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| pubmed-article:15328326 | lifeskim:mentions | umls-concept:C0030421 | lld:lifeskim |
| pubmed-article:15328326 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:15328326 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:15328326 | lifeskim:mentions | umls-concept:C1709982 | lld:lifeskim |
| pubmed-article:15328326 | lifeskim:mentions | umls-concept:C1419907 | lld:lifeskim |
| pubmed-article:15328326 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:15328326 | lifeskim:mentions | umls-concept:C2348519 | lld:lifeskim |
| pubmed-article:15328326 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:15328326 | pubmed:dateCreated | 2004-8-25 | lld:pubmed |
| pubmed-article:15328326 | pubmed:abstractText | Germline mutations of the genes encoding succinate dehydrogenase subunits B (SDHB) and D (SDHD) predispose to paraganglioma syndromes type 4 (PGL-4) and type 1 (PGL-1), respectively. In both syndromes, pheochromocytomas as well as head and neck paragangliomas occur; however, details for individual risks and other clinical characteristics are unknown. | lld:pubmed |
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| pubmed-article:15328326 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:15328326 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:15328326 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15328326 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:15328326 | pubmed:issn | 1538-3598 | lld:pubmed |
| pubmed-article:15328326 | pubmed:author | pubmed-author:SchipperJörgJ | lld:pubmed |
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| pubmed-article:15328326 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:15328326 | pubmed:day | 25 | lld:pubmed |
| pubmed-article:15328326 | pubmed:volume | 292 | lld:pubmed |
| pubmed-article:15328326 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15328326 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15328326 | pubmed:pagination | 943-51 | lld:pubmed |
| pubmed-article:15328326 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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| pubmed-article:15328326 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15328326 | pubmed:articleTitle | Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. | lld:pubmed |
| pubmed-article:15328326 | pubmed:affiliation | Department of Nephrology and Hypertension, Albert-Ludwigs-University, Freiburg, Germany. neumann@med1.ukl.uni-freiburg.de | lld:pubmed |
| pubmed-article:15328326 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15328326 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:15328326 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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