المؤلفون: MacLennan, Alastair, 1943-

المصدر: Scope, Art, Aug 2012; p.51-59

URL الوصول: https://www.thescopes.org/assets/Uploads/fc70c02da3/007-051-MacLennan-11-12.pdf
https://ndhadeliver.natlib.govt.nz/delivery/DeliveryManagerServlet?dps_pid=IE26770369

المؤلفون: MacLennan, Alastair, 1943-

المصدر: Scope, Art, Aug 2012; p.39-49

URL الوصول: https://www.thescopes.org/assets/Uploads/e0d73e5b93/007-039-MacLennan-11-12.pdf
https://ndhadeliver.natlib.govt.nz/delivery/DeliveryManagerServlet?dps_pid=IE26770369

المؤلفون: MacLennan, Alastair

المصدر: New Zealand patient management, Aug 1996; v.25 n.8:p.71-72

المؤلفون: Wang, Yangong, Xu, Yiran, Zhou, Chongchen, Cheng, Ye, Qiao, Niu, Shang, Qing, Xia, Lei, Song, Juan, Gao, Chao, Qiao, Yimeng, Zhang, Xiaoli, Li, Ming, Ma, Caiyun, Fan, Yangyi, Peng, Xirui, Wu, Silin, Lv, Nan, Li, Bingbing, Sun, Yanyan, Zhang, Bohao, Li, Tongchuan, Li, Hongwei, Zhang, Jin, Su, Yu, Li, Qiaoli, Yuan, Junying, Liu, Lei, Moreno-De-Luca, Andres, Maclennan, Alastair H., Gecz, Jozef, Zhu, Dengna, Wang, Xiaoyang, 1965, Zhu, Changlian, Xing, Qinghe

المصدر: NATURE MEDICINE. 30:1395-1405

مصطلحات موضوعية: Medical Genetics and Genomics, Medicinsk genetik och genomik

URL الوصول: https://gup.ub.gu.se/publication/338889

المؤلفون: MacLennan, Alastair

المصدر: Irish Arts Review (2002-), 2021 Jul 01. 38(2), 62-63.

URL الوصول: https://www.jstor.org/stable/45388777

المؤلفون: Helbig, Katherine L, Lauerer, Robert J, Bahr, Jacqueline C, Souza, Ivana A, Myers, Candace T, Uysal, Betül, Schwarz, Niklas, Gandini, Maria A, Huang, Sun, Keren, Boris, Mignot, Cyril, Afenjar, Alexandra, de Villemeur, Thierry Billette, Héron, Delphine, Nava, Caroline, Valence, Stéphanie, Buratti, Julien, Fagerberg, Christina R, Soerensen, Kristina P, Kibaek, Maria, Kamsteeg, Erik-Jan, Koolen, David A, Gunning, Boudewijn, Schelhaas, H Jurgen, Kruer, Michael C, Fox, Jordana, Bakhtiari, Somayeh, Jarrar, Randa, Padilla-Lopez, Sergio, Lindstrom, Kristin, Jin, Sheng Chih, Zeng, Xue, Bilguvar, Kaya, Papavasileiou, Antigone, Xing, Qinghe, Zhu, Changlian, Boysen, Katja, Vairo, Filippo, Lanpher, Brendan C, Klee, Eric W, Tillema, Jan-Mendelt, Payne, Eric T, Cousin, Margot A, Kruisselbrink, Teresa M, Wick, Myra J, Baker, Joshua, Haan, Eric, Smith, Nicholas, Sadeghpour, Azita, Davis, Erica E, Katsanis, Nicholas, Genomics, Task Force for Neonatal, Allori, Alexander, Angrist, Misha, Ashley, Patricia, Bidegain, Margarita, Boyd, Brita, Chambers, Eileen, Cope, Heidi, Cotten, C Michael, Curington, Theresa, Ellestad, Sarah, Fisher, Kimberley, French, Amanda, Gallentine, William, Goldberg, Ronald, Hill, Kevin, Kansagra, Sujay, Katsanis, Sara, Kurtzberg, Joanne, Marcus, Jeffrey, McDonald, Marie, Mikati, Mohammed, Miller, Stephen, Murtha, Amy, Perilla, Yezmin, Pizoli, Carolyn, Purves, Todd, Ross, Sherry, Smith, Edward, Wiener, John, Corbett, Mark A, MacLennan, Alastair H, Gecz, Jozef, Biskup, Saskia, Goldmann, Eva, Rodan, Lance H, Kichula, Elizabeth, Segal, Eric, Jackson, Kelly E, Asamoah, Alexander, Dimmock, David, McCarrier, Julie, Botto, Lorenzo D, Filloux, Francis, Tvrdik, Tatiana, Cascino, Gregory D

المصدر: American Journal of Human Genetics. 103(5)

مصطلحات موضوعية: Medical Physiology, Biomedical and Clinical Sciences, Neurodegenerative, Brain Disorders, Neurosciences, Epilepsy, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Neurological, Adolescent, Adult, Calcium Channels, R-Type, Cation Transport Proteins, Child, Child, Preschool, Contracture, Dyskinesias, Female, Genetic Variation, Humans, Infant, Male, Megalencephaly, Neurodevelopmental Disorders, Spasms, Infantile, Task Force for Neonatal Genomics, Deciphering Developmental Disorders Study, CACNA1E, ion channel, arthrogryposis, calcium channel, epilepsy, Biological Sciences, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2061z9kg

المؤلفون: Kayumi, Sayaka, Pérez-Jurado, Luis A, Palomares, María, Rangu, Sneha, Sheppard, Sarah E, Chung, Wendy K, Kruer, Michael C, Kharbanda, Mira, Amor, David J, McGillivray, George, Cohen, Julie S, García-Miñaúr, Sixto, van Eyk, Clare L, Harper, Kelly, Jolly, Lachlan A, Webber, Dani L, Barnett, Christopher P, Santos-Simarro, Fernando, Pacio-Míguez, Marta, Pozo, Angela Del, Bakhtiari, Somayeh, Deardorff, Matthew, Dubbs, Holly A, Izumi, Kosuke, Grand, Katheryn, Gray, Christopher, Mark, Paul R, Bhoj, Elizabeth J, Li, Dong, Ortiz-Gonzalez, Xilma R, Keena, Beth, Zackai, Elaine H, Goldberg, Ethan M, Perez de Nanclares, Guiomar, Pereda, Arrate, Llano-Rivas, Isabel, Arroyo, Ignacio, Fernández-Cuesta, María Ángeles, Thauvin-Robinet, Christel, Faivre, Laurence, Garde, Aurore, Mazel, Benoit, Bruel, Ange-Line, Tress, Michael L, Brilstra, Eva, Fine, Amena Smith, Crompton, Kylie E, Stegmann, Alexander P A, Sinnema, Margje, Stevens, Servi C J, Nicolai, Joost, Lesca, Gaetan, Lion-François, Laurence, Haye, Damien, Chatron, Nicolas, Piton, Amelie, Nizon, Mathilde, Cogne, Benjamin, Srivastava, Siddharth, Bassetti, Jennifer, Muss, Candace, Gripp, Karen W, Procopio, Rebecca A, Millan, Francisca, Morrow, Michelle M, Assaf, Melissa, Moreno-De-Luca, Andres, Joss, Shelagh, Hamilton, Mark J, Bertoli, Marta, Foulds, Nicola, McKee, Shane, MacLennan, Alastair H, Gecz, Jozef, Corbett, Mark A

المساهمون: Genetica Klinische Genetica, Brain

مصطلحات موضوعية: Autism, Cerebral palsy, Familial exudative vitreoretinopathy, Microcephaly, Wnt beta catenin signaling pathway, Genetics(clinical), Journal Article

وصف الملف: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/447367

الاتاحة: https://dspace.library.uu.nl/handle/1874/447367

المؤلفون: van Eyk, Clare L., Webber, Dani L., Minoche, André E., Pérez Jurado, Luis Alberto, Corbett, Mark A., Gardner, Alison E., Berry, Jesia G., Harper, Kelly, MacLennan, Alastair H., Gecz, Jozef

مصطلحات موضوعية: Genetic testing, Medical genomics, Molecular medicine, Neonatal brain damage, Neurodevelopmental disorders

وصف الملف: application/pdf

Relation: NPJ Genom Med. 2021;6(1):74; http://hdl.handle.net/10230/48712

الاتاحة: http://hdl.handle.net/10230/48712
https://doi.org/10.1038/s41525-021-00238-0

المؤلفون: MacLennan, Alastair

المصدر: Art Journal, 1997 Dec 01. 56(4), 4-85.

URL الوصول: https://www.jstor.org/stable/777713

المؤلفون: Pham, Ryan, Mol, Ben W, Gecz, Jozef, MacLennan, Alastair H, MacLennan, Suzanna C, Corbett, Mark A, van Eyk, Clare L, Webber, Dani L, Palmer, Lyle J, Berry, Jesia G

المساهمون: Cerebral Palsy Alliance Research Foundation, National Health and Medical Research Council

المصدر: Developmental Medicine & Child Neurology ; volume 62, issue 9, page 1024-1030 ; ISSN 0012-1622 1469-8749

الاتاحة: http://dx.doi.org/10.1111/dmcn.14585
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fdmcn.14585
https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.14585
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/dmcn.14585

المؤلفون: MacLennan, Alastair H., Pérez Jurado, Luis Alberto, Gecz, Jozef

مصطلحات موضوعية: Causation, Cerebral palsy, Clinical definition, Genomics

وصف الملف: application/pdf

Relation: J Child Neurol. 2019; 34(8):472-476; http://hdl.handle.net/10230/41984; http://dx.doi.org/10.1177/0883073819840449

الاتاحة: http://hdl.handle.net/10230/41984
https://doi.org/10.1177/0883073819840449

المؤلفون: Corbett, Mark A., van Eyk, Clare L., Webber, Dani L., Bent, Stephen J., Newman, Morgan, Harper, Kelly, Berry, Jesia G., Azmanov, Dimitar N., Woodward, Karen J., Gardner, Alison E., Slee, Jennie, Pérez-Jurado, Luís A., MacLennan, Alastair H., Gecz, Jozef

المصدر: npj Genomic Medicine ; volume 4, issue 1 ; ISSN 2056-7944

الاتاحة: https://doi.org/10.1038/s41525-019-0086-7
https://www.nature.com/articles/s41525-019-0086-7.pdf
https://www.nature.com/articles/s41525-019-0086-7

المؤلفون: Braillon, Alain, Maclennan, Alastair, Marron, Loretta, Dervaux, Alain

المصدر: Women and Birth ; volume 32, issue 2, page e284-e285 ; ISSN 1871-5192

الاتاحة: http://dx.doi.org/10.1016/j.wombi.2018.06.002
https://api.elsevier.com/content/article/PII:S1871519218301379?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1871519218301379?httpAccept=text/plain

المؤلفون: van Eyk, Clare, MacLennan, Suzanna C., MacLennan, Alastair H.

المصدر: JAMA Pediatrics ; volume 177, issue 5, page 455 ; ISSN 2168-6203

الاتاحة: http://dx.doi.org/10.1001/jamapediatrics.2023.0015
https://jamanetwork.com/journals/jamapediatrics/articlepdf/2801967/jamapediatrics_van_eyk_2023_ed_230001_1682695718.09204.pdf

المؤلفون: MacLennan, Alastair, Connolly, Brian, Thorpe, Dominic, Johnston, Sandra

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::403b944d85f3158e652227a9908afbf5

المؤلفون: Corbett, Mark A., van Eyk, Clare L., Webber, Dani L., Bent, Stephen J., Newman, Morgan, Harper, Kelly, Berry, Jesia G., Azmanov, Dimitar N., Woodward, Karen J., Gardner, Alison E., Slee, Jennie, Pérez Jurado, Luis Alberto, MacLennan, Alastair H., Gecz, Jozef

مصطلحات موضوعية: Cervell -- Malalties -- Aspectes genètics

وصف الملف: application/pdf

Relation: NPJ Genomic Medicine. 2018 Dec 14;3:33; http://hdl.handle.net/10230/41847

الاتاحة: http://hdl.handle.net/10230/41847
https://doi.org/10.1038/s41525-018-0073-4

المؤلفون: MacLennan, Alastair H, Kruer, Michael C, Baynam, Gareth, Moreno‐De‐Luca, Andres, Wilson, Yana A, Zhu, Changlian, Wintle, Richard F, Gecz, Jozef

المصدر: Developmental Medicine & Child Neurology ; volume 60, issue 2, page 209-210 ; ISSN 0012-1622 1469-8749

الاتاحة: http://dx.doi.org/10.1111/dmcn.13643
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fdmcn.13643
https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.13643

المؤلفون: MacLennan, Alastair, Gecz, Jozef, Pérez‐Jurado, Luis

المصدر: Annals of Clinical and Translational Neurology ; volume 5, issue 8, page 1011-1011 ; ISSN 2328-9503 2328-9503

الاتاحة: http://dx.doi.org/10.1002/acn3.591
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Facn3.591
https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.591

المؤلفون: van Eyk, Clare L., Corbett, Mark A., Gardner, Alison, van Bon, Bregje W., Broadbent, Jessica L., Harper, Kelly, MacLennan, Alastair H., Gecz, Jozef

المصدر: Translational Psychiatry ; volume 8, issue 1 ; ISSN 2158-3188

الاتاحة: http://dx.doi.org/10.1038/s41398-018-0136-4
https://www.nature.com/articles/s41398-018-0136-4.pdf
https://www.nature.com/articles/s41398-018-0136-4

المؤلفون: Fahey, Michael C., Maclennan, Alastair H, Kretzschmar, Doris, Gecz, Jozef, Kruer, Michael C.

المصدر: Fahey , M C , Maclennan , A H , Kretzschmar , D , Gecz , J & Kruer , M C 2017 , ' The genetic basis of cerebral palsy ' , Developmental Medicine & Child Neurology , vol. 59 , no. 5 , pp. 462-469 . https://doi.org/10.1111/dmcn.13363

وصف الملف: application/pdf

الاتاحة: https://research.monash.edu/en/publications/011b60ea-b58d-451f-a5f2-7dfabced1d35
https://doi.org/10.1111/dmcn.13363
https://researchmgt.monash.edu/ws/files/289347632/56444820_oa.pdf
http://www.scopus.com/inward/record.url?scp=85009188317&partnerID=8YFLogxK