Glycogen Storage Disease and Nutrition
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Neurology Article | Glycogen Storage Disease
mdlinx.com — “Challenges in diagnosis and treatment of late-onset Pompe disease” View full resource at mdlinx.com
Most Recently Shared on September 10, 2011 at 10:31 am By:
Sandeep Pulim MD Doctor, Health Communicator, and Physician
Challenges in diagnosis and treatment of late-onset Pompe disease: Current Opinion in Neurology http://t.co/AEryDxe #neuro
Glycogen Storage Disease, Type IV: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:03 pm By:
Type IV glycogen storage disease is also known as Andersen disease, and is a result of transglucosidase deficiency. http://bit.ly/boizB9
Glycogen Storage Disease, Type VI: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:06 pm By:
Hers disease, also called type VI glycogen storage disease, is characterized by phosphorylase deficiency. http://bit.ly/aBvj7k
Glycogen Storage Disease, Type Ib: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 6:59 pm By:
Unfortunately, no specific treatment or cure exists for type Ib glycogen storage disease. Learn symptoms. http://bit.ly/cDomLM
Glycogen Storage Disease, Type Ia: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 6:58 pm By:
Type Ia glycogen storage disease can cause seizures or cardiomegaly. Learn more specifics. http://bit.ly/9dAIVV
Glycogen Storage Disease, Type III: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) results from the absence of enzymes that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the defect has systemic consequences, but, in ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:02 pm By:
Type III glycogen storage disease is also called Forbes-Cori disease, & is a result of debranching enzyme deficiecy. http://bit.ly/aGgc9e
Glycogen Storage Disease, Type V: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:04 pm By:
McArdle disease, or type V glycogen storage disease is myophosphorylase deficiency. Learn more. http://bit.ly/cPhOaH
Glycogen Storage Disease, Type VII: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:08 pm By:
Type VII glycogen storage disease is also called Tarui disease and is due to phosphofructokinase deficiency. Learn more.http://bit.ly/d8jUrn
Glycogen Storage Disease, Type II (Pompe Disease): eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to monosaccharides, of which glucose is the predominant component. Enzyme deficiency results in glycogen ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:01 pm By:
Type II glycogen storage disease, or Pompe disease, is a result of acid maltase deficiency. More about type II GSD. http://bit.ly/bQYTVx
Glycogen Storage Diseases Types I-VII: eMedicine Dermatology
emedicine.medscape.com — “Overview: Glycogen storage disease type IGlycogen storage disease (GSD) type I is also known as von Gierke disease or hepatorenal glycogenosis. von Gierke1 described the first patient with GSD type I in 1929 under the name ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 8:08 pm By:
Susan Scroggins Active Health Library and Health Advocate
Glycogen storage diseases occur due to the body's inability to break down or use glycogen. Learn about these diseases.http://bit.ly/dekuIN
Discovery Of Source Of Glycogen "Manufacturing" Errors Sheds Light On Fatal Disease
medicalnewstoday.com — “Indiana University scientists have solved a perplexing mystery regarding one of the body's main energy storage molecules, in the process shedding light on a possible route to treatment of a rare b” View full resource at medicalnewstoday.com
Most Recently Shared on March 3, 2011 at 10:05 am By:
MNT Neurology News Neurology and Health News
Discovery Of Source Of Glycogen "Manufacturing" Errors Sheds Light On Fatal Disease http://mnt.to/3RNK #neurology
Glycogen storage disease type I and G6Pase-[beta] deficiency: etiology and therapy : Abstract : Nature Reviews Endocrinology
nature.com — “Glycogen storage disease type I and G6Pase-[beta] deficiency: etiology and therapy : Abstract : Nature Reviews Endocrinology” View full resource at nature.com
Most Recently Shared on October 26, 2010 at 11:56 am By:
NatureRevEndocrinol Endocrinology and Medical Journal
Now available online: Glycogen storage disease type I and G6Pase-? deficiency: etiology and therapy by J. Y. Chou et al. http://ow.ly/31uM5
Discovery of source of glycogen 'manufacturing' errors sheds light on fatal disease
sciencedaily.com — “Scientists have solved a perplexing mystery regarding one of the body's main energy storage molecules, in the process shedding light on a possible route to treatment of a rare but deadly disease in teenagers.” View full resource at sciencedaily.com
Most Recently Shared on March 1, 2011 at 9:08 pm By:
Discovery of source of glycogen 'manufacturing' errors sheds light on fatal disease: Scientists have solved a pe... http://bit.ly/fEgHEq
Discovery of source of glycogen 'manufacturing' errors sheds light on fatal disease
sciencedaily.com — “Scientists have solved a perplexing mystery regarding one of the body's main energy storage molecules, in the process shedding light on a possible route to treatment of a rare but deadly disease in teenagers.” View full resource at sciencedaily.com
Most Recently Shared on March 1, 2011 at 9:45 pm By:
#teenhealth Discovery of source of glycogen 'manufacturing' errors sheds light on fatal disease http://sns.ly/rDbMy8
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