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Results 1 - 10 for Johann PompeJohann Pompe - Wikipedia, the free encyclopediaJoannes Cassianus Pompe (1901-1945) was a Dutch pathologist. [1] He characterized the condition now known as Glycogen storage disease type II in 1932. [2] http://wiki.healthhaven.com/Johann_Pompe open pop Glycogen storage disease type II - Wikipedia, the free encyclopedia The disease is named after Johann Pompe, who characterized it in 1932. [1] [2] ... Their recommendation was to provide funding to treat a very small subset of Pompe ... http://wiki.healthhaven.com/Pompe open pop Glycogen storage disease type II: Definition from Answers.com The disease is named after Johann Pompe, who characterized it in 1932. [1] [2] ... Pompe's disease is one of the infiltrative causes of restrictive cardiomyopathy. http://www.answers.com/topic/pompe-s-disease open pop Pompe disease definition - Medical Dictionary definitions of popular ... It is named for a Dutch physician, Johann Cassianius Pompe. Last Editorial Review: 4/25/2000. Common Misspellings: pompe diease, pompe desease http://www.medterms.com/script/main/art.asp?articlekey=11417 open pop MDA / Quest Vol 16 No 1 / Myozyme Rescued Lives Credit for the first accurate description of Pompe (pronounced either “pom-PAY” or “POM-puh”) disease is generally given to Dutch pathologist Johann Pompe. http://www.mda.org/publications/Quest/q161RescuedLives.html open pop Orphan Drugs Doctoral Seminar Pompe disease • First described by Johann Pompe in 1932. • Infantile, or early onset – Noticed shortly after birth – Symptoms: severe lack of muscle tone, weakness, enlarged ... http://www.scribd.com/doc/6461612/Orphan-Drugs-Doctoral-Seminar open pop Update of the Pompe disease mutation database with...[Hum Mutat. 2008 ... PubMed is a service of the U.S. National Library of Medicine that includes over 18 million citations from MEDLINE and other life science journals for biomedical articles back to ... http://www.ncbi.nlm.nih.gov/pubmed/18425781 open pop Fabry Disease: History In 1898, two physicians – Johann Fabry in Germany, and William Anderson in England ... General information: Gaucher Disease: Fabry Disease: MPS I Disease: Pompe Disease http://www.lysomed.be/hcp/fabry/lyso_hcp_fa_history_en.asp open pop Li Jennifer[au] - PubMed Result 14: Smith PB, Benjamin DK Jr, Murphy MD, Johann-Liang R, Iyasu S, Gould B, Califf RM, Li ... after enzyme replacement therapy with acid alpha-glucosidase for infants with Pompe ... http://www.ncbi.nlm.nih.gov/pubmed?term=Li+Jennifer[au] open pop Fabry Disease MPS I: Pompe ... disease, was first described independently by Drs. William Anderson in England and Johann ... http://www.lysomed.be/hcp/fabry/lyso_hcp_fa_intro_en.asp open pop |
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