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Quoted phrase not found in phrase index: "Glycogen storage disease IIIb"
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Reversal of glycogen storage disease type IIIa-related cardiomyopathy with modification of diet.
Dagli AI, Zori RT, McCune H, Ivsic T, Maisenbacher MK, Weinstein DA. Dagli AI, et al. J Inherit Metab Dis. 2009 Dec;32 Suppl 1(0 1):S103-6. doi: 10.1007/s10545-009-1088-x. Epub 2009 Mar 30. J Inherit Metab Dis. 2009. PMID: 19322675 Free PMC article.
Glycogen storage disease type III (GSD III) is caused by a deficiency in debranching enzyme, which leads to an accumulation of abnormal glycogen called limit dextrin in affected tissues. ...While studies are lacking regarding the best treatment for ske …
Glycogen storage disease type III (GSD III) is caused by a deficiency in debranching enzyme, which leads to an accumula …
Epilepsy and electrophysiological findings in polish twins with glycogenosis type IIIb.
Kroczka S, Biedroń A, Kaciński M. Kroczka S, et al. Clin EEG Neurosci. 2014 Jul;45(3):201-4. doi: 10.1177/1550059413500276. Clin EEG Neurosci. 2014. PMID: 24357677
Glycogen storage diseases are rare genetic disorders, mostly autosomal recessively inherited. Abnormal accumulation is because of the lack of one of the enzymes involved in glycogen metabolism. Neurological manifestation of the diseases involves muscle weakne …
Glycogen storage diseases are rare genetic disorders, mostly autosomal recessively inherited. Abnormal accumulation is because …
Reduction in bone mineral density in glycogenosis type III may be due to a mixed muscle and bone deficit.
Mundy HR, Williams JE, Lee PJ, Fewtrell MS. Mundy HR, et al. J Inherit Metab Dis. 2008 Jun;31(3):418-23. doi: 10.1007/s10545-008-0830-0. Epub 2008 Apr 4. J Inherit Metab Dis. 2008. PMID: 18392743
Glycogen storage disease type III (GSD III; OMIM 232400) is an autosomal recessive deficiency of the glycogen debrancher enzyme, amylo-1,6-glucosidase (EC 3.2.1.33). ...Lower bone mass was found at all sites for GSD IIIa patients (combined liver and mu …
Glycogen storage disease type III (GSD III; OMIM 232400) is an autosomal recessive deficiency of the glycogen de …