| pubmed-article:11223846 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11223846 | lifeskim:mentions | umls-concept:C0337514 | lld:lifeskim |
| pubmed-article:11223846 | lifeskim:mentions | umls-concept:C0949595 | lld:lifeskim |
| pubmed-article:11223846 | lifeskim:mentions | umls-concept:C0349588 | lld:lifeskim |
| pubmed-article:11223846 | lifeskim:mentions | umls-concept:C0220981 | lld:lifeskim |
| pubmed-article:11223846 | lifeskim:mentions | umls-concept:C0034897 | lld:lifeskim |
| pubmed-article:11223846 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:11223846 | pubmed:dateCreated | 2001-3-6 | lld:pubmed |
| pubmed-article:11223846 | pubmed:abstractText | Gonadal (ovarian) dysgenesis in 46,XX individuals is genetically heterogeneous. We report on two sisters who, in addition to primary ovarian failure, have marked short stature and recurrent episodes of dehydration with metabolic acidosis. Studies performed during one of these episodes suggested mitochondrial dysfunction; however, results of biochemical analysis of electron transport chain activity in skeletal muscle and mitochondrial DNA studies were normal. We discuss the phenotype in relation to previously described conditions of 46,XX gonadal dysgenesis. We suggest this constellation of findings represents a new syndrome. | lld:pubmed |
| pubmed-article:11223846 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11223846 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11223846 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11223846 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11223846 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:11223846 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11223846 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11223846 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11223846 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:11223846 | pubmed:issn | 0148-7299 | lld:pubmed |
| pubmed-article:11223846 | pubmed:author | pubmed-author:VladutiuG DGD | lld:pubmed |
| pubmed-article:11223846 | pubmed:author | pubmed-author:ZemelSS | lld:pubmed |
| pubmed-article:11223846 | pubmed:author | pubmed-author:PoberB RBR | lld:pubmed |
| pubmed-article:11223846 | pubmed:author | pubmed-author:HisamaF MFM | lld:pubmed |
| pubmed-article:11223846 | pubmed:author | pubmed-author:CherniskeE... | lld:pubmed |
| pubmed-article:11223846 | pubmed:copyrightInfo | Copyright 2001 Wiley-Liss, Inc. | lld:pubmed |
| pubmed-article:11223846 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11223846 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:11223846 | pubmed:volume | 98 | lld:pubmed |
| pubmed-article:11223846 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11223846 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11223846 | pubmed:pagination | 121-4 | lld:pubmed |
| pubmed-article:11223846 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:meshHeading | pubmed-meshheading:11223846... | lld:pubmed |
| pubmed-article:11223846 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11223846 | pubmed:articleTitle | 46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters. | lld:pubmed |
| pubmed-article:11223846 | pubmed:affiliation | Department of Neurology, Yale University School of Medicine, New Haven, CT 06510, USA. | lld:pubmed |
| pubmed-article:11223846 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11223846 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:11223846 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:11223846 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
