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Displaying mucopolysaccharidosis PowerPoint Presentations

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Presentation Summary : mucopolysaccharidosis. I: Findings from the MPS I Registry. Eur. J . Pediatr, 171, 911-919. MPS I Newborn Screening. Low IDUA enzyme activity. Detected in . dried ...

Source : http://www.hrsa.gov/advisorycommittees/mchbadvisory/heritabledisorders/meetings/2014/third/mucopolysaccharidosistype1.pptx

UMBILICAL CORD STEM CELLS - University of Pittsburgh PPT

Presentation Summary : Metabolic storage diseases Hurler syndrome- Severe form of mucopolysaccharidosis type I, causes progressive deterioration of the CNS and death in childhood.

Source : http://www.pitt.edu/~super4/37011-38001/37341.ppt

PowerPoint Presentation PPT

Presentation Summary : Hypoxic ischemic encephalopathy Mucopolysaccharidosis type 3 Hydranencephaly Jacobsen / Paris-Trousseau Spinal muscular ...

Source : http://www.pennstatehershey.org/c/document_library/get_file?folderId=757477&name=DLFE-9214.ppt

Inborn Errors of Metabolic Etiology - School of Medicine ... PPT

Presentation Summary : Lysosomal storage disease (mucopolysaccharidosis) How would you confirm a specific diagnosis? Enzyme assay, urine mucopolysaccharies (glycosaminoglycans), ...

Source : http://www.medschool.lsuhsc.edu/pediatrics/residents/docs/Inborn%20Errors%20of%20Metabolism.ppt

PowerPoint Presentation PPT

Presentation Summary : Introduction Meeting subject Aldurazyme (laronidase) for the treatment of Mucopolysaccharidosis I (MPS I) Recombinant human –L-iduronidase (rhIDU) ...

Source : http://www.fda.gov/ohrms/dockets/ac/03/slides/3917S3_01_BioMarin.ppt

Inborn Errors of Metabolism - Wikispaces PPT

Presentation Summary : 1.1. Types of Metabolic Storage Disorders. Glycogen storage diseases (GSD) Mucopolysaccharidosis (MPS) Lysosomal storage diseases or lipidosis (LSD)

Source : http://med1mcst.wikispaces.com/file/view/I%20E%20M%20%20SDK%20Dec%2018%202012%20Lecture%202.ppsx/394476990/I%20E%20M%20%20SDK%20Dec%2018%202012%20Lecture%202.ppsx

Inborn Errors of Metabolic Etiology - School of Medicine ... PPT

Presentation Summary : Lysosomal storage disease (mucopolysaccharidosis) How would you confirm a specific diagnosis? Enzyme assay Mucopolysaccharidosis Hurler Syndrome: ...

Source : http://www.medschool.lsuhsc.edu/pediatrics/residents/docs/Metabolic%20-%20Dr.%20Marble.ppt

Current Therapy of Genetic Disorders - New York University PPT

Presentation Summary : ... Mucopolysaccharidosis I Approved 2003 (EU & US) Mucopolysaccharidosis VI Approved, 2005 (US& EU) Mucopolysaccharidosis II Approved, 2006 (US) Pompe Disease ...

Source : http://education.med.nyu.edu/courses/molecular/lectures/therapy/therapy.ppt

Teaching With Technology - University at Buffalo Libraries PPT

Presentation Summary : A specialist finally discovered that Andrue had mucopolysaccharidosis type I, or MPS I, an inherited disease that leads to problems with the heart, lungs, ...

Source : http://library.buffalo.edu/libraries/projects/cases/conference/2005/brickman.ppt

Gaucher Therapeutic Goals - Shire's Brave Community - News ... PPT

Presentation Summary : Mucopolysaccharidosis type II. eMedicine Journal [serial online]. 2006. 2Neufeld, Muenzer. In: The Metabolic and Molecular Bases of Inherited Disease. 2001:3421–3452.

Source : http://www.bravecommunity.com/healthcare-providers/educational-resources/additional-resources/Hunter-Learning-Lab-Presentation.ppt

Cellular Disorders - Texas A+M University PPT

Presentation Summary : ... and Gaucher's disease — both caused by a failure to produce an enzyme needed to break down things sphingolipids Mucopolysaccharidosis I (MPS-I).

Source : http://peer.tamu.edu/NSF_Files/Cellular%20Disorders.ppt

PowerPoint Presentation PPT

Presentation Summary : ... Mixed cryoglobulinemia Mucopolysaccharidosis Multicentric reticulohistiocytosis Multiple epiphyseal dysplasia Mycoplasmal arthritis Myofascial pain syndrome ...

Source : http://www.lionden.com/slides/ap/Arthritis%20facts.pps

PowerPoint Presentation PPT

Presentation Summary : Lethal Irradiation and Bone Marrow Transplantation in the Mouse Model of Mucopolysaccharidosis Type IIIB Angela A. Mensah1, Elizabeth Snella2, Eman Mohammed2, ...

Source : http://www.reu.iastate.edu/2010/2010poster2.ppt

Approach to Floppy Infant - IAP NEUROLOGY PPT

Presentation Summary : ... mucopolysaccharidosis and cerebral lipidosis. Spinal cord lesions Anterior horn cell disease – werdnig Hoffman spinal muscular atrophy, poliomyelitis.

Source : http://iapneurologyindia.com/download/presentation/Approach%20to%20Floppy%20Infant.ppt

Glycosaminoglycans - Rawal Institute of Health Sceinces ... PPT

Presentation Summary : Changes in the amounts of certain GAGs in the skin are also observed with aging. Mucopolysaccharidosis Several genetically inherited diseases, ...

Source : http://www.rihs.com.pk/web/wordpress/wp-content/uploads/class/biochemistry/GAGs.ppt

Poster 8 - REU Program PPT

Presentation Summary : Production of a Conditional Mouse Model for the Deficient Enzyme in Mucopolysaccharidosis IIIC: Acetyl-coenzyme A:alpha-glucosaminide N-acetyltransferase

Source : http://www.reu.iastate.edu/2008/2008poster8.ppt


Presentation Summary : ... anomalies Anomalous origin of Left coronary Inborn errors of metabolism Glycogen storage dses (Pompe’s dse) Mucopolysaccharidosis Disorders of fatty acid ...

Source : http://elpaso.ttuhsc.edu/fostersom/pediatrics/neonatology/documents/presentations/cardiomyopathyandthenewborn.ppt

PowerPoint Presentation PPT

Presentation Summary : ... (Most common) Obesity GERD (Laryngeal/pharyngeal edema) Neuromuscular Disorders : MD Achondroplasia Mucopolysaccharidosis Nasal Polyps (CF) ...

Source : http://www.inosteo.org/UserFiles/File/PowerPoint/2012%20IOA%20Annual%20Convention/Friday/Pediatric%20Obstructive%20Sleep%20Apnea.Morgenstein.ppt

Lysosomal Storage Diseases - Anything to make this fun PPT

Presentation Summary : What accumulates? Inheritance Pattern? Mucopolysaccharidosis NO Corneal clouding, developmental delay, gargoylism, airway obstr, HSM, ...

Source : http://akreczko.files.wordpress.com/2009/03/lysosomal-storage-diseases.ppt

Accelerating Biotechnology Innovation for Rare Diseases PPT

Presentation Summary : Mucopolysaccharidosis I (MPS I)Hurler, Hurler-Scheie and Scheie Syndrome A lysosomal storage disorder. Deficiency of lysosomal enzyme -L-iduronidase

Source : http://www.med.upenn.edu/orphandisease/documents/02-KakkisDevofRareDiseaseTreatments.pptx

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