Titre : Mixed function oxygenases

Mixed function oxygenases : Questions médicales fréquentes

Termes MeSH sélectionnés :

Data Collection
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"Question", "name": "Quels tests sont utilisés pour évaluer l'activité des oxydases ?", "position": 2, "acceptedAnswer": { "@type": "Answer", "text": "Des tests de métabolisme des médicaments et des analyses biochimiques sont utilisés." } }, { "@type": "Question", "name": "Les tests génétiques sont-ils utiles pour ces enzymes ?", "position": 3, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les tests génétiques peuvent identifier des mutations affectant l'activité enzymatique." } }, { "@type": "Question", "name": "Quels symptômes peuvent indiquer une anomalie enzymatique ?", "position": 4, "acceptedAnswer": { "@type": "Answer", "text": "Des symptômes comme la toxicité médicamenteuse ou des réactions indésirables peuvent survenir." } }, { "@type": "Question", "name": "Comment les antécédents médicaux aident-ils au diagnostic ?", "position": 5, "acceptedAnswer": { "@type": "Answer", "text": "Les antécédents d'exposition à des médicaments ou toxines peuvent orienter le diagnostic." } }, { "@type": "Question", "name": "Quels sont les symptômes d'une déficience en oxydases ?", "position": 6, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes incluent des réactions médicamenteuses imprévues et une toxicité accrue." } }, { "@type": "Question", "name": "Peut-on observer des symptômes neurologiques ?", "position": 7, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des symptômes neurologiques peuvent survenir en raison d'une accumulation de toxines." } }, { "@type": "Question", "name": "Les symptômes varient-ils selon les individus ?", "position": 8, "acceptedAnswer": { "@type": "Answer", "text": "Oui, la gravité et le type de symptômes peuvent varier selon la génétique et l'environnement." } }, { "@type": "Question", "name": "Quels signes cliniques sont associés à une suractivité enzymatique ?", "position": 9, "acceptedAnswer": { "@type": "Answer", "text": "Une suractivité peut entraîner une dégradation rapide des médicaments et des effets secondaires." } }, { "@type": "Question", "name": "Les symptômes peuvent-ils être confondus avec d'autres maladies ?", "position": 10, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les symptômes peuvent ressembler à ceux d'autres maladies métaboliques ou hépatiques." } }, { "@type": "Question", "name": "Comment prévenir les dysfonctionnements des oxydases ?", "position": 11, "acceptedAnswer": { "@type": "Answer", "text": "Éviter l'exposition à des médicaments et toxines connus pour affecter ces enzymes." } }, { "@type": "Question", "name": "L'éducation des patients est-elle importante ?", "position": 12, "acceptedAnswer": { "@type": "Answer", "text": "Oui, informer les patients sur les risques liés aux médicaments est essentiel pour la prévention." } }, { "@type": "Question", "name": "Les bilans de santé réguliers aident-ils ?", "position": 13, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des bilans réguliers peuvent détecter précocement des anomalies enzymatiques." } }, { "@type": "Question", "name": "Les habitudes alimentaires influencent-elles la fonction enzymatique ?", "position": 14, "acceptedAnswer": { "@type": "Answer", "text": "Oui, une alimentation équilibrée peut soutenir la santé enzymatique et métabolique." } }, { "@type": "Question", "name": "Les vaccinations ont-elles un impact sur la fonction enzymatique ?", "position": 15, "acceptedAnswer": { "@type": "Answer", "text": "Certaines vaccinations peuvent influencer le métabolisme, mais les effets varient." } }, { "@type": "Question", "name": "Quels traitements sont disponibles pour les dysfonctionnements enzymatiques ?", "position": 16, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements incluent des ajustements médicamenteux et des thérapies de soutien." } }, { "@type": "Question", "name": "Les suppléments peuvent-ils aider à la fonction enzymatique ?", "position": 17, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certains suppléments peuvent améliorer la fonction enzymatique, selon le cas." } }, { "@type": "Question", "name": "Comment la pharmacogénétique influence-t-elle le traitement ?", "position": 18, "acceptedAnswer": { "@type": "Answer", "text": "La pharmacogénétique permet de personnaliser les traitements en fonction du profil enzymatique." } }, { "@type": "Question", "name": "Les traitements sont-ils différents pour les enfants et les adultes ?", "position": 19, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les dosages et les choix de médicaments peuvent varier entre enfants et adultes." } }, { "@type": "Question", "name": "Des thérapies géniques sont-elles envisagées ?", "position": 20, "acceptedAnswer": { "@type": "Answer", "text": "Des recherches sont en cours sur les thérapies géniques pour corriger les déficiences enzymatiques." } }, { "@type": "Question", "name": "Quelles complications peuvent survenir avec une dysfonction enzymatique ?", "position": 21, "acceptedAnswer": { "@type": "Answer", "text": "Des complications incluent des réactions médicamenteuses graves et des maladies hépatiques." } }, { "@type": "Question", "name": "Les complications sont-elles réversibles ?", "position": 22, "acceptedAnswer": { "@type": "Answer", "text": "Certaines complications peuvent être réversibles avec un traitement approprié, d'autres non." } }, { "@type": "Question", "name": "Comment les complications affectent-elles la qualité de vie ?", "position": 23, "acceptedAnswer": { "@type": "Answer", "text": "Les complications peuvent réduire la qualité de vie en limitant les options de traitement." } }, { "@type": "Question", "name": "Les complications sont-elles plus fréquentes chez certains groupes ?", "position": 24, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines populations peuvent être plus à risque en raison de facteurs génétiques." } }, { "@type": "Question", "name": "Les complications peuvent-elles être prévenues ?", "position": 25, "acceptedAnswer": { "@type": "Answer", "text": "Certaines complications peuvent être évitées par une surveillance et un traitement précoce." } }, { "@type": "Question", "name": "Quels sont les principaux facteurs de risque pour les dysfonctionnements enzymatiques ?", "position": 26, "acceptedAnswer": { "@type": "Answer", "text": "Les facteurs incluent des antécédents familiaux, l'exposition à des toxines et certains médicaments." } }, { "@type": "Question", "name": "L'âge influence-t-il le risque de dysfonctionnement ?", "position": 27, "acceptedAnswer": { "@type": "Answer", "text": "Oui, le risque peut augmenter avec l'âge en raison de changements métaboliques." } }, { "@type": "Question", "name": "Les maladies chroniques augmentent-elles le risque ?", "position": 28, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines maladies chroniques peuvent affecter la fonction enzymatique et augmenter le risque." } }, { "@type": "Question", "name": "Le mode de vie joue-t-il un rôle dans le risque ?", "position": 29, "acceptedAnswer": { "@type": "Answer", "text": "Oui, un mode de vie malsain, comme une mauvaise alimentation, peut augmenter le risque." } }, { "@type": "Question", "name": "Les interactions médicamenteuses sont-elles un facteur de risque ?", "position": 30, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines interactions médicamenteuses peuvent altérer l'activité des oxydases à fonction mixte." } } ] } ] }

Sous-catégories

25 au total
└─

Benzoate 4-monooxygenase

Benzoate 4-Monooxygenase D050565 - D08.811.682.690.708.062
└─

Catechol oxidase

Catechol Oxidase D004156 - D08.811.682.690.708.125
└─

Dopamine beta-monooxygenase

Dopamine beta-Hydroxylase D004299 - D08.811.682.690.708.292
└─

Fatty acid desaturases

Fatty Acid Desaturases D044943 - D08.811.682.690.708.392
└─

gamma-butyrobetaine dioxygenase

gamma-Butyrobetaine Dioxygenase D050563 - D08.811.682.690.708.401
└─

Heme oxygenase (decyclizing)

Heme Oxygenase (Decyclizing) D006419 - D08.811.682.690.708.410
└─

4-Hydroxybenzoate 3-monooxygenase

4-Hydroxybenzoate-3-Monooxygenase D015109 - D08.811.682.690.708.425
└─

Kynurenine 3-monooxygenase

Kynurenine 3-Monooxygenase D050601 - D08.811.682.690.708.557
└─

Phenylalanine 4-monooxygenase

Phenylalanine Hydroxylase D010651 - D08.811.682.690.708.601
└─

Procollagen-lysine, 2-oxoglutarate 5-dioxygenase

Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase D008240 - D08.811.682.690.708.660
└─

Prolyl hydroxylases

Prolyl Hydroxylases D064828 - D08.811.682.690.708.694
└─

Prostaglandin-endoperoxide synthases

Prostaglandin-Endoperoxide Synthases D011451 - D08.811.682.690.708.715
└─

Squalene monooxygenase

Squalene Monooxygenase D050603 - D08.811.682.690.708.749
└─

Trans-cinnamate 4-monooxygenase

Trans-Cinnamate 4-Monooxygenase D050564 - D08.811.682.690.708.826
└─

Tryptophane 5-monooxygenase

Tryptophan Hydroxylase D014365 - D08.811.682.690.708.870
└─

Vitamin K epoxide reductases

Vitamin K Epoxide Reductases D064417 - D08.811.682.690.708.961
└─└─

Monophenol monooxygenase

Monophenol Monooxygenase D014442 - D08.811.682.690.708.125.500
└─└─

beta-Carotene 15,15'-monooxygenase

beta-Carotene 15,15'-Monooxygenase D050559 - D08.811.682.690.708.392.312
└─└─

Delta-5 fatty acid desaturase

Delta-5 Fatty Acid Desaturase D000090943 - D08.811.682.690.708.392.390
└─└─

Linoleoyl-CoA desaturase

Linoleoyl-CoA Desaturase D050602 - D08.811.682.690.708.392.468
└─└─

Acyl-(acyl-carrier-protein)desaturase

Stearoyl-CoA Desaturase D013230 - D08.811.682.690.708.392.625
└─└─

Heme oxygenase-1

Heme Oxygenase-1 D051547 - D08.811.682.690.708.410.500
└─└─

Hypoxia-inducible factor-proline dioxygenases

Hypoxia-Inducible Factor-Proline Dioxygenases D064799 - D08.811.682.690.708.694.500
└─└─

Procollagen-Proline Dioxygenase

Procollagen-Proline Dioxygenase D011393 - D08.811.682.690.708.694.750
└─└─└─

7-Alkoxycoumarin O-dealkylase

7-Alkoxycoumarin O-Dealkylase D015660 - D08.811.682.690.708.170.010.024

Sources (10000 au total)

User perspectives on systematic data collection regarding back pain managed in general practice - a qualitative study.

Back pain is a main driver of disability and the most prevalent reason why people in Demark visit a general practitioner (GP). However, little is known about back pain management in primary care. For ... We applied an adapted exploratory sequential design using focus groups and individual interviews. Seven GPs and ten patients with back pain participated, and four focus groups and seventeen individual... Both GPs and patients with back pain found that 1) recruitment to a cohort should take place through the GPs, 2) the heterogeneity of patients with back pain and their need for individualized treatmen... GPs and patients with back pain both considered the nationwide cohort with the overall aim to investigate back pain management as being extremely relevant in relation to improve t the patient pathway....

Harmonization of maternal balanced energy-protein supplementation studies for individual participant data (IPD) meta-analyses - finding and creating similarities in variables and data collection.

Public health and clinical recommendations are established from systematic reviews and retrospective meta-analyses combining effect sizes, traditionally, from aggregate data and more recently, using i... We developed an initiative including seven clinical intervention studies of balanced energy-protein (BEP) supplementation during pregnancy and/or lactation that are being conducted (or recently conclu... We have fostered extensive communication between investigators from different studies, and importantly, created a large set of harmonized variable definitions within a prospective meta-analysis framew...

Retrospective dataset and survey analyses identify gaps in data collection for craniopharyngioma and priorities of patients and families affected by the disease.

Craniopharyngioma is a rare, low-grade tumor located in the suprasellar region of the brain, near critical structures like the pituitary gland. Here, we concurrently investigate the status of clinical... Clinical, genomic, and outcome data for a retrospective cohort of patients with craniopharyngioma were collected and reviewed through the Children's Brain Tumor Network (CBTN) database. An anonymous s... The CBTN repository revealed a large proportion of patients (40 - 70%) with specimens that are available for sequencing but lacked relevant quality of life (QoL) and functional outcomes. Frequencies o... This work highlights the importance of prospective collection of QoL and functional metrics alongside robust clinical and molecular correlates in individuals with craniopharyngioma. Such comprehensive...

Beyond standard data collection - the promise and potential of BRAIN (Brain tumour Registry Australia INnovation and translation registry).

Real-world data (RWD) is increasingly being embraced as an invaluable source of information to address clinical and policy-relevant questions that are unlikely to ever be answered by clinical trials. ... BRAIN was designed by a panel of clinicians in conjunction with BIOGRID to capture comprehensive clinical data on patients diagnosed with brain tumours from diagnosis through treatment to recurrence o... Between February 2021 and December 2021, a total of 350 new patients from 10 sites, including one private and two regional, were entered into BRAIN. Additionally, BRAIN supports the world's first regi... Here we report on the first data collection effort in brain tumours for Australia, which we believe to be unique worldwide given the number of sites and patients involved and the extent to which the r...