Lysosomal Storage Diseases
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Scientists Successfully Reprogram Blood Cells to Correct Lysosomal Storage Disease
newswise.com — “Researchers have transplanted genetically modified hematopoietic stem cells into mice so that their developing red blood cells produce a critical lysosomal enzyme " preventing or reducing organ and central nervous system damage from the often-fatal genetic disorder Hurler's syndrome.” View full resource at newswise.com
Most Recently Shared on November 9, 2009 at 9:39 pm By:
Scientists Successfully Reprogram Blood Cells to Correct Lysosomal Storage Disease http://bit.ly/pySwH
Researchers Receive NIH Grant For The Move Toward Clinical Trials Targeting The Lysosomal Storage Disease MPSIIIB
medicalnewstoday.com — “Investigators at Nationwide Children's have received a grant from the National Institutes of Health (NIH) to help move a therapy for MPS IIIB that has been shown effective in mice toward clinical” View full resource at medicalnewstoday.com
Most Recently Shared on May 26, 2011 at 7:05 am By:
Researchers Receive NIH Grant For The Move Toward Clinical Trials Targeting The Lysosomal Storage Disease MPSIIIB http://mnt.to/3WmL
CTD Holdings Receives Large Order From Brazil For Trappsol CycloTM Which May Provide Benefit In Many Lysosomal Storage Diseases
medicalnewstoday.com — “CTD Holdings, Inc. (OTCBB: CTDH) (FRANKFURT: CDJ) announced that a significant order has been placed by a Brazilian healthcare organization for Trappsol Cyclo™ for the experimental treatmen” View full resource at medicalnewstoday.com
Most Recently Shared on March 23, 2010 at 12:18 pm By:
MNT Cholesterol News Health News
CTD Holdings Receives Large Order From Brazil For Trappsol CycloTM Which May Provide Benefit In Many Lysosomal Storage... http://mnt.to/3zgp
Storage Disorders Ppt Powerpoint Presentation slides-Medical Slideshow The Lysosomes and lysosomal storage disorders (LSD)
slideworld.org — “Powerpoint Storage Disorders Slides by Prakash The Lysosomes and lysosomal storage disorders (LSD) Download Free Medical Powerpoint Presentations” View full resource at slideworld.org
Most Recently Shared on August 2, 2010 at 3:38 am By:
Medical Templates Health Organization
Storage Disorders: Glycogen storage disorders http://bit.ly/9DR9cZ
Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria : The Lancet
thelancet.com — “Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria. By - Thomas P Mechtler MD, Susanne Stary PhD, Thomas F Metz MSc, Víctor R De Jesús ...” View full resource at thelancet.com
Most Recently Shared on November 30, 2011 at 6:02 pm By:
Lysosomal storage disorders more common than thought in children in developed countries raising q's around screening http://t.co/KhFiYY1q
New biotechnological and nanomedicine strategies for treatment of lysosomal storage disorders - WIREs Nanomedicine and Nanobiotechnology
wires.wiley.com — “New biotechnological and nanomedicine strategies for treatment of lysosomal storage disorders” View full resource at wires.wiley.com
Most Recently Shared on February 5, 2010 at 9:18 pm By:
Wiley Health Medical Health Site
RT @WIREsNanomed: "New biotechnological and nanomedicine strategies for treatment of lysosomal storage disorders" http://ow.ly/14o4m
Neonatal screening for lysosomal storage disorders: f... [Lancet. 2011] - PubMed - NCBI
ncbi.nlm.nih.gov — “PubMed comprises more than 21 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content from PubMed Central and publisher web sites.” View full resource at ncbi.nlm.nih.gov
Most Recently Shared on December 3, 2011 at 5:13 pm By:
Tom Heston, MD Doctor, Family Medicine Doctor, and Physician
Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationw... http://t.co/psUadGig #health
Screening patients referred to a metabolic clinic for lysosomal storage disorders -- Fuller et al. 48 (6): 422 -- Journal of Medical Genetics
jmg.bmj.com — “Fuller, Maria; Tucker, Justin N; Lang, Debbie L; Dean, Caroline J; Fietz, Michael J; Meikle, Peter J; Hopwood, John J” View full resource at jmg.bmj.com
Most Recently Shared on June 2, 2011 at 8:15 pm By:
Symposier Endocrino Health Site
Screening patients referred to a metabolic clinic for lysosomal storage disorders. http://bit.ly/kukx1E
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
Researchers identify a fundamental process in lysosomal function and protein degradation
labspaces.net — “The degradation of proteins and other macromolecules in cells is vital to survival. Disruption of this process can result in serious disease.” View full resource at labspaces.net
Most Recently Shared on June 15, 2010 at 8:16 pm By:
Researchers identify a fundamental process in lysosomal function and protein degradation - http://is.gd/cQBGw
Fabry Disease: eMedicine Pediatrics: Genetics and Metabolic Disease
emedicine.medscape.com — “Overview: Fabry disease is an X-linked lysosomal storage disease that is caused by deficient activity of lysosomal enzyme a-galactosidase A (a-Gal A). Most males with no a-Gal A activity develop the classic phenotype of ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 9, 2009 at 6:56 pm By:
Medscape Pediatrics Health Site and Pediatrics
eMedicine article Fabry Disease updated for 2009. http://bit.ly/beP4n #pediatrics #health #medicine #fabrydisease #childrensmedicine
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
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