Hasil Pencarian - Pia Ostergaard

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  1. 1
    A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon

    A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon oleh Noeline Nadarajah, Dörte Schulte, Vivienne McConnell, Silvia Martin-Almedina, Christina Karapouliou, Peter S. Mortimer, Steve Jeffery, Stefan Schulte-Merker, Kristiana Gordon, Sahar Mansour, Pia Ostergaard

    Diterbitkan 2018-08-01
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  2. 2
    Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies

    Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies oleh René Hägerling, Malou Van Zanten, Rose Yinghan Behncke, Sascha Ulferts, Nils R. Hansmeier, Bruno Märkl, Christian Witzel, Bernard Ho, Vaughan Keeley, Katie Riches, Sahar Mansour, Kristiana Gordon, Pia Ostergaard, Peter S. Mortimer

    Diterbitkan 2023-10-01
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  3. 3
    Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions

    Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions oleh Julian Pearce, Julian Pearce, Linda Hadcocks, Sahar Mansour, Sahar Mansour, Sahar Mansour, Malou van Zanten, Steve Jeffery, Kristiana Gordon, Pia Ostergaard, Peter Mortimer, Peter Mortimer, Derek C. Macallan, Derek C. Macallan

    Diterbitkan 2023-11-01
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  4. 4
    Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program

    Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program oleh Maike Frye, Andrea Taddei, Cathrin Dierkes, Ines Martinez-Corral, Matthew Fielden, Henrik Ortsäter, Jan Kazenwadel, Dinis P. Calado, Pia Ostergaard, Marjo Salminen, Liqun He, Natasha L. Harvey, Friedemann Kiefer, Taija Mäkinen

    Diterbitkan 2018-04-01
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  5. 5
    Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort

    Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort oleh Dionysios Grigoriadis, Ege Sackey, Katie Riches, Malou van Zanten, Glen Brice, Ruth England, Mike Mills, Sara E. Dobbins, Li Ling Lee, Steve Jeffery, Liang Dong, David B. Savage, Peter S. Mortimer, Vaughan Keeley, Alan Pittman, Kristiana Gordon, Pia Ostergaard

    Diterbitkan 2022-01-01
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  6. 6
    Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

    Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis oleh Elisavet Fotiou, Silvia Martin-Almedina, Michael A. Simpson, Shin Lin, Kristiana Gordon, Glen Brice, Giles Atton, Iona Jeffery, David C. Rees, Cyril Mignot, Julie Vogt, Tessa Homfray, Michael P. Snyder, Stanley G. Rockson, Steve Jeffery, Peter S. Mortimer, Sahar Mansour, Pia Ostergaard

    Diterbitkan 2019-04-01
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  7. 7
    Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort.

    Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort. oleh Dionysios Grigoriadis, Ege Sackey, Katie Riches, Malou van Zanten, Glen Brice, Ruth England, Mike Mills, Sara E Dobbins, Li Ling Lee, Lipoedema Consortium, Genomics England Research Consortium, Steve Jeffery, Liang Dong, David B Savage, Peter S Mortimer, Vaughan Keeley, Alan Pittman, Kristiana Gordon, Pia Ostergaard

    Diterbitkan 2022-01-01
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  8. 8
    Mutations in EPHB4 cause human venous valve aplasia

    Mutations in EPHB4 cause human venous valve aplasia oleh Oliver Lyons, James Walker, Christopher Seet, Mohammed Ikram, Adam Kuchta, Andrew Arnold, Magda Hernández-Vásquez, Maike Frye, Gema Vizcay-Barrena, Roland A. Fleck, Ashish S. Patel, Soundrie Padayachee, Peter Mortimer, Steve Jeffery, Siren Berland, Sahar Mansour, Pia Ostergaard, Taija Makinen, Bijan Modarai, Prakash Saha, Alberto Smith

    Diterbitkan 2021-09-01
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  9. 9
    Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma.

    Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma. oleh Naushin H Waseem, Sancy Low, Amna Z Shah, Deepa Avisetti, Pia Ostergaard, Michael Simpson, Katarzyna A Niemiec, Belen Martin-Martin, Hebah Aldehlawi, Saima Usman, Pak Sang Lee, Anthony P Khawaja, Jonathan B Ruddle, Ameet Shah, Ege Sackey, Alexander Day, Yuzhen Jiang, Geoff Swinfield, Ananth Viswanathan, Giovanna Alfano, Christina Chakarova, Heather J Cordell, David F Garway-Heath, Peng T Khaw, Shomi S Bhattacharya, Ahmad Waseem, Paul J Foster

    Diterbitkan 2020-04-01
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