10.1002/mus.24552.

PMID:
25556768
15.

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.

16.

Glutaric acidemia type II: neuroimaging and spectroscopy evidence for developmental encephalomyopathy.

Shevell MI, Didomenicantonio G, Sylvain M, Arnold DL, O'Gorman AM, Scriver CR.

Pediatr Neurol. 1995 May;12(4):350-3.

PMID:
7546009
17.

Late-onset form of beta-electron transfer flavoprotein deficiency.

Curcoy A, Olsen RK, Ribes A, Trenchs V, Vilaseca MA, Campistol J, Osorio JH, Andresen BS, Gregersen N.

Mol Genet Metab. 2003 Apr;78(4):247-9.

PMID:
12706375
19.

Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes.

Loehr JP, Goodman SI, Frerman FE.

Pediatr Res. 1990 Mar;27(3):311-5.

PMID:
2320399

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