By Icon Health Publications
ISBN-10: 0497004496
ISBN-13: 9780497004491
ISBN-10: 1417556617
ISBN-13: 9781417556618
It is a 3-in-1 reference e-book. It provides an entire scientific dictionary overlaying countless numbers of phrases and expressions on the subject of Gaucher ailment. It additionally provides vast lists of bibliographic citations. eventually, it offers info to clients on how you can replace their wisdom utilizing quite a few web assets. The publication is designed for physicians, scientific scholars getting ready for Board examinations, clinical researchers, and sufferers who are looking to familiarize yourself with learn devoted to Gaucher affliction. in the event that your time is efficacious, this ebook is for you. First, you won't waste time looking the web whereas lacking loads of correct info. moment, the booklet additionally saves you time indexing and defining entries. ultimately, you won't waste time and cash printing hundreds of thousands of websites.
Read or Download Gaucher Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References PDF
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Extra resources for Gaucher Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References
Example text
Author(s): Hodson P, Goldblatt J, Beighton P. Source: Archives of Disease in Childhood. 1979 September; 54(9): 707-9. cmd=Retrieve&db=pubmed&dopt=A bstract&list_uids=518109 • Non-pseudogene-derived complex acid beta-glucosidase mutations causing mild type 1 and severe type 2 Gaucher disease. Author(s): Grace ME, Ashton-Prolla P, Pastores GM, Soni A, Desnick RJ. Source: The Journal of Clinical Investigation. 1999 March; 103(6): 817-23. cmd=Retrieve&db=pubmed&dopt=A bstract&list_uids=10079102 • Norrbottnian type of Gaucher disease--clinical, biochemical and molecular biology aspects: successful treatment with bone marrow transplantation.
Cmd=Retrieve&db=pubmed&dopt=A bstract&list_uids=8982958 • Neuronopathic juvenile glucosylceramidosis due to sap-C deficiency: clinical course, neuropathology and brain lipid composition in this Gaucher disease variant. Author(s): Pampols T, Pineda M, Giros ML, Ferrer I, Cusi V, Chabas A, Sanmarti FX, Vanier MT, Christomanou H. Source: Acta Neuropathologica. 1999 January; 97(1): 91-7. cmd=Retrieve&db=pubmed&dopt=A bstract&list_uids=9930900 • Neuropathology of the Norrbottnian type of Gaucher disease.
Cmd=Retrieve&db=pubmed&dopt=A bstract&list_uids=11600137 • Mutation analysis of type II Gaucher disease in five Taiwanese children: identification of two novel mutations. Author(s): Tsai FJ, Lee CC, Wu MC, Lin SP, Lin CY, Tsai CH, Kodama H, Wu JY. Source: Acta Paediatr Taiwan. 2001 July-August; 42(4): 231-5. cmd=Retrieve&db=pubmed&dopt=A bstract&list_uids=11550412 Studies 41 • Mutation prevalence among 51 unrelated Spanish patients with Gaucher disease: identification of 11 novel mutations. Author(s): Alfonso P, Cenarro A, Perez-Calvo JI, Giralt M, Giraldo P, Pocovi M.
Gaucher Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by Icon Health Publications
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