Hakutulokset - Harinder Gill

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  1. 1
    Extranodal Natural-Killer/T-Cell Lymphoma, Nasal Type

    Extranodal Natural-Killer/T-Cell Lymphoma, Nasal Type Tekijä Harinder Gill, Raymond Liang, Eric Tse

    Julkaistu 2010
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  2. 2
    Patterns of recurrence of congenital heart disease

    Patterns of recurrence of congenital heart disease Tekijä Harinder Gill, Miranda Splitt, Gurleen Sharland, John Simpson

    Julkaistu 2003
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  3. 3
    Fetal ventricular tachycardia secondary to long QT syndrome treated with maternal intravenous magnesium: case report and review of the literature

    Fetal ventricular tachycardia secondary to long QT syndrome treated with maternal intravenous magnesium: case report and review of the literature Tekijä John Simpson, D. J. Maxwell, Éric Rosenthal, Harinder Gill

    Julkaistu 2009
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  4. 4
    Molecular and Cellular Mechanisms of Myelodysplastic Syndrome: Implications on Targeted Therapy

    Molecular and Cellular Mechanisms of Myelodysplastic Syndrome: Implications on Targeted Therapy Tekijä Harinder Gill, Anskar Y.H. Leung, Yok‐Lam Kwong

    Julkaistu 2016
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  5. 5
    Autozygosity Mapping of a Seckel Syndrome Locus to Chromosome 3q22.1-q24

    Autozygosity Mapping of a Seckel Syndrome Locus to Chromosome 3q22.1-q24 Tekijä Judith Goodship, Harinder Gill, Joan Carter, Andrew P. Jackson, Miranda Splitt, Michael Wright

    Julkaistu 2000
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  6. 6
    SURPASS-ET: phase III Study of Ropeginterferon Alfa-2b versus Anagrelide as Second-Line Therapy in Essential Thrombocythemia

    SURPASS-ET: phase III Study of Ropeginterferon Alfa-2b versus Anagrelide as Second-Line Therapy in Essential Thrombocythemia Tekijä Srđan Verstovšek, Norio Komatsu, Harinder Gill, Jie Jin, Sung‐Eun Lee, Hsin‐An Hou, Toshiaki Sato, Albert Qin, Raymond Urbanski, Weichung Shih, Oleh Zagrijtschuk, Craig Zimmerman, Ruben A. Mesa

    Julkaistu 2022
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  7. 7
    Type II enteropathy‐associated T‐cell lymphoma: A multicenter analysis from the Asia Lymphoma Study Group

    Type II enteropathy‐associated T‐cell lymphoma: A multicenter analysis from the Asia Lymphoma Study Group Tekijä Eric Tse, Harinder Gill, Florence Loong, Seok Jin Kim, Siok‐Bian Ng, Tiffany Tang, Young Hyeh Ko, Wee Joo Chng, Soon Thye Lim, Won Seog Kim, Yok‐Lam Kwong

    Julkaistu 2012
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  8. 8
    Disseminated Infections with<i>Talaromyces</i><i>marneffei</i>in Non-AIDS Patients Given Monoclonal Antibodies against CD20 and Kinase Inhibitors

    Disseminated Infections with<i>Talaromyces</i><i>marneffei</i>in Non-AIDS Patients Given Monoclonal Antibodies against CD20 and Kinase Inhibitors Tekijä Jasper Fuk‐Woo Chan, Thomas S. Y. Chan, Harinder Gill, Frank Y.F. Lam, Nigel J. Trendell‐Smith, Siddharth Sridhar, Herman Tse, Susanna K. P. Lau, Ivan Fan‐Ngai Hung, Kwok‐Yung Yuen, Patrick C. Y. Woo

    Julkaistu 2015
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  9. 9
    Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes

    Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes Tekijä Renske Oegema, Thomas D. Cushion, Ian G. Phelps, Seo‐Kyung Chung, Jennifer C. Dempsey, Sarah Collins, Jonathan G.L. Mullins, Tracy Dudding, Harinder Gill, Andrew Green, William B. Dobyns, Gisele E. Ishak, Mark I. Rees, Dan Doherty

    Julkaistu 2015
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  10. 10
    Long-term outcome of relapsed acute promyelocytic leukemia treated with oral arsenic trioxide-based reinduction and maintenance regimens: A 15-year prospective study

    Long-term outcome of relapsed acute promyelocytic leukemia treated with oral arsenic trioxide-based reinduction and maintenance regimens: A 15-year prospective study Tekijä Harinder Gill, Rita Yim, Harold K. K. Lee, Vivien Mak, Shek‐Ying Lin, Bonnie Kho, Sze‐Fai Yip, June S. M. Lau, Wah Li, Ho‐Wan Ip, Yu‐Yan Hwang, Thomas S. Y. Chan, Eric Tse, Wing‐Yan Au, Cyrus R. Kumana, Yok‐Lam Kwong

    Julkaistu 2018
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  11. 11
    Acute promyelocytic leukaemia: population-based study of epidemiology and outcome with ATRA and oral-ATO from 1991 to 2021

    Acute promyelocytic leukaemia: population-based study of epidemiology and outcome with ATRA and oral-ATO from 1991 to 2021 Tekijä Harinder Gill, Radha Raghupathy, Carmen Y.Y. Lee, Yammy Yung, Hiu-Tung Chu, Michael Y. Ni, Xiao Xiao, Francis P. Flores, Rita Yim, Paul Lee, Lynn Gencianeo Chin, Vivian Li, Lester Au, Wing‐Yan Au, Edmond S.K., Diwakar Mohan, Cyrus R. Kumana, Yok‐Lam Kwong

    Julkaistu 2023
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  12. 12
    Next-generation sequencing with a myeloid gene panel in core-binding factor AML showed KIT activation loop and TET2 mutations predictive of outcome

    Next-generation sequencing with a myeloid gene panel in core-binding factor AML showed KIT activation loop and TET2 mutations predictive of outcome Tekijä Chae‐Yin Cher, GM Leung, Chun Hang Au, Tsun‐Leung Chan, Edmond S.K., Joycelyn Sim, Harinder Gill, Albert K. W. Lie, Raymond Liang, K.F. Wong, Lisa L. P. Siu, Christy Sp Tsui, C.C So, Hera Wong, Sze‐Fai Yip, H K K Lee, H S Y Liu, Jeremy Lau, T H Luk, Chi Kuen Lau, S.-Y. Lin, Yok‐Lam Kwong, Anskar Y.H. Leung

    Julkaistu 2016
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  13. 13
    Further delineation of CANT1 phenotypic spectrum and demonstration of its role in proteoglycan synthesis

    Further delineation of CANT1 phenotypic spectrum and demonstration of its role in proteoglycan synthesis Tekijä Mathilde Nizon, Céline Huber, Fabio De Leonardis, Rodolphe Merrina, Antonella Forlino, Mélanie Fradin, Beyhan Tüysüz, Bassam Abu‐Libdeh, Yasemin Alanay, Beate Albrecht, Lihadh Al‐Gazali, Sarenur Yilmaz Basaran, Jill Clayton‐Smith, Julie Désir, Harinder Gill, Marie T. Greally, Erkan Koparir, Merel C. van Maarle, Sara MacKay, Geert Mortier, Jenny Morton, David Sillence, Catheline Vilain, Ian Young, Klaus Zerres, Martine Le Merrer, Arnold Münnich, Carine Le Goff, Antonio Rossi, Valérie Cormier‐Daire

    Julkaistu 2012
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  14. 14
    Clinical delineation, sex differences, and genotype–phenotype correlation in pathogenic KDM6A variants causing X-linked Kabuki syndrome type 2

    Clinical delineation, sex differences, and genotype–phenotype correlation in pathogenic KDM6A variants causing X-linked Kabuki syndrome type 2 Tekijä Víctor Faúndes, Stephanie Goh, Rhoda Akilapa, Heidre Bezuidenhout, Hans T. Björnsson, Lisa Bradley, Angela F. Brady, Elise Brischoux‐Boucher, Han G. Brunner, Saskia Bulk, Natalie Canham, Declan Cody, Maria Lisa Dentici, M. Cristina Digilio, Frances Elmslie, Andrew E. Fry, Harinder Gill, Jane A. Hurst, Diana Johnson, Sophie Julia, Katherine Lachlan, Robert Roger Lebel, Melissa Byler, Eric Gershon, Edmond G. Lemire, Maria Gnazzo, Francesca Romana Lepri, Antonia Marchèse, Meriel McEntagart, Julie McGaughran, Seiji Mizuno, Nobuhiko Okamoto, Claudine Rieubland, Jonathan Rodgers, Erina Sasaki, Emmanuel Scalais, Ingrid Scurr, Mohnish Suri, Ineke van der Burgt, Naomichi Matsumoto, Noriko Miyake, Valérie Benoît, Damien Lederer, Siddharth Banka

    Julkaistu 2021
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  15. 15
    How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

    How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum Tekijä Siddharth Banka, Ratna Veeramachaneni, William Reardon, Emma Howard, Sancha Bunstone, Nicola Ragge, Michael Parker, Yanick J. Crow, Bronwyn Kerr, Helen Kingston, Kay Metcalfe, Kate Chandler, Alex Magee, Fiona Stewart, Vivienne McConnell, Deirdre E. Donnelly, Siren Berland, Gunnar Houge, Jenny E.V. Morton, Christine Oley, Nicole Revençu, Soo-Mi Park, Sally Davies, Andrew E. Fry, Sally Ann Lynch, Harinder Gill, Susann Schweiger, Wayne Lam, John Tolmie, Shehla Mohammed, Emma Hobson, Audrey Smith, Moira Blyth, Christopher Bennett, Pradeep Vasudevan, Sixto García‐Miñaúr, Alex Henderson, Judith Goodship, Michael Wright, Richard Fisher, Richard J. Gibbons, Susan Price, Deepthi C. de Silva, I. Karen Temple, Amanda Collins, Katherine Lachlan, Frances Elmslie, Meriel McEntagart, Bruce Castle, Jill Clayton‐Smith, Graeme Black, Dian Donnai

    Julkaistu 2011
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  16. 16
    Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

    Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders Tekijä Víctor Faúndes, William G. Newman, Laura Bernardini, Natalie Canham, Jill Clayton‐Smith, Bruno Dallapiccola, Sally Davies, Michelle Demos, Amy Goldman, Harinder Gill, Rachel Horton, Bronwyn Kerr, Dhavendra Kumar, Anna Lehman, Shane McKee, Jenny Morton, Michael Parker, Julia Rankin, Lisa Robertson, I. Karen Temple, Siddharth Banka, Shelin Adam, Christèle du Souich, Alison M. Elliott, Anna Lehman, Jill Mwenifumbo, Tanya N. Nelson, Clara van Karnebeek, Jan M. Friedman, Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Stuart Aitken, Nadia Akawi, Mohsan Alvi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones, Daniel King, Netravathi Krishnappa, Laura E. Mason, Tarjinder Singh, Adrian R. Tivey, Munaza Ahmed, Uruj Anjum, Hayley Archer, Ruth Armstrong, Jana Awada, Meena Balasubramanian, Siddharth Banka, Diana Baralle, Angela Barnicoat, Paul Batstone, David Baty, Chris Bennett, Jonathan Berg, Birgitta Bernhard, A. Paul Bevan, Maria Bitner‐Glindzicz, Edward Blair, Moira Blyth, David Bohanna, Louise Bourdon, David Bourn, Lisa Bradley, Angela F. Brady, Simon Brent, Carole Brewer, Kate Brunstrom, David J. Bunyan, John Burn, Natalie Canham, Bruce Castle, Kate Chandler, Elena Chatzimichali, Deirdre Cilliers, Angus Clarke, Susan Clasper, Jill Clayton‐Smith, Virginia Clowes, Andrea Coates, Trevor Cole, Irina Colgiu, Amanda Collins, Morag N. Collinson, Fiona Connell, Nicola Cooper, Helen Cox, Lara Cresswell, Gareth Cross, Yanick J. Crow, Mariella D’Alessandro, Tabib Dabir, Rosemarie Davidson

    Julkaistu 2017
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