전문 번역가, 번역 회사, 웹 페이지 및 자유롭게 사용할 수 있는 번역 저장소 등을 활용합니다.
upper hunter or
upper hunter jew
마지막 업데이트: 2014-11-14
사용 빈도: 2
품질:
hunter - hunter valley
hunter — hunter valley
마지막 업데이트: 2014-11-14
사용 빈도: 2
품질:
upper hunter valley or
upper hunter valley jew
마지막 업데이트: 2014-11-14
사용 빈도: 2
품질:
upper hunter river valley
upper hunter river valley
마지막 업데이트: 2014-11-14
사용 빈도: 2
품질:
elaprase is used to treat patients with hunter syndrome.
elaprase jintuża biex jikkura l-pazjenti bis-sindrome ta' hunter.
마지막 업데이트: 2017-04-26
사용 빈도: 1
품질:
it represents a source of income and contributes to the subsistence of the hunter.
tirrappreżenta sors ta’ dħul u tikkontribwixxi għall-għixien tal-kaċċatur.
마지막 업데이트: 2017-04-06
사용 빈도: 1
품질:
it replaces the enzyme that is missing or defective in patients with hunter syndrome.
din tissostitwixxi l-enzima li hi nieqsa jew difettuża fil-pazjenti bis-sindrome ta' hunter.
마지막 업데이트: 2017-04-26
사용 빈도: 1
품질:
jackie hunter (chair) (uk) ceo of oi pharma partners ltd.
jackie hunter (president) (uk) president ta' oi pharma partners ltd.
마지막 업데이트: 2017-04-06
사용 빈도: 1
품질:
abnormal behaviour or disturbance of the general condition of the live animal reported by the hunter;
aġir anormali jew disturb tal-kondizzjoni ġenerali ta' l-annimal ħaj irrappurtat mill-kaċċatur;
마지막 업데이트: 2014-10-18
사용 빈도: 2
품질:
patients with hunter syndrome do not produce an enzyme called iduronate-2-sulfatase.
pazjenti bis-sindrome ta' hunter ma jipproduċux enzima msejħa iduronate-2-sulfatase.
마지막 업데이트: 2017-04-26
사용 빈도: 1
품질:
this means that because hunter syndrome is rare, it has not been possible to obtain complete information about elaprase.
dan ifisser li billi s-sindrome ta' hunter huwa wieħed rari, ma kienx possibbli li jinkiseb tagħrif sħiħ dwar elaprase.
마지막 업데이트: 2017-04-26
사용 빈도: 1
품질:
2 jankovic j, hunter c, dolimbek bz, dolimbek gs, adler ch, brashear a, et al.
2 jankovic j, hunter c, dolimbek bz, dolimbek gs, adler ch, brashear a, et al.
마지막 업데이트: 2011-10-23
사용 빈도: 1
품질:
경고: 이 정렬은 잘못되었을 수 있습니다.
잘못된 경우 삭제해 주십시오.
hunter syndrome, which is also known as mucopolysaccharidosis ii, is a rare, inherited disease that primarily affects male patients.
is-sindrome ta' hunter, li huwa magħruf ukoll bħala mukopolisakkaridożi ii, huwa marda rari li tintiret li taffettwa primarjament lill-pazjenti rġiel.
마지막 업데이트: 2017-04-26
사용 빈도: 1
품질:
requirements are specified as to secure that the seal and/or the hunter is sufficiently stable and that the target can be properly visualised.
huma speċifikati rekwiżiti biex jiġi żgurat li l-foka u/jew il-kaċċatur ikunu stabbli biżżejjed u li l-mira tkun tista’ tiġi viżwalizzata kif xieraq.
마지막 업데이트: 2017-04-06
사용 빈도: 1
품질:
elaprase is indicated for the long-term treatment of patients with hunter syndrome (mucopolysaccharidosis ii, mps ii).
elaprase huwa indikat għat-trattament fuq tul ta’ żmien ta’ pazjenti bis-sindromu ta’ hunter (mucopolysaccharidosis ii, mps ii).
마지막 업데이트: 2017-04-26
사용 빈도: 3
품질:
hunter syndrome is an x-linked disease caused by insufficient levels of the lysosomal enzyme iduronate-2-sulfatase.
is-sindromu hunter huwa marda tat-tip x-linked ikkaġunata minn livelli insuffiċjenti ta’ l-enzima liżożomali iduronate-2-sulfatase.
마지막 업데이트: 2017-04-26
사용 빈도: 3
품질:
small numbers of wild game, unskinned or unplucked, and, in the case of small wild game, ineviscerated, supplied directly by the hunter to the consumer or to the retailer;
selvaġġina fi kwantitajiet zġħar, mhux imqaxxra jew imnittfa, u, fil-każ ta' selvaġġina żgħira, mhux imnaddfa, fornita direttament mill-kaċċatur lill-konsumatur jew lill-bejjiegħ bl-imnut;
마지막 업데이트: 2014-10-18
사용 빈도: 2
품질:
the hunter (either inuit/indigenous hunter or licensed hunter for resource management purposes) – having a unique identification number;
il-kaċċatur (jew kaċċatur inuit/indiġenu jew kaċċatur liċenzjat għal skopijiet ta’ ġestjoni tar-riżorsi) għandu jkollu numru ta’ identifikazzjoni uniku;
마지막 업데이트: 2017-04-06
사용 빈도: 1
품질:
elaprase is used as enzyme replacement therapy to treat hunter syndrome (mucopolysaccharidosis ii) when the level of iduronate-2-sulfatase in the body is lower than normal.
elaprase jintuża bħala terapija ta ’ sostituzzjoni ta ’ l- enzimi biex jitratta s- sindromu ta ’ hunter (mucopolysaccharidosis ii) meta l- livell ta ’ iduronate- 2- sulfatase fil- ġisem ikun iktar baxx mis- soltu.
마지막 업데이트: 2012-04-10
사용 빈도: 2
품질:
due to the missing or defective iduronate-2-sulfatase enzyme in patients with hunter syndrome, glycosaminoglycans progressively accumulate in the cells, leading to cellular engorgement, organomegaly, tissue destruction, and organ system dysfunction.
minħabba l-enzima iduronate-2-sulfatase nieqsa jew difettuża f’pazjenti bis- sindromu hunter, il-glycoaminoglycans jakkumulaw progressivament fiċ-ċelloli, u jwasslu għal nefħa ċellolari, organomegalija, qerda tat-tessuti, u funzjoni ħażina tas-sistema ta’ l-organi.
마지막 업데이트: 2017-04-26
사용 빈도: 3
품질: