Self-care treatment for lymphoedema of lymphatic filariasis using integrative medicine
Narahari, Saravu R, Aggithaya, Madhur G, Ryan, Terence J, Muralidharan, Kunnathody, Franks, Peter J, Moffatt, Christine, Mortimer, Peter S
Published in British journal of dermatology (1951) (20.12.2023)
Published in British journal of dermatology (1951) (20.12.2023)
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EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis
Martin-Almedina, Silvia, Martinez-Corral, Ines, Holdhus, Rita, Vicente, Andres, Fotiou, Elisavet, Lin, Shin, Petersen, Kjell, Simpson, Michael A, Hoischen, Alexander, Gilissen, Christian, Jeffery, Heather, Atton, Giles, Karapouliou, Christina, Brice, Glen, Gordon, Kristiana, Wiseman, John W, Wedin, Marianne, Rockson, Stanley G, Jeffery, Steve, Mortimer, Peter S, Snyder, Michael P, Berland, Siren, Mansour, Sahar, Makinen, Taija, Ostergaard, Pia
Published in The Journal of clinical investigation (01.08.2016)
Published in The Journal of clinical investigation (01.08.2016)
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Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort
Grigoriadis, Dionysios, Sackey, Ege, Riches, Katie, van Zanten, Malou, Brice, Glen, England, Ruth, Mills, Mike, Dobbins, Sara E, Lee, Li Ling, Jeffery, Steve, Dong, Liang, Savage, David B, Mortimer, Peter S, Keeley, Vaughan, Pittman, Alan, Gordon, Kristiana, Ostergaard, Pia
Published in PloS one (13.10.2022)
Published in PloS one (13.10.2022)
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Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
Ostergaard, Pia, Simpson, Michael A., Mendola, Antonella, Vasudevan, Pradeep, Connell, Fiona C., van Impel, Andreas, Moore, Anthony T., Loeys, Bart L., Ghalamkarpour, Arash, Onoufriadis, Alexandros, Martinez-Corral, Ines, Devery, Sophie, Leroy, Jules G., van Laer, Lut, Singer, Amihood, Bialer, Martin G., McEntagart, Meriel, Quarrell, Oliver, Brice, Glen, Trembath, Richard C., Schulte-Merker, Stefan, Makinen, Taija, Vikkula, Miikka, Mortimer, Peter S., Mansour, Sahar, Jeffery, Steve
Published in American journal of human genetics (10.02.2012)
Published in American journal of human genetics (10.02.2012)
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Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
Gordon, Kristiana, Moore, Matthew, Van Zanten, Malou, Pearce, Julian, Itkin, Maxim, Madden, Brendan, Ratnam, Lakshmi, Mortimer, Peter S, Nagaraja, Rani, Mansour, Sahar
Published in Frontiers in genetics (27.09.2022)
Published in Frontiers in genetics (27.09.2022)
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PSENEN and NCSTN Mutations in Familial Hidradenitis Suppurativa (Acne Inversa)
Pink, Andrew E., Simpson, Michael A., Brice, Glen W., Smith, Catherine H., Desai, Nemesha, Mortimer, Peter S., Barker, Jonathan N.W.N., Trembath, Richard C.
Published in Journal of investigative dermatology (01.07.2011)
Published in Journal of investigative dermatology (01.07.2011)
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A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon
Nadarajah, Noeline, Schulte, Dörte, McConnell, Vivienne, Martin-Almedina, Silvia, Karapouliou, Christina, Mortimer, Peter S, Jeffery, Steve, Schulte-Merker, Stefan, Gordon, Kristiana, Mansour, Sahar, Ostergaard, Pia
Published in International journal of molecular sciences (01.08.2018)
Published in International journal of molecular sciences (01.08.2018)
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Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
Fotiou, Elisavet, Martin-Almedina, Silvia, Simpson, Michael A., Lin, Shin, Gordon, Kristiana, Brice, Glen, Atton, Giles, Jeffery, Iona, Rees, David C., Mignot, Cyril, Vogt, Julie, Homfray, Tessa, Snyder, Michael P., Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Mansour, Sahar, Ostergaard, Pia
Published in Nature communications (26.04.2019)
Published in Nature communications (26.04.2019)
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New developments in clinical aspects of lymphatic disease
Mortimer, Peter S, Rockson, Stanley G
Published in The Journal of clinical investigation (01.03.2014)
Published in The Journal of clinical investigation (01.03.2014)
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Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies
Hägerling, René, Van Zanten, Malou, Behncke, Rose Yinghan, Ulferts, Sascha, Hansmeier, Nils R, Märkl, Bruno, Witzel, Christian, Ho, Bernard, Keeley, Vaughan, Riches, Katie, Mansour, Sahar, Gordon, Kristiana, Ostergaard, Pia, Mortimer, Peter S
Published in JCI insight (23.10.2023)
Published in JCI insight (23.10.2023)
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Popliteal Node Visualization During Standard Pedal Lymphoscintigraphy for a Swollen Limb Indicates Impaired Lymph Drainage
BURNAND, Katherine M, GLASS, Daphne M, SUNDARAIYA, Sumati, MORTIMER, Peter S, MICHAEL PETERS, A
Published in American journal of roentgenology (1976) (01.12.2011)
Published in American journal of roentgenology (1976) (01.12.2011)
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Lymphatic drainage in the muscle and subcutis of the arm after breast cancer treatment
Stanton, Anthony W. B, Modi, Stephanie, Bennett Britton, Thomas M, Purushotham, Anand D, Peters, A. Michael, Levick, J. Rodney, Mortimer, Peter S
Published in Breast cancer research and treatment (01.10.2009)
Published in Breast cancer research and treatment (01.10.2009)
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Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
Fotiou, Elisavet, Martin-Almedina, Silvia, Simpson, Michael A., Lin, Shin, Gordon, Kristiana, Brice, Glen, Atton, Giles, Jeffery, Iona, Rees, David C., Mignot, Cyril, Vogt, Julie, Homfray, Tessa, Snyder, Michael P., Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Mansour, Sahar, Ostergaard, Pia
Published in Nature communications (03.09.2015)
Published in Nature communications (03.09.2015)
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Mutations in FOXC2 in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency
Mellor, Russell H., Tate, Naomi, Stanton, Anthony W.B., Hubert, Charlotte, Mäkinen, Taija, Smith, Alberto, Burnand, Kevin G., Jeffery, Steve, Levick, J. Rodney, Mortimer, Peter S.
Published in Journal of vascular research (01.01.2011)
Published in Journal of vascular research (01.01.2011)
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Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
Mansour, Sahar, Ostergaard, Pia, Simpson, Michael A, Connell, Fiona C, Steward, Colin G, Brice, Glen, Woollard, Wesley J, Dafou, Dimitra, Kilo, Tatjana, Smithson, Sarah, Lunt, Peter, Murday, Victoria A, Hodgson, Shirley, Keenan, Russell, Pilz, Daniela T, Martinez-Corral, Ines, Makinen, Taija, Mortimer, Peter S, Jeffery, Steve, Trembath, Richard C
Published in Nature genetics (01.10.2011)
Published in Nature genetics (01.10.2011)
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