41. Searchalot Directory For Barth Syndrome Related Web Sites. barth syndrome Family Network Offers details aboutthe disease, message board, research sites, events and private chats. http://www.searchalot.com/Top/Health/ConditionsandDiseases/RareDisorders/BarthSy

Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases Rare Disorders : Barth Syndrome Related Web Sites Barth Syndrome Family Network - Offers details about the disease, message board, research sites, events and private chats. Numerous links to other resources. Barth Syndrome Foundation - Promotes knowledge about this disease among families, physicians and scientists, serving as a focal point for data and research for scientists. The group offers support to families learning to cope with the disorder. Clinical Mass Spectrometry Laboratory - An article about Barth Syndrome with a description, clinical manifestations, etiology, epidemiology, diagnosis, prognosis and management. Related Categories Health: Conditions and Diseases: Cardiovascular Disorders: Heart Disease: Cardiomyopathy Health: Conditions and Diseases: Genetic Disorders All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite

42. 02-392 Barth Syndrome Foundation Date 05/16/2002. To RGS Fundopp. Re 02-392 barth syndrome Foundation.TO RGS Fundopp Subscribers 02-392 Subject barth syndrome http://alpha.ddm.uci.edu/zotmail/archive/2002/20020516107.html

Date: To: RGS - Fundopp Re: 02-392 Barth Syndrome Foundation

43. Current E-news barth syndrome Foundation to Award Research Grants Deadline for letters of intentJune 30 The barth syndrome Foundation will award its first grants for http://www.med.umich.edu/medschool/enews/archive/june14.htm

Submission deadline: 5 p.m., Wednesday Published Friday by the Department of Public information, contact Lisa Copeland at 647-4890 or e-mail at lisacc@umich.edu Many internal computer users will need to cut- and-paste the e-mail and web addresses. E-News June 14, 2002 Submit an event for the E-News Submission guidelines E-News archive U-M Medical School Home He Will Be Missed Dean Allen S. Lichter offers the following words in remembrance of Donald Fredrickson, M.D. "We at the Medical School are saddened by the passing of Donald Fredrickson, a distinguished U-M Medical School alumnus, former director of the National Institutes of Health and past president of the Howard Hughes Medical Research Institute in Bethesda. Our sympathies are with his wife and two sons. Dr. Fredrickson received both his bachelor of science and medical degrees from U-M. After graduating from the Medical School in 1949, he began a career in research and scientific leadership. Dr. Fredrickson discovered two genetic disorders and helped to illuminate our understanding of plasma lipoproteins. While serving as the NIH director, he smoothed the way for our society's acceptance of genetic engineering and the safety of recombinant DNA technology.

44. NINDS: Organization Contact Information (help). Contact us My privacy NINDS is part of the National Institutes ofHealth. Organization Contact Information. barth syndrome Foundation, Inc. http://www.ninds.nih.gov/find_people/vol_org.htm?index=801&webcode=A1

45. Finding Funders - Web Sites Of Grantmaking Public Charities - B (6/18/01). barth syndrome Foundation, Inc. (FL) The Perry, Floridabasedbarth syndrome Foundation was established in 1997 by three http://fdncenter.org/funders/grantmaker/gws_pubch/pubch_b.html

Although classified as public charities by the IRS, community foundations are listed separately on our site under Web Sites of Corporate Grantmakers (The sites listed below are launched in new browsers.) Bainbridge Arts and Crafts (WA) Bainbridge Arts and Crafts was founded in 1948 on Bainbridge Island in Washington "to inspire interest in the visual arts, advance creative achievement in craft and fine art, support the development of local and regional artists, and fund arts education." The nonprofit organization and gallery offers a wide variety of charitable support and programs, including scholarships for local arts students, educational programs and funds for the community, a cultural grant to individuals and community arts organizations, an Art Apprentice Program and the quarterly ART NEWS publication. Visitors to the Bainbridge Arts and Crafts Web site will find information on current and upcoming exhibits, general news on the organization and contact information. Bainbridge Foundation, Inc. (WA) The Bainbridge Foundation supports community organizations on and near Bainbridge Island, Washington. The Foundation runs the "One Call for All" funding drive in order to support these agencies. The Foundation's Web site lists Island agencies and Off-Island agencies that it funds, and maintains an online feedback and pledge form for donors. The Bainbridge Island (Washington) Arts and Humanities Council was established in 1986. The group's mission is to "provide access to the arts and humanities for every Island citizen, and to assist individuals and organizations delivering cultural services and programs." The elegant site includes a searchable database of cultural resources and artists in the area. There is also information on current exhibits and events, a calendar of cultural events in the community, a page of links to related sites, and a membership form. The site does not offer any information on applying for a grant.

46. Children’s Cardiomyopathy Foundation – Related Disorders Links And Resources The barth syndrome Foundation The Foundation's mission is to guide the search fora cure, to educate and support physicians and to create a caring community http://www.childrenscardiomyopathy.org/main/related.htm

Search the Site LINKS AND RESOURCES HEART DIAGRAMS ABOUT CARDIOMYOPATHY HEART TRANSPLANTS RELATED DISORDERS ... ADDITIONAL RESOURCES DISORDERS RELATED TO CARDIOMYOPATHY The National Organization Of Rare Disorders (N.O.R.D.) Dedicated towards the prevention, treatment and cure of rare "orphan" diseases. Maintains databases on diseases, organizations, drug developments and news. N.I.H. - Office of Rare Diseases Patient Support Groups National Institute of Health list of various online databases of voluntary health organizations for specific disorders. National Ataxia Foundation Home Page Established in 1957 with the primary mission of encouraging and supporting research into hereditary ataxia, a group of neurological disorder. International Network of Ataxia Friends Provides medical and general information, mailing lists, newsletters, and assistance in finding a national or local support group. Friedreich's Ataxia Parents Group Formed by a small group of parents, site provides online support, FAQ's, and information about research articles.

47. Children’s Cardiomyopathy Foundation – Possible Genetic Disorders Associated W Possible Genetic Disorders Associated with Dilated Cardiomyopathy Disease/Syndrome. Symptoms Characteristics. Incidence Cause. barth syndrome. http://www.childrenscardiomyopathy.org/main/chart1.htm

Possible Genetic Disorders Associated with Hypertrophic Cardiomyopathy Disease/ Syndrome Noonan Syndrome Distinctive physical/facial appearance: broad or webbed neck, short stature, low set ears, wide set eyes, small jaw, chest deformity, extra skin folds, congenital heart defects Skeletal malformations, malformations of blood and lymph vessels, cardiomyopathy, blood clotting, mild mental retardation Incidence of 1 in 2,500 live births Autosomal dominant inheritance 50% of cases due to genetic mutation in PTPN11 gene Pompe Disease Excess glycogen accumulated in lysosomes Poor muscle tone Incidence of 1 in 100,000 Enzyme deficiency of acid maltase (glycogen storage disease type II) Autosomal recessive disease Fatty Acid Oxidation (carnitine deficiency, CPT, MCAD, VLCAD, LCHAD, LCAD, SCHAD, glutaric acidemia II, beta oxidation spiral defects) Recurrent episodes of illness caused by fasting or reduced food intake when sick, vomiting, severe lethargy that can progress to coma Hypoglycemia, respiratory distress, congestive heart failure with or without arrhythmias, muscle weakness, low muscle tone Incidence of 1 in 10,000 live births (MCAD - most common form of FOD)

48. WebGuest - Open Directory : Health : Conditions And Diseases : Rare Disorders : Sites barth syndrome Family Network Offers details about the disease,message board, research sites, events and private chats. http://directory.webguest.com/index.cgi/Health/Conditions_and_Diseases/Rare_Diso

Browse thru 1000's of books about health, mind and body: About Us Privacy Statement Acceptable Use Policy Legal Notices ... Contact Us the entire directory only in Top Health Conditions and Diseases Rare Disorders : Barth Syndrome See also: Health: Conditions and Diseases: Cardiovascular Disorders: Heart Disease: Cardiomyopathy Health: Conditions and Diseases: Genetic Disorders Sites: Barth Syndrome Family Network - Offers details about the disease, message board, research sites, events and private chats. Numerous links to other resources. Barth Syndrome Foundation - Promotes knowledge about this disease among families, physicians and scientists, serving as a focal point for data and research for scientists. The group offers support to families learning to cope with the disorder. Clinical Mass Spectrometry Laboratory - An article about Barth Syndrome with a description, clinical manifestations, etiology, epidemiology, diagnosis, prognosis and management. Last update: 4:20 PT, Friday, March 16, 2001 Help build the largest human-edited directory on the web.

49. Websites En Adressen Kenmerken Diagnose+behandeling Websites+ www.barthsyndrome.org logo barth syndrome Family Network, link naar www.barthsyndrome.orgDit is de pagina van de barth syndrome Foundation, opgericht in de http://www.stofwisselingsziekten.nl/ziekten/barthsyn/barweb.html

Websites en Adressen kenmerken diagnose+behandeling websites+adressen andere ziekten Nuttige websites en adressen: Deze lijst zal binnenkort worden uitgebreid. www.barthsyndrome.org Dit is de pagina van de Barth Syndrome Foundation, opgericht in de Verenigde Staten van Amerika door het Barth Syndrome Family Network. Bij dit Barth Syndrome Family Network zijn families van over de hele wereld aangesloten en al deze families hebben zelf met het Barth Syndroom te maken. Op deze pagina is veel informatie over het Barth Syndroom te vinden met veel nuttige links naar andere websites. Het is allemaal in het Engels. Als dit een probleem is, neem dan contact op met Joke van Loo . Zij kan de informatie op deze pagina voor U vertalen. De informatie op deze pagina staat onder supervisie van Pr. Dr. P.G. Barth, kinderneuroloog, verbonden aan het Emma Kinderziekenhuis / Academisch Medisch Centrum in Amsterdam.

50. Directory :: Look.com barth syndrome (3) See Also. Sites. barth syndrome Family Network Offers detailsabout the disease, message board, research sites, events and private chats. http://www.look.com/searchroute/directorysearch.asp?p=524632

51. AD HOC BIBLIO - INDEX SUJETS LETTRE B Compilé Le 14/01/03 Reliability and responsiveness of the BarryAlbright Dystonia Scale .a;barth syndrome Gross motor development of a toddler http://www.cidg.com/~marienf/k/i/mid1b.htm

B B-Sarcoglycan... Prenatal diagnosis in a family affected with B-sarcoglycan muscular dystrophy.... [a] Disability-related electronic bulletin boards.... [a] Interests and participation on disability-related computer bulletin boards.... [a] Baby Behavior Questionaire (BBQ)... Behavioral dimensions in one-year-olds and dimensional stability in infancy.... [a] Balaieur... Toward task transparency in alternative computer access: selection of text throu... [m] Wivik-2 scan : 1-5 switch scanning access.... [m] Balance... Clinical assessment of balance disorders... [a] [m] Vestibular proprioceptive functions in four year olds: normative and regression ... [m] Balance dynamique... Characterization of normal and pathological sway dynamics.... [m] Dynamic balance testing with electrically evoked perturbation: A test of reliabi... [a] Evaluation of a model that determines the stability limits of dynamic balance.... [a] Functional reach : does it really measure dynamic balance ?... [a] Monaural and binaural galvanic vestibular stimulation in human dynamic balance f... [a] Balance Master Test...

52. MEDLINEplus: Genetic Disorders Specific Conditions/Aspects About barth syndrome (barth syndrome Foundation);Angelman Syndrome (National Institute of Neurological Disorders and Stroke); http://www.nlm.nih.gov/medlineplus/geneticdisorders.html

Skip navigation Other health topics: A B C D ... List of All Topics Genetic Disorders Contents of this page: News From the NIH General/Overviews Anatomy/Physiology ... Teenagers Search MEDLINE for recent research articles on Genetic Disorders: General Fragile X Syndrome You may also be interested in these MEDLINEplus related pages: Birth Defects Celiac Disease Cleft Lip and Palate Cystic Fibrosis ... Genetics/Birth Defects Latest News Fetal Genetic Info Found in Mom's Blood (03/17/2003, Reuters Health) From the National Institutes of Health Frequently Asked Questions About Genetics (National Human Genome Research Institute) General/Overviews Genes and Populations (National Institute of General Medical Sciences) Also available in: Spanish Genetic Disorders in Pregnancy (American College of Obstetricians and Gynecologists) Introduction to Chromosome Abnormalities (Chromosome Deletion Outreach) JAMA Patient Page: Genetics (American Medical Association) Anatomy/Physiology Gene-Environment Interaction Fact Sheet (National Center for Environmental Health) Genes and Birth Defects: Common Forms of Inheritance (March of Dimes Birth Defects Foundation) Late-Appearing Defects (March of Dimes Birth Defects Foundation) Multifactorial Inheritance (March of Dimes Birth Defects Foundation) Clinical Trials ClinicalTrials.gov: Genetic Diseases, Inborn

53. Whats New: Funding Announcements: Barth Syndrome Foundation Announces 2002 Resea barth syndrome Foundation Announces 2002 Research Grant Program. For complete grantand application guidelines, see the barth syndrome Foundation Web site. http://www.omhrc.gov/OMH/WhatsNew/2pgwhatsnew/funding257.htm

Barth Syndrome Foundation Announces 2002 Research Grant Program Deadline: June 30, 2002 (Letters of intent) In 2002, the Barth Syndrome Foundation will award its first grants for research on the natural history, biochemical basis, and treatment of Barth syndrome. The foundation anticipates awarding up to $100,000, divided among several one- or two-year grants ranging in size from $10,000 to $40,000. Barth syndrome is an X-linked recessive, cardioskeletal myopathy associated with neutropenia, growth delay, and diverse biochemical abnormalities, among which are defects in mitochondrial metabolism and phospholipid biosynthesis. Because many clinical and biochemical abnormalities of Barth syndrome remain poorly understood, the foundation is seeking proposals for research that may shed light on any aspect of the syndrome. The foundation hopes to find improved treatments and ultimately a cure for this rare but serious disorder. The Barth Syndrome Foundation awards grants to principal investigators who are affiliated with nonprofit institutions. The foundation is interested in providing seed money to experienced investigators for the testing of initial hypotheses and collection of preliminary data leading to successful long-term funding by NIH and other major granting institutions, and in attracting new investigators to the field of Barth syndrome research.

54. Cardiomyopathy A condition known as barth syndrome, a rare and relatively unknown geneticallylinked cardiac disease, can cause dilated cardiomyopathy. http://www.americanheart.org/presenter.jhtml?identifier=4468

55. June 14, 2002 -- SSTI Weekly Digest Funding Supplement barth syndrome Foundation The barth syndrome Foundation serves to help finda cure for barth syndrome and to educate and support physicians. http://www.ssti.org/Digest/2002/Supplements/061402supplement.htm

In the June 14, 2002 Supplement: Low-income Communities Get Boost from New Markets Tax Credit Program Federal Research Opportunities National Institutes of Health National Science Foundation Foundation Research Opportunities Barth Syndrome Foundation Community Technology Fund of Ohio Cure Autism Now Flight Attendant Medical Research Institute ... Verizon Foundation SSTI Weekly Digest Digest do not necessarily reflect the official position of the U.S. Department of Commerce. Subscription to the SSTI Weekly Digest is free. If you are reading a forwarded copy of this issue and would like to receive your own copy each week directly, please subscribe at: http://www.ssti.org/Digest/digform.htm Requests to unsubscribe should be sent to sstiwd@ssti.org Low-income Communities Get Boost from New Markets Tax Credit Program The Department of Treasury recently announced the first competitive round for the allocation of tax credits under the New Markets Tax Credit Program ( NMTC), a program designed to stimulate private sector investment in the economic development of low-income communities.

56. IComm: File Not Found! barth syndrome ..CardiomyopathyNeutropeniaSyndrome). barth syndrome at UMDF http//www.umdf.org. http://www.icomm.ca/geneinfo/b.htm

File Not Found We're sorry, but the file you're looking for can't be found. You might want to try starting at our front page or a list of iComm accountholders , or you can search the site This site was last updated on 30 August 2002. iComm Questions regarding the iComm web site should be sent to our webmaster

57. IComm: File Not Found! Lethal Infantile Cardiomyopathy (LIC) .barth syndrome), barth syndromeat UMDF United Mitochondrial Foundation http//www.umdf.org http://www.icomm.ca/geneinfo/l.htm

File Not Found We're sorry, but the file you're looking for can't be found. You might want to try starting at our front page or a list of iComm accountholders , or you can search the site This site was last updated on 30 August 2002. iComm Questions regarding the iComm web site should be sent to our webmaster

58. B Barotrauma. Barrett Esophagus. barth syndrome ( Cardiomyopathy, Congestive).Basal Cell Nevus Syndrome. barth syndrome. Bartonella Infections. http://www.mashhadkit.com/iranmedicine/diseases-list/diseases-b.htm

B Babesiosis Back Pain Bacteremia Baker's Cyst ... Bronchiolitis Obliterans Organizing Pneumonia (BOOP) Bronchitis Bronchopulmonary Dysplasia Brown (Tendon Sheath) Syndrome Brown-Sequard Syndrome ... Buruli Ulcer

59. Mitochondrial Conditions 5070 International Mitochondrial Disease Network (IMDFN) Website www.imdn.org Email info@imdn.org barth syndrome Family Network Web site www.barthsyndrome http://www.kumc.edu/gec/support/mitochon.html

Mitochondrial Conditions Alpers Disease (Progressive Infantile Poliodystrophy); Barth syndrome (Cardiomyopathy-Neutropenia Syndrome) / Lethal Infantile Cardiomyopathy (LIC); Beta-oxidation Defects; Carnitine Deficiency and Disorders; Chronic Progressive External Ophthalmoplegia Syndrome (CPEO); Kearns-Sayre Syndrome (KSS); Lactic Acidosis; Leber Hereditary Optic Neuropathy (LHON); Leigh Disease (Subacute Necrotizing Encephalomyelopathy); Long-Chain Acyl-CoA Dehydrogenase (LCAD) Deficiency; Luft Disease; Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency; Mitochondrial Cytopathy; Mitochondrial Encephalomyopathy Lactic Acidosis and Strokelike Episodes (MELAS); Mitochondrial Encephalopathy; Mitochondrial Myopathy; Multiple Acyl-CoA Dehydrogenase (MAD) Deficiency / Glutaric Aciduria Type II; Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); Myoneurogastointestinal Disorder and Encephalopathy (MNGIE); Neuropathy Ataxia and Retinitis Pigmentosa (NARP); Pearson Syndrome; Pyruvate Carboxylase Deficiency; Pyruvate Dehydrogenase Deficiency (PHD); Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency Respiratory Chain Disorders: Complex I: NADH dehydrogenase (NADH-CoQ reductase) deficiency, Complex II: Succinate dehydrogenase deficiency, Complex III: Ubiquinone-cytochrome c oxidoreductase deficiency, Complex IV: Cytochrome c oxidase (COX) deficiency, Complex V: ATP synthase deficiency

60. Congenital Heart Defects / Cardiovascular Conditions barth syndrome Family Network; Down Syndrome; Familial Dilated Cardiomyopathy(FDC) Project, Oregon Health Sciences University (OHSU); http://www.kumc.edu/gec/support/conghart.html

Heart / Cardiology Conditions Congenital Heart Defects including: atrial septal defect (ASD), ventricular septal defect (VSD), patent ductus arteriosus (PDA), endocardial cushion defect, aortic stenosis, pulmonary stenosis, coarctation of the aorta, tetralogy of Fallot, tricuspid atresia, transposition of the great arteries, truncus arteriosus, Ebstein anomaly, anomalous pulmonary venous connection, hypoplastic left heart syndrome, endocardial fibroelastosis, Long QT, other conditions and syndromes (Marfan, Down, Holt Oram, Barth, Hypertrophic Cardiomyopathy, Kawasaki, Noonan, Turner , Velo-Cardio-Facial, other) Cardiovascular conditions including: hyperlipidemia, coronary artery disease, angina, cholesterol and lipid conditions, heart disease/stroke CHASER (Congenital Heart Anomalies Support, Education, and Resources) c/o Jim and Anita Myers 2112 North Wilkins Road Swanton, OH 43558 Phone: (419) 825-5575 Fax: (419) 825-2880 E-mail: myer106w@wonder.em.cdc.gov or 75050.2742@compuserve.com

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