81. THE GRANT ADVISOR - JUNE 2002 barth syndrome FOUNDATION RESEARCH GRANT PROGRAM DUE JUN http://www.grantadvisor.com/sample.txt

< > SEP 5 AI Arts International: The Fund for U.S. Artists at International Festivals 2/02 212/674-9744 and Exhibitions http://www.artsinternational.org >>> Also due: JAN16 MAY 2 < > SEP15 MDC MacDowell Colony Residencies for Writers, Composers, and Artists 10/01 603/924-3886 http://www.macdowellcolony.org >>> Also due: JAN15 APR15 < JUN 1 SLU St. Louis Univ./Vatican Film Library: Andrew W. Mellon Fellowship Program 12/01 314/977-3090 >>> Also due: OCT 1 MAR 1 < JUN17 CAN Canadian Studies Program Enhancement Grant 5/94 202/682-1740 JUN17 CAN Canadian Studies Conference Grant Program 5/94 202/682-1740 JUN30 HAGLEY Hagley Museum and Library: Short-Term Grants-in-Aid 3/02 302/658-2400 >>> Also due: OCT29 MAR31 < JUN30 HAGLEY Hagley Museum and Library: Henry Belin du Pont Fellowship 3/02 302/658-2400 >>> Also due: OCT29 MAR31 < JUL 1 NEH Nat'l Endow. for the Humanities: Preservation, Access, and Reference Works 4/02 202/606-8570 JUL15 KRESS Samuel H. Kress Foundation: Old Masters in Context 212/861-4993 >>> Also due: JAN15

82. Health Library - barth syndrome. Important It is possible that the main title of the report barth syndrome is not the name you expected. Please check http://myhealth.barnesjewish.org/library/healthguide/illnessconditions/topic.asp

83. NodeWorks - Rare Disorders: Barth Syndrome barth syndrome is a rare but serious genetic disorder that affects males. thumbnail, 1. barth syndrome Foundation Promotes knowledge http://dir.nodeworks.com/Health/Conditions_and_Diseases/Rare_Disorders/Barth_Syn

in entire NodeWorks Directory in Health in Rare Disorders in ++ Barth Syndrome Top Health Rare Disorders Barth Syndrome Barth Syndrome is a rare but serious genetic disorder that affects males. 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. NINDS - Barth Syndrome Information Information sheet compiled by the National Institute of Neurological Disorders and Stroke. The Complete Barth Syndrome Homepage List of clinical symptoms, history of the condition, current news, and links to support groups. NodeWorks boosts web surfing! Page Returned in seconds - HTML Compressed Help build the largest human-edited directory on the web. Submit a Site Update a Site Open Directory Project Become an Editor

84. Program Nr 1352 Program Nr 1352 Frequency of new mutations and allele dropout in barth syndrome. IL Gonzalez, J. Johnston, V. Funanage, R. Proujansky. http://www.faseb.org/genetics/ashg00/f1352.htm

Program Nr: 1352 Frequency of new mutations and allele drop-out in Barth syndrome. I.L. Gonzalez, J. Johnston, V. Funanage, R. Proujansky. DuPont Hospital for Children, Wilmington, DE. We have also found a surprisingly high frequency of new mutations in Barth families and have ascertained the origin of the mutation in families that are informative for linked polymorphisms. G4.5 mutations have originated de novo in mothers, and in both male and female grand- and great-grand-parents. * LE-pcr consists of a linear multiplication stage followed by an exponential amplification stage. Protocol will be provided.

85. Research Matters At UGA Funding Opportunities (Where to Look for Money). barth syndrome Foundation, Inc. (BSF) is pleased to announce the availability http://www.ovpr.uga.edu/researchmatters/funding/2003/may/bsf.htm

UGA MAIN OVPR MAIN SPONSORED PROGRAMS SEARCH: May 2003 Vol. 1, No. 7 Main Page Stuff You Need To Know Funding Opportunities Teachable Moments ... Contact Us Funding Opportunities (Where to Look for Money) Barth Syndrome Foundation, Inc. (BSF) - www.barthsyndrome.org for Letter of Intent guidelines and requirements. Previous Page Subscribe Here Unsubscribe Here

86. MedlinePlus: Genetic Disorders barth syndrome (National Institute of Neurological Disorders and Stroke); Genes and Disease (National Center for Biotechnology Information); http://www.nlm.nih.gov/medlineplus/geneticdisorders.html

@import url(http://www.nlm.nih.gov/medlineplus/images/advanced.css); 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 ... Women Search MEDLINE for recent research articles on Genetic Disorders 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 Prenatal Testing Has Cut Amnio Use (05/31/2004, Reuters Health) Umbilical Cord Blood Treats Rare Inherited Disorder (05/06/2004, Reuters Health) From the National Institutes of Health Genes and Disease (National Center for Biotechnology Information) Genes and Populations (National Institute of General Medical Sciences) Also available in: Spanish Genetics Home Reference (National Library of Medicine) Learning about Genetics (National Human Genome Research Institute) General/Overviews Introduction to Chromosome Abnormalities (Chromosome Deletion Outreach) JAMA Patient Page: Genetics (American Medical Association) Your Genes, Your Health

87. Euromit 4: Submitted Abstract A case of barth syndrome with massive 3methylglutaconic and 3-methylglutaric aciduria. keywords barth syndrome, children, mitochondria http://www.gen.cam.ac.uk/euromit/abs/nikolaeva.html

A case of Barth syndrome with massive 3-methylglutaconic and 3-methylglutaric aciduria. E.A. Nikolaeva, I.V. Leontieva, V. Semenov, T. Chentsova, I.A. Sebeleva, L.Z. Kazantseva Institute of Paediatrics and Children Surgery, Moscow, Russia X-linked mitochondrial Barth's cardioskeletal myopathy with neutropenia has been delineated in 1983. We observed a boy 6 years old with this disease. The syndrome manifestations included: severe growth deficiency, mild retardation of psychomotoric development, myopathy, hypertrophic non-obstructive cardiomyopathy (echo enddiastolic septal wall thickness - 11,8 mm, the normal value is 5,5-6 mm), neutropenia ( <900/mm3), recurrent hypoglycaemia 2.0 mmol/l, hyperlactatacidemia 2.6 mmol/l (the normal value is 1.0-1.7). GC-MS analysis of organic acids revealed a marked increase of 3-methylglutaconic (two isomers), 3-methylglutaric acid excretion and moderate increase of 3-hydroxy-3-methylglutaric, fumaric, adipic acid excretion. Therapy with cytochrome C, coenzyme Q10, L- carnitine demonstrated significant clinical and biochemical efficacy. In 1,5 year echo enddiastolic septal wall thickness diminished to 6,5 mm (N). 3-Methylglutaconic, 3-methylglutaric acid excretion decreased 3 times. Excretion of 3-hydroxy-3-methylglutaric, fumaric, adipic acid disappeared. keywords: Barth syndrome, children, mitochondria

88. E-news: June, 14, 2002 barth syndrome Foundation to Award Research Grants Deadline for letters of intent June 30 The barth syndrome Foundation will award its first grants for http://www.med.umich.edu/medschool/enews/archive/june14.htm

dqmcodebase="/medschool/templates/script/" 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.

89. UMB 1809 CASE IDENTIFICATION CODE. UMB 1809. DISORDER barth s syndrome AGE 13 year(s) 294 day(s) SEX Male RACE Caucasian POST MORTEM INTERVAL 7 hour(s) CAUSE OF DEATH http://medschool.umaryland.edu/BTBank/UMB_1809.htm

UNIVERSITY OF MARYLAND BRAIN AND TISSUE BANK FOR DEVELOPMENTAL DISORDERS email: btbumab@umaryland.edu phone: 1-800-847-1539 CASE IDENTIFICATION CODE UMB#1809 DISORDER: Barth's Syndrome AGE: 13 year(s) 294 day(s) SEX: Male RACE: Caucasian POST MORTEM INTERVAL: 7 hour(s) CAUSE OF DEATH: Complication of Disorder KARYOTYPE AVAILABLE? No FINDINGS: HIV STATUS: - HBSAG STATUS: - LENGTH OF TIME IN STORAGE AS OF MARCH 2004: 178 days AVAILABLE TISSUE ....FIXED.... BRAIN (Protocol Method 2) CEREBRUM- Hemi Coronal Section(2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30), MID BRAIN/PONS- Section(2, 4, 6, 8, 10), CEREBELLUM- Section (2, 4, 6, 8, 10) OTHER ORGAN SYSTEMS ENDOCRINE- (Pituitary), SPINAL CORD- (Lumbar) ....FROZEN.... BRAIN (Protocol Method 2) CEREBRUM- Hemi Coronal Section(1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25), MID BRAIN/PONS- Section(1, 3, 5, 7, 9), CEREBELLUM- Section(1, 3, 5, 7) OTHER ORGAN SYSTEMS CARDIOVASCULAR- (Heart), ENDOCRINE- (Adrenal), GASTROINTESTINAL- (Jejunum), INTEGUMENTARY- (Skin), OTHER TISSUE- (Tissue(s) nrc)

90. Reactive Arthritis (Reiter's Syndrome) - August 1999 - American Academy Of Famil August 1999 AFP. Reactive Arthritis (Reiter s syndrome). WERNER F. barth, MD, and KINIM SEGAL, MD Washington Hospital Center Washington, DC, http://www.aafp.org/afp/990800ap/499.html

Advanced Search Reactive Arthritis (Reiter's Syndrome) WERNER F. BARTH, M.D., and KINIM SEGAL, M.D. Washington Hospital Center Washington, D.C. A patient information handout on reactive arthritis, written by the authors of this article, is provided on page 507. Reactive arthritis, also called Reiter's syndrome, is the most common type of inflammatory polyarthritis in young men. It is sometimes the first manifestation of human immunodeficiency virus infection. An HLA-B27 genotype is a predisposing factor in over two thirds of patients with reactive arthritis. The syndrome most frequently follows genitourinary infection with Chlamydia trachomatis , but other organisms have also been implicated. Treatment with doxycycline or its analogs sometimes shortens the course or aborts the onset of the arthritis. Reactive arthritis may also follow enteric infections with some strains of Salmonella or Shigella, but use of antibiotics in these patients has not been shown to be effective. Reactive arthritis should always be considered in young men who present with polyarthritis. Symptoms may persist for long periods and may, in some cases, cause long-term disability. Initial treatment consists of high doses of potent nonsteroidal anti-inflammatory drugs. Patients with large-joint involvement may also benefit from intra-articular corticosteroid injection. (Am Fam Physician 1999;60:499-507.) I n 1984 in Ontario, Canada, an outbreak of

91. Electricbrain Home: Index: Health: Conditions And Diseases: Rare Disorders: Bart Health Conditions and Diseases Rare Disorders barth syndrome News at 0417 on May 16, 2004 Random quote There are http://www.electricbrain.com/index/Health/Conditions_and_Diseases/Rare_Disorders

electricbrain Index Health Conditions and Diseases ... Rare Disorders : Barth Syndrome home index write privacy ... cache Quote of the Minute... A bug in the code is worth two in the documentation. Find someone: Old Friends New Friends Lost Love New Love ... privacy

92. BARTH SYNDROOM (OMIM 302060) Index Welkom op deze pagina over het barth Syndroom (OMIM 302060). Comité barth Syndroom Nederland. Comité barth Syndroom Nederland http://www.wapenveld.com/BarthSyndroom/

laatste update vragen? reageren? Welkom op deze pagina over het Barth Syndroom (OMIM 302060) Het Barth syndroom is een erfelijke aangeboren stofwisselingsziekte. Medisch wetenschappelijke literatuur hierover is te vinden onder registratienummer OMIM 302060. De ziekte is genoemd naar Pr. Dr. P.G. Barth, die dit syndroom als eerste in de medische literatuur beschreven heeft in 1981. Pr. Dr. P.G. Barth is momenteel als kinderneuroloog verbonden aan het Emma Kinderziekenhuis / Academisch Medisch Centrum in Amsterdam. De informatie over het Barth Syndroom op deze website staat onder zijn supervisie. Op deze website vindt U informatie over: Symptomen 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. Diagnose, ziekteverloop en behandeling Hier wordt beschreven hoe de diagnose vastgesteld wordt, hoe de ziekte verloopt en welke behandelingen mogelijk zijn. 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. Nuttige websites en adressen Een lijst van nuttige websites en adressen.

93. Gimenei >> Health >> Conditions_and_Diseases >> Rare_Disorders >> Barth_Syndrome Gimenei.com, Search for Scope All Words, Results per page 10. Request Timeout 2, http://www.gimenei.com/directory/top/Health/Conditions_and_Diseases/Rare_Disorde

Search for: Scope: All Words Any Word Phrase Results per page: Request Timeout: Search Depth: Gimenei Health Conditions and Diseases Rare Disorders Barth Syndrome Music: The Recorded Viola - Volume IV - This is a good recording, full of virtuoustic performances. There is a good representation of violist with recordings of Rivka Golani, Joseph De Pasquale, Yizhak Schotten, among others. However some very important violists are missing here. I hope there will be a volume five with recordings of Roberto Diaz, Robert Vernon, Cynthia Phelps, Burton Fine, Richard Fields and Patricia McCarty. Software: The Sims House Party Expansion Pack ( Mac ) - this game was bought for my niece and son.installed the game and it constantly shuts off.screen flickers,you can't use the keyboard correctly and then it just shuts off.they say it won't work with intel chipsets,well i have a via chipset and amd processor.so i guess they're wrong there.i'm using an ati radeon 9700 pro card,amd athlon 2200+ so there is plenty of power.tried the latest via and ati drivers with no help at all.don't waste your money and thank god i only wasted 9.99 at target.i also tried to totally clean the registry of all traces and it doesn't help.even a fresh install of xp didn't help.so there you have it.one last thing,there are no patches to download and support is like talking to a brick wall,except the wall might be more helpfull cause you can at least smash the cd off it. Software: Strawberry Shortcake Amazing Cookie Party - Very little educational value in this title. My daughter was bored after about 15 minutes. The whole underlying game is poorly planned and very disjointed. It was slapped together quickly to cash in on the name. The background music was the best part. For this price, perhaps it will kill a rainy afternoon and get your kid smiling. But don't expect much after that. I would highly recommend the I Spy series (only two now). They are much more engaging and kids get a sense of accomplishment AND learn in the process. Oh and if you have a mac, forget it. We couuldn't get past the start menu. We have PCs in the house - it was fine on them. But don't waste your energy if you are mac only.

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