Titre : One-carbon group transferases

One-carbon group transferases : Questions médicales fréquentes

Questions fréquentes et termes MeSH associés

Diagnostic 5

#1

Comment diagnostiquer une déficience en transférases un-carbon ?

Des tests sanguins et des analyses génétiques peuvent identifier des déficiences enzymatiques.
Déficience enzymatique Tests sanguins
#2

Quels tests sont utilisés pour évaluer l'activité des transférases ?

Des tests enzymatiques spécifiques mesurent l'activité des transférases dans des échantillons biologiques.
Tests enzymatiques Échantillons biologiques
#3

Quels symptômes peuvent indiquer un problème avec ces enzymes ?

Des symptômes comme la fatigue, des troubles neurologiques ou des anomalies métaboliques peuvent survenir.
Symptômes Troubles neurologiques
#4

Les tests génétiques sont-ils nécessaires pour le diagnostic ?

Oui, les tests génétiques peuvent confirmer des mutations associées aux déficiences enzymatiques.
Tests génétiques Mutations
#5

Peut-on utiliser l'imagerie pour diagnostiquer des troubles liés ?

L'imagerie peut aider à évaluer des complications, mais n'est pas spécifique pour ces enzymes.
Imagerie médicale Complications

Symptômes 5

#1

Quels sont les symptômes d'une déficience en transférases un-carbon ?

Les symptômes incluent fatigue, troubles cognitifs, et anomalies de croissance.
Fatigue Troubles cognitifs
#2

Les troubles neurologiques sont-ils fréquents ?

Oui, des troubles neurologiques peuvent survenir en raison d'un métabolisme altéré.
Troubles neurologiques Métabolisme
#3

Y a-t-il des symptômes digestifs associés ?

Des troubles digestifs comme des nausées ou des vomissements peuvent se manifester.
Troubles digestifs Nausées
#4

Les symptômes varient-ils selon l'âge ?

Oui, les symptômes peuvent varier en fonction de l'âge et de la gravité de la déficience.
Âge Gravité
#5

Des anomalies cutanées peuvent-elles se produire ?

Certaines anomalies cutanées peuvent être observées, mais elles ne sont pas spécifiques.
Anomalies cutanées Symptômes

Prévention 5

#1

Peut-on prévenir les déficiences en transférases un-carbon ?

Certaines déficiences peuvent être évitées par une nutrition adéquate et un suivi médical.
Prévention Nutrition
#2

Les femmes enceintes doivent-elles se soucier de ces enzymes ?

Oui, une carence en nutriments essentiels peut affecter le développement fœtal.
Femmes enceintes Développement fœtal
#3

Des tests de dépistage sont-ils recommandés ?

Des tests de dépistage peuvent être recommandés pour les familles à risque.
Dépistage Familles à risque
#4

L'éducation nutritionnelle est-elle importante ?

Oui, l'éducation nutritionnelle peut aider à prévenir les carences et à promouvoir la santé.
Éducation nutritionnelle Carences
#5

Les suppléments sont-ils nécessaires pour tous ?

Non, les suppléments ne sont nécessaires que pour ceux qui présentent des risques spécifiques.
Suppléments Risques spécifiques

Traitements 5

#1

Quels traitements sont disponibles pour ces déficiences ?

Les traitements incluent des suppléments nutritionnels et des thérapies ciblées.
Suppléments nutritionnels Thérapies ciblées
#2

La thérapie génique est-elle une option ?

La thérapie génique est en recherche, mais pas encore largement disponible pour ces déficiences.
Thérapie génique Recherche
#3

Les modifications alimentaires peuvent-elles aider ?

Oui, des régimes spécifiques peuvent aider à gérer les symptômes et améliorer la santé.
Modifications alimentaires Régimes spécifiques
#4

Des médicaments sont-ils prescrits pour ces conditions ?

Des médicaments peuvent être prescrits pour traiter des symptômes spécifiques ou des complications.
Médicaments Complications
#5

Y a-t-il des traitements expérimentaux disponibles ?

Des essais cliniques peuvent offrir des traitements expérimentaux pour certaines déficiences.
Essais cliniques Traitements expérimentaux

Complications 5

#1

Quelles complications peuvent survenir avec ces déficiences ?

Des complications incluent des troubles neurologiques, des problèmes de croissance et des malformations.
Complications Troubles neurologiques
#2

Les complications sont-elles réversibles ?

Certaines complications peuvent être réversibles avec un traitement précoce et approprié.
Réversibilité Traitement précoce
#3

Y a-t-il un risque accru de maladies chroniques ?

Oui, les déficiences peuvent augmenter le risque de maladies métaboliques chroniques.
Maladies chroniques Risque accru
#4

Les complications affectent-elles la qualité de vie ?

Oui, les complications peuvent significativement affecter la qualité de vie des patients.
Qualité de vie Complications
#5

Des soins palliatifs sont-ils nécessaires dans certains cas ?

Oui, des soins palliatifs peuvent être nécessaires pour gérer des symptômes graves.
Soins palliatifs Symptômes graves

Facteurs de risque 5

#1

Quels sont les facteurs de risque pour ces déficiences ?

Les facteurs incluent des antécédents familiaux, des régimes alimentaires pauvres et des maladies métaboliques.
Facteurs de risque Antécédents familiaux
#2

L'âge joue-t-il un rôle dans le risque ?

Oui, certains risques augmentent avec l'âge, notamment pour les maladies métaboliques.
Âge Maladies métaboliques
#3

Les habitudes alimentaires influencent-elles le risque ?

Oui, une alimentation déséquilibrée peut augmenter le risque de déficiences enzymatiques.
Habitudes alimentaires Risque
#4

Les facteurs environnementaux sont-ils significatifs ?

Oui, l'exposition à certains toxines peut influencer le risque de déficiences.
Facteurs environnementaux Toxines
#5

Les maladies génétiques augmentent-elles le risque ?

Oui, des maladies génétiques peuvent prédisposer les individus à des déficiences en transférases.
Maladies génétiques Prédisposition
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expérimentaux disponibles ?", "url": "https://questionsmedicales.fr/mesh/D019875#section-traitements" }, { "@type": "MedicalWebPage", "name": "Complications", "headline": "Complications sur One-carbon group transferases", "description": "Quelles complications peuvent survenir avec ces déficiences ?\nLes complications sont-elles réversibles ?\nY a-t-il un risque accru de maladies chroniques ?\nLes complications affectent-elles la qualité de vie ?\nDes soins palliatifs sont-ils nécessaires dans certains cas ?", "url": "https://questionsmedicales.fr/mesh/D019875#section-complications" }, { "@type": "MedicalWebPage", "name": "Facteurs de risque", "headline": "Facteurs de risque sur One-carbon group transferases", "description": "Quels sont les facteurs de risque pour ces déficiences ?\nL'âge joue-t-il un rôle dans le risque ?\nLes habitudes alimentaires influencent-elles le risque ?\nLes facteurs environnementaux sont-ils significatifs ?\nLes maladies génétiques augmentent-elles le risque ?", "url": "https://questionsmedicales.fr/mesh/D019875#section-facteurs de risque" } ] }, { "@type": "FAQPage", "mainEntity": [ { "@type": "Question", "name": "Comment diagnostiquer une déficience en transférases un-carbon ?", "position": 1, "acceptedAnswer": { "@type": "Answer", "text": "Des tests sanguins et des analyses génétiques peuvent identifier des déficiences enzymatiques." } }, { "@type": "Question", "name": "Quels tests sont utilisés pour évaluer l'activité des transférases ?", "position": 2, "acceptedAnswer": { "@type": "Answer", "text": "Des tests enzymatiques spécifiques mesurent l'activité des transférases dans des échantillons biologiques." } }, { "@type": "Question", "name": "Quels symptômes peuvent indiquer un problème avec ces enzymes ?", "position": 3, "acceptedAnswer": { "@type": "Answer", "text": "Des symptômes comme la fatigue, des troubles neurologiques ou des anomalies métaboliques peuvent survenir." } }, { "@type": "Question", "name": "Les tests génétiques sont-ils nécessaires pour le diagnostic ?", "position": 4, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les tests génétiques peuvent confirmer des mutations associées aux déficiences enzymatiques." } }, { "@type": "Question", "name": "Peut-on utiliser l'imagerie pour diagnostiquer des troubles liés ?", "position": 5, "acceptedAnswer": { "@type": "Answer", "text": "L'imagerie peut aider à évaluer des complications, mais n'est pas spécifique pour ces enzymes." } }, { "@type": "Question", "name": "Quels sont les symptômes d'une déficience en transférases un-carbon ?", "position": 6, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes incluent fatigue, troubles cognitifs, et anomalies de croissance." } }, { "@type": "Question", "name": "Les troubles neurologiques sont-ils fréquents ?", "position": 7, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des troubles neurologiques peuvent survenir en raison d'un métabolisme altéré." } }, { "@type": "Question", "name": "Y a-t-il des symptômes digestifs associés ?", "position": 8, "acceptedAnswer": { "@type": "Answer", "text": "Des troubles digestifs comme des nausées ou des vomissements peuvent se manifester." } }, { "@type": "Question", "name": "Les symptômes varient-ils selon l'âge ?", "position": 9, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les symptômes peuvent varier en fonction de l'âge et de la gravité de la déficience." } }, { "@type": "Question", "name": "Des anomalies cutanées peuvent-elles se produire ?", "position": 10, "acceptedAnswer": { "@type": "Answer", "text": "Certaines anomalies cutanées peuvent être observées, mais elles ne sont pas spécifiques." } }, { "@type": "Question", "name": "Peut-on prévenir les déficiences en transférases un-carbon ?", "position": 11, "acceptedAnswer": { "@type": "Answer", "text": "Certaines déficiences peuvent être évitées par une nutrition adéquate et un suivi médical." } }, { "@type": "Question", "name": "Les femmes enceintes doivent-elles se soucier de ces enzymes ?", "position": 12, "acceptedAnswer": { "@type": "Answer", "text": "Oui, une carence en nutriments essentiels peut affecter le développement fœtal." } }, { "@type": "Question", "name": "Des tests de dépistage sont-ils recommandés ?", "position": 13, "acceptedAnswer": { "@type": "Answer", "text": "Des tests de dépistage peuvent être recommandés pour les familles à risque." } }, { "@type": "Question", "name": "L'éducation nutritionnelle est-elle importante ?", "position": 14, "acceptedAnswer": { "@type": "Answer", "text": "Oui, l'éducation nutritionnelle peut aider à prévenir les carences et à promouvoir la santé." } }, { "@type": "Question", "name": "Les suppléments sont-ils nécessaires pour tous ?", "position": 15, "acceptedAnswer": { "@type": "Answer", "text": "Non, les suppléments ne sont nécessaires que pour ceux qui présentent des risques spécifiques." } }, { "@type": "Question", "name": "Quels traitements sont disponibles pour ces déficiences ?", "position": 16, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements incluent des suppléments nutritionnels et des thérapies ciblées." } }, { "@type": "Question", "name": "La thérapie génique est-elle une option ?", "position": 17, "acceptedAnswer": { "@type": "Answer", "text": "La thérapie génique est en recherche, mais pas encore largement disponible pour ces déficiences." } }, { "@type": "Question", "name": "Les modifications alimentaires peuvent-elles aider ?", "position": 18, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des régimes spécifiques peuvent aider à gérer les symptômes et améliorer la santé." } }, { "@type": "Question", "name": "Des médicaments sont-ils prescrits pour ces conditions ?", "position": 19, "acceptedAnswer": { "@type": "Answer", "text": "Des médicaments peuvent être prescrits pour traiter des symptômes spécifiques ou des complications." } }, { "@type": "Question", "name": "Y a-t-il des traitements expérimentaux disponibles ?", "position": 20, "acceptedAnswer": { "@type": "Answer", "text": "Des essais cliniques peuvent offrir des traitements expérimentaux pour certaines déficiences." } }, { "@type": "Question", "name": "Quelles complications peuvent survenir avec ces déficiences ?", "position": 21, "acceptedAnswer": { "@type": "Answer", "text": "Des complications incluent des troubles neurologiques, des problèmes de croissance et des malformations." } }, { "@type": "Question", "name": "Les complications sont-elles réversibles ?", "position": 22, "acceptedAnswer": { "@type": "Answer", "text": "Certaines complications peuvent être réversibles avec un traitement précoce et approprié." } }, { "@type": "Question", "name": "Y a-t-il un risque accru de maladies chroniques ?", "position": 23, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les déficiences peuvent augmenter le risque de maladies métaboliques chroniques." } }, { "@type": "Question", "name": "Les complications affectent-elles la qualité de vie ?", "position": 24, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les complications peuvent significativement affecter la qualité de vie des patients." } }, { "@type": "Question", "name": "Des soins palliatifs sont-ils nécessaires dans certains cas ?", "position": 25, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des soins palliatifs peuvent être nécessaires pour gérer des symptômes graves." } }, { "@type": "Question", "name": "Quels sont les facteurs de risque pour ces déficiences ?", "position": 26, "acceptedAnswer": { "@type": "Answer", "text": "Les facteurs incluent des antécédents familiaux, des régimes alimentaires pauvres et des maladies métaboliques." } }, { "@type": "Question", "name": "L'âge joue-t-il un rôle dans le risque ?", "position": 27, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certains risques augmentent avec l'âge, notamment pour les maladies métaboliques." } }, { "@type": "Question", "name": "Les habitudes alimentaires influencent-elles le risque ?", "position": 28, "acceptedAnswer": { "@type": "Answer", "text": "Oui, une alimentation déséquilibrée peut augmenter le risque de déficiences enzymatiques." } }, { "@type": "Question", "name": "Les facteurs environnementaux sont-ils significatifs ?", "position": 29, "acceptedAnswer": { "@type": "Answer", "text": "Oui, l'exposition à certains toxines peut influencer le risque de déficiences." } }, { "@type": "Question", "name": "Les maladies génétiques augmentent-elles le risque ?", "position": 30, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des maladies génétiques peuvent prédisposer les individus à des déficiences en transférases." } } ] } ] }
Dr Olivier Menir

Contenu validé par Dr Olivier Menir

Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale


Validation scientifique effectuée le 26/08/2026

Contenu vérifié selon les dernières recommandations médicales

Sous-catégories

39 au total
└─

Amidinotransferases

Amidinotransferases D000579 - D08.811.913.555.150
└─

Carboxyl and carbamoyl transferases

Carboxyl and Carbamoyl Transferases D019878 - D08.811.913.555.275
└─

Hydroxymethyl et formyl transferases

Hydroxymethyl and Formyl Transferases D019877 - D08.811.913.555.400
└─

Methyltransferases

Methyltransferases D008780 - D08.811.913.555.500
└─└─

Aspartate carbamoyltransferase

Aspartate Carbamoyltransferase D001221 - D08.811.913.555.275.200
└─└─

Ornithine carbamoyltransferase

Ornithine Carbamoyltransferase D009954 - D08.811.913.555.275.600
└─└─

Aminomethyltransferase

Aminomethyltransferase D050960 - D08.811.913.555.400.100
└─└─

Glutamate formimidoyltransferase

Glutamate Formimidoyltransferase D051042 - D08.811.913.555.400.300
└─└─

Glycine hydroxymethyltransferase

Glycine Hydroxymethyltransferase D012696 - D08.811.913.555.400.500
└─└─

Phosphoribosylaminoimidazolecarboxamide formyltransferase

Phosphoribosylaminoimidazolecarboxamide Formyltransferase D051027 - D08.811.913.555.400.625
└─└─

Phosphoribosylglycinamide formyltransferase

Phosphoribosylglycinamide Formyltransferase D051026 - D08.811.913.555.400.750
└─└─

Acetylserotonin O-Methyltransferase

Acetylserotonin O-Methyltransferase D000121 - D08.811.913.555.500.100
└─└─

Betaine-homocysteine S-methyltransferase

Betaine-Homocysteine S-Methyltransferase D050940 - D08.811.913.555.500.175
└─└─

Catechol O-methyltransferase

Catechol O-Methyltransferase D002394 - D08.811.913.555.500.250
└─└─

DNA modification methylases

DNA Modification Methylases D015254 - D08.811.913.555.500.350
└─└─

Glycine N-methyltransferase

Glycine N-Methyltransferase D050938 - D08.811.913.555.500.387
└─└─

Guanidinoacetate N-methyltransferase

Guanidinoacetate N-Methyltransferase D050937 - D08.811.913.555.500.425
└─└─

Histamine N-methyltransferase

Histamine N-Methyltransferase D006637 - D08.811.913.555.500.500
└─└─

Homocysteine S-methyltransferase

Homocysteine S-Methyltransferase D050904 - D08.811.913.555.500.625
└─└─

5-Methyltetrahydrofolate-homocysteine s-methyltransferase

5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase D013766 - D08.811.913.555.500.645
└─└─

Nicotinamide N-methyltransferase

Nicotinamide N-Methyltransferase D050903 - D08.811.913.555.500.650
└─└─

Phenylethanolamine n-methyltransferase

Phenylethanolamine N-Methyltransferase D010625 - D08.811.913.555.500.700
└─└─

Phosphatidyl-N-methylethanolamine N-methyltransferase

Phosphatidyl-N-Methylethanolamine N-Methyltransferase D050941 - D08.811.913.555.500.710
└─└─

Phosphatidylethanolamine N-methyltransferase

Phosphatidylethanolamine N-Methyltransferase D050918 - D08.811.913.555.500.712
└─└─

Protein Methyltransferases

Protein Methyltransferases D011496 - D08.811.913.555.500.800
└─└─

Thymidylate synthase

Thymidylate Synthase D013940 - D08.811.913.555.500.862
└─└─

T-RNA methyltransferases

tRNA Methyltransferases D012359 - D08.811.913.555.500.925
└─└─└─

DNA-Cytosine Methylases

DNA-Cytosine Methylases D015257 - D08.811.913.555.500.350.100
└─└─└─

Site-specific DNA-methyltransferase (adenine-specific)

Site-Specific DNA-Methyltransferase (Adenine-Specific) D015265 - D08.811.913.555.500.350.700
└─└─└─

Histone méthyltransférases

Histone Methyltransferases D000076983 - D08.811.913.555.500.800.200
└─└─└─

O(6)-methylguanine-DNA methyltransferase

O(6)-Methylguanine-DNA Methyltransferase D019853 - D08.811.913.555.500.800.650
└─└─└─

Protein-arginine N-methyltransferases

Protein-Arginine N-Methyltransferases D011484 - D08.811.913.555.500.800.750
└─└─└─

Protein O-methyltransferase

Protein O-Methyltransferase D011497 - D08.811.913.555.500.800.800
└─└─└─

AlkB Homolog 8, tRNA methyltransferase

AlkB Homolog 8, tRNA Methyltransferase D000071503 - D08.811.913.555.500.925.500
└─└─└─└─

DNA (cytosine-5-)-methyltransferase

DNA (Cytosine-5-)-Methyltransferases D004248 - D08.811.913.555.500.350.100.500
└─└─└─└─

Site-Specific DNA-Methyltransferase (Cytosine-N(4)-Specific)

Site-Specific DNA-Methyltransferase (Cytosine-N4-Specific) D057265 - D08.811.913.555.500.350.100.750
└─└─└─└─

Histone-lysine N-methyltransferase

Histone-Lysine N-Methyltransferase D011495 - D08.811.913.555.500.800.200.500
└─└─└─└─

Protein D-aspartate-L-isoaspartate methyltransferase

Protein D-Aspartate-L-Isoaspartate Methyltransferase D026601 - D08.811.913.555.500.800.800.700
└─└─└─└─└─

DNA methyltransferase 3A

DNA Methyltransferase 3A D000090205 - D08.811.913.555.500.350.100.500.750

Auteurs principaux

Miyako Yamamoto

2 publications dans cette catégorie

Affiliations :
  • Laboratory of Immunohematology and Glycobiology, Josep Carreras Leukaemia Research Institute (IJC), Campus Can Ruti, Camí de les Escoles, Badalona, Barcelona, 08916, Spain.

Emili Cid

2 publications dans cette catégorie

Affiliations :
  • Laboratory of Immunohematology and Glycobiology, Josep Carreras Leukaemia Research Institute (IJC), Campus Can Ruti, Camí de les Escoles, Badalona, Barcelona, 08916, Spain.
  • Program of Predictive and Personalized Medicine of Cancer (PMPPC), Institut d'Investigació Germans Trias i Pujol (IGTP), Campus Can Ruti, Camí de les Escoles, Badalona, Barcelona, 08916, Spain.

Fumiichiro Yamamoto

2 publications dans cette catégorie

Affiliations :
  • Laboratory of Immunohematology and Glycobiology, Josep Carreras Leukaemia Research Institute (IJC), Campus Can Ruti, Camí de les Escoles, Badalona, Barcelona, 08916, Spain. fyamamoto@carrerasresearch.org.
  • Program of Predictive and Personalized Medicine of Cancer (PMPPC), Institut d'Investigació Germans Trias i Pujol (IGTP), Campus Can Ruti, Camí de les Escoles, Badalona, Barcelona, 08916, Spain. fyamamoto@carrerasresearch.org.

Jianguo Xu

2 publications dans cette catégorie

Affiliations :
  • College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing, Zhejiang 314001, P. R. China. jgxu0816@163.com.

Adam G Maynard

2 publications dans cette catégorie

Affiliations :
  • Department of Pathology, Boston Children's Hospital, Boston, Massachusetts, USA; Graduate Program in Biological and Biomedical Sciences, Harvard Medical School, Boston, Massachusetts, USA.
Publications dans "One-carbon group transferases" :

Naama Kanarek

2 publications dans cette catégorie

Affiliations :
  • Department of Pathology, Boston Children's Hospital, Boston, Massachusetts, USA; Harvard Medical School, Boston, Massachusetts, USA; The Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA. Electronic address: Naama.Kanarek@childrens.harvard.edu.
Publications dans "One-carbon group transferases" :

Nafisa M Jadavji

2 publications dans cette catégorie

Affiliations :
  • College of Veterinary Medicine, Midwestern University, Glendale, AZ 85308, USA.
  • Biomedical Sciences Program, Midwestern University, Glendale, AZ 85308, USA.
  • Department of Neuroscience, Carleton University, Ottawa, ON K1S 5B6, Canada.
Publications dans "One-carbon group transferases" :

Fabio Coppedè

2 publications dans cette catégorie

Affiliations :
  • Department of Translational Research and of New Surgical and Medical Technologies, University of Pisa, Via Roma 55, 56126, Pisa, Italy. Electronic address: fabio.coppede@med.unipi.it.
Publications dans "One-carbon group transferases" :

Zhaohui Huang

1 publication dans cette catégorie

Affiliations :
  • The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China.
Publications dans "One-carbon group transferases" :

Hui Chen

1 publication dans cette catégorie

Affiliations :
  • The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China. Electronic address: chenhui86@wust.edu.cn.
Publications dans "One-carbon group transferases" :

Lei Zhao

1 publication dans cette catégorie

Affiliations :
  • The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China; Department of Materials Science, School of Materials and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China. Electronic address: zhaolei@wust.edu.cn.
Publications dans "One-carbon group transferases" :

Wei Fang

1 publication dans cette catégorie

Affiliations :
  • The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China.
Publications dans "One-carbon group transferases" :

Xuan He

1 publication dans cette catégorie

Affiliations :
  • The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China.
Publications dans "One-carbon group transferases" :

Weixin Li

1 publication dans cette catégorie

Affiliations :
  • The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China.
Publications dans "One-carbon group transferases" :

Pan Tian

1 publication dans cette catégorie

Affiliations :
  • The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science & Technology, Wuhan 430081, PR China.
Publications dans "One-carbon group transferases" :

Logan Tenney

1 publication dans cette catégorie

Vanha N Pham

1 publication dans cette catégorie

Christopher J Chang

1 publication dans cette catégorie

David Fernández-Ramos

1 publication dans cette catégorie

Affiliations :
  • Precision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Technology Park of Bizkaia, 48160 Derio, Bizkaia, Spain.
Publications dans "One-carbon group transferases" :

Fernando Lopitz-Otsoa

1 publication dans cette catégorie

Affiliations :
  • Precision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Technology Park of Bizkaia, 48160 Derio, Bizkaia, Spain.
Publications dans "One-carbon group transferases" :

Sources (10000 au total)

One-to-one counselling and school attendance in the UK: a single group pre-post study.

Absence rates remain high in UK schools, with negative implications for attainment, life chances and inequality. Reasons for non-attendance are complex but include psychosocial factors. Few UK-based s... Secondary analysis of routine data, collected by a national mental health provider in primary and secondary schools.... 7405 pupils aged 4-19 years, with complete school attendance records at Time1 (pre-counselling term) and Time2 (the term when counselling ended).... All participants received school-based one-to-one counselling with a trained counsellor between August 2016 and December 2019.... Percentage of school sessions attended (continuous) and persistent absence (binary; attending ≤90% of sessions) in a term. Potential moderators included sociodemographics, mental health and school eng... Median Time1 attendance was 96%. 23.6% of participants were persistently absent. The intervention was not associated with improved percentage attendance (0.028%, 95% CI -0.160-0.216%) but was associat... One-to-one counselling may improve school attendance among persistently absent pupils, particularly at younger ages. Improving mental health and pupil engagement/enjoyment are potential intervention t...