المؤلفون: Vu, An Dan, Vo-Thanh, Tan, Nguyen, Thi Tuyet Mai, Bui, Ha Linh, Pham, Tan Nhat

المصدر: In Heliyon 15 January 2024 10(1)

المؤلفون: Beauregard-Lacroix, Éliane, Scott, Alexandra, Nguyen, Thi Tuyet Mai, Wierenga, Klaas J., Purcarin, Gabriela, Karstensen, Anne B., Carvalho, Daniel R., Alessandri, Jean-Luc, Payet, Frédérique, Girisha, Katta M., Ferron, Mathieu, Campeau, Philippe M.

المصدر: In Genetics in Medicine Open 2024 2

المؤلفون: Johnstone, Devon L., Nguyen, Thi Tuyet Mai, Zambonin, Jessica, Kernohan, Kristin D., St-Denis, Anik, Baratang, Nissan V., Hartley, Taila, Geraghty, Michael T., Richer, Julie, Majewski, Jacek, Bareke, Eric, Guerin, Andrea, Pendziwiat, Manuela, Pena, Loren D.M., Braakman, Hilde M.H., Gripp, Karen W., Edmondson, Andrew C., He, Miao, Spillmann, Rebecca C., Eklund, Erik A., Bayat, Allan, McMillan, Hugh J., Boycott, Kym M., Campeau, Philippe M.

المصدر: Journal of Inherited Metabolic Disease. 43(6):1321-1332

مصطلحات موضوعية: epileptic encephalopathy, exome sequencing, GPI, IGD, PIGQ, rare diseases, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Neurovetenskaper, Medical and Health Sciences, Basic Medicine, Neurosciences

URL الوصول: https://lup.lub.lu.se/record/6ef070d0-a2d7-4b12-a18c-a9170d2b7094
http://dx.doi.org/10.1002/jimd.12278

المؤلفون: Ha-Huy, Thai, Nguyen, Thi Tuyet Mai

المصدر: In Journal of Mathematical Economics December 2022 103

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المؤلفون: Nguyen, Thi Tuyet Mai, Tran, Quoc Trung

المصدر: In North American Journal of Economics and Finance November 2022 62

المؤلفون: Nguyen, Thi Tuyet Mai, Murakami, Yoshiko, Wigby, Kristen M, Baratang, Nissan V, Rousseau, Justine, St-Denis, Anik, Rosenfeld, Jill A, Laniewski, Stephanie C, Jones, Julie, Iglesias, Alejandro D, Jones, Marilyn C, Masser-Frye, Diane, Scheuerle, Angela E, Perry, Denise L, Taft, Ryan J, Le Deist, Françoise, Thompson, Miles, Kinoshita, Taroh, Campeau, Philippe M

المصدر: American Journal of Human Genetics. 103(4)

مصطلحات موضوعية: Neurodegenerative, Congenital Structural Anomalies, Pediatric, Brain Disorders, Rare Diseases, Genetics, Human Genome, Neurosciences, 2.1 Biological and endogenous factors, Aetiology, Abnormalities, Multiple, Acyltransferases, Arthrogryposis, Cell Line, Cerebellar Ataxia, Child, Child, Preschool, Developmental Disabilities, Epilepsy, Generalized, Female, HEK293 Cells, Humans, Intellectual Disability, Male, Muscle Hypotonia, Mutation, Nervous System Malformations, Pedigree, Seizures, Syndrome, Whole Exome Sequencing, Exome Sequencing, PIGS, epilepsy, glycosylphosphatidylinositol, glycosylphosphatidylinositol biosynthesis defect, inherited GPI deficiency, seizures, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4bj18588

المؤلفون: Tremblay-Laganière, Camille, Maroofian, Reza, Nguyen, Thi Tuyet Mai, Karimiani, Ehsan Ghayoor^{Aff3, Aff4}, Kirmani, Salman, Akbar, Fizza, Ibrahim, Shahnaz, Afroze, Bushra, Doosti, Mohammad, Ashrafzadeh, Farah, Babaei, Meisam, Efthymiou, Stephanie, Christoforou, Marilena, Sultan, Tipu, Ladda, Roger L., McLaughlin, Heather M., Truty, Rebecca, Mahida, Sonal, Cohen, Julie S.^{Aff11, Aff12}, Baranano, Kristin^{Aff11, Aff12}, Ismail, Fatima Y.^{Aff12, Aff13}, Patel, Millan S., Lehman, Anna, Edmondson, Andrew C., Nagy, Amanda, Walker, Melissa A., Mercimek-Andrews, Saadet^{Aff17, Aff18}, Maki, Yuta^{Aff19, Aff20}, Sachdev, Rani^{Aff21, Aff22}, Macintosh, Rebecca, Palmer, Elizabeth E.^{Aff21, Aff22}, Mancini, Grazia M. S., Barakat, Tahsin Stefan, Steinfeld, Robert, Rüsch, Christina T., Stettner, Georg M., Wagner, Matias^{Aff25, Aff26}, Wortmann, Saskia B.^{Aff27, Aff28}, Kini, Usha, Brady, Angela F., Stals, Karen L., Ismayilova, Naila, Ellard, Sian^{Aff31, Aff33}, Bernardo, Danilo, Nugent, Kimberly, McLean, Scott D., Antonarakis, Stylianos E., Houlden, Henry, Kinoshita, Taroh^{Aff37, Aff38}, Campeau, Philippe M.^Aff1, Murakami, Yoshiko^{Aff37, Aff38}

المصدر: Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 23(10):1873-1881

المؤلفون: Salian, Smrithi, Benkerroum, Hind, Nguyen, Thi Tuyet Mai, Nampoothiri, Sheela, Kinoshita, Taroh, Félix, Têmis Maria, Stewart, Fiona, Sisodiya, Sanjay M., Murakami, Yoshiko, Campeau, Philippe M.^Aff1

المصدر: Human Genetics. 140(6):879-884