Comparative study between computed tomography guided superior hypogastric plexus block and the classic posterior approach: A prospective randomized study

por Ghoneim, Ayman A., Mansour, Sahar M.
Publicado 2014

Use of somatostatin analogues to treat chylothorax in a child with Generalised Lymphatic Dysplasia

por Brodlie, Malcolm, Abdelgalil, Sara, Mansour, Sahar, Spencer, David A.
Publicado 2011

Impact of three dimensional tomosynthesis on the detection and diagnosis of breast lesions

por Mansour, Sahar, Adel, Lamia, Mokhtar, Omina, Omar, Omar Sherif
Publicado 2014

Diffusion-weighted MR imaging and assessment of ovarian carcinomas with vaginal deposit accidentally detected during pregnancy

por Hamed, Soha, Kamal, Rasha, Sheeba, Mamdouh, El-Toukhy, Marwan Mohamed, Mansour, Sahar
Publicado 2016

Ataxia-Pancytopenia Syndrome due to a de Novo SAMD9L Mutation

por King-Robson, Josh, Marshall, Joseph, Smith, Frances, Willoughby, Leanne, Mansour, Sahar, Sztriha, Laszlo
Publicado 2021

Comparison of mean platelet volume levels in coronary artery ectasia and healthy people: systematic review and meta-analysis

por Moghadam, Reza Heidary, Shahmohammadi, Afshar, Asgari, Nader, Azizi, Koorosh, Mansour, Sahar Mehr, Roozbahani, Mohammad
Publicado 2018

Scintigraphy has the potential to replace thyroid stimulating hormone and ultrasonography in hyperthyroidism diagnosis

por Almohammed, Huda I., Mansour, Sahar, Alhulwah, Arwa H., Mayhoub, Fareed H., Arafah, Ahnaf M.
Publicado 2020

Update and audit of the St George’s classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis

por Gordon, Kristiana, Varney, Ruth, Keeley, Vaughan, Riches, Katie, Jeffery, Steve, Van Zanten, Malou, Mortimer, Peter, Ostergaard, Pia, Mansour, Sahar
Publicado 2020

Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions

por Pearce, Julian, Hadcocks, Linda, Mansour, Sahar, van Zanten, Malou, Jeffery, Steve, Gordon, Kristiana, Ostergaard, Pia, Mortimer, Peter, Macallan, Derek C.
Publicado 2023

Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition

por Gordon, Kristiana, Moore, Matthew, Van Zanten, Malou, Pearce, Julian, Itkin, Maxim, Madden, Brendan, Ratnam, Lakshmi, Mortimer, Peter S., Nagaraja, Rani, Mansour, Sahar
Publicado 2022

A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders

por King, Daniel A., Fitzgerald, Tomas W., Miller, Ray, Canham, Natalie, Clayton-Smith, Jill, Johnson, Diana, Mansour, Sahar, Stewart, Fiona, Vasudevan, Pradeep, Hurles, Matthew E.
Publicado 2014

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

por 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
Publicado 2018

Detection of structural mosaicism from targeted and whole-genome sequencing data

por King, Daniel A., Sifrim, Alejandro, Fitzgerald, Tomas W., Rahbari, Raheleh, Hobson, Emma, Homfray, Tessa, Mansour, Sahar, Mehta, Sarju G., Shehla, Mohammed, Tomkins, Susan E., Vasudevan, Pradeep C., Hurles, Matthew E.
Publicado 2017

Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies

por 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.
Publicado 2023

Short amplicon reverse transcription‐polymerase chain reaction detects aberrant splicing in genes with low expression in blood missed by ribonucleic acid sequencing analysis for cl...

por Wai, Htoo A., Constable, Matthew, Drewes, Cosima, Davies, Ian C., Svobodova, Eliska, Dempsey, Esther, Saggar, Anand, Homfray, Tessa, Mansour, Sahar, Douzgou, Sofia, Barr, Kate, Mercer, Catherine, Hunt, David, Douglas, Andrew G. L., Baralle, Diana
Publicado 2022

Pierpont Syndrome: A Collaborative Study

por Wright, Emma MM Burkitt, Suri, Mohnish, White, Susan M, de Leeuw, Nicole, Silfhout, Anneke T Vulto-van, Stewart, Fiona, McKee, Shane, Mansour, Sahar, Connell, Fiona C, Chopra, Maya, Kirk, Edwin P, Devriendt, Koen, Reardon, Willie, Brunner, Han, Donnai, Dian
Publicado 2011

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

por 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
Publicado 2015

Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders

por Pagnamenta, Alistair T, Murakami, Yoshiko, Taylor, John M, Anzilotti, Consuelo, Howard, Malcolm F, Miller, Venessa, Johnson, Diana S, Tadros, Shereen, Mansour, Sahar, Temple, I Karen, Firth, Rachel, Rosser, Elisabeth, Harrison, Rachel E, Kerr, Bronwen, Popitsch, Niko, Kinoshita, Taroh, Taylor, Jenny C, Kini, Usha
Publicado 2017

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

por 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
Publicado 2019

Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts

por Mansour, Sahar, Josephs, Katherine S, Ostergaard, Pia, Gordon, Kristiana, Van Zanten, Malou, Pearce, Julian, Jeffery, Steve, Keeley, Vaughan, Riches, Katie, Kreuter, Alexander, Wieland, Ulrike, Hägerling, René, Ratnam, Lakshmi, Sackey, Ege, Grigoriadis, Dionysios, Ho, Bernard, Smith, Frances, Rauter, Elisabeth, Mortimer, Peter, Macallan, Derek
Publicado 2023