HuGE Literature Finder
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| HLA Genotyping in Romanian Adult Patients with Celiac Disease, their First-degree Relatives and Healthy Persons. Journal of gastrointestinal and liver diseases : JGLD 2022 Jun 31 (2): 191-197. Maruntelu Ion, Preda Carmen Monica, Sandra Irina, Istratescu Doina, Chifulescu Andreea Elena, Manuc Mircea, Diculescu Mircea, Talangescu Adriana, Tugui Letitia, Manuc Teodora, Stroie Tudor, Andrei Adriana Corina, Tieranu Cristian, Constantinescu Ilea |
| Venetoclax plus azacitidine and donor lymphocyte infusion in treating acute myeloid leukemia patients who relapse after allogeneic hematopoietic stem cell transplantation. Annals of hematology 2021 Sep . Zhao Peng, Ni Ming, Ma Dan, Fang Qin, Zhang Yan, Li Yanju, Huang Yi, Chen Ying, Chai Xiao, Zhan Yun, Li Yan, Kang Qian, Zhao Mei, Liu Min, Zhang Fengqi, Huang Shisi, Wen Shuangshuang, Deng Bo, Wang Jis |
| Prognostic factors for survival in patients with mucosal and ocular melanoma treated with ipilimumab: Turkish Oncology Group study. Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners 2019 Mar 1078155219840796. Arzu Yasar H, Turna Hande, Esin Ece, Murat Sedef A, Alkan Ali, Oksuzoglu Berna, Ozdemir Nuriye, Sendur Ma Nahit, Sezer Ahmet, Kilickap Saadettin, Utkan Gungor, Akbulut Hakan, Celik Ismail, Abali Huseyin, Urun Yuks |
| Assessment of glucose-6-phosphate dehydrogenase activity using CareStart G6PD rapid diagnostic test and associated genetic variants in Plasmodium vivax malaria endemic setting in Mauritania. PloS one 2019 14 (9): e0220977. Djigo Oum Kelthoum Mamadou, Bollahi Mohamed Abdallahi, Hasni Ebou Moina, Ould Ahmedou Salem Mohamed Salem, Tahar Rachida, Bogreau Hervé, Basco Leonardo, Ould Mohamed Salem Boukhary A |
| Association of genetic polymorphisms with erythrocyte traits: Verification of SNPs reported in a previous GWAS in a Japanese population. Gene 2017 Nov . Seiki Toshio, Naito Mariko, Hishida Asahi, Takagi Sahoko, Matsunaga Takashi, Sasakabe Tae, Hattori Yuta, Kawai Sayo, Okada Rieko, Yin Guang, Hamajima Nobuyuki, Wakai Ken |
| Development of a new real-time PCR screening kit for HbS and common beta-thalassemia mutations observed in Turkey. Turkish journal of medical sciences 2017 Jun 47 (3): 973-978. Kan Karaer Derya, Ergün Mehmet Ali, Ruhi Hatice Ilg?n, Öztürk Jale, Kara Halil, Reiso?lu Çakmak Deniz, Aydo?mu? Talihanur, Perçin Emriye Fer |
| [Association between clinical outcome and gene mutation in children with Fanconi anemia]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2016 Aug 18 (8): 742-5. Chang Li-Xian, Ren Ruan-Ruan, Yang Wen-Yu, Zhang Jia-Yuan, Wan Yang, Liu Tian-Feng, Zhang Li, Chen Xiao-Juan, Zhu Shuai, Ruan Min, Chen Xia, Liu Xiao-Ming, Qi Ben-Quan, Zhang Ran-Ran, Zou Yao, Chen Yu-Mei, Zhu Xiao-F |
| Efficacy and Safety of Midostaurin in Advanced Systemic Mastocytosis. The New England journal of medicine 2016 Jun 374 (26): 2530-41. Gotlib Jason, Kluin-Nelemans Hanneke C, George Tracy I, Akin Cem, Sotlar Karl, Hermine Olivier, Awan Farrukh T, Hexner Elizabeth, Mauro Michael J, Sternberg David W, Villeneuve Matthieu, Huntsman Labed Alice, Stanek Eric J, Hartmann Karin, Horny Hans-Peter, Valent Peter, Reiter Andre |
| Mastocytosis among elderly patients: A multicenter retrospective French study on 53 patients. Medicine 2016 Jun 95 (24): e3901. Rouet Audrey, Aouba Achille, Damaj Gandhi, Soucié Erinn, Hanssens Katia, Chandesris Marie-Olivia, Livideanu Cristina Bulai, Dutertre Marine, Durieu Isabelle, Grandpeix-Guyodo Catherine, Barète Stéphane, Bachmeyer Claude, Soria Angèle, Frenzel Laurent, Fain Olivier, Grosbois Bernard, de Gennes Christian, Hamidou Mohamed, Arlet Jean-Benoit, Launay David, Lavigne Christian, Arock Michel, Lortholary Olivier, Dubreuil Patrice, Hermine Olivier, Georgin-Lavialle Soph |
| Nilotinib in patients with systemic mastocytosis: analysis of the phase 2, open-label, single-arm nilotinib registration study. Journal of cancer research and clinical oncology 2015 Nov 141 (11): 2047-60. Hochhaus Andreas, Baccarani Michele, Giles Francis J, le Coutre Philipp D, Müller Martin C, Reiter Andreas, Santanastasio Helene, Leung Mimi, Novick Steven, Kantarjian Hagop |
| Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The Istanbul Perspective. Turkish journal of haematology : official journal of Turkish Society of Haematology 2015 Aug . Koç Beg |
| Pre-treatment role of inosine triphosphate pyrophosphatase polymorphism for predicting anemia in Egyptian hepatitis C virus patients. World journal of gastroenterology : WJG 2013 Mar 19 (9): 1387-95. Ahmed Walaa H, Furusyo Norihiro, Zaky Saad, Eldin Abeer Sharaf, Aboalam Hany, Ogawa Eiichi, Murata Masayuki, Hayashi J |
| ITPA gene polymorphisms significantly affect hemoglobin decline and treatment outcomes in patients coinfected with HIV and HCV. Journal of medical virology 2012 Jul 84 (7): 1106-14. Osinusi Anu, Naggie Susanna, Poonia Seerat, Trippler Martin, Hu Zonghui, Funk Emily, Schlaak Joerg, Fishbein Dawn, Masur Henry, Polis Michael, Kottilil Shy |
| Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia in HIV/HCV-coinfected patients with all HCV genotypes. The Journal of infectious diseases 2012 Feb 205 (3): 376-83. Naggie Susanna, Rallon Norma I, Benito José M, Morello Judith, Rodriguez-Novoa Sonia, Clark Paul J, Thompson Alexander J, Shianna Kevin V, Vispo Eugenia, McHutchison John G, Goldstein David B, Soriano Vince |
| Prevalence of glutathione S-transferase gene deletions and their effect on sickle cell patients. Revista brasileira de hematologia e hemoterapia 2012 34 (2): 100-2. Sanjay Pandey, Mani Mishra Rahasy, Sweta Pandey, Vineet Shah, Kumar Ahuja Rajesh, Renu Saxe |
| A prospective, multicenter, phase 2 study of imatinib mesylate in korean patients with metastatic or unresectable gastrointestinal stromal tumor. Oncology 2009 Mar 76 (5): 5. Ryu MH, Kang WK, Bang YJ, Lee KH, Shin DB, Ryoo BY, Roh JK, Kang JH, Lee H, Kim TW, Chang HM, Park JO, Park YS, Kim TY, Kim MK, Lee WK, Kang HJ, Kang YK |
| Bloom syndrome and Fanconi's anemia: rate and ethnic origin of mutation carriers in Israel. The Israel Medical Association journal : IMAJ 2002 Feb 4 (2): 95-7. Peleg Leah, Pesso Rachel, Goldman Boleslaw, Dotan Keren, Omer Merav, Friedman Eitan, Berkenstadt Michal, Reznik-Wolf Haike, Barkai G |
| Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population. Pakistan journal of medical sciences 0 33 (2): 411-416. Shahid Saba, Nadeem Muhammad, Zahid Danish, Hassan Jawad, Ansari Saqib, Shamsi Tah |
| HLA - DQ genotyping in celiac disease in western India. Tropical gastroenterology : official journal of the Digestive Diseases Foundation 0 36 (3): 174-8. Amarapurkar Deepak N, Somani Vaibhav S, Shah Apurva S, Kankonkar Sharada |
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- Page last updated:Feb 03, 2023
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