61. Publications: Michael Dean, Ph.D A liverspecific ATP-binding cassette gene (ABCG5) from the ABCG (White) gene subfamilymaps to human chromosome 2p21 in the region of the sitosterolemia locus http://home.ncifcrf.gov/ccr/lgd/about/staff/deanm_pn.asp

ABOUT LGD STAFF PUBLICATIONS PROJECTS ... by Topic Research Human Genetics Comparative Genomic Wildlife FIV Projects Bioinformatics Conferences Courses Conservation Genetics LGD Spotlight News Staff Michael Dean, Ph.D. Principal Investigator, Human Genetics NCI-Frederick Building 560, Room 21-18 Frederick, Maryland 21702-1201 Phone: (301) 846-5931 Biography Research Recent Publications Publications: top Annilo, T., Shulenin, S., Chen, Z.Q., Arnould, I., Prades, C., Lemoine, C., Maintoux-Larois, C., Devaud, C., Dean, M. , Denèfle, P., and Rosier, M.: Identification and characterization of a novel ABCA subfamily member, ABCA12, located in the lamellar ichthyosis region on 2q34. Cytogenet. Genome. Res. (in press, 2003). Prades, C., Arnould, I., Annilo, T., Shulenin, S., Chen, Z.Q., Orosco, L., Triunfol, M., Devaud, C., Maintoux-Larois, C., Lafargue, C., Lemoine, C., Denèfle, P., Rosier, M., and Dean, M.

62. ILDS: ICD-10 - By Code [E039 - E80109] E75501 Syndrome Ruvalcaba Myhre Smith, E75502 sitosterolemia andxanthomatosis, E75502 Xanthomatosis with sitosterolemia, E75503 http://www.ilds.org/icd10/bycode/E-01.html

Application to Dermatology of ICD-10 Alphabetized by ICD Code, E039 - E80109: Return to Alphabetical listing... ICD Code: Disorder Myxedema diffuse Diffuse myxedema Myxedema pretibial Pretibial myxedema Acropachy thyroid Thyroid acropachy Hyperthyroidism (NOS) Thyrotoxicosis (NOS) Dermopathy diabetic Diabetic dermopathy Rubeosis diabetic Diabetic rubeosis Gangrene wet of feet in diabetic Wet gangrene of feet diabetic Necrobiosis lipoidica diabeticorum Cheiroarthropathy Erythema necrolytic migratory Glucagonoma syndrome Migratory necrolytic erythema Necrolytic migratory erythema Syndrome glucagonoma Zollinger Ellison syndrome Flushing Zollinger Ellison Syndrome Zollinger Ellison Hyperparathyroidism (NOS) Sheehan's syndrome Syndrome Sheehan's Adiposogenital dystrophy Dystrophia adiposogenital Nelson's syndrome Syndrome Nelson's Cushing's syndrome drug-induced Syndrome Cushing's drug-induced Cushing's syndrome (NOS) Syndrome Cushing's (NOS) Adrenogenital syndrome congenital Congenital adrenogenital syndrome Syndrome adrenogenital congenital Acquired adrenogenital syndrome Adrenogenital syndrome acquired Syndrome adrenogenital acquired Adrenogenital syndrome (NOS) Syndrome adrenogenital (NOS) Addison's disease Disease Addison's Flushing due to pheochromocytoma Pheochromocytoma flushing Polycystic ovary syndrome Syndrome Stein Leventhal Syndrome polycystic ovary Stein Leventhal syndrome Achard Thiers syndrome Syndrome Achard Thiers Poems syndrome Syndrome Poems Carcinoid flushing Carcinoid syndrome

63. Riesgo De Hipoglicemía En Diabéticos Translate this page de colesterol en el tracto digestivo. sitosterolemia y transportadoresdependientes de ATP. Por razones hasta hace poco desconocidas http://www.galenored.com/galeno/galeno/avances/colesterol.htm

Novedosos hallazgos sobre metabolismo intracelular del colesterol En años recientes, diferentes grupos de investigadores han hecho importantes descubrimientos relacionados con el transporte intracelular de colesterol. Tales avances han permitido comprender mejor el metabolismo de los lípidos y abren enormes posibilidades para el desarrollo de medicamentos, con el fin de controlar condiciones clínicas adversas como dislipidemias y aterosclerosis. En este contexto, resultan de enorme importancia dos estudios recientes que revelan aspectos desconocidos hasta el momento sobre la absorción y transporte de colesterol en el tracto digestivo. Sitosterolemia y transportadores dependientes de ATP Por razones hasta hace poco desconocidas, sólo 5% de los homólogos vegetales del colesterol (sitosterol, estigmasterol, campestrol), presentes en la dieta, son absorbidos en el intestino. En una rara enfermedad, denominada sitosterolemia, hay un paso masivo de tales moléculas a la circulación sanguínea. Los pacientes afectados desarrollan hipercolesterolemia, aterosclerosis y enfermedad coronaria a temprana edad. Con el fin de identificar el defecto subyacente, investigadores de

64. ATP ABCG5 sitosterolemia; ABCG8 sitosterolemia; ATPbinding protein(torsinA) Torsion dystonia (DYT1), Early-onset. Cyclic nucleotide http://www.neuro.wustl.edu/neuromuscular/mother/atp.htm

Front Index Search Links ... Patient Information ATP Adenosine (P1) receptors ATPase types ATP Receptors ATP-related Disorders ... P2 Receptors External link: Klotho ATP metabolism Precursors ADP Synthesizing enzymes Phosphorylases Metabolizing enzymes Phosphatases ATPases Metabolites ADP AMP Adenosine Inosine ATP Receptors (P2 purin oceptors) Receptor subtypes Agonists Antagonists Second messenger Principal tissue a b -Me-ATP ATP a b -Me-ATP (desensitizes) Suramin Cation channel Ca Influx into cell Smooth muscle Sensory ganglia Cerebellum (Postsynaptic) Heart; Platelets g -S PPADS Suramin Cation channel Ca : Influx into cell Autonomic ganglia Brain; Pituitary Sensory ganglia Smooth muscle Retina TNP-ATP PPADS a b -Me-ATP (desensitizes) Suramin Ion channel Sensory ganglia Solitary tract neurons Sympathetic neurons a b -Me-ATP Cation channel Ca : Influx into cell Brain; Pancreas Testes; Colon Smooth muscle a b -Me-ATP PPADS Suramin Ion channel Heart; Gut; Bladder Autonomic ganglia Skin (Proliferating cells) Thymus; Spinal cord No function as homomultimer Ion channel Skeletal muscle Brain Spinal motor neurons Autonomic ganglia Coomassie brilliant blue Cation channel Large pore with prolonged activation Apoptotic cells Macrophages Lymphocytes Microglia Skin 2-Me-S-ATP G q /G n PLC- b activation Muscle: NMJs Epithelium; Endothelium

65. Display The Complete GeneCard For This Gene (ABCD4) More Like lines in the GeneCard text contribute to matching your query LITERATURE 11099417 Accumulation of dietary cholesterol in sitosterolemia caused by http://www.sfu.ca/~zyzhao/abc/GeneCard.html

GeneCard Report for ABC Transporters Display the complete GeneCard for this gene More like this Gene: ABCD4 = ATP-binding cassette, sub-family D (ALD), member 4 [Locus: 14q24.3] The following lines in the GeneCard text contribute to matching your query: - SWISSPROT: similarity: belongs to the atp-binding transport protein family ( abc transporters ). ald subfamily. ABC transporter ABC-transporter Display the complete GeneCard for this gene More like this Gene: ABCD1 = ATP-binding cassette, sub-family D (ALD), member 1 [Locus: Xq28] The following lines in the GeneCard text contribute to matching your query: - SWISSPROT: similarity: belongs to the atp-binding transport protein family ( abc transporters ). ald subfamily. ABC transporters - BLOCKS: BL00211, ABC transporters family proteins.; Display the complete GeneCard for this gene More like this Gene: ABCB7 = ATP-binding cassette, sub-family B (MDR/TAP), member 7 [Locus: Xq13.1-q13.3] The following lines in the GeneCard text contribute to matching your query: - SWISSPROT: atp-binding cassette transporter 7 precursor ( abc transporter - SWISSPROT: similarity: belongs to the atp-binding transport protein family ( abc transporters ). mdr subfamily.

66. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : S Diseases Da syndrome see Multiple endocrine neoplasia type 2a Sirolimus Sisomicin Sister MaryJoseph's nodule Sitosterolaemia see sitosterolemia sitosterolemia Situational http://www.diseasesdatabase.com/sieve/disease_index_s.asp

Diseases Database [Previous page] [Search] [Index] [Feedback] Diseases Database disease, symptom, sign, etc alphabetical index : S Saber shin see Sabre tibia Sabia virus Sabin vaccine Sabre tibia ... Sacrosidase SAD see Seasonal affective disorder Saddle nose deformity Saethre-Chotzen syndrome see Chotzen syndrome SAH see Subarachnoid haemorrhage Sakurai-Lisch nodule Salaam attacks Salazopyrine see Sulphasalazine Salbutamol Salcatonin see Calcitonin Saldino-Noonan syndrome see Short rib-polydactyly syndrome type 1 Salicylates Salicylic acid Salicylsalicylic acid Salivary calculus see Sialolithiasis Salivary gland cancer Salivary gland enlargement Salivary gland mass see Salivary gland enlargement Salivary hypersecretion see Hypersialisis Salivary secretion decreased see Xerostomia Salivation excessive see Hypersialisis Salk vaccine Salla disease Salmeterol ... Salmonella typhi Salmonellosis see Salmonella Salpingitis and oophoritis see Pelvic inflammatory disease Salsalate see Salicylsalicylic acid Salt (dietary) Salt depletion see Depletional hyponatraemia Salt losing nephropathy Salt overload see Sodium overload Salzmann's nodular degeneration of cornea Sampatrilat San Joaquin fever see Coccidioidomycosis Sand flea see Tungiasis Sandfly species Sandhoff's disease Sanfilippo disease Sanguinarine see Epidemic dropsy Sanjad-Sakati syndrome Santavuori-Haltia disease see Ceroid lipofuscinosis, neuronal 1, infantile

67. DiabetoValens.com - The Diabetes Guide The FDA also approved ZETIA for use in two rare genetic disorders homozygousfamilial hypercholesterolemia and homozygous sitosterolemia. http://my.diabetovalens.com/diab_update/latestnews.asp?newsid=363

68. Rabbit Polyclonal To ABCG8 The mutated form of this transporter can lead to sterol accumulation and atherosclerosisor sitosterolemia, a rare autosomal recessive disorder, characterized http://www.novus-biologicals.com/data_sheet.php/4389/N

Home About Us Collaborations New Products ... Terms and Conditions Product Search Shopping Cart Your Cart is Empty. New Products Home New Products ABCG8 Polyclonal Antibody (fusion protein) Rabbit Polyclonal to ABCG8 Catalog Number NB 400-111 Price $225.00 Add to Cart Background: ATP-binding cassette (ABC) transporter genes are involved in the regulation of the amount of dietary cholesterol retained in the body. ABCG8, expressed at high levels in the liver and intestine, normally cooperates with ABCG5 to limit intestinal absorption and promote biliary excretion of sterols. The mutated form of this transporter can lead to sterol accumulation and atherosclerosis or sitosterolemia, a rare autosomal recessive disorder, characterized by hyperabsorption of sterols and the inability to excrete sterols into bile. Specificity: This antibody is specific for human ABCG8 Immunogen: ABCG8 fusion protein Host: Rabbit Species Reactivity: Human and mouse ABCG8. Other species have not been tested. Uses and Dilutions: A band around 75.7 kDa, in Western analysis, represents ABCG8 protein. Western blot dilution - 1:1,000-1:5,000

69. Annual Report On The Rare Diseases And Conditions Research Activities Of The Nat disease. sitosterolemia sitosterolemia is characterized by severepremature coronary artery disease, anemia, and painful joints. http://rarediseases.info.nih.gov/news-reports/FY97annual/NHGRI.htm

Office of Rare Diseases Annual Report on the Rare Diseases and Conditions Research Activities of the National Institutes of Health National Human Genome Research Institute (NHGRI) The National Human Genome Research Institute (NHGRI) leads the National Institutes of Health's effort in the Human Genome Project. The NHGRI's Division of Extramural Research (DER) funds Human Genome Project research in laboratories throughout the country. Research on genetic and physical mapping, DNA sequencing, database development, technology development for genome research, and studies of the ethical, legal, and social implications of genetics research are supported by the extramural arm of the NHGRI. NHGRI's Division of Intramural Research (DIR) applies the tools of the Human Genome Project to the study of human genetic diseases, their diagnosis and treatment. Recent Scientific Advances in Tools for Gene Discovery Detailed Maps of Human Chromosomes: Earlier this year, the Human Genome Project passed an important milestone when the human X chromosome was fully mapped with landmarks spaced about 75,000 base pairs apart. This map of a human chromosome was the first to meet or exceed the Human Genome Project goal of markers every 100,000 base pairs. The map will greatly benefit research into X-linked disease genes. In August 1997, a team headed by NHGRI DIR scientists completed a map of human chromosome 7, which contains an estimated 5 percent of the human genome and a total of 170 million base pairs. Scientists are now starting to sequence that chromosome from beginning to end, which will provide important information to study such human genetic diseases as cerebral cavernous malformations (CCM1), Pendred syndrome, Charcot-Marie-Tooth syndrome (CMT2D), and Williams syndrome.

70. Merck Newsroom Other indications. The FDA also approved ZETIA for use in two rare genetic disordershomozygous familial hypercholesterolemia and homozygous sitosterolemia. http://www.merck.com/newsroom/press_releases/102502.html

Full Prescribing Information Patient Product Information FDA Approves ZETIA TM (ezetimibe) for Cholesterol Reduction First New Class To Treat Cholesterol Since Statins Introduced 15 Years Ago; Studies Show Significant Reductions in LDL Cholesterol When Added to All Statins Tested WHITEHOUSE STATION and KENILWORTH, N.J., Oct. 25, 2002 Following a 10-month review, the FDA has approved ZETIA TM (ezetimibe), the first in a new class of cholesterol-lowering agents that inhibits the intestinal absorption of cholesterol, Merck/Schering-Plough Pharmaceuticals announced today. The once-daily tablet of ZETIA 10 mg was approved for use either by itself or together with statins in patients with high cholesterol to reduce LDL "bad" cholesterol and total cholesterol. Cholesterol-lowering medicines should be used in addition to an appropriate diet when the response to diet and exercise has been inadequate. In clinical trials, ZETIA was generally well tolerated with an overall side effect profile similar to placebo.

71. EHS: Mosby's Drug Consult - Drug Updates - Ezetimibe 003574 Categories, Drug Classes, Brand Names Cost Of Therapy. CATEGORIES Hypercholesterolemia;Hyperlipidemia; sitosterolemia; Pregnancy; FDA Approved 2002 Oct. http://www.mosbysdrugconsult.com/DrugConsult/003574.html

Drug Consult Home Log In Drug Updates Description ... Contact Us Ezetimibe (3574) CATEGORIES: Hypercholesterolemia; Hyperlipidemia; Sitosterolemia; Pregnancy; FDA Approved 2002 Oct Drug Classes: Antihyperlipidemics Brand Names: Zetia Description Ezetimibe is in a class of lipid-lowering compounds that selectively inhibits the intestinal absorption of cholesterol and related phytosterols. The chemical name of ezetimibe is 1-(4-fluorophenyl)-3(R)-[3-(4-fluorophenyl)-3(S)-hydroxypropyl]-4(S)-(4-hydroxyphenyl)-2-azetidinone. The empirical formula is C H F NO . Its molecular weight is 409.4. Clinical Pharmacology Background Clinical studies have demonstrated that elevated levels of total cholesterol (total-C), low density lipoprotein cholesterol (LDL-C) and apolipoprotein B (Apo B), the major protein constituent of LDL, promote human atherosclerosis. In addition, decreased levels of high density lipoprotein cholesterol (HDL-C) are associated with the development of atherosclerosis. Epidemiologic studies have established that cardiovascular morbidity and mortality vary directly with the level of total-C and LDL-C and inversely with the level of HDL-C. Like LDL, cholesterol-enriched triglyceride-rich lipoproteins, including very-low-density lipoproteins (VLDL), intermediate-density lipoproteins (IDL), and remnants, can also promote atherosclerosis. The independent effect of raising HDL-C or lowering triglycerides (TG) on the risk of coronary and cardiovascular morbidity and mortality has not been determined.

72. Sitosterolemia Information Sites Reviewed sitosterolemia sites, by people who know sitosterolemia andwork with sitosterolemia. HEALTHorgs.com. Search The Largest http://www.healthorgs.com/ConditionsandDiseases/NutritionandMetabolismDisorders/

HEALTHorgs.com Search The Largest Human Reviewed Health Database on Internet (Not sure of spelling? Use first letters and * such as abc* or abcd* or abcde*) Match:.. All Any Format: Long Short Search Words: Search the Internet (Not sure of spelling? Use first letters and * such as abc* or abcd* or abcde*) Match:.. All Any Format: Long Short Search Words: Top Health Conditions and Diseases Nutrition and Metabolism Disorders ... Cholesterol and Other Fats : Sitosterolemia Sitosterolemia - A press release with a brief explanation of this disease. Sitosterolemia - An article about this uncommon genetic lipid disorder and the gene that is responsible for it. Scientists Closer To Locating Gene That May Explain Cholesterol Absorption - An article about a study of 10 families with sitosterolemia, a rare, recessively inherited disease. Click Here for a fast ON-LINE APPLICATION FREE HOME LOAN APPRAISAL (on approved loans) The content of the SPYorg.com directory is based on the Open Directory and is enhanced using Spyorg.com technology. Privacy Statement Add Your Site to SPYorg.com

73. ML_ADDƒŠƒ\[ƒXF‚Ž‰ŒŒÇŽ¡—Öò Homozygous sitosterolemiaZETIA is indicated as adjunctive therapy to dietfor the reduction of elevated sitosterol and campesterol levels in patients http://www.fukumi.co.jp/mm/add/mp_hyperlipemia.htm

DGDispatch: ASHP: Statins Use Poor in Patients Requiring Cholesterol Management By Bonnie Darves :Special to DG News ATLANTA, GA December 12, 2002 Patient education, provider knowledge of cli nical guidelines and appropriately aggressive treatment of patients with dangero usly high triglyceride levels are still generally lacking, despite the fact that reductions in cholesterol are known to reduce coronary heart disease (CHD) mortality. @¡‰ñÌ‚èã‚°‚½‰–Ž_ƒRƒŒƒZƒxƒ‰ƒ€‚Í‚±‚ÌŒn“B@‚µ‚©‚µA‚±‚̐»•i‚Ì‘æ‚Q¢‘ã‰ü—Ç•iƒIƒƒKƒWƒFƒ‹‚ªŠù‚ɃtƒF[ƒY‚QI—¹‚µ‘ÛŠJ”­‚Ì’iŠK‚É‚ ‚èAƒRƒŒƒXƒ`ƒ‰ƒ~ƒ“‚Ì1/5‚̏­—Ê‚Å“¯“™‚ÌLDL-C’ቺì—p‚ð”­Œ»A‚³‚ç‚É• •”–c–žŠ´‚â•Ö”é“™‚Ì•›ì—p‚à­‚È‚¢‚Æ‚¢‚¤‚±‚Æ‚©‚çƒVƒ‡[ƒgƒŠƒŠ[ƒt‚ÆŒ©‚ç‚ê‚éB yŽsêz ¢ŠE‚Ì–òŒø•ª—ޕʈã–ò•i”„ã‚2000/1999/1998”N“x‚ŁA‚Ž‰ŒŒÇŽ¡—Ü‚Í‘æ‚QˆÊ159/134/96‰­ƒhƒ‹i‘O”N”ä+21/+21/+20%jB[(2000)IMS Health;(99-98)Scrip no.2549/no.2424]@‰~Š·ŽZ‚Å–ñ2’›‰~ •Ä‘Žå—v»•i”„ã‚ãˆÊ20 [2000/1999/1998”N]‚ŁA‘æ2/2/3ˆÊƒŠƒsƒg[ƒ‹[Pfizer] 4,100/2,420/1,544•S–œƒhƒ‹(+38.3/+57/+165%)A‘æ4/6/4ˆÊƒ]ƒR[ƒ‹[ƒƒ‹ƒN] 2,800/1,720/1,481•S–œƒhƒ‹(+21.7/+16/+7%)A‘æ?/17/13ˆÊƒvƒ‰ƒoƒR[ƒ‹[BMS] 1,127/950/880•S–œƒhƒ‹(+18.6/+8/+14%)B[(2000)IMS Health;(99-98)Scrip no.2516/no.2428] ŒŽŠ§ƒ~ƒNƒX28(6)44-66(May 2000)uƒXƒyƒVƒƒƒ‹F‚Ž‰ŒŒÇŽ¡—–ò‚̐V‚½‚È“WŠJv‚ÉŽ¡—AŽsê‚È‚Ç‚Ì’²¸•ñ‚ª“Z‚ß‚ç‚ê‚Ä‚¢‚éB 00.03.13 atorvastatin‚Æsuperstatin

74. GeneCards: List Of Disease Genes ABCG5, ATPbinding cassette, sub-family G (WHITE), member 5 (sterolin1), 2p21, sitosterolemia. ABCG8, ATP-binding cassette, sub-family http://genecards.bcgsc.ca/cgi-bin/listdiseasecards?type=full

75. Sitosterolemia Websites From Linkspider.org The Best Results for sitosterolemia from the Linkspider Organization.Click here for sitosterolemia listings. Complete Directory http://www.linkspider.org/Health/ConditionsandDiseases/NutritionandMetabolismDis

Directory Results for Sitosterolemia from Linkspider.org Keyword: Sitosterolemia Linkspider Organization Sitosterolemia Search for Directory Tree: Top Health Conditions and Diseases Nutrition and Metabolism Disorders ... Cholesterol and Other Fats : Sitosterolemia (3) Add URL Advertise Here! Personalize Amazon ... Sitosterolemia - A press release with a brief explanation of this disease. Sitosterolemia - An article about this uncommon genetic lipid disorder and the gene that is responsible for it. Scientists Closer To Locating Gene That May Explain Cholesterol Absorption - An article about a study of 10 families with sitosterolemia, a rare, recessively inherited disease.

76. Diseases Solved After Completion Of The June 2001 Analysis R50954, 10.0, 35, 56, 7, sitosterolemia, 5453902 NP_006214, protein (peptidylprolylcis/trans isomerase) NIMA-interacting, 4 (parvulin) Homo sapiens, 0.000912, http://www.bork.embl-heidelberg.de/g2d/table_resolved.html

Diseases solved after completion of the June 2001 analysis Id Size (Mb) r e ... Beckwith-Wiedemann syndrome tumor suppressing subtransferable candidate 3; imprinted in placenta and liver; tumor-supressing STF cDNA 3; Tumor-suppressing subtransferable candidate-3 [Homo sapiens] Knobloch syndrome(2) phosphodiesterase 9A [Mus musculus] May-Hegglin anomaly zinc finger protein 146 [Homo sapiens] No match to Ensembl Lymphedema with distichiasis procollagen (type III) N-endopeptidase; protease, metallo, 1, 33kD [Homo sapiens] No match to Ensembl Leukoencephalopathy, vacuoliting megalencephalic, with subcortical cysts arylsulfatase B precursor [Homo sapiens] No match to Ensembl Smith-Lemli-Opitz syndrome insulin-like growth factor binding protein, acid labile subunit [Mus musculus] No match to RefSeq Sitosterolemia protein (peptidyl-prolyl cis/trans isomerase) NIMA-interacting, 4 (parvulin) [Homo sapiens] No match to RefSeq No match to Ensembl Netherton syndrome alpha internexin neuronal intermediate filament protein [Mus musculus] No match to RefSeq No match to Ensembl arthroophthalmopathy, progressive (Stickler syndrome)

77. List Of Tests Cholestanol (Cerebrotendinous xanthomatosis). Sitosterol (sitosterolemia, Phytosterolemia).Free Fatty Acids Total level and qualitative analysis. Desmosterol. http://www.genetics.kennedykrieger.org/TestList.htm

Accreditation Faculty History List of Tests ... Print all test forms To view forms in PDF (Portable Document Format), you must download Adobe Acrobat Reader which is free from Adobe at http://www.adobe.com/prodindex/acrobat/readstep.html If you wish to print all test forms at once please use the following link: All Forms Clinical Mass Spectrometry Section Organic acid gas chromatography/mass spectrometry N-acetyl-l-aspartic acid (Canavan disease) Canavan disease - prenatal diagnosis 3-Methylglutaconic acid ... Mevalonic Acid Peroxisomal Diseases Section Plasma Very Long Chain Fatty Acids: Includes Phytanic Acid (screening test for peroxisomal disorders) Red Blood Cell Plasmalogen Content (screening test for rhizomelic chondrodysplasia punctata) Plasma Total Lipid Fatty Acid Profile: Includes C8 to C26 saturated, monounsaturated, polyunsaturated, trans and branched chain fatty acids Red Blood Cell Total Lipid Fatty Acid Profile: Includes C8 to C26 saturated, monounsaturated, polyunsaturated fatty acids and plasmalogens ... DNA Testing for X-Linked Adrenoleukodystrophy Site best viewed with:

78. IX Sitosterolemia Nutrition and Metabolism Disorders, Cholesterol and Other Fats, sitosterolemia, sitosterolemiaT A press release with a brief explanation of this disease. http://ix.joal.net/en/Health/Conditions_and_Diseases/Nutrition_and_Metabolism_Di

79. Sitosterolemia In Health > Conditions And Diseases > Nutrition And Metabolism Di Similar pages ScheringPlough SP in the News Other indications The FDA also approved ZETIA for use in two rare genetic disordershomozygous familial hypercholesterolemia and homozygous sitosterolemia. http://ilectric.com/browse/web/Health/Conditions_and_Diseases/Nutrition_and_Meta

Metasearch Directory News Multi-Search ... Login/Out Choose a Search Metasearch - The Web Metasearch - This Site Metasearch - News Metasearch - Auctions Metasearch - Forums Metasearch - Images Metasearch - Shopping Directory - Within This Category Only Directory - Entire Directory - Adult Directory - Arts Directory - Business Directory - Computers Directory - Games Directory - Health Directory - Home Directory - News Directory - Recreation Directory - Reference Directory - Regional Directory - Science Directory - Shopping Directory - Society Directory - Sports Directory - World Shopping - All products Shopping - Books Shopping - Electronics Shopping - Popular music Shopping - Classical music Shopping - DVD's Shopping - VHS Videos Shopping - In Theaters Shopping - Toys Shopping - Computer Hardware Shopping - Software Shopping - Magazines Shopping - Photo Shopping - Garden / Outdoor Living Shopping - Baby Shopping - Kitchen Lookup - Domain in Whois Lookup - Domain Availability Lookup - HTTP Source Lookup - DNS Record W eb Directory Categories Related Sponsored Sites Sites ... Cholesterol and Other Fats Sitosterolemia Try your search at Amazon in - The United States Canada United Kingdom Germany ... Japan Sponsored Sites: Sites: Sitosterolemia A press release with a brief explanation of this disease.

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