| pubmed-article:12105778 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12105778 | lifeskim:mentions | umls-concept:C0008059 | lld:lifeskim |
| pubmed-article:12105778 | lifeskim:mentions | umls-concept:C0005961 | lld:lifeskim |
| pubmed-article:12105778 | lifeskim:mentions | umls-concept:C0035222 | lld:lifeskim |
| pubmed-article:12105778 | lifeskim:mentions | umls-concept:C0398689 | lld:lifeskim |
| pubmed-article:12105778 | lifeskim:mentions | umls-concept:C0449450 | lld:lifeskim |
| pubmed-article:12105778 | lifeskim:mentions | umls-concept:C0439608 | lld:lifeskim |
| pubmed-article:12105778 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:12105778 | pubmed:dateCreated | 2002-7-9 | lld:pubmed |
| pubmed-article:12105778 | pubmed:abstractText | We describe a 10-month-old boy diagnosed with X-linked hyper-IgM syndrome (XHIM) after suffering from life-threatening acute respiratory distress syndrome (ARDS) caused by Pneumocystis carinii pneumonia (PCP), although his previous clinical history and first level laboratory tests investigating immunological function did not indicate immunodeficiency. When the patient's overall condition was good, elective bone marrow transplantation from an HLA-matched older brother was performed successfully. We describe how correct diagnosis and successful treatment were made possible thanks to the involvement of a network of specialists. | lld:pubmed |
| pubmed-article:12105778 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12105778 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12105778 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:12105778 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12105778 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12105778 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12105778 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:12105778 | pubmed:issn | 0268-3369 | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:TommasiniAA | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:VenturaAA | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:LeoniJJ | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:CampelloCC | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:AndolinaMM | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:NotarangeloL... | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:RuntiGG | lld:pubmed |
| pubmed-article:12105778 | pubmed:author | pubmed-author:De... | lld:pubmed |
| pubmed-article:12105778 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12105778 | pubmed:volume | 30 | lld:pubmed |
| pubmed-article:12105778 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12105778 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12105778 | pubmed:pagination | 49-52 | lld:pubmed |
| pubmed-article:12105778 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:meshHeading | pubmed-meshheading:12105778... | lld:pubmed |
| pubmed-article:12105778 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12105778 | pubmed:articleTitle | Elective bone marrow transplantation in a child with X-linked hyper-IgM syndrome presenting with acute respiratory distress syndrome. | lld:pubmed |
| pubmed-article:12105778 | pubmed:affiliation | Department of Pediatrics IRCCS Burlo Garofolo, University of Trieste, Trieste, Italy. | lld:pubmed |
| pubmed-article:12105778 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12105778 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:12105778 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
