Zobrazeno 1 - 10
of 2 851
pro vyhledávání: '"Jesus Hernandez"'
Autor:
DOHERTY, SUSAN
Publikováno v:
Principal; Sep/Oct2024, Vol. 104 Issue 1, p40-41, 2p
Autor:
Keiko Taniguchi-Ponciano, Silvia Hinojosa-Alvarez, Jesus Hernandez-Perez, Rocio A. Chavez-Santoscoy, Ilan Remba-Shapiro, Gerardo Guinto, Erika Magallon-Gayon, Benjamin Telles-Ramirez, Rodrigo Ponce de Leon-Conconi, Sandra Vela-Patiño, Sergio Andonegui-Elguera, Amayrani Cano-Zaragoza, Florencia Martinez-Mendoza, Jacobo Kerbel, Marco Loza-Mejia, Juan Rodrigo-Salazar, Alonso Mendez-Perez, Cristina Aguilar-Flores, Antonieta Chavez-Gonzalez, Elenka Ortiz-Reyes, Erick Gomez-Apo, Laura C. Bonifaz, Daniel Marrero-Rodriguez, Moises Mercado
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-20 (2024)
Abstract Pituitary neuroendocrine tumors (PitNET) represent the vast majority of sellar masses. Some behave aggressively, growing rapidly and invading surrounding tissues, with high rates of recurrence and resistance to therapy. Our aim was to establ
Externí odkaz:
https://doaj.org/article/1b6c1939f3f746799fce58209502bf76
Autor:
Hernández, Jesús Hernández
This work is the extension of the results by the author in [7] and [6] for low-genus surfaces. Let $S$ be an orientable, connected surface of finite topological type, with genus $g \leq 2$, empty boundary, and complexity at least $2$; as a complement
Externí odkaz:
http://arxiv.org/abs/2307.15161
Akademický článek
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Autor:
Paulo José Lorenzoni, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci, Otto Jesus Hernandez Fustes, Paula Raquel do Vale Pascoal Rodrigues, Raquel Cristina Arndt, Rosana Herminia Scola, Lineu Cesar Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 02, Pp 001-004 (2024)
Carnitine palmitoyltransferase II (CPT II) deficiency is an autosomal recessive inherited disorder related to lipid metabolism affecting skeletal muscle. The first cases of CPT II deficiency causing myopathy were reported in 1973. In 1983, Werneck et
Externí odkaz:
https://doaj.org/article/ef0fa6c811994542ac3af4f780a87966
Autor:
Santiró, Ernest Sánchez
Publikováno v:
Historia Mexicana, 2014 Oct 01. 642 (254), 792-800.
Externí odkaz:
https://www.jstor.org/stable/24369058
Autor:
Vázquez, Josefina Zoraida
Publikováno v:
Historia Mexicana, 2014 Apr 01. 634 (252), 2062-2071.
Externí odkaz:
https://www.jstor.org/stable/43744195
Autor:
Cristhiam de Jesus Hernandez Martinez, Joseph Glessner, Livia Sertori Finoti, Pedro Felix Silva, Michel Messora, Ricardo Della Coletta, Hakon Hakonarson, Daniela Bazan Palioto
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 14 (2024)
ObjectiveThe study delved into the epigenetic factors associated with periodontal disease in two lineages of mice, namely C57bl/6 and Balb/c. Its primary objective was to elucidate alterations in the methylome of mice with distinct genetic background
Externí odkaz:
https://doaj.org/article/3fb7e4f396b84e208811b02c823f84ab
Autor:
Paula Raquel do Vale Pascoal Rodrigues, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci, Marco Antonio Takashi Utiumi, Otto Jesus Hernandez Fustes, Lineu Cesar Werneck, Paulo José Lorenzoni, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 01, Pp 001-007 (2024)
Background Myasthenia gravis (MG) is an autoimmune disease usually caused by antibodies against the acetylcholine receptor (AChR-Abs), muscle-specific tyrosine kinase (MuSK-Abs), or low-density lipoprotein receptor-related protein 4 (LRP4-Abs). Howev
Externí odkaz:
https://doaj.org/article/f1f761e852df46bfb0c8abb739988a34
Autor:
Renata Dal-Prá Ducci, Michelle Zonkowski Ribas, Enzo Oku Martinazzo, Otto Jesus Hernandez Fustes, Paulo José Lorenzoni, Claudia Suemi Kamoi Kay, Rosana Hermínia Scola
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 59, Iss 1, Pp 1-4 (2023)
Abstract Background Gaucher disease (GD) is an autosomal recessive disease characterized by an inborn metabolic error. Although pain attributed to skeletal involvement is one of the most frequent symptoms of this condition, some patients may have neu
Externí odkaz:
https://doaj.org/article/d842150c2ea2475a84cc398f47de3195