المؤلفون: Rashidghamat, Elham, Kadiyirire, Tendai, Ayis, Salma, Petrof, Gabriela, Liu, Lu, Pullabhatla, Venu, Ainali, Chrysanthi, Guy, Alyson, Aristodemou, S, McMillan, James R., Ozoemena, L, Mee, John, Pramanik, Rashida, Saxena, Alka, Nuamah, Rosamond, de Rinaldis, Emanuele, Serrano, Sonia, Maurin, Clarisse, Martinez-Queipo, Magdalena, Lwin, Su, Ilic, Dusko, Martinez, Anna E., Dazzi, Francesco, Slaper-Cortenbach, Ineke, Westinga, Kasper, Zeddies, Sabrina, van den Broek, Marcel, Onoufriadis, Alexandros, Mellerio, J, McGrath, John A.

المصدر: Rashidghamat , E , Kadiyirire , T , Ayis , S , Petrof , G , Liu , L , Pullabhatla , V , Ainali , C , Guy , A , Aristodemou , S , McMillan , J R , Ozoemena , L , Mee , J , Pramanik , R , Saxena , A , Nuamah , R , de Rinaldis , E , Serrano , S , Maurin , C , Martinez-Queipo , M , Lwin , S , Ilic , D , Martinez , A E , Dazzi , F , Slaper-Cortenbach , I , ....

مصطلحات موضوعية: BM-MSC, RDEB, epidermolysis bullosa, mesenchymal stromal cells

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/970f9dbe-ddea-4328-bfab-c8e1ec205517

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/970f9dbe-ddea-4328-bfab-c8e1ec205517
https://doi.org/10.1016/j.jaad.2019.11.038

المؤلفون: Vahidnezhad, H., Youssefian, L., Saeidian, A.H., Mahmoudi, H., Touati, A., Abiri, M., Kajbafzadeh, A.-M., Aristodemou, S., Liu, L., McGrath, J.A., Ertel, A., Londin, E., Kariminejad, A., Zeinali, S., Fortina, P., Uitto, J.

مصطلحات موضوعية: WR Dermatology, QZ Pathology

Relation: Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Mahmoudi, H. and Touati, A. and Abiri, M. and Kajbafzadeh, A.-M. and Aristodemou, S. and Liu, L. and McGrath, J.A. and Ertel, A. and Londin, E. and Kariminejad, A. and Zeinali, S. and Fortina, P. and Uitto, J. (2018) Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biology, 66. pp. 22-33.

الاتاحة: http://eprints.iums.ac.ir/5875/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85035090558&doi=10.1016%2fj.matbio.2017.11.003&partnerID=40&md5=dcdcfeb264eaf9d2f6fdcf47e6a7b5cc

المؤلفون: Lee, J.Y.W., Liu, L., Hsu, C., Aristodemou, S., Ozoemena, L., Ogboli, M., Moss, C., Martinez, A.E., Mellerio, J.E., McGrath, J.

المصدر: Lee , J Y W , Liu , L , Hsu , C , Aristodemou , S , Ozoemena , L , Ogboli , M , Moss , C , Martinez , A E , Mellerio , J E & McGrath , J 2017 , ' 515 Mutations in KLHL24 add to the molecular heterogeneity of epidermolysis bullosa simplex : SID 2017 Annual Meeting Abstract SupplementSociety for Investigative Dermatology Annual Meeting ' , Journal of Investigative Dermatology , vol. 137 , no. 5, Supplement 1 , pp. S88 . https://doi.org/10.1016/j.jid.2017.02.535

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/515-mutations-in-klhl24-add-to-the-molecular-heterogeneity-of-epidermolysis-bullosa-simplex(da634e3a-3123-41cd-b4db-2ee8c328dfbc).html
https://doi.org/10.1016/j.jid.2017.02.535

المؤلفون: Mahmoodi, P, Aristodemou, S, Ransing, RS, Owen, N, Friswell, MI

المصدر: Proceedings of the Institution of Mechanical Engineers, Part C: Journal of Mechanical Engineering Science ; volume 231, issue 17, page 3093-3103 ; ISSN 0954-4062 2041-2983

الاتاحة: https://doi.org/10.1177/0954406216643110
https://journals.sagepub.com/doi/pdf/10.1177/0954406216643110
https://journals.sagepub.com/doi/full-xml/10.1177/0954406216643110

المؤلفون: Pohler, E., Cunningham, F., Sandilands, A., Cole, C., Digby, S., McMillan, J. R., Aristodemou, S., McGrath, J. A., Smith, F. J. D., Mclean, W. H. I., Munro, C. S., Zamiri, M.

المصدر: Pohler , E , Cunningham , F , Sandilands , A , Cole , C , Digby , S , McMillan , J R , Aristodemou , S , McGrath , J A , Smith , F J D , Mclean , W H I , Munro , C S & Zamiri , M 2015 , ' Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis ' British Journal of Dermatology , vol 173 , no. 5 , pp. 1292-1294 . DOI:10.1111/bjd.13895

مصطلحات موضوعية: /dk/atira/pure/subjectarea/asjc/2700/2708, Dermatology

وصف الملف: application/pdf

الاتاحة: http://discovery.dundee.ac.uk/portal/en/research/novel-autosomal-dominant-mutation-in-loricrin-presenting-as-prominent-ichthyosis(18741c42-709c-4ac4-a411-ac09c4eea738).html
https://doi.org/10.1111/bjd.13895
http://hdl.handle.net/10588/18741c42-709c-4ac4-a411-ac09c4eea738
http://discovery.dundee.ac.uk/ws/files/10292879/Pohler_et_al_2015_British_Journal_of_Dermatology.pdf
http://www.scopus.com/inward/record.url?scp=84939865188&partnerID=8YFLogxK

المؤلفون: Liu, L, Mellerio, J E, Martinez, A E, McMillan, J R, Aristodemou, S, Parsons, Madeline, McGrath, J A

المصدر: Liu , L , Mellerio , J E , Martinez , A E , McMillan , J R , Aristodemou , S , Parsons , M & McGrath , J A 2014 , ' Mutations in EXPH5 result in autosomal recessive inherited skin fragility ' , British Journal of Dermatology , vol. 170 , no. 1 , N/A , pp. 196-199 . https://doi.org/10.1111/bjd.12723

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/bcd8a256-2688-44d1-8c12-263901df2eb1
https://doi.org/10.1111/bjd.12723

المؤلفون: Lwin, SM, Syed, F, Di, W-L, Kadiyirire, T, Liu, L, Guy, A, Petrova, A, Abdul-Wahab, A, Reid, F, Phillips, R, Elstad, M, Georgiadis, C, Aristodemou, S, Lovell, PA, McMillan, JR, Mee, J, Miskinyte, S, Titeux, M, Ozoemena, L, Pramanik, R, Serrano, S, Rowles, R, Maurin, C, Orrin, E, Martinez-Queipo, M, Rashidghamat, E, Tziotzios, C, Onoufriadis, A, Chen, M, Chan, L, Farzaneh, F, Del Rio, M, Tolar, J, Bauer, JW, Larcher, F, Antoniou, MN, Hovnanian, A, Thrasher, AJ, Mellerio, JE, Qasim, W, McGrath, JA

المصدر: 19 ; 1

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Medicine, Research & Experimental, Research & Experimental Medicine, REAL-TIME PCR, VII COLLAGEN, CELL THERAPY, SKIN, COL7A1, TRANSPLANTATION, KERATINOCYTES, EXPRESSION, INJECTION, DIAGNOSIS, Dermatology, Gene therapy, Genetic diseases, Genetics

Relation: JCI insight; http://hdl.handle.net/10044/1/74451

الاتاحة: http://hdl.handle.net/10044/1/74451
https://doi.org/10.1172/jci.insight.126243

المؤلفون: Takeichi, T., Nanda, A., Aristodemou, S., McMillan, J. R., Lee, J., Akiyama, M., Al-Ajmi, H., Simpson, M. A., McGrath, J. A.

المصدر: Takeichi , T , Nanda , A , Aristodemou , S , McMillan , J R , Lee , J , Akiyama , M , Al-Ajmi , H , Simpson , M A & McGrath , J A 2015 , ' Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family ' , British Journal of Dermatology , vol. 172 , no. 5 , pp. 1407-1411 . https://doi.org/10.1111/bjd.13473

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/3b2fe7fd-34ec-4d2a-aca0-c3b590d4da36
https://doi.org/10.1111/bjd.13473
http://www.scopus.com/inward/record.url?scp=84929131073&partnerID=8YFLogxK

المؤلفون: Takeichi, T, Nanda, A, Liu, L, Aristodemou, S, McMillan, J R, Sugiura, K, Akiyama, M, Al-Ajmi, H, Simpson, M A, McGrath, J A

المصدر: Takeichi , T , Nanda , A , Liu , L , Aristodemou , S , McMillan , J R , Sugiura , K , Akiyama , M , Al-Ajmi , H , Simpson , M A & McGrath , J A 2015 , ' Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait ' , British Journal of Dermatology , vol. 172 , no. 2 , pp. 527-31 . https://doi.org/10.1111/bjd.13294

مصطلحات موضوعية: Blister, Carrier Proteins, Codon, Nonsense, Consanguinity, Cytoskeletal Proteins, Epidermolysis Bullosa Simplex, Female, Foot Dermatoses, Founder Effect, Genotype, Hand Dermatoses, Heterozygote, Homozygote, Humans, Kuwait, Male, Nerve Tissue Proteins, Pedigree, Phenotype, Recurrence

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/founder-mutation-in-dystonine-underlying-autosomal-recessive-epidermolysis-bullosa-simplex-in-kuwait(eca4cb14-d991-42bd-8224-07ba3cfadb70).html
https://doi.org/10.1111/bjd.13294

المؤلفون: Kyriacou, K, Michael, T, Zenios, A, Aristodemou, S, Papacharalambous, R, Kyriakides, T

مصطلحات موضوعية: 9th Congress of the Mediterranean Society of Myology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmc_________::1e28e81512304de28189a31afd15c684
https://europepmc.org/articles/PMC2859661/

المؤلفون: Richardson, C C, Jensen, R, Aristodemou, S, Taylor, P D, Poston, L, Christie, M R

المصدر: Richardson , C C , Jensen , R , Aristodemou , S , Taylor , P D , Poston , L & Christie , M R 2005 , ' Reduced pancreatic insulin content in offspring of rats fed high saturated fat during pregnancy ' , Diabetologia , vol. 48 , pp. 486 .

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/8377fd00-7851-47b4-b015-d3f8f350d1d1

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/8377fd00-7851-47b4-b015-d3f8f350d1d1

المؤلفون: Mahmoodi, P., Aristodemou, S., Ransing, R. S., Owen, N., Friswell, M. I.

المصدر: Proceedings of the Institution of Mechanical Engineers, Part C: Journal of Mechanical Engineering Science (Sage Publications, Ltd.); Sep2017, Vol. 231 Issue 17, p3093-3103, 11p

المؤلفون: Takeichi, T., Nanda, A., Liu, L., Aristodemou, S., McMillan, J.R., Sugiura, K., Akiyama, M., Al ‐ Ajmi, H., Simpson, M.A., McGrath, J.A.

المصدر: British Journal of Dermatology; Feb2015, Vol. 172 Issue 2, p527-531, 5p

مصطلحات موضوعية: GENETIC mutation, DYSTONIN, EPIDERMOLYSIS bullosa, BLISTERS, SKIN diseases

المؤلفون: Liu, L., Mellerio, J.E., Martinez, A.E., McMillan, J.R., Aristodemou, S., Parsons, M., McGrath, J.A.

المصدر: British Journal of Dermatology; Jan2014, Vol. 170 Issue 1, p196-199, 4p

مصطلحات موضوعية: SKIN diseases, AUTOSOMAL recessive polycystic kidney, GENETIC mutation, KERATINOCYTES, IMMUNOCYTOCHEMISTRY, GENETIC polymorphisms

المؤلفون: Lee, J.Y.W., Liu, L., Hsu, C., Aristodemou, S., Ozoemena, L., Ogboli, M., Moss, C., Martinez, A.E., Mellerio, J.E., McGrath, J.

المصدر: Journal of Investigative Dermatology; May 2017, Vol. 137 Issue: 5, Number 5 Supplement 1 pS88-S88, 1p