檢索結果 - Diana Alcantara
- Showing 1 - 17 results of 17
-
1
-
2
-
3
-
4
APASL practical recommendations for the management of hepatocellular carcinoma in the era of COVID-19 由 Shiina, Shuichiro, Gani, Rino A., Yokosuka, Osamu, Maruyama, Hitoshi, Nagamatsu, Hiroaki, Payawal, Diana Alcantara, Dokmeci, A. Kadir, Lesmana, Laurentius A., Tanwandee, Tawesak, Lau, George, Sarin, Shiv Kumar, Omata, Masao
出版 2020Text -
5
Liver Disease Trends in the Asia-Pacific Region for the Next 50 Years 由 Shuichiro Shiina, Javkhlan Maikhuu, Deng Qing, Terguunbileg Batsaikhan, Lariza Marie Canseco, Maki Tobari, Hitoshi Maruyama, Hiroaki Nagamatsu, Diana Alcantara‐Payawal, Rino Alvani Gani, Yi‐Hsiang Huang, Tawesak Tanwandee, Giovanni Galati, Yoon Jun Kim
出版 2025Revisão -
6
Somatic PDGFRB Activating Variants in Fusiform Cerebral Aneurysms 由 Yigit Karasozen, Joshua W. Osbun, Carolina A. Parada, Tina Busald, Philip D. Tatman, Luis F. Gonzalez‐Cuyar, Christopher J. Hale, Diana Alcantara, Mark O’Driscoll, William B. Dobyns, Mitzi L. Murray, Louis J. Kim, Peter H. Byers, Michael O. Dorschner, Manuel Ferreira
出版 2019Artigo -
7
Mutations in PIK3R1 Cause SHORT Syndrome 由 David A. Dyment, Amanda Smith, Diana Alcantara, Jeremy Schwartzentruber, Lina Basel‐Vanagaite, Cynthia J. Curry, I. Karen Temple, William Reardon, Sahar Mansour, Mushfequr R. Haq, Rodney D. Gilbert, Ordan J. Lehmann, Megan R. Vanstone, Chandree L. Beaulieu, Jacek Majewski, Dennis E. Bulman, Mark O’Driscoll, Kym M. Boycott, A. Micheil Innes
出版 2013Artigo -
8
Understanding the impact of 1q21.1 copy number variant 由 Chansonette Harvard, Emma Strong, Eloi Mercier, Rita Colnaghi, Diana Alcantara, Eva W. C. Chow, Sally Martell, Christine Tyson, Monica Hrynchak, Barbara McGillivray, Sara Hamilton, Sandra L. Marles, Aziz Mhanni, Angelika J. Dawson, Paul Pavlidis, Ying Qiao, J.J.A. Holden, M. E. Suzanne Lewis, Mark O’Driscoll, Evica Rajcan‐Separovic
出版 2011Artigo -
9
Asia–Pacific clinical practice guidelines on the management of hepatocellular carcinoma: a 2017 update 由 Omata, Masao, Cheng, Ann-Lii, Kokudo, Norihiro, Kudo, Masatoshi, Lee, Jeong Min, Jia, Jidong, Tateishi, Ryosuke, Han, Kwang-Hyub, Chawla, Yoghesh K., Shiina, Shuichiro, Jafri, Wasim, Payawal, Diana Alcantara, Ohki, Takamasa, Ogasawara, Sadahisa, Chen, Pei-Jer, Lesmana, Cosmas Rinaldi A., Lesmana, Laurentius A., Gani, Rino A., Obi, Shuntaro, Dokmeci, A. Kadir, Sarin, Shiv Kumar
出版 2017Text -
10
Expert consensus on the diagnosis and treatment of end-stage liver disease complicated by infections 由 Tao Chen, Guang Chen, Guiqiang Wang, Sombat Treeprasertsuk, Cosmas Rinaldi Adithya Lesmana, Han‐Chieh Lin, Mamun Al‐Mahtab, Yogesh Chawla, Soek-Siam Tan, Jia‐Horng Kao, Man‐Fung Yuen, Guan Huei Lee, Diana Alcantara‐Payawal, Nobuaki Nakayama, Zaigham Abbas, Wasim Jafri, Dong Joon Kim, Ashok Choudhury, Rakhi Mahiwall, Jinlin Hou, Saeed Hamid, Jidong Jia, Jasmohan S. Bajaj, Fusheng Wang, Shiv Kumar Sarin, Qin Ning
出版 2024Artigo -
11
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis 由 James T. Bennett, Tiong Yang Tan, Diana Alcantara, Martine Tétrault, Andrew E. Timms, Dana M. Jensen, Sarah Collins, Małgorzata J.M. Nowaczyk, Marjorie J. Lindhurst, Katherine Christensen, Stephen R. Braddock, Heather A. Brandling‐Bennett, Raoul C. M. Hennekam, Brian Hon‐Yin Chung, Anna Lehman, John Su, SuYuen Ng, David J. Amor, Jacek Majewski, Les Biesecker, Kym M. Boycott, William B. Dobyns, Mark O’Driscoll, Ute Moog, Laura M. McDonell
出版 2016Artigo -
12
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly–capillary malformation syndrome 由 Laura M. McDonell, Ghayda Mirzaa, Diana Alcantara, Jeremy Schwartzentruber, Melissa T. Carter, Leo J. Lee, Carol L. Clericuzio, John M. Graham, Deborah Morris‐Rosendahl, Tilman Polster, Gyula Acsádi, Sharron Townshend, Simon Williams, Anne Halbert, Bertrand Isidor, Albert David, Christopher D. Smyser, Alex R. Paciorkowski, Marcia Willing, John Woulfe, Soma Das, Chandree L. Beaulieu, Janet Marcadier, Michael T. Geraghty, Brendan J. Frey, Jacek Majewski, Dennis E. Bulman, William B. Dobyns, Mark O’Driscoll, Kym M. Boycott
出版 2013Artigo -
13
An expert review on the use of tenofovir alafenamide for the treatment of chronic hepatitis B virus infection in Asia 由 Charlton, Michael R., Alam, Altaf, Shukla, Akash, Dashtseren, Bekhbold, Lesmana, Cosmas Rinaldi Adithya, Duger, Davadoorj, Payawal, Diana Alcantara, Duy Cuong, Do, Jargalsaikhan, Ganbolor, Cua, Ian Homer Yee, Sollano, Jose Decena, Singh, Karam Romeo, Madan, Kaushal, Win, Khin Maung, Kyi, Khin Pyone, Tun, Kyaw Soe, Salih, Mohd., Rastogi, Mukul, Saraf, Neeraj, Thuy, Pham Thi Thu, Hien, Pham Tran Dieu, Gani, Rino Alvani, Mohamed, Rosmawati, Tanwandee, Tawesak, Piratvisuth, Teerha, Sukeepaisarnjaroen, Wattana, Naing, Win, Hashmi, Zahid Yasin
出版 2020Text -
14
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly 由 Diana Alcantara, Andrew E. Timms, Karen W. Gripp, Laura Baker, Kaylee Park, Sarah Collins, Chi Vicky Cheng, Fiona Stewart, Sarju Mehta, Anand Saggar, László Sztriha, Melinda Zombor, Oana Caluseriu, Ronit Mesterman, Margot I. Van Allen, Adeline Jacquinet, Sofia Ygberg, Jonathan A. Bernstein, Aaron M. Wenger, Harendra Guturu, Gill Bejerano, Natalia Gomez‐Ospina, Anna Lehman, Enrico Alfei, Chiara Pantaleoni, Valerio Conti, Renzo Guerrini, Ute Moog, John M. Graham, Robert F. Hevner, William B. Dobyns, Mark O’Driscoll, Ghayda Mirzaa
出版 2017Artigo -
15
Primary brain calcification: an international study reporting novel variants and associated phenotypes 由 Eliana Marisa Ramos, Miryam Carecchio, Roberta R. Lemos, Joana Ferreira, Andrea Legati, Renee Sears, Sandy Hsu, Celeste Panteghini, Luca Magistrelli, Ettore Salsano, Silvia Esposito, Franco Taroni, Anne‐Claire Richard, Christine Tranchant, Mathieu Anheim, Xavier Ayrignac, Cyril Goizet, Marie Vidailhet, David Maltête, David Wallon, Thierry Frébourg, Lylyan Fragoso Pimentel, Daniel H. Geschwind, Olivier Vanakker, Douglas Galasko, Brent L. Fogel, A. Micheil Innes, Alison Ross, William B. Dobyns, Diana Alcantara, Mark O’Driscoll, Didier Hannequin, Dominique Campion, João Ricardo Mendes de Oliveira, Barbara Garavaglia, Giovanni Coppola, Gaël Nicolas
出版 2018Artigo -
16
Asia–Pacific association for study of liver guidelines on management of ascites in liver disease 由 Virendra Singh, Arka De, Rohit Mehtani, Paolo Angeli, Rakhi Maiwall, Sanjaya K. Satapathy, Ashwini K. Singal, Anoop Saraya, Barjesh Chander Sharma, C. E. Eapen, Padaki Nagaraja Rao, Akash Shukla, S. Shalimar, Narendra S. Choudhary, Diana Alcantara‐Payawal, Vinod Arora, Guruprasad P. Aithal, Anand V. Kulkarni, Akash Roy, Ananta Shrestha, Mamun Al Mahtab, Madunil Anuk Niriella, Tan Soek Siam, Chunqing Zhang, Guan Huei Lee, Ming‐Lung Yu, Stuart K. Roberts, Cheng‐Yuan Peng, Tao Chen, Jacob George, Vincent Wai‐Sun Wong, Yusuf Yılmaz, Sombat Treeprasertsuk, Juferdy Kurniawan, Seung Up Kim, Zobair M. Younossi, Shiv Kumar Sarin
出版 2023Artigo -
17
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes 由 Jean-Baptiste Rivière, Ghayda Mirzaa, Brian J. O’Roak, Margaret Beddaoui, Diana Alcantara, Robert L. Conway, Judith St‐Onge, Jeremy Schwartzentruber, Karen W. Gripp, Sarah M. Nikkel, Thea Worthylake, Christopher T. Sullivan, Thomas Ward, Hailly E Butler, Nancy Kramer, Beate Albrecht, Christine M. Armour, Linlea Armstrong, Oana Caluseriu, Cheryl Cytrynbaum, Beth A. Drolet, A. Micheil Innes, Julie Lauzon, Angela E. Lin, Grazia M.S. Mancini, Wendy S. Meschino, James D. Reggin, Anand Saggar, Tally Lerman‐Sagie, Gökhan Uyanık, Rosanna Weksberg, Birgit Zirn, Chandree L. Beaulieu, Jacek Majewski, Dennis E. Bulman, Mark O’Driscoll, Jay Shendure, John M. Graham, Kym M. Boycott, William B. Dobyns
出版 2012Artigo
相關主題
Biology
Genetics
Medicine
Gene
Internal medicine
Mutation
Liver disease
Microcephaly
Abdominal surgery
Cancer research
Cell biology
Colorectal surgery
Disease
Epilepsy
General surgery
Geography
Hepatology
Intensive care medicine
Megalencephaly
Neuroscience
PDGFRB
PI3K/AKT/mTOR pathway
Paleontology
Pediatrics
Phenotype
Polymicrogyria
Receptor
Sanger sequencing
AKT1
AKT3