Intravenous glycerol-sodium ascorbate combination as osmotic agent to reduce intraocular pressure

Por Ray Swapna, Thomas Anna
Publicado em 1977-01-01

An unusual presentation of femoral neck fracture in a young patient

Por Thomas, Anna, Mason, Fiona, Deshpande, Shreeram
Publicado no J Surg Case Rep (2014)

Observable indicators and behaviors for the identification of problem gamblers in venue environments

Por Delfabbro, Paul, Thomas, Anna, Armstrong, Andrew
Publicado no J Behav Addict (2016)

Evaluating non-coding nucleotide repeat expansions in amyotrophic lateral sclerosis

Por Figley, Matthew D., Thomas, Anna, Gitler, Aaron D.
Publicado em 2013

Association between Patient-Provider Communication and Lung Cancer Stigma

Por Shen, Megan Johnson, Hamann, Heidi A., Thomas, Anna J., Ostroff, Jamie S.
Publicado no Support Care Cancer (2015)

How can mental health and substance use services become dual diagnosis capable? Moving from theory into practice

Por Staiger, Petra, Howard, Alexandra, Thomas, Anna C, Young, Greg, McCabe, Marita
Publicado em 2014

Feeling Bad and Looking Worse: Negative Affect Is Associated with Reduced Perceptions of Face-Healthiness

Por Mirams, Laura, Poliakoff, Ellen, Zandstra, Elizabeth H., Hoeksma, Marco, Thomas, Anna, El-Deredy, Wael
Publicado em 2014

Pleasant and Unpleasant Odors Influence Hedonic Evaluations of Human Faces: An Event-Related Potential Study

Por Cook, Stephanie, Fallon, Nicholas, Wright, Hazel, Thomas, Anna, Giesbrecht, Timo, Field, Matt, Stancak, Andrej
Publicado no Front Hum Neurosci (2015)

Premature Terminal Differentiation and a Reduction in Specific Proteases Associated with Loss of ABCA12 in Harlequin Ichthyosis

Por Thomas, Anna C., Tattersall, Daniel, Norgett, Elizabeth E., O'Toole, Edel A., Kelsell, David P.
Publicado em 2009

Heightened eating drive and visual food stimuli attenuate central nociceptive processing

Por Wright, Hazel, Li, Xiaoyun, Fallon, Nicholas B., Giesbrecht, Timo, Thomas, Anna, Harrold, Joanne A., Halford, Jason C. G., Stancak, Andrej
Publicado no J Neurophysiol (2014)

Differential effects of hunger and satiety on insular cortex and hypothalamic functional connectivity

Por Wright, Hazel, Li, Xiaoyun, Fallon, Nicholas B., Crookall, Rebecca, Giesbrecht, Timo, Thomas, Anna, Halford, Jason C.G., Harrold, Joanne, Stancak, Andrej
Publicado no Eur J Neurosci (2016)

A Deafness Associated Mutant Human Connexin 26 Improves The Epithelial Barrier In Vitro

Por Man, Y.K. Stella, Trolove, Caroline, Tattersall, Daniel, Thomas, Anna C., Papakonstantinopoulou, Annie, Patel, Drashnika, Scott, Claire, Chong, Jiehan, Jagger, Daniel J., O’Toole, Edel A., Navsaria, Harshad, Curtis, Michael A., Kelsell, David P.
Publicado em 2007

Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight

Por Demetriou, Charalambos, Abu-Amero, Sayeda, Thomas, Anna C., Ishida, Miho, Aggarwal, Reena, Al-Olabi, Lara, Leon, Lydia J., Stafford, Jaime L., Syngelaki, Argyro, Peebles, Donald, Nicolaides, Kypros H., Regan, Lesley, Stanier, Philip, Moore, Gudrun E.
Publicado em 2014

Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

Por Kinsler, Veronica A, Thomas, Anna C, Ishida, Miho, Bulstrode, Neil W, Loughlin, Sam, Hing, Sandra, Chalker, Jane, McKenzie, Kathryn, Abu-Amero, Sayeda, Slater, Olga, Chanudet, Estelle, Palmer, Rodger, Morrogh, Deborah, Stanier, Philip, Healy, Eugene, Sebire, Neil J, Moore, Gudrun E
Publicado em 2013

Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models

Por Mendioroz, Maite, Do, Catherine, Jiang, Xiaoling, Liu, Chunhong, Darbary, Huferesh K., Lang, Charles F., Lin, John, Thomas, Anna, Abu-Amero, Sayeda, Stanier, Philip, Temkin, Alexis, Yale, Alexander, Liu, Meng-Min, Li, Yang, Salas, Martha, Kerkel, Kristi, Capone, George, Silverman, Wayne, Yu, Y. Eugene, Moore, Gudrun, Wegiel, Jerzy, Tycko, Benjamin
Publicado no Genome Biol (2015)

Erratum to: Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models

Por Mendioroz, Maite, Do, Catherine, Jiang, Xiaoling, Liu, Chunhong, Darbary, Huferesh K., Lang, Charles F., Lin, John, Thomas, Anna, Abu-Amero, Sayeda, Stanier, Philip, Temkin, Alexis, Yale, Alexander, Liu, Meng-Min, Li, Yang, Salas, Martha, Kerkel, Kristi, Capone, George, Silverman, Wayne, Yu, Y. Eugene, Moore, Gudrun, Wegiel, Jerzy, Tycko, Benjamin
Publicado no Genome Biol (2016)

The role and interaction of imprinted genes in human fetal growth

Por Moore, Gudrun E., Ishida, Miho, Demetriou, Charalambos, Al-Olabi, Lara, Leon, Lydia J., Thomas, Anna C., Abu-Amero, Sayeda, Frost, Jennifer M., Stafford, Jaime L., Chaoqun, Yao, Duncan, Andrew J., Baigel, Rachel, Brimioulle, Marina, Iglesias-Platas, Isabel, Apostolidou, Sophia, Aggarwal, Reena, Whittaker, John C., Syngelaki, Argyro, Nicolaides, Kypros H., Regan, Lesley, Monk, David, Stanier, Philip
Publicado no Philos Trans R Soc Lond B Biol Sci (2015)

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

Por Thomas, Anna C., Zeng, Zhiqiang, Rivière, Jean-Baptiste, O’Shaughnessy, Ryan, Al-Olabi, Lara, St.-Onge, Judith, Atherton, David J., Aubert, Hélène, Bagazgoitia, Lorea, Barbarot, Sébastien, Bourrat, Emmanuelle, Chiaverini, Christine, Chong, W. Kling, Duffourd, Yannis, Glover, Mary, Groesser, Leopold, Hadj-Rabia, Smail, Hamm, Henning, Happle, Rudolf, Mushtaq, Imran, Lacour, Jean-Philippe, Waelchli, Regula, Wobser, Marion, Vabres, Pierre, Patton, E. Elizabeth, Kinsler, Veronica A.
Publicado no J Invest Dermatol (2016)

Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

Por Thomas, Anna C., Williams, Hywel, Setó-Salvia, Núria, Bacchelli, Chiara, Jenkins, Dagan, O’Sullivan, Mary, Mengrelis, Konstantinos, Ishida, Miho, Ocaka, Louise, Chanudet, Estelle, James, Chela, Lescai, Francesco, Anderson, Glenn, Morrogh, Deborah, Ryten, Mina, Duncan, Andrew J., Pai, Yun Jin, Saraiva, Jorge M., Ramos, Fabiana, Farren, Bernadette, Saunders, Dawn, Vernay, Bertrand, Gissen, Paul, Straatmaan-Iwanowska, Anna, Baas, Frank, Wood, Nicholas W., Hersheson, Joshua, Houlden, Henry, Hurst, Jane, Scott, Richard, Bitner-Glindzicz, Maria, Moore, Gudrun E., Sousa, Sérgio B., Stanier, Philip
Publicado no Am J Hum Genet (2014)

Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

Por Thomas, Anna C., Williams, Hywel, Setó-Salvia, Núria, Bacchelli, Chiara, Jenkins, Dagan, O’Sullivan, Mary, Mengrelis, Konstantinos, Ishida, Miho, Ocaka, Louise, Chanudet, Estelle, James, Chela, Lescai, Francesco, Anderson, Glenn, Morrogh, Deborah, Ryten, Mina, Duncan, Andrew J., Pai, Yun Jin, Saraiva, Jorge M., Ramos, Fabiana, Farren, Bernadette, Saunders, Dawn, Vernay, Bertrand, Gissen, Paul, Straatmaan-Iwanowska, Anna, Baas, Frank, Wood, Nicholas W., Hersheson, Joshua, Houlden, Henry, Hurst, Jane, Scott, Richard, Bitner-Glindzicz, Maria, Moore, Gudrun E., Sousa, Sérgio B., Stanier, Philip
Publicado no Am J Hum Genet (2015)