المؤلفون: Charlton R

المصدر: Therapeutics and Clinical Risk Management, Vol 2012, Iss default, Pp 173-179 (2012)

مصطلحات موضوعية: Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: http://www.dovepress.com/optimal-management-of-giant-cell-arteritis-and-polymyalgia-rheumatica-a9640; https://doaj.org/toc/1176-6336; https://doaj.org/toc/1178-203X

URL الوصول: https://doaj.org/article/27740a16c9c94352850b900daa43b091

المؤلفون: Pfeiffer, Kathryn M., Brod, Meryl, Smith, Alden, Gianettoni, Jill, Viuff, Dorthe, Ota, Sho, Charlton, R. Will

المصدر: Quality of Life Research, 2021 Jan 01. 30(1), 203-219.

URL الوصول: https://www.jstor.org/stable/48750740

المؤلفون: Ellard S, Morgan S, Wynn SL, Walker S, Parrish A, Mein R, Juett A, Ahn JW, Berry I, Cassidy E-J, Durkie M, Fish L, Hall R, Howard E, Rankin J, Wright CF, Deans ZC, Scott RH, Hill SL, Baple EL, Taylor RW, Baty D, Berg J, Blair E, Bowdin S, Bownass L, Bradley T, Campbell J, Charlton R, Clouston P, Constantinou P, Cooper N, Delon I, Downes K, Ellis D, Elmslie F, Ghali N, Hagan R, Heggarty S, Higgs J, Hunt D, Jenkins L, McAnulty C, McCann E, McDevitt T, McMullan D, Miedzybrodzka Z, Moore D, Newman W, O'Sullivan D, Parker M, Porteous M, Ramsden S, Rea G, Ruddy D, Ryan G, Sarkar A, Sheridan E, Short J, Thomas E, Thomas S, Varghese V, Vasudevan P, Wakeling E, Williams A, Wright M

المصدر: Journal of Medical Genetics, 2024

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/301579; https://eprints.ncl.ac.uk/fulltext.aspx?url=301579/293258B2-88BF-418F-9A6C-4E0F9F01F96E.pdf&pub_id=301579

الاتاحة: https://eprints.ncl.ac.uk/301579

المؤلفون: Torenvliet, C, Groenman, A P, Van der Burg, E, Charlton, R C, Hamilton, C J, Geurts, H M

المصدر: Torenvliet , C , Groenman , A P , Van der Burg , E , Charlton , R C , Hamilton , C J & Geurts , H M 2024 , ' Memory strategies in autistic and older adults ' , Autism Research , vol. 17 , no. 10 , pp. 2092-2104 . https://doi.org/10.1002/aur.3195

الاتاحة: https://research.vu.nl/en/publications/32227985-18ff-4432-9706-1a0ddeac7a6f
https://doi.org/10.1002/aur.3195
https://hdl.handle.net/1871.1/32227985-18ff-4432-9706-1a0ddeac7a6f

المؤلفون: O'Nions, E, Brown, J, Buckman, JEJ, Charlton, R, Cooper, C, El Baou, C, Happé, F, Hoare, S, Lewer, D, Manthorpe, J, McKechnie, DGJ, Richards, M, Saunders, R, Mandy, W, Stott, J

Relation: The Lancet Regional Health - Europe; https://qmro.qmul.ac.uk/xmlui/handle/123456789/97572

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/97572
https://doi.org/10.1016/j.lanepe.2024.100907

المؤلفون: O'Nions, E, Lewer, D, Petersen, I, Brown, J, Buckman, JEJ, Charlton, R, Cooper, C, El Baou, C, Happé, F, Manthorpe, J, McKechnie, DGJ, Richards, M, Saunders, R, Zanker, C, Mandy, W, Stott, J

مصطلحات موضوعية: Autism, Intellectual disability, Life expectancy, Premature mortality

وصف الملف: 100776 - ?

Relation: Lancet Reg Health Eur; https://qmro.qmul.ac.uk/xmlui/handle/123456789/97560

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/97560
https://doi.org/10.1016/j.lanepe.2023.100776

المؤلفون: Hany, U., Watson, C.M., Liu, L., Smith, C.E.L., Harfoush, A., Poulter, J.A., Nikolopoulos, G., Balmer, R., Brown, C.J., Patel, A., Simmonds, J., Charlton, R., Acosta de Camargo, M.G., Rodd, H.D., Jafri, H., Antanaviciute, A., Moffat, M., Al-Jawad, M., Inglehearn, C.F., Mighell, A.J.

وصف الملف: text

Relation: https://eprints.whiterose.ac.uk/205978/1/jmg-2023-109510.full.pdf; Hany, U. orcid.org/0000-0002-4486-1625 , Watson, C.M. orcid.org/0000-0003-2371-1844 , Liu, L. et al. (17 more authors) (2024) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics, 61 (4). pp. 347-355. ISSN 0022-2593

الاتاحة: https://eprints.whiterose.ac.uk/205978/

المؤلفون: Hany U, Watson CM, Liu L, Smith CEL, Harfoush A, Poulter JA, Nikolopoulos G, Balmer R, Brown CJ, Patel A, Simmonds J, Charlton R, Acosta De Camargo MG, Rodd HD, Jafri H, Antanaviciute A, Moffat M, Al-Jawad M, Inglehearn CF, Mighell AJ

المصدر: Journal of Medical Genetics, 2023

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/295346; https://eprints.ncl.ac.uk/fulltext.aspx?url=295346/C773BABC-AAEE-4FFF-B679-3C580E1A97BF.pdf&pub_id=295346

الاتاحة: https://eprints.ncl.ac.uk/295346

المؤلفون: ONions, E, Petersen, I, Buckman, JEJ, Charlton, R, Cooper, C, Corbett, A, Happe, F, Manthorpe, J, Richards, M, Saunders, R, Zanker, C, Mandy, W, Stott, J

مصطلحات موضوعية: Autism spectrum condition, Primary care, Underdiagnosis, Under-diagnosis, Incidence, Prevalence

Relation: LANCET REGIONAL HEALTH-EUROPE; ARTN 100626; https://qmro.qmul.ac.uk/xmlui/handle/123456789/92394

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/92394
https://doi.org/10.1016/j.lanepe.2023.100626

المؤلفون: Hany, U., Watson, C.M., Liu, L., Smith, C.E.L., Harfoush, A., Poulter, J.A., Nikolopoulos, G., Balmer, R., Brown, C.J., Patel, A., Simmonds, J., Charlton, R., Acosta de Camargo, M.G., Rodd, H.D., Jafri, H., Antanaviciute, A., Moffat, M., Al-Jawad, M., Inglehearn, C.F., Mighell, A.J.

وصف الملف: text

Relation: https://eprints.whiterose.ac.uk/207220/1/jmg-2023-109510.full.pdf; Hany, U. orcid.org/0000-0002-4486-1625 , Watson, C.M. orcid.org/0000-0003-2371-1844 , Liu, L. et al. (17 more authors) (2023) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics. ISSN 0022-2593

الاتاحة: https://eprints.whiterose.ac.uk/207220/
https://eprints.whiterose.ac.uk/207220/1/jmg-2023-109510.full.pdf

المؤلفون: Khattab, Ahmed, Charlton, R. Will

المصدر: Frontiers in Endocrinology ; volume 14 ; ISSN 1664-2392

الاتاحة: http://dx.doi.org/10.3389/fendo.2023.1127558
https://www.frontiersin.org/articles/10.3389/fendo.2023.1127558/full

المؤلفون: Torenvliet, C., Groenman, A. P., Van der Burg, E., Charlton, R. C., Hamilton, C. J., Geurts, H. M.

المصدر: Autism Research: Official Journal of the International Society for Autism Research; Oct2024, Vol. 17 Issue 10, p2092-2104, 13p

المؤلفون: Andoni, T, Wiggins, J, Robinson, R, Charlton, R, Sandberg, M, Eeles, R

المساهمون: Eeles, Rosalind

مصطلحات موضوعية: Humans, Neoplasms, Genetic Predisposition to Disease, Incidence, Risk Assessment, Retrospective Studies, Genetic Counseling, Germ-Line Mutation, Adolescent, Adult, Aged, 80 and over, Middle Aged, State Medicine, England, Female, Male, Young Adult, Genetic Testing, Biomarkers, Tumor

وصف الملف: Electronic; ?; application/pdf

Relation: Scientific reports, 2022, 12 (1), pp. 2507 - ?; https://repository.icr.ac.uk/handle/internal/5104

الاتاحة: https://repository.icr.ac.uk/handle/internal/5104
https://doi.org/10.1038/s41598-022-06376-4

المؤلفون: Breinholt, Vibeke Miller, Mygind, Per Holse, Christoffersen, Eva Dam, Zhang, Ying, Ota, Sho, Will Charlton, R., Viuff, Dorthe

المصدر: British Journal of Clinical Pharmacology ; volume 88, issue 11, page 4763-4772 ; ISSN 0306-5251 1365-2125

الاتاحة: http://dx.doi.org/10.1111/bcp.15369
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bcp.15369
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/bcp.15369
https://bpspubs.onlinelibrary.wiley.com/doi/pdf/10.1111/bcp.15369

المؤلفون: Geurts, H.M., Charlton, R., Bishop, L.

المساهمون: Putnam, M., Bigby, C.

المصدر: Geurts , H M , Charlton , R & Bishop , L 2021 , Ageing when Being Autistic . in M Putnam & C Bigby (eds) , Handbook on Ageing with Disability . Routledge handbooks , New York , pp. 148-157 . https://doi.org/10.4324/9780429465352-13

وصف الملف: application/pdf

Relation: https://dare.uva.nl/personal/pure/en/publications/ageing-when-being-autistic(82690f32-4fdb-4570-b8b9-268293d21f98).html; urn:ISBN:9781138611498

الاتاحة: https://dare.uva.nl/personal/pure/en/publications/ageing-when-being-autistic(82690f32-4fdb-4570-b8b9-268293d21f98).html
https://doi.org/10.4324/9780429465352-13
https://hdl.handle.net/11245.1/82690f32-4fdb-4570-b8b9-268293d21f98
https://pure.uva.nl/ws/files/76023881/10.4324_9780429465352_13_chapterpdf.pdf
http://www.scopus.com/inward/record.url?scp=85106929869&partnerID=8YFLogxK

المؤلفون: Pfeiffer, Kathryn M., Brod, Meryl, Smith, Alden, Viuff, Dorthe, Ota, Sho, Charlton, R. Will

المصدر: American Journal of Medical Genetics Part A ; volume 188, issue 2, page 454-462 ; ISSN 1552-4825 1552-4833

الاتاحة: https://doi.org/10.1002/ajmg.a.62534
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62534
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/ajmg.a.62534

المؤلفون: Pfeiffer, Kathryn M., Brod, Meryl, Smith, Alden, Viuff, Dorthe, Ota, Sho, Charlton, R. Will

المساهمون: Ascendis Pharma Growth Disorders, A/S

المصدر: Orphanet Journal of Rare Diseases ; volume 16, issue 1 ; ISSN 1750-1172

الاتاحة: http://dx.doi.org/10.1186/s13023-021-01978-z
https://link.springer.com/content/pdf/10.1186/s13023-021-01978-z.pdf
https://link.springer.com/article/10.1186/s13023-021-01978-z/fulltext.html

المؤلفون: Saggers, R T, Charlton, R, Nongena, P, Velaphi, S C

المصدر: South African Journal of Child Health ; volume 15, issue 4, page 224-225 ; ISSN 1994-3032 1999-7671

الاتاحة: http://dx.doi.org/10.7196/sajch.2021.v15i4.1815

المؤلفون: Topf, A., Bengoechea, R., Duff, J., Charlton, R., Mroczek, M., Garcia, S. Kapetanovic, Dominguez, C., Alsaman, A., Findlay, A., Ravenscroft, G., Weihl, C., Straub, V.

المصدر: Neuromuscular Disorders ; volume 31, page S160 ; ISSN 0960-8966

الاتاحة: http://dx.doi.org/10.1016/j.nmd.2021.07.389
https://api.elsevier.com/content/article/PII:S0960896621005769?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0960896621005769?httpAccept=text/plain

المؤلفون: Beckemeyer, R J, Charlton, R E

المساهمون: BioStor

المصدر: 111:84-96

URL الوصول: http://www.biodiversitylibrary.org/part/15154