61. The Health Library — Nutritional & Metabolic MPS II (Hunter Syndrome)National MPS Society. mps iii (Sanfilippo Syndrome)NationalMPS Society. MPS IV (Morquio Syndrome)National MPS Society. http://healthlibrary.stanford.edu/resources/internet/bodysystems/nutrition4.html

Diseases and Disorders Use these links to jump directly to your topic of interest: Caffeine Carbohydrates Fats Fiber ... Page 7 Metabolic Disease (General) Metabolic Disorders:MEDLINEplus Metabolic Disorders:Merck What Is a Metabolic Disease:Canadian Society for Metabolic Disease How Many Are There? (overview of the more frequently-encountered metabolic diseases):Canadian Society for Metabolic Disease ... Adult Metabolic Transition Project (for young adults with metabolic diseases):University of Washington Metabolic Diseases (A -F) Acid-Base Imbalance Acidosis:MEDLINEplus Medical Encyclopedia Metabolic Acidosis:Hendrick Health System Leucine Metabolism Disorders:Mead Johnson Renal Tubular Acidosis:NIDDK ... Respiratory Alkalosis:Hendrick Health System Adrenoleukodystrophy Adrenoleukodystrophy:NINDS Adrenoleukodystrophy:United Leukodystrophy Foundation Genes and Disease: Adreno-Leukodystrophy:National Center for Biotechnology Information X-Linked Adrenoleukodystrophy :GeneReviews, University of Washington Alexander Disease Alexander Disease:NINDS Alexanders Disease:United Leukodystrophy Foundation Alexander Disease:GeneReviews, University of Washington Amyloidosis What is Amyloidosis?:Amyloidosis Support Network

62. Priser XAL Timesag II. 15.600. MPS I. 23.400. MPS II. 62.400. mps iii. 31.200. Løn I, eksklusivstamrecords. 16.600. Løn II Udvidet. 7.800. Løn III Personaleadministration. 7.800. http://www.datacomfort.dk/Navision/Xal.htm

Navision C5 Navision C5 Light Navision XAL C5 Ver. 3.0 Info ... Priser C5 [ Priser XAL ] CONCORDE XAL - PRISER kr. APPLIKATIONSMODULER: Grundpakke inkl. 1 bruger, jobafvikling, databaselog og dansk sprogmodul Finans I Finans II Udvidet Debitor Kreditor Lager Salgsordre incl. Fakturering Indkøbsordre Timesag I Timesag II MPS I MPS II MPS III Løn I, eksklusiv stamrecords Løn II Udvidet Løn III Personaleadministration Anlæg (version 3.1) Dokumentstyring (version 3.1) Avanceret product konfigurator (version 3.1) Salg -og Marketingstyring (version 3.1) eOrdre eButik eForretning VÆRKTØJSMODULER Basis Udvikling Ubegrænsede rapporttilretninger Ubegrænsede formstilretninger 5 Rapporttilretninger 5 Formstilretninger UDVIDELSESMODULER Flere regnskaber, pr. applikationsmodul # 1 Specialapplikations-afvikling BUS-lag afvikling (godkendte specialappl.) CUS-lag udvikling og afvikling CUS-lag afvikling Lønstamrecords - 100 stamrecords - 500 stamrecords - ubegrænset antal stamrecords Operativsystem-Afviklere Windows 32-bit, afvikling

63. THE LIGHTNING HYPERTEXT OF DISEASE. Packet No. 14 52560 POLYDYSTROPHIC OLIGOPHRENIA Sanfilippo's Syndrome Mucopolysaccharidosis3 mps iii A mps iii B mps iii C mps iii D San Filippo's Syndrome http://www.pathinfo.com/cgi-bin/lh.cgi?tx=oligophrenia

64. The Contact A Family Directory - MUCOPOLYSACCHARIDE DISEASES And Associated Dise MPS II) alphaL-iduronidase-2-sulphate-sulphatase deficiency Sanfilippo (mps iii)Four distinct enzyme abnormalities, same clinical patterns Morquio (MPS IV) A http://www.cafamily.org.uk/Direct/m42.html

printer friendly MUCOPOLYSACCHARIDE DISEASES and associated diseases home more about us in your area conditions information ... how you can help search this site These rare lysosomal diseases are each caused by a different enzyme deficiency. This results in Mucopolysaccharides being stored in cells of the body causing progressive damage. In most children growth is restricted and some diseases cause progressive mental as well as physical disability. Many of the diseases are associated with death in childhood. At present there is no cure for these conditions. Bone marrow transplantation is an option for a small number of these conditions. Enzyme replacement therapy for Fabry disease and MPS I has been developed. Phase 3 human clinical trials for MPS II and MPS VI are currently taking place. The Mucopolysaccharide diseases are classified as MPS I-IX. They are named after the doctor who first described them: Hurler (MPS IH) alpha-L-iduronidase deficiency Hurler Scheie (MPS IHS) alpha-L-iduronidase deficiency (formerly MPS V) Scheie (MPS IS) alpha-L-iduronidase deficiency Hunter (MPS II) alpha-L-iduronidase-2-sulphate-sulphatase deficiency Sanfilippo (MPS III) Four distinct enzyme abnormalities, same clinical patterns

65. The Contact A Family Directory - Index M see Mucopolysaccharide Diseases and associated diseases MPS II see MucopolysaccharideDiseases and associated diseases mps iii see Mucopolysaccharide Diseases http://www.cafamily.org.uk/Idx/m.html

printer friendly home more about us in your area ... how you can help search this site Please use the Index below to access the condition on which you require information. If you do not find what you want in the Index then try our search facility in the navigator on the left. Contact a Family also has information on many other specific conditions and rare disorders. If you cannot find the information you require in The Contact a Family Directory Online , you may wish to use our Contact a Family Helpline service. MAD see Fatty Acid Oxidation Disorders MCAD see Fatty Acid Oxidation Disorders M-CMTC Syndrome MDA see MDS see Lissencephaly ME see Myalgic Encephalomyelitis MEB Disease see Lissencephaly MED see Perthes Disease MELAS see Metabolic Diseases and see Mitochondrial Cytopathies and Related Disorders MERRF see Mitochondrial Cytopathies and Related Disorders MG see Myasthenia Gravis and other Myasthenic Syndromes MH see Malignant Hyperthermia ML I see Mucopolysaccharide Diseases and associated diseases ML II see Mucopolysaccharide Diseases and associated diseases ML III see Mucopolysaccharide Diseases and associated diseases ML IV see Mucopolysaccharide Diseases and associated diseases MNGIE see Mitochondrial Cytopathies and Related Disorders MPHD see Growth Hormone Deficiency MPS I see Mucopolysaccharide Diseases and associated diseases MPS II see Mucopolysaccharide Diseases and associated diseases MPS III see Mucopolysaccharide Diseases and associated diseases MPS IV see Mucopolysaccharide Diseases and associated diseases MPS VI see

66. Healthfinder® — MPS III - Sanfilippo mps iii Sanfilippo. internet URL. http//www.mpssociety.org/mps3.html.sponsoring agency. National MPS Society, Inc. description. A http://www.healthfinder.gov/Scripts/ShowDocDetail.asp?doc=2351&lang=1

67. The Society For Mucopolysaccharide Diseases HurlerScheie Syndrome, MPS I-HS. Hunter Syndrome, MPS II. Sanfilippo SyndromeA,B,C,D, mps iii. Morquio Syndrome A and B, MPS IV. Maroteaux-Lamy Syndrome, MPSVI. http://www.mpssociety.co.uk/faq.htm

home the society faq hurler/scheie ... international contacts Frequently Asked Questions What is the definition of Mucopolysaccharide? What are Mucopolysaccharide diseases? What is the cause of these diseases? How are they inherited? ... Which diseases are classified as Mucopolysaccharide Diseases? Definition ^top^ Mucopolysaccharides are long molecular chains of sugar. They are used by the body in the building of connective tissues. The word "Mucopolysaccharide" can be broken down as follows: "muco" refers to the thick jelly-like consistency of the molecules "poly" means many "saccharide" is a general term for a sugar molecule What are Mucopolysaccharide diseases? ^top^ These rare metabolic diseases are reffered to as MPS I-VII or more commonly by the name of the doctor who first described the condition. These commonly include:- Hurler Scheie Hunter Sanfilippo Morquio Maroteaux Lamy Sly Included also are the Mucolipidoses, other 'storage diseases' and the following conditions which are similar to Mucopolysaccharide:-

68. Mucopolysaccharidoses These conditions are often referred to as MPS I, MPS II, mps iii, MPSIV, MPS VI, MPS VII, and MPS IX. mps iii (Sanfilippo syndrome). http://www.healthatoz.com/healthatoz/Atoz/ency/mucopolysaccharidoses.html

Encyclopedia Index M Home Encyclopedia Encyclopedia Index M Mucopolysaccharidoses Definition Description Mucopolysaccharides are long chains of sugar molecules that are essential for building the bones, cartilage, skin, tendons, and other tissues in the body. Normally, the human body continuously breaks down and builds mucopolysaccharides. Another name for mucopolysaccharides is glycosaminoglycans (GAGs). There are many different types of GAGs and specific GAGs are unable to be broken down in each of the MPS conditions. There are several enzymes involved in breaking down each GAG and a deficiency or absence of any of the essential enzymes can cause the GAG to not be broken down completely and result in its accumulation in the tissues and organs in the body. In some MPS conditions, in addition to the GAG being stored in the body, some of the incompletely broken down GAGs can leave the body via the urine. When too much GAG is stored, organs and tissues can be damaged or not function properly. Genetic profile pregnancy to have a child affected with the disease. Some individuals with MPS do have children of their own. Children of parents who have an autosomal recessive condition are all carriers of that condition. These children are not at risk to develop the condition unless the other parent is a carrier or affected with the same autosomal recessive condition.

69. Mukopolysacharidosa MPS I Hurler (težší forma) - Scheie (lehcí forma); MPS II - Hunter;mps iii - Sanfilippo; MPS IV - Morquio; MPS VI - Maroteaux Lamy; MPS VII - Sly. http://www.mukopoly.cz/MPS/mukopolysacharidosa.htm

Chaloupky 35 773 00 Olomouc spmps@seznam.cz tel./fax: 585315787 IÈO: 61985112 è.ú: 108775975/0300 Spoleènost pro mukopolysacharidosu charitativní obèanské sdružení Homepage O Spoleènosti Mukopolysacharidosa Pomozte dìtem ... Fotogalerie Nemoc MPS Typ I Typ II Typ III Typ IV Typ VI a VII Bankovní spojení IPB Olomouc, Spoleènost pro MPS zastupuje její pøedseda Dr. Jan Michalík Odkazy: MPS v zahranièí Nìmecko Kanada Rakousko USA ... Velká Británie Mukopolysacharidosa - MPS Jedná se o vrozená, dìdiènì podmínìná onemocnìní látkové výmìny, která jsou zpùsobena chybìním konkrétního životnì dùležitého enzymu. Následkem toho dochází k hromadìní produktù metabolismu, jež se usazují ve tkáních èetných orgánù (játra, slezina, srdce, mozek ap.) s následující poruchou jejich funkce. Z toho poté vyplývají èetné závažné patoogické projevy onemocnìní. Zpoèátku se vìtšinou dìti vyvíjejí normálnì, k nástupu obtíží dochází až v dalším vývoji, pøièemž rozvoj a intenzita pøíznakù mohou být velmi rozdílné. Onemocnìní se vyskytují zøídka a oznaèují se jako MPS I. - VII. Každý z typù nemoci se ještì nazývá jménem (zpravidla podle jména lékaøe, který typ objevil a popsal). MPS I - Hurler (t잚í forma) - Scheie (lehèí forma) MPS II - Hunter MPS III - Sanfilippo MPS IV - Morquio MPS VI - Maroteaux Lamy MPS VII - Sly Vedle dìtí s mukopolysacharidosou se èleny Spoleènosti stávají i rodiny s dìtmi nemocnými obdobnými onemocnìními. Jedná se zejména o Mannosidózu a onemocnìní syndromem Niemmann-Pick. Všechna onemocnìní jsou však v klinickém obrazu velmi podobná.

70. The Mucopolysaccharidoses Fact Sheet mps iii, Sanfilippo syndrome, is marked by severe neurological symptoms. Mostpersons with mps iii live into their teenage years, and some live longer. http://www.ninds.nih.gov/health_and_medical/pubs/mps.htm

National Institute of Neurological Disorders and Stroke Accessible version Science for the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system Browse all disorders Browse all health organizations More about a disorder Studies with patients Research literature Press releases Search NINDS... (help) Contact us My privacy NINDS is part of the National Institutes of Health The Mucopolysaccharidoses Fact Sheet Get Web page suited for printing Email this to a friend or colleague Request free mailed brochure Table of Contents What are the mucopolysaccharidoses? Who is at risk? What are the signs and symptoms? What are the different types of the mucopolysaccharidoses? ... Where can I go for more information? What are the mucopolysaccharidoses? The mucopolysaccharidoses are a group of inherited metabolic diseases caused by the absence or malfunctioning of certain enzymes needed to break down molecules called glycosaminoglycans - long chains of sugar carbohydrates in each of our cells that help build bone, cartilage, tendons, corneas, skin, and connective tissue. Glycosaminoglycans (formerly called mucopolysaccharides) are also found in the fluid that lubricates our joints.  People with a mucopolysaccharidosis either do not produce enough of one of the 11 enzymes required to break down these sugar chains into proteins and simpler molecules or they produce enzymes that do not work properly. Over time, these glycosaminoglycans collect in the cells, blood, and connective tissues. The result is permanent, progressive cellular damage that affects the individual's appearance, physical abilities, organ and system functioning, and, in most cases, mental development.

71. OHSU BIOCHEMICAL GENETICS TEST DETAIL Morquio B (MPS IV B) betaGalactosidase. Sanfilippo A (mps iii A) Heparan-n-sulfatase.Sanfilippo B (mps iii B) N-Acetyl-ad-glucosaminidase. http://www.ohsu.edu/som-MedGen/bclab.htm

BIOCHEMICAL GENETICS LABORATORY Oregon Health Sciences University 3181 S.W. Sam Jackson Park Road Mail Code L-473, BH 2029 Portland, Oregon 97201-3098 phone: (503) 494-8392 (800) 452-3563 ext. 8392 fax: (503) 494-7645 TESTS OFFERED SPECIMEN:MUST BE ARRANGED WITH LAB IN ADVANCE; contact (503) 494-8392. 3 mL free flowing whole blood added immediately to special tube, pre-cooled in ice and obtained from this lab. Deliver on ice immediately. COMMENTS:To evaluate patients with unexplained hypoglycemia, lactic acidosis, dicarboxylic aciduria or possible defects of carnitine or fatty acid metabolism. ACYLCARNITINES BY GC/MS, PLASMA SPECIMEN:1 - 3 mL, GREEN-top, heparinized plasma, refrigerated and delivered to lab within four hours or separate, freeze, and transport frozen. Additive: Sodium heparin. AMINO ACID / METABOLIC SCREEN, URINE SPECIMEN: Minimum 6 mL random urine (first morning sample preferred but not essential) or aliquot of 24 hr collection. Refrigerate and deliver within 4 hr or freeze and transport frozen. List clinical indication, and all medications from previous 48 hr. COMMENTS:NOTE: This is the preferred test for initial screening for inborn errors of metabolism since it covers a WIDE range of abnormalities.

72. Mucopolisacaridosis Translate this page Comparto tu opinión al respecto, soy padre de tres hijos de los cuales dos presentarónla enfermedad mps iii C, mi hijo mayor murio a los 12 años hace 5 http://boards1.melodysoft.com/app?ID=CRECER&msg=43

73. National MPS Society - Understanding Mucopolysaccharide And Mucolipidosis (MPS) mps 6 Disorder Link. mps 7 Disorder Link. ICell disorder Cell disorder.ML-iii was described by Dr. Maroteaux and Dr. Lamy from France. They http://www.mpssociety.org/mps-disorders.html

Home MPS and Mucolipidoses (ML) are rare genetically determined disorders caused by the body's inability to produce certain enzymes. This results in an abnormal deposit of complex sugars in tissues and cells. This process causes progressive damage which can range in severity from strictly bone and joint involvement to massive complications in all organ systems. MPS and ML belong to a larger group of genetically inherited disorders known as the Lysosomal Storage Diseases , all of which share an enzymatic defect resulting in lysosomal accumulation. For a layman-friendly explanation of the biochemical process resulting in these diseases see Human Genetic Diseases: A Layman's Approach The National MPS Society provides support to families and promotes research initiatives that affect the following disorders : I-Cell disorder and Pseudo-Hurler Poldystrophy are forms of a condition known as mucolipidoses. They are also known as ML-II and ML-IIII. The name I-Cell comes from the characteristic appearance of cells under a microscope. One of the first doctors to write about the condition in the 1960's was a Dr. Jules Lerory from Belgium and his name is sometimes used to refer to I-Cell disorder.

74. Mucopolysaccharidosis (MPS) III (A, B, C, D) View the Full Record Syndrome, mucopolysaccharidosis (mps) iii (A, B, C, D).Synonyms, Sanfilippo disease (A, B, C, D). Sanfilippo syndrome (A, B, C, D). http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome465.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome mucopolysaccharidosis (MPS) III (A, B, C, D) Synonyms Sanfilippo disease (A, B, C, D) Sanfilippo syndrome (A, B, C, D) heparitinuria HS-mucopolysaccharidosis mucopolysaccharide storage disease III polydystrophic oligophrenia Summary Major Features Head and neck: Dull and slightly coarse facies, sclerotic mastoid bones, and thick posterior calvaria. Nose: Slightly sunken bridge. Mouth and oral structures: Protruding tongue in advanced stages. Abdomen: Visceromegaly. Hand and foot: Claw hand. Extremities: Restricted joint mobility of elbows and knees. Spine: Biconvexity of vertebral bodies. Muscles: Atrophy. Bones and joints: Mild dysostosis multiplex. Skin appendages: Abundant, coarse, and triangular in cross section hair. Nervous system: Deposits of heparan sulfate, ceramide polyhexoside, and GM1 ganglioside in the brain. Biochemical and metabolic features: Faulty degradation and urinary excretion of heparan sulfate with abnormal storage of glycosoaminoglycan in various tissues. Deficiencies of heparan sulfatase, N-acetyl-alpha-D-glusaminidase, aceyl-CoA:alpha-glucosamide N-acetyltransferase, and N-acetylglucosamine-6-sulfate sulfatase are the cause. Growth and development: Mental, motor, and speech deterioration and minimal growth retardation.

75. MPS-Service Translate this page mps-Typ. Bereich. Untergruppe. Tipp. Bezugsquelle. Tipp von. iii A. Draussen. Bewegung.Therapie-Tandem von Fa. Hoening (Kind sitzt vorne (fixiert)). www.hoening.de. http://mps.muc.dtag.de/service.htm

Service Unsere Broschüren Forum Aktuelles Tagungen/Regionaltreffen/Kongresse und Berichte ... Archiv/Rundbriefe Aktuelles BioMarin and Genzyme-Pressemeldung über die ersten Ergebnisse zur abgeschlossenen MPS I Studie. Die Studie Phase III zeigt in der vorläufigen Auswertung positive Ergebnisse.Statistisch relevant ist die positive Beeinflussung der Lungenfunktion und der 6-minütigem Gehtest. Weiterhin kam es zu einer Reduzierung der Lebergröße und der im Urin nachweisbaren GAG´s. Die Nebenwirkungen waren Fieber,Kopfschmerz, laufende Nase und ein Hautausschlag. In keinem Fall ist von einem schweren Nebenwirkungsfall im Zusammenhang mit dem Medikament berichtet worden. BioMarin and Genzyme to file for Marketing Approval for Aldurazyme based on Phase 3 Trial Results: November 2, 2001 BioMarin Pharmaceutical Inc. and Genzyme General announced November 2 positive results from a preliminary analysis of data from the Phase 3 clinical trial of Aldurazyme(tm)(laronidase), an investigational enzyme replacement therapy for patients with mucopolysaccharidosis I (MPS I). Based on the strength of the trial's results, the companies plan to meet with U.S., Canadian, and European regulatory authorities to discuss applications to market Aldurazyme. The Phase 3 trial enrolled 45 patients at five sites in the U.S., Europe, and Canada in a randomized, double-blind, placebo-controlled study designed to evaluate the safety and efficacy of Aldurazyme in patients with MPS I.

76. Warcraft III - Northrend - MPS - Player Profile Full Game Listings, Player Name mps Clan Name Homepage wc3addicts.com reps more // aka StaTiciS Additional Information http://www.battle.net/war3/ladder/war3-player-profile.aspx?PlayerName=MPS&Gatewa

77. Warcraft III - Northrend - Master[MPS] - Player Profile Player Name Mastermps Clan Name Homepage Additional Information Last LadderGame Thursday, February 06, 2003 157 PM UTC Play History Wins, Losses, Win %. http://www.battle.net/war3/ladder/war3-player-profile.aspx?PlayerName=Master[MPS

78. Ciara's Sunshine Foundation - Welcome Sanfilippo Syndrome is a mucopolysaccharide disorder and is alsoknown as mpsiii. mps-iii children are missing an enzyme which http://www.goldrush.com/~wlverine/ciara/

Facing the future together The Bennett family struggles to cope as all three children have a rare, deadly disease John and Alicia Bennett of I one recently discovered that all three of their children from left, 4-year-old Hunter, 2-year-old Tommy and 5-year-old Ciara have Sanfilippo syndrome. About one in 70,000 babies is afflicted with the genetic disorder, which usually leads to pre-teenage death. The Bennetts are hoping new medical techniques will help their offspring. Sacramento Bee/Anne Chadwick Williams FULL ARTICLE By Cynthia Hubert Bee Staff Writer Published 2:15 a.m. PDT Wednesday, May 29, 2002 http://www.sacbee.com *** View the original article About Ciara Ciara is a beautiful 6 year old who was recently diagnosed with Sanfilippo Syndrome. Sanfilippo Syndrome is a mucopolysaccharide disorder and is also known as MPS-III. MPS-III children are missing an enzyme which is essential in the breakdown of the sugar molecules in their bodies. The incomplete broken down sugars remain stored in the cells in the body causing progressive damage. MPS-III is a very rare disorder and only 24,000 babies a year are born with it. Children with Sanfilippo usually don't live past the age of 10-15 years old. At present there is no cure, various experimental methods have been used to try to replace the missing enzyme, but none so fare have been of any long-term benefit.

79. Wizards Of Storms - Warcraft III Turniere Who is playing in it? Is it a Warcraft iii only Clan, or do you playother games? iSmps Its a warcraft iii only clan. iSeNvious http://wizards-of-storms.de/turnier/phpmytourney/interview_infinit.php

Allgemeines News Champions FAQ Forum ... Passwort-Mailer 2vs2 Turniere 15. 2vs2 Freitagsturnier [Playing] Turnier Details Anmelden Team bearbeiten Check In ... Aufstellung/Grid 1vs1 Turniere DA] - 1on1 Turniere (zur Zeit finden keine 1vs1 Turniere statt) zur DA] 1on1 Turniere-Page Interview zum 7.Warcraft III 2on2 Turnier: Gewinner: Team Infinit Skill Wizards of Storms: Hello MPS, hello Kawa (aka eNvious)! You are playing in the Clan [iS] (Infinit Skill). Thus you are one of the top clans in europe. It would be very good, if you can present yourself in a few sentences, because there are some player among us, who are not familiar with the warcraft III scene. [iS]MPS: Me and Kawa are playing WC3 from beginning on and we started playing as a team 1 or 2 month ago [iS]eNvious: And we are really good team but we have lost many times for noobs ;o. [iS]MPS: At the beginning we just played for some stats but at the point we got 20:0 we started realising we are not that bad and then we played more games and reached 40:0 then we wanted to get rank 50 in 2002. Fnally it got rank 5 :) [iS]MPS: Then we thought about being in same clan cause i played at team-equalize and he played for e1 then we got invited by [iS] and here we are.

80. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE See also ZIEKTE van HURLER HURLER's DISEASE mpsIH See also ZIEKTE van SAN FILIPPOSAN FILIPPO's DISEASE mps-iii See also ZIEKTE van SCHEIE SCHEIE's DISEASE http://www.vada.nl/medisch/medmru.htm

VADA - GEZONDHEID en ZIEKTE HEALTH and DISEASE MR - MU OPGELET - ATTENTION Patienten en leken die raadgevingen/adviezen/informatie zoeken via deze verzameling links wordt dringend geadviseerd de verzamelde informatie te bespreken met de (behandelend) arts/specialist/hulpverlener. Patients and lay persons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. MUCOEPIDERMOID CARCINOMA See also: NEOPLASTIC THORACIC DISEASES Mucoepidermoid Carcinoma MUCOLIPIDOSE MUCOLIPIDOSIS SIALIDOSE MUCOLIPIDOSE II MUCOLIPIDOSIS III I-CELL DISEASE MUCOLIPIDOSE III PSEUDO-HURLER MUCOLIPIDOSE IV See also: See also: STOFWISSELINGSZIEKTEN METABOLIC DISEASES See also: MUCOLIPIDOSIS I GALACTOSIALIDOSIS SIALIDOSIS Lysosomale Stapelingsziekten O.a. Mucolipidose I (Sialidose), Mucolipidose II (I-Cell Disease), Mucolipidose III (Pseudo-Hurler) Lysosomal Storage Diseases Mucolipidosis IV Foundation - Home Page Mucolipidosis Type IV Who to Contact. Where to Go to Chat with Others. Learn More About It. Web Sites Lysosomal Storage Diseases: Mucolipidosis The Canadian MPS Society Mucolipidosis Type II and Type III MUCOPOLYSACCHARIDE DISORDERS MPS MUCOPOLYSACCHARIDE MUCOPOLYSACCHARIDOSIS MUCOPOLYSACCHARIDOSES See also: ZIEKTE van HURLER HURLER's DISEASE MPS-I H See also: ZIEKTE van SAN FILIPPO SAN FILIPPO's DISEASE MPS-III See also: ZIEKTE van SCHEIE SCHEIE's DISEASE SCHEIE SYNDROME MPS-I S See also:

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