Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Kelly Gonzalez"'
Publikováno v:
Journal of Economics Finance and Administrative Science, Vol 20, Iss 39, Pp 84-93 (2015)
This paper describes the changes in ownership and internationalization of the brokerage firms in Colombia as a result of the regional integration process of its stock exchange market through the Latin American Integrated Market (MILA). It proposes th
Externí odkaz:
https://doaj.org/article/f7c7111530204eaea7199f606415bfc8
Autor:
Kelly Gonzalez
Publikováno v:
Journal of the Medical Library Association, Vol 105, Iss 4 (2017)
A profile of Barbara Epstein, AHIP, FMLA, Medical Library Association President, 2017–2018.
Externí odkaz:
https://doaj.org/article/74908790f05c43f698090a3d560ac335
Autor:
Sofía Romero Gil, Marina Morcillo Martin, Paula Pereira Velicia, Kelly González Anselmo, José María Ramada, Fernando G. Benavides
Publikováno v:
Archivos de Prevención de Riesgos Laborales, Vol 27, Iss 3 (2024)
En España, entender si una enfermedad está relacionada con el trabajo puede ser complicado. Desde 2010, la Unidad de Patología Laboral del Hospital de Mar en Barcelona ha jugado un papel clave examinando 228 casos de enfermedades que podrían veni
Externí odkaz:
https://doaj.org/article/9cad01e960f44214bd3f219f4dab0bf2
Written for all gaming enthusiasts, this book fuses Latinx studies and video game studies to document how Latinx masculinities are portrayed in high-budget action-adventure video games, inviting Latinxs and others to insert their experiences into gam
Publikováno v:
Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral NutritionReference. 34(6)
Autor:
Kelly Gonzalez
Publikováno v:
Journal of Hospital Librarianship. 16:250-254
The transformation of an academic medical center library into a digital library seems like an impossible task. The Library at the University of Texas Southwestern Medical Center (UTSW) took the fir...
Autor:
Antonia R. Sepulveda, Lea Tuzovic, Ashley Wilson, Charles A. LeDuc, Kwame Anyane-Yeboa, Luis Rohena, Kelly Gonzalez, Ashley Mills, Xiang Li, Sha Tang, Russell Miller, Kenneth Glassberg, Jiancheng Guo, Wendy K. Chung, Layla Shahmirzadi, Heidi Rotterdam, Wenqi Zeng
Publikováno v:
Fetal Diagnosis and Therapy. 38:296-306
Objective: To identify the molecular basis for prenatally suspected cases of megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) (MIM 249210) in 3 independent families with clinical and radiographic evidence of MMIHS. Methods: Whole-exo
Autor:
Masayuki Endo, Jennifer Alphonse, Luc De Catte, Jan Deprest, Mamak Shariat, Takumi Ishiodori, Ashley Wilson, Abhijit Kulkarni, Alec W. Welsh, Kiyotake Ichizuka, Wenqi Zeng, Nobuaki Mitsuda, Linda Wu, Luis Rohena, Mahdi Sheikh, Naoto Yonetani, Negar Mahmoodian, Philip DeKoninck, Satz Mengensatzproduktion, Aki Mabuchi, Kelly Gonzalez, Keisuke Ishii, Seigo Gomi, Asma Khalil, Joost Akkermans, Xiang Li, Tatsuya Arakaki, Hiroko Takita, Kenneth Glassberg, Jiancheng Guo, Masakazu Abe, Shusaku Hayashi, Neama Meriki, Heidi Rotterdam, Basky Thilaganathan, Layla Shahmirzadi, Yukiko Ban, Druckerei Stückle, Masamitsu Nakamura, Junichi Hasegawa, Shoko Hamada, Wendy K. Chung, Ashley Mills, Frans J.C.M. Klumper, Charles A. LeDuc, Junko Shiono, Antonia R. Sepulveda, Amanda Henry, Hiroshi Kawamura, Lea Tuzovic, Sha Tang, Russell Miller, Suzanne H.P. Peeters, Takashi Murakami, Kwame Anyane-Yeboa, Hitoshi Horigome, Sedigheh Hantoushzadeh, Amar Bhide, Tessa Homfray, Enrico Lopriore, Dick Oepkes, Aris T. Papageorghiou, Johanna M. Middeldorp, Akihiko Sekizawa, Sanaz Mousavi, Aditi Mahajan
Publikováno v:
Fetal Diagnosis and Therapy. 38:I-IV
Autor:
Melissa C. Parra, Elizabeth C. Chao, Kelly Gonzalez, Erika Palmaer, Sha Tang, Layla Shahmirzadi
Publikováno v:
Genetics in Medicine. 16:395-399
Exome sequencing of a single individual for a clinical indication may result in the identification of incidental deleterious variants unrelated to the indication for testing (secondary findings). Given the recent availability of clinical exome testin
Autor:
Kwame Anyane-Yeboa, Patrick P. Koty, Wenqi Zeng, Christiane Zweier, Guntram Borck, Nils Rahner, Rüstem Yilmaz, Dorothy K. Grange, Heinrich Sticht, Lina Basel-Vanagaite, Nathalie Boddaert, Christian Kubisch, Heather Feenstra, Tamison Jewett, André Reis, Sha Tang, Megan Mortenson, Miriam S. Reuter, Julie Désir, Kelly Gonzalez
Publikováno v:
Human Genetics. 133:939-949
Biallelic mutations of UBE3B have recently been shown to cause Kaufman oculocerebrofacial syndrome (also reported as blepharophimosis-ptosis-intellectual disability syndrome), an autosomal recessive condition characterized by hypotonia, developmental