000 | 01907 a2200541 4500 | ||
---|---|---|---|
005 | 20250516064548.0 | ||
264 | 0 | _c20130502 | |
008 | 201305s 0 0 eng d | ||
022 | _a1522-1709 | ||
024 | 7 |
_a10.1007/s11325-011-0614-x _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBittencourt, Lia Rita Azeredo | |
245 | 0 | 0 |
_aLate-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report. _h[electronic resource] |
260 |
_bSleep & breathing = Schlaf & Atmung _cDec 2012 |
||
300 |
_a951-5 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aContinuous Positive Airway Pressure |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aDNA Repeat Expansion _xgenetics |
650 | 0 | 4 | _aFollow-Up Studies |
650 | 0 | 4 |
_aHomeodomain Proteins _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aHypoventilation _xcongenital |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aPatient Compliance |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aPolysomnography |
650 | 0 | 4 | _aRecurrence |
650 | 0 | 4 |
_aRespiratory Distress Syndrome, Newborn _xdiagnosis |
650 | 0 | 4 |
_aSleep Apnea, Central _xdiagnosis |
650 | 0 | 4 | _aTracheotomy |
650 | 0 | 4 |
_aTranscription Factors _xgenetics |
700 | 1 | _aPedrazzoli, Mario | |
700 | 1 | _aYagihara, Fabiana | |
700 | 1 | _aLuz, Gabriela Pontes | |
700 | 1 | _aGarbuio, Silvério | |
700 | 1 | _aMoreira, Gustavo Antonio | |
700 | 1 | _aPerfeito, João Aléssio J | |
700 | 1 | _aTufik, Sergio | |
773 | 0 |
_tSleep & breathing = Schlaf & Atmung _gvol. 16 _gno. 4 _gp. 951-5 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1007/s11325-011-0614-x _zAvailable from publisher's website |
999 |
_c21329391 _d21329391 |