000 | 01227 a2200337 4500 | ||
---|---|---|---|
005 | 20250515195511.0 | ||
264 | 0 | _c20100401 | |
008 | 201004s 0 0 eng d | ||
022 | _a1521-0669 | ||
024 | 7 |
_a10.3109/08880010903116413 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aDemirel, Nihal | |
245 | 0 | 0 |
_aSevere purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation. _h[electronic resource] |
260 |
_bPediatric hematology and oncology _cNov 2009 |
||
300 |
_a597-600 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Letter | ||
650 | 0 | 4 | _aHomozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMethylenetetrahydrofolate Reductase (NADPH2) _xgenetics |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 |
_aProtein C Deficiency _xgenetics |
650 | 0 | 4 |
_aPurpura Fulminans _xetiology |
700 | 1 | _aBas, Ahmet Yagmur | |
700 | 1 | _aOkumus, Nurullah | |
700 | 1 | _aZenciroglu, Ayşegul | |
700 | 1 | _aYarali, Nese | |
773 | 0 |
_tPediatric hematology and oncology _gvol. 26 _gno. 8 _gp. 597-600 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.3109/08880010903116413 _zAvailable from publisher's website |
999 |
_c19337599 _d19337599 |