Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Sharif, Saghira Malik"'
Autor:
Malawsky, Daniel S., van Walree, Eva, Jacobs, Benjamin M., Heng, Teng Hiang, Huang, Qin Qin, Sabir, Ataf H., Rahman, Saadia, Sharif, Saghira Malik, Khan, Ahsan, Mirkov, Maša Umićević, Kuwahara, Hiroyuki, Gao, Xin, Alkuraya, Fowzan S., Posthuma, Danielle, Newman, William G., Griffiths, Christopher J., Mathur, Rohini, van Heel, David A., Finer, Sarah, O’Connell, Jared, Martin, Hilary C.
Publikováno v:
In Cell 12 October 2023 186(21):4514-4527
Autor:
Lee, Jeong Ho, Silhavy, Jennifer L., Lee, Ji Eun, Al-Gazali, Lihadh, Thomas, Sophie, Davis, Erica E., Bielas, Stephanie L., Hill, Kiley J., Iannicelli, Miriam, Brancati, Francesco, Gabriel, Stacey B., Russ, Carsten, Logan, Clare V., Sharif, Saghira Malik, Bennett, Christopher P., Abe, Masumi, Hildebrandt, Friedhelm, Diplas, Bill H., Attié-Bitach, Tania, Katsanis, Nicholas, Rajab, Anna, Koul, Roshan, Sztriha, Laszlo, Waters, Elizabeth R., Ferro-Novick, Susan, Woods, C. Geoffrey, Johnson, Colin A., Valente, Enza Maria, Zaki, Maha S., Gleeson, Joseph G.
Publikováno v:
Science, 2012 Feb . 335(6071), 966-969.
Externí odkaz:
http://dx.doi.org/10.1126/science.1213506
Akademický článek
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Autor:
Begum-Ali, Jannath, Kolesnik-Taylor, Anna, Quiroz, Isabel, Mason, Luke, Garg, Shruti, Green, Jonathan, Johnson, Mark H., Jones, Emily J. H., Holman, Rebecca, Kalwarowsky, Sarah, Pirazzoli, Laura, Taylor, Chloë, Vassallo, Grace, Burkitt-Wright, Emma, Eelloo, Judith, Evans, D. Gareth, West, Siobhan, Hupton, Eileen, Lewis, Lauren, Robinson, Louise, Dobbie, Angus, Drimer, Ruth, Sharif, Saghira Malik, Bethell, Helen, Jones, Rachel, Musson, Susan, Prem, Catherine, Splitt, Miranda, Horridge, Karen, Baralle, Diana, Redman, Carolyn, Tomkins, Helen
Background: Sensory modulation difficulties are common in children with conditions such as Autism Spectrum Disorder (ASD) and could contribute to other social and non-social symptoms. Positing a causal role for sensory processing differences requires
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6d2e42e2b50aad3ec54f4bc4f01b2ab
Autor:
Kolesnik, Anna May, Jones, Emily Jane Harrison, Garg, Shruti, Green, Jonathan, Charman, Tony, Johnson, Mark Henry, Baron-Cohen, Simon, Begum-Ali, Jannath, Bolton, Patrick, Cheung, Celeste, Dafner, Leila, Davies, Kim, Elsabbagh, Mayada, Fernandes, Janice, Fish, Laurel, Gammer, Isobel, Greensmith, Marian, Gliga, Teodora, Kalwarowsky, Sarah, Liew, Michelle, Pasco, Greg, Pickles, Andrew, Ribeiro, Helena, Salomone, Erica, Taylor, Chloe, Tucker, Leslie, Wass, Sam, Burkitt-Wright, Emma, Evans, D. Gareth, Vassallo, Grace, Eelloo, Judith, West, Siobhan, Howard, Elizabeth, Hupton, Eileen, Huson, Sue, Lewis, Lauren, Tricker, Karen, Dobbie, Angus, Drimer, Ruth, Sharif, Saghira Malik, Baralle, Diane, Redman, Carolyn, Sharif, Saba, Symth, Carolyn, Lam, Wayne, Bradbury, Alyson, Harrower, Neil, Quarrell, Oliver, Bethell, Helen, Jones, Rachel, Musson, Susan, Prem, Catherine, Splitt, Miranda, Horridge, Karen, Steiger, Christine, Jim, Carly
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-13 (2017)
Molecular Autism
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M 2017, ' Early development of infants with Neurofibromatosis Type 1 : A case series ', Molecular Autism, vol. 8, no. 62 . https://doi.org/10.1186/s13229-017-0178-0
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M H, Baron-Cohen, S, Begum-Ali, J, Bolton, P, Cheung, C, Dafner, L, Davies, K, Elsabbagh, M, Fernandes, J, Fish, L, Gammer, I, Greensmith, M, Gliga, T, Kalwarowsky, S, Liew, M, Pasco, G, Pickles, A, Ribeiro, H, Salomone, E, Taylor, C, Tucker, L, Wass, S, Burkitt-Wright, E, Evans, D G, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S M, Baralle, D, Redman, C, Sharif, S, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R & Eden-Basis Team 2017, ' Early development of infants with neurofibromatosis type 1 : a case series ', Molecular Autism, vol. 8, no. 1, 62 . https://doi.org/10.1186/s13229-017-0178-0
Molecular Autism
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M 2017, ' Early development of infants with Neurofibromatosis Type 1 : A case series ', Molecular Autism, vol. 8, no. 62 . https://doi.org/10.1186/s13229-017-0178-0
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M H, Baron-Cohen, S, Begum-Ali, J, Bolton, P, Cheung, C, Dafner, L, Davies, K, Elsabbagh, M, Fernandes, J, Fish, L, Gammer, I, Greensmith, M, Gliga, T, Kalwarowsky, S, Liew, M, Pasco, G, Pickles, A, Ribeiro, H, Salomone, E, Taylor, C, Tucker, L, Wass, S, Burkitt-Wright, E, Evans, D G, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S M, Baralle, D, Redman, C, Sharif, S, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R & Eden-Basis Team 2017, ' Early development of infants with neurofibromatosis type 1 : a case series ', Molecular Autism, vol. 8, no. 1, 62 . https://doi.org/10.1186/s13229-017-0178-0
Background Prospective studies of infants at familial risk for autism spectrum disorder (ASD) have yielded insights into the earliest signs of the disorder but represent heterogeneous samples of unclear aetiology. Complementing this approach by study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1e2521880839ccacdf90fd22c2f3fa4
http://link.springer.com/article/10.1186/s13229-017-0178-0
http://link.springer.com/article/10.1186/s13229-017-0178-0
Autor:
Hartill, Verity, Szymanska, Katarzyna, Sharif, Saghira Malik, Wheway, Gabrielle, Johnson, Colin A.
Publikováno v:
Frontiers in Pediatrics
Meckel-Gruber syndrome (MKS) is a lethal autosomal recessive congenital anomaly syndrome caused by mutations in genes encoding proteins that are structural or functional components of the primary cilium. Conditions that are caused by mutations in cil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f0f09fe3630d70058629f483cf2d12a3
http://europepmc.org/articles/PMC5701918
http://europepmc.org/articles/PMC5701918
Akademický článek
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Akademický článek
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Autor:
Stella Zhang, Sharif, Saghira Malik, Ya-Chun Chen, Valente, Enza-Maria, Ahmed, Mushtaq, Sheridan, Eamonn, Bennett, Christopher, Woods, Geoffrey
Publikováno v:
Journal of Medical Genetics; Aug2016, Vol. 53 Issue 8, p533-535, 3p
Autor:
Smith, Ursula M., Consugar, Mark, Tee, Louise J., McKee, Brandy M., Esther N.Maina, Whelan, Shelly, Neil V.Morgan, Goranson, Erin, Gissen, Paul, Lilliquist, Stacie, Aligianis, Irene A., Ward, Christopher J., Pasha, Shanaz, Punyashthiti, Rachaneekorn, Sharif, Saghira Malik, Batman, Philip A., Bennett, Christopher P., Woods, C. Geoffrey, McKeown, Carole, Bucourt, Martine
Publikováno v:
Nature Genetics; Feb2006, Vol. 38 Issue 2, p191-196, 6p, 2 Black and White Photographs, 3 Diagrams, 1 Chart, 1 Graph