There are indications that preexisting mitochondrial disorders or beta-oxidation defects
predispose for propofol infusion syndrome. This review aimed at investigating if propofol …

This review aims at summarizing and discussing previous and recent findings concerning
the cerebral manifestations of mitochondrial disorders (MIDs). MIDs frequently present as …

RESUMO A escolha do tipo de anestésico a ser utilizado em pacientes com variações
genéticas requer um estudo detalhado das alterações genéticas e monitoramento constante …

SUPPLEMENT NR. 2 | 2021 ANÄSTHESIOLOGIE & INTENSIVMEDIZIN Page 1 O ffizielles
Organ: Deutsche Gesellschaft für Anästhesiologie und Intensivmedizin eV (DGAI) Berufsverband …

El objetivo de este estudio de caso fue conocer el tratamiento odontológico integral bajo
anestesia general de un paciente con encefalopatía necrosante subaguda o enfermedad …

Leigh syndrome (LS) is an extremely rare neurodegenerative disease with multi-organ
involvement; and is associated with genetic abnormalities, which affect mitochondrial …

Leigh sendromu nadir görülen bir infant ve çocukluk dönemi hastalığıdır. Hastalık;
nörodejenerasyon, subakut nekrotizan ensefalomiyelopati ile progresyon göstermekte ve …

Leigh syndrome is a rare inherited neurodegenerative disorder of infancy and childhood
and is characterized by developmental delay of nervous system function and respiratory …

抄録 Leigh 脳症に対する開腹による胃瘻造設術の全身麻酔を経験した. 症例は 33 歳男性, 2 歳 5
ヵ月で Leigh 脳症と診断され, 4 歳で気管切開術を受け, 人工呼吸管理を継続して …

抄録 Leigh encephalopathy (LE) is a clinical subtype of mitochondrial encephalomyopathy
characterized by delayed development of psychomotor functions and regression from …