ALK-positive histiocytosis: an expanded clinicopathologic spectrum and frequent presence of KIF5B-ALK fusion
Chang, Kenneth Tou En, Tay, Amos Zhi En, Kuick, Chik Hong, Chen, Huiyi, Algar, Elizabeth, Taubenheim, Nadine, Campbell, Janine, Mechinaud, Francoise, Campbell, Martin, Super, Leanne, Chantranuwat, Chavit, Yuen, S T, Chan, John K C, Chow, Chung W
Published in Modern pathology (01.05.2019)
Published in Modern pathology (01.05.2019)
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Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5
Scerri, Thomas, Riseley, Jessica R., Gillies, Greta, Pope, Kate, Burgess, Rosemary, Mandelstam, Simone A., Dibbens, Leanne, Chow, Chung W., Maixner, Wirginia, Harvey, Anthony Simon, Jackson, Graeme D., Amor, David J., Delatycki, Martin B., Crino, Peter B., Berkovic, Samuel F., Scheffer, Ingrid E., Bahlo, Melanie, Lockhart, Paul J., Leventer, Richard J.
Published in Annals of clinical and translational neurology (01.05.2015)
Published in Annals of clinical and translational neurology (01.05.2015)
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Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility
Leventer, Richard J., Jansen, Floor E., Mandelstam, Simone A., Ho, Alice, Mohamed, Ismail, Sarnat, Harvey B., Kato, Mitsuhiro, Fukasawa, Tatsuya, Saitsu, Hirotomo, Matsumoto, Naomichi, Itoh, Masayuki, Kalnins, Renate M., Chow, Chung W., Harvey, A. Simon, Jackson, Graeme D., Crino, Peter B., Berkovic, Samuel F., Scheffer, Ingrid E.
Published in Epilepsia (Copenhagen) (01.03.2014)
Published in Epilepsia (Copenhagen) (01.03.2014)
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Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients
Gill, Anthony J, Hes, Ondrej, Papathomas, Thomas, Šedivcová, Monika, Tan, Puay Hoon, Agaimy, Abbas, Andresen, Per Arne, Kedziora, Andrew, Clarkson, Adele, Toon, Christopher W, Sioson, Loretta, Watson, Nicole, Chou, Angela, Paik, Julie, Clifton-Bligh, Roderick J, Robinson, Bruce G, Benn, Diana E, Hills, Kirsten, Maclean, Fiona, Niemeijer, Nicolasine D, Vlatkovic, Ljiljana, Hartmann, Arndt, Corssmit, Eleonora P M, van Leenders, Geert J L H, Przybycin, Christopher, McKenney, Jesse K, Magi-Galluzzi, Cristina, Yilmaz, Asli, Yu, Darryl, Nicoll, Katherine D, Yong, Jim L, Sibony, Mathilde, Yakirevich, Evgeny, Fleming, Stewart, Chow, Chung W, Miettinen, Markku, Michal, Michal, Trpkov, Kiril
Published in The American journal of surgical pathology (01.12.2014)
Published in The American journal of surgical pathology (01.12.2014)
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A toddler with a cough and wheeze refractory to treatment
Shanthikumar, Shivanthan, Lwin, Tommy, Chow, Chung W, Crameri, Joe, Harrison, Jo
Published in Thorax (01.10.2017)
Published in Thorax (01.10.2017)
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Infantile Hemangioma with Minimal or Arrested Growth: Further Observations on Clinical and Histopathologic Findings of this Unique but Underrecognized Entity
Ma, Ellen Hui, Robertson, Susan J., Chow, Chung W., Bekhor, Philip S.
Published in Pediatric dermatology (01.01.2017)
Published in Pediatric dermatology (01.01.2017)
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Can celiac serology alone be used as a marker of duodenal mucosal recovery in children with celiac disease on a gluten-free diet?
Bannister, Elizabeth G, Cameron, Donald J, Ng, Jessica, Chow, Chung W, Oliver, Mark R, Alex, George, Catto-Smith, Anthony G, Heine, Ralf G, Webb, Annette, McGrath, Kathleen, Simpson, Diane, Hardikar, Winita
Published in The American journal of gastroenterology (01.09.2014)
Published in The American journal of gastroenterology (01.09.2014)
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Effect of a 4-Food Elimination Diet and Omeprazole in Children with Eosinophilic Esophagitis – A Randomized, Controlled Trial
Heine, Ralf G., Peters, Rachel, Cameron, Don J., Alex, George, Oliver, Mark R., Hardikar, Winita, Chow, Chung W., McWilliam, Vicki L., Moore, David J., Kakakios, Alyson M., Cheah, Eric, O'Loughlin, Edward V., Axelrad, Christine, Allen, Katrina
Published in Journal of allergy and clinical immunology (01.02.2019)
Published in Journal of allergy and clinical immunology (01.02.2019)
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Germline SDHC mutation presenting as recurrent SDH deficient GIST and renal carcinoma
Gill, Anthony J., Lipton, Lara, Taylor, Jessica, Benn, Diane E., Richardson, Anne Louise, Frydenberg, Mark, Shapiro, Jeremy, Clifton-Bligh, Roderick J., Chow, Chung W., Bogwitz, Michael
Published in Pathology (01.12.2013)
Published in Pathology (01.12.2013)
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Persistent Folliculitis in An Immunocompetent Child
Wen, Sophie CH, Lee, Lai‐yang, Daley, Andrew J, Chow, Chung W, Phillips, Roderic, Gwee, Amanda
Published in Journal of paediatrics and child health (01.11.2018)
Published in Journal of paediatrics and child health (01.11.2018)
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Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay
Myers, Kenneth A., Bennett, Mark F., Chow, Chung W., Carden, Susan M., Mandelstam, Simone A., Bahlo, Melanie, Scheffer, Ingrid E.
Published in American journal of medical genetics. Part A (01.01.2018)
Published in American journal of medical genetics. Part A (01.01.2018)
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Neuropathology of childhood‐onset basal ganglia degeneration caused by mutation of VAC14
Stutterd, Chloe, Diakumis, Peter, Bahlo, Melanie, Fanjul Fernandez, Miriam, Leventer, Richard J., Delatycki, Martin, Amor, David, Chow, Chung W., Stephenson, Sarah, Meisler, Miriam H., Mclean, Catriona, Lockhart, Paul J.
Published in Annals of clinical and translational neurology (01.12.2017)
Published in Annals of clinical and translational neurology (01.12.2017)
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Immunoreactivity for high-affinity choline transporter colocalises with VAChT in human enteric nervous system
Harrington, Andrea M, Lee, Margaret, Ong, Sim-Yee, Yong, Eric, Farmer, Pamela, Peck, Cristal J, Chow, Chung W, Hutson, John M, Southwell, Bridget R
Published in Cell and tissue research (01.07.2010)
Published in Cell and tissue research (01.07.2010)
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Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen
Frew, John, Lim, Shueh W, Klausseger, Alfred, Chow, Chung W, Tran, Kim, Su, John, Orchard, David, Varigos, George, Sawamura, Daisuke, Nishie, Wataru, Shimizu, Hiroshi, Murrell, Dédée F
Published in Australasian journal of dermatology (01.11.2011)
Published in Australasian journal of dermatology (01.11.2011)
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Journal Article
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC 5
Scerri, Thomas, Riseley, Jessica R., Gillies, Greta, Pope, Kate, Burgess, Rosemary, Mandelstam, Simone A., Dibbens, Leanne, Chow, Chung W., Maixner, Wirginia, Harvey, Anthony Simon, Jackson, Graeme D., Amor, David J., Delatycki, Martin B., Crino, Peter B., Berkovic, Samuel F., Scheffer, Ingrid E., Bahlo, Melanie, Lockhart, Paul J., Leventer, Richard J.
Published in Annals of clinical and translational neurology (01.05.2015)
Published in Annals of clinical and translational neurology (01.05.2015)
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Esophageal Eosinophilia In Children With Dysphagia
Cheung, Ka Ming, Oliver, Mark R., Cameron, Donald J. S., Catto‐Smith, Anthony G., Chow, Chung W.
Published in Journal of pediatric gastroenterology and nutrition (01.10.2003)
Published in Journal of pediatric gastroenterology and nutrition (01.10.2003)
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