Monogenic causes of stroke: now and the future von Tan, Rhea Y. Y., Markus, Hugh S.

Volltext

Encephalopathy in a Large Cohort of British Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients von Drazyk, Anna M, Tan, Rhea Y.Y, Tay, Jonathan, Traylor, Matthew, Das, Tilak, Markus, Hugh S

Volltext

How common are single gene mutations as a cause for lacunar stroke?: A targeted gene panel study von Tan, Rhea Y.Y, Traylor, Matthew, Megy, Karyn, Duarte, Daniel, Deevi, Sri V.V, Shamardina, Olga, Mapeta, Rutendo P, Ouwehand, Willem H, Gräf, Stefan, Downes, Kate, Markus, Hugh S

Volltext

CADASIL: Migraine, Encephalopathy, Stroke and Their Inter-Relationships von Tan, Rhea Yan Ying, Markus, Hugh Stephen

Volltext

Whole-genome sequencing of patients with rare diseases in a national health system von Turro, Ernest, Astle, William J., Megy, Karyn, Gräf, Stefan, Greene, Daniel, Shamardina, Olga, Allen, Hana Lango, Sanchis-Juan, Alba, Frontini, Mattia, Thys, Chantal, Stephens, Jonathan, Mapeta, Rutendo, Burren, Oliver S., Downes, Kate, Haimel, Matthias, Tuna, Salih, Deevi, Sri V. V., Aitman, Timothy J., Bennett, David L., Calleja, Paul, Carss, Keren, Caulfield, Mark J., Chinnery, Patrick F., Dixon, Peter H., Gale, Daniel P., James, Roger, Koziell, Ania, Laffan, Michael A., Levine, Adam P., Maher, Eamonn R., Markus, Hugh S., Morales, Joannella, Morrell, Nicholas W., Mumford, Andrew D., Ormondroyd, Elizabeth, Rankin, Stuart, Rendon, Augusto, Richardson, Sylvia, Roberts, Irene, Roy, Noemi B. A., Saleem, Moin A., Smith, Kenneth G. C., Stark, Hannah, Tan, Rhea Y. Y., Themistocleous, Andreas C., Thrasher, Adrian J., Watkins, Hugh, Webster, Andrew R., Wilkins, Martin R., Williamson, Catherine, Whitworth, James, Humphray, Sean, Bentley, David R., Kingston, Nathalie, Walker, Neil, Bradley, John R., Ashford, Sofie, Penkett, Christopher J., Freson, Kathleen, Stirrups, Kathleen E., Raymond, F. Lucy, Ouwehand, Willem H.

Volltext

Brief Screening of Vascular Cognitive Impairment in Patients With Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Without Dementia von Brookes, Rebecca L, Hollocks, Matthew J, Tan, Rhea Y.Y, Morris, Robin G, Markus, Hugh S

Volltext

Semiconductor diode laser device adjuvanting intradermal vaccine von Kimizuka, Yoshifumi, Callahan, John J, Huang, Zilong, Morse, Kaitlyn, Katagiri, Wataru, Shigeta, Ayako, Bronson, Roderick, Takeuchi, Shu, Shimaoka, Yusuke, Chan, Megan P.K, Zeng, Yang, Li, Binghao, Chen, Huabiao, Tan, Rhea Y.Y, Dwyer, Conor, Mulley, Tyler, Leblanc, Pierre, Goudie, Calum, Gelfand, Jeffrey, Tsukada, Kosuke, Brauns, Timothy, Poznansky, Mark C, Bean, David, Kashiwagi, Satoshi

Volltext

Near-Infrared 1064 nm Laser Modulates Migratory Dendritic Cells To Augment the Immune Response to Intradermal Influenza Vaccine von Morse, Kaitlyn, Kimizuka, Yoshifumi, Chan, Megan P K, Shibata, Mai, Shimaoka, Yusuke, Takeuchi, Shu, Forbes, Benjamin, Nirschl, Christopher, Li, Binghao, Zeng, Yang, Bronson, Roderick T, Katagiri, Wataru, Shigeta, Ayako, Sîrbulescu, Ruxandra F, Chen, Huabiao, Tan, Rhea Y Y, Tsukada, Kosuke, Brauns, Timothy, Gelfand, Jeffrey, Sluder, Ann, Locascio, Joseph J, Poznansky, Mark C, Anandasabapathy, Niroshana, Kashiwagi, Satoshi

Volltext

NEXT GENERATION SEQUENCING IN FAMILIAL CEREBRAL SMALL VESSEL DISEASE - AN ONGOING STUDY von Tan, Rhea, Markus, Hugh

Volltext

THE SPECTRUM OF MIGRAINE IN 306 PATIENTS WITH CADASIL von Tan, Rhea, Markus, Hugh

Volltext

Impaired DNA Damage Response in the Pathogenesis of Multiple System Atrophy: A Histopathological Study (P3.016) von Tan, Rhea Yan Ying, Ota, Kiyobumi, Mizusawa, Hidehiro, Yokota, Takanori, Ishikawa, Kinya

Volltext

Whole-genome sequencing of patients with rare diseases in a national health system von Turro, Ernest, Astle, William, Megy, Karyn, Gräf, Stefan, Greene, Daniel, Shamardina, Olga, Allen, Hana Lango, Sanchis-Juan, Alba, Frontini, Mattia, Thys, Chantal, Stephens, Jonathan, Mapeta, Rutendo, Burren, Oliver, Downes, Kate, Haimel, Matthias, Tuna, Salih, Deevi, Sri, Aitman, Timothy, Bennett, David, Calleja, Paul, Carss, Keren, Caulfield, Mark, Chinnery, Patrick, Dixon, Peter, Gale, Daniel, James, Roger, Koziell, Ania, Laffan, Michael, Levine, Adam, Maher, Eamonn, Markus, Hugh, Morales, Joannella, Morrell, Nicholas, Mumford, Andrew, Ormondroyd, Elizabeth, Rankin, Stuart, Rendon, Augusto, Richardson, Sylvia, Roberts, Irene, Roy, Noemi, Saleem, Moin, Smith, Kenneth, Stark, Hannah, Tan, Rhea, Themistocleous, Andreas, Thrasher, Adrian, Watkins, Hugh, Webster, Andrew, Wilkins, Martin, Williamson, Catherine, Whitworth, James, Humphray, Sean, Bentley, David, Abbs, Stephen, Abulhoul, Lara, Adlard, Julian, Ahmed, Munaza, Alachkar, Hana, Allsup, David, Almeida-King, Jeff, Ancliff, Philip, Antrobus, Richard, Armstrong, Ruth, Arno, Gavin, Ashford, Sofie, Attwood, Anthony, Aurora, Paul, Babbs, Christian, Bacchelli, Chiara, Bakchoul, Tamam, Banka, Siddharth, Bariana, Tadbir, Barwell, Julian, Batista, Joana, Baxendale, Helen, Beales, Phil, Bierzynska, Agnieszka, Biss, Tina, Bitner-Glindzicz, Maria, Black, Graeme, Bleda, Marta, Blesneac, Iulia, Bockenhauer, Detlef, Bogaard, Harm, Bourne, Christian, Boyce, Sara, Bradley, John, Bragin, Eugene, Breen, Gerome, Brennan, Paul, Brewer, Carole, Brown, Matthew, Browning, Andrew, Browning, Michael, Buchan, Rachel, Buckland, Matthew, Bueser, Teofila, Diz, Carmen Bugarin, Burn, John, Burns, Siobhan

Volltext

Whole-genome sequencing of patients with rare diseases in a national health system von Turro, Ernest, Astle, William J, Megy, Karyn, Graef, Stefan, Greene, Daniel, Shamardina, Olga, Allen, Hana Lango, Sanchis-Juan, Alba, Frontini, Mattia, Thys, Chantal, Stephens, Jonathan, Mapeta, Rutendo, Burren, Oliver S, Downes, Kate, Haimel, Matthias, Tuna, Salih, Deevi, Sri V.V, Aitman, Timothy J, Bennett, David L, Calleja, Paul, Carss, Keren, Caulfield, Mark J, Chinnery, Patrick F, Dixon, Peter H, Gale, Daniel P, James, Roger, Koziell, Ania, Laffan, Michael A, Levine, Adam P, Maher, Eamonn R, Markus, Hugh S, Morales, Joannella, Morrell, Nicholas W, Mumford, Andrew D, Ormondroyd, Elizabeth, Rankin, Stuart, Rendon, Augusto, Richardson, Sylvia, Roberts, Irene, Roy, Noemi B.A, Saleem, Moin A, Smith, Kenneth G.C, Stark, Hannah, Tan, Rhea Y.Y, Themistocleous, Andreas C, Thrasher, Adrian J, Watkins, Hugh, Webster, Andrew R, Wilkins, Martin R, Williamson, Catherine, Whitworth, James, Humphray, Sean, Bentley, David R, Kingston, Nathalie, Walker, Neil, Bradley, John R, Ashford, Sofie, Penkett, Christopher J, Freson, Kathleen, Stirrups, Kathleen E, Raymond, F. Lucy, Ouwehand, Willem H

Volltext

Whole-genome sequencing of patients with rare diseases in a national health system von Turro, Ernest, Astle, William, Megy, Karyn, Gräf, Stefan, Greene, Daniel, Shamardina, Olga, Allen, Hana Lango, Sanchis-Juan, Alba, Frontini, Mattia, Thys, Chantal, Stephens, Jonathan, Mapeta, Rutendo, Burren, Oliver, Downes, Kate, Haimel, Matthias, Tuna, Salih, Deevi, Sri, Aitman, Timothy, Bennett, David, Calleja, Paul, Carss, Keren, Caulfield, Mark, Chinnery, Patrick, Dixon, Peter, Gale, Daniel, James, Roger, Koziell, Ania, Laffan, Michael, Levine, Adam, Maher, Eamonn, Markus, Hugh, Morales, Joannella, Morrell, Nicholas, Mumford, Andrew, Ormondroyd, Elizabeth, Rankin, Stuart, Rendon, Augusto, Richardson, Sylvia, Roberts, Irene, Roy, Noemi, Saleem, Moin, Smith, Kenneth, Stark, Hannah, Tan, Rhea, Themistocleous, Andreas, Thrasher, Adrian, Watkins, Hugh, Webster, Andrew, Wilkins, Martin, Williamson, Catherine, Whitworth, James, Humphray, Sean, Bentley, David, Abbs, Stephen, Abulhoul, Lara, Adlard, Julian, Ahmed, Munaza, Alachkar, Hana, Allsup, David, Almeida-King, Jeff, Ancliff, Philip, Antrobus, Richard, Armstrong, Ruth, Arno, Gavin, Ashford, Sofie, Attwood, Anthony, Aurora, Paul, Babbs, Christian, Bacchelli, Chiara, Bakchoul, Tamam, Banka, Siddharth, Bariana, Tadbir, Barwell, Julian, Batista, Joana, Baxendale, Helen, Beales, Phil, Bierzynska, Agnieszka, Biss, Tina, Bitner-Glindzicz, Maria, Black, Graeme, Bleda, Marta, Blesneac, Iulia, Bockenhauer, Detlef, Bogaard, Harm, Bourne, Christian, Boyce, Sara, Bradley, John, Bragin, Eugene, Breen, Gerome, Brennan, Paul, Brewer, Carole, Brown, Matthew, Browning, Andrew, Browning, Michael, Buchan, Rachel, Buckland, Matthew, Bueser, Teofila, Diz, Carmen Bugarin, Burn, John, Burns, Siobhan

Volltext

Near-infrared 1064 nm laser modulates migratory dendritic cells to adjuvant the immune response to intradermal influenza vaccine von Morse, Kaitlyn, Kimizuka, Yoshifumi, Chan, Megan P. K., Shibata, Mai, Shimaoka, Yusuke, Takeuchi, Shu, Forbes, Benjamin, Nirschl, Christopher, Li, Binghao, Zeng, Yang, Bronson, Roderick T., Katagiri, Wataru, Shigeta, Ayako, Sîrbulescu, Ruxandra F., Chen, Huabiao, Tan, Rhea Y. Y., Tsukada, Kosuke, Brauns, Timothy, Gelfand, Jeffrey, Sluder, Ann, Locascio, Joseph J., Poznansky, Mark C., Anandasabapathy, Niroshana, Kashiwagi, Satoshi

Volltext

Genetics of Cerebral Small Vessel Disease von Tan, Yan Ying Rhea

Volltext bestellen

Encephalopathy in a Large Cohort of British Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients von Drazyk, Anna M, Tan, Rhea YY, Tay, Jonathan, Traylor, Matthew, Das, Tilak, Markus, Hugh S

Volltext bestellen

How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study von Tan, Rhea YY, Traylor, Matthew, Megy, Karyn, Duarte, Daniel, Deevi, Sri VV, Shamardina, Olga, Mapeta, Rutendo P, NIHR BioResource: Rare Diseases Consortium, Ouwehand, Willem H, Gräf, Stefan, Downes, Kate, Markus, Hugh S

Volltext bestellen

Brief Screening of Vascular Cognitive Impairment in Patients With Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Without Dementia von Brookes, Rebecca L, Hollocks, Matthew J, Tan, Rhea YY, Morris, Robin G, Markus, Hugh S

Volltext bestellen

Whole-genome sequencing of patients with rare diseases in a national health system von Turro, Ernest, Astle, William J, Megy, Karyn, Gräf, Stefan, Greene, Daniel, Shamardina, Olga, Allen, Hana Lango, Sanchis-Juan, Alba, Frontini, Mattia, Thys, Chantal, Stephens, Jonathan, Mapeta, Rutendo, Burren, Oliver S, Downes, Kate, Haimel, Matthias, Tuna, Salih, Deevi, Sri VV, Aitman, Timothy J, Bennett, David L, Calleja, Paul, Carss, Keren, Caulfield, Mark J, Chinnery, Patrick F, Dixon, Peter H, Gale, Daniel P, James, Roger, Koziell, Ania, Laffan, Michael A, Levine, Adam P, Maher, Eamonn R, Markus, Hugh S, Morales, Joannella, Morrell, Nicholas W, Mumford, Andrew D, Ormondroyd, Elizabeth, Rankin, Stuart, Rendon, Augusto, Richardson, Sylvia, Roberts, Irene, Roy, Noemi BA, Saleem, Moin A, Smith, Kenneth GC, Stark, Hannah, Tan, Rhea YY, Themistocleous, Andreas C, Thrasher, Adrian J, Watkins, Hugh, Webster, Andrew R, Wilkins, Martin R, Williamson, Catherine, Whitworth, James, Humphray, Sean, Bentley, David R, NIHR BioResource for the 100,000 Genomes Project, Kingston, Nathalie, Walker, Neil, Bradley, John R, Ashford, Sofie, Penkett, Christopher J, Freson, Kathleen, Stirrups, Kathleen E, Raymond, F Lucy, Ouwehand, Willem H

Volltext bestellen