QJMed -- Abstracts: Rigante And Caradonna 97 (4): 205 97 no. 4 (c) Association of Physicians 2004; all rights reserved. Secondary skeletal involvement in sanfilippo syndrome. D. Rigante 1 and P. Caradonna 2 http://qjmed.oupjournals.org/cgi/content/abstract/97/4/205
Extractions: Download to Citation Manager Q J Med 2004; D. Rigante and P. Caradonna From the Departments of Pediatric Sciences and Received 17 October 2003 and in revised form 19 January 2004 Background: Sanfilippo syndrome, or mucopolysaccharidosis (MPS) type III, is a rare lysosomal storage disease, resulting from errors in the catabolism of heparan sulphate. Aim: To evaluate bone turnover and bone mineral density (BMD) in MPS type III patients. Design: Clinical and observational study. Methods: We evaluated serum markers of bone formation or resorption, and measured BMD using dual-energy X-ray absorptiometry (DEXA), in three patients with MPS type III.
Rural Nurse Organization Clinic Digital Library sanfilippo syndrome Clinical Resources. Lysosomal (Keyword search) List of documents. Miscellaneous sanfilippo syndrome Clinical Resources http://ruralnurseorganization-dl.slis.ua.edu/clinical/metabolism/inborn/lysosoma
Extractions: Clinical Resources by Topic: Metabolic Disorders Sanfilippo Syndrome Clinical Resources Pediatrics Radiology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Neurology (eMedicine): Table of contents Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes: List of documents Pediatrics Resources See also General Pediatrics Resources Dermatology (eMedicine): Table of contents Orthopedic Surgery (eMedicine): Table of contents Radiology Resources See also General Radiology Resources Genetics Resources See also General Genetics Resources Clinical Guidelines
Entrez PubMed Click here to read The molecular basis of sanfilippo syndrome type B. Zhao HG, Li HH, Bach G, Schmidtchen A, Neufeld EF. Department http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8
Entrez PubMed Genetic heterogeneity and clinical variability in the sanfilippo syndrome (types A, B, and C). van de Kamp JJ, Niermeijer MF, von Figura K, Giesberts MA. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra
The Molecular Basis Of Sanfilippo Syndrome Type B Proc Natl Acad Sci US A. 1996 June 11; 93 (12) 6101 6105 The Molecular Basis of sanfilippo syndrome Type B. HG Zhao, HH Li, G Bach http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=39196&rendertype=abstr
Health Library - sanfilippo syndrome. Synonyms urine. There are four types of sanfilippo syndrome; types A and B are the most common forms. Resources. http://www.stjhs.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=nord29
New Page 1 sanfilippo syndrome assoicated to Health Just The Best Results from the Linkspider Organization. Click here for sanfilippo syndrome http://www.linkspider.org/index.cgi/Health/ConditionsandDiseases/GeneticDisorder
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Genetic Disorders / Sanfilippo Syndrome Genetic Disorders / sanfilippo syndrome. Categories related to sanfilippo syndrome http://paloweb.com/Health/Conditions_and_Diseases/Genetic_Disorders/Sanfilippo_S
Health Library - sanfilippo syndrome. Important It is possible that the main title of the report sanfilippo syndrome is not the name you expected. http://yourhealth.healtheast.org/Library/HealthGuide/IllnessConditions/topic.asp
Sanfilippo's Syndrome Browse entry words starting with A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Other characters, sanfilippo s syndrome,. Print this article, http://www.amershamhealth.com/medcyclopaedia/medical/Volume III 1/SANFILIPPOS SY
Extractions: Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Sanfilippo's syndrome, (Sylvester J. Sanfilippo, 20th century, American paediatrician), a group of diseases (types A, B, C and D) that constitute type III mucopolysaccharidosis . In all of these disorders a deficiency of lysosomal enzymes involved in the degradation of heparan sulfate is present. Among the features of this syndrome are limitation of joint motion, hepatosplenomegaly and a mild gibbus deformity
The CDGS Family Network,Inc. information and support for a Carbohydratedeficient Glycoprotein syndrome which is also now referred to as Congenital http://www.cdgs.com/
NORD - National Organization For Rare Disorders, Inc. Search NORD s Databases Read about diseases in NORD s Rare Disease Database. Find an organization in our Organizational Database. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Craniosynosto
