Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Alfredo Adolfo Reza-Albarran"'
Autor:
Marcia Janneth Bermeo Cabrera, Pablo Roberto Ordoñez Chacha, Alfredo Adolfo Reza‐Albarrán, Ana Karina Ordoñez Chacha, Marcy Acosta Acero, Agustin Rodas Serrano
Publikováno v:
Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract X‐linked hypophosphatemia (XLH) is a rare disexase in which patients present with severe bowing of the legs, joint pain, and mobility problems. XLH has major adverse repercussions on the quality of life.
Externí odkaz:
https://doaj.org/article/fe70a8f8675b47329f5a49945c30e08d
Autor:
Alejandro Terrones-Lozano, Alan Hernández-Hernández, Edgar Nathal Vera, Gerardo Yoshiaki Guinto-Nishimura, Jorge Luis Balderrama-Bañares, Claudia Ramírez-Rentería, Judith de la Serna-Soto, Alfredo Adolfo Reza-Albarran, Lesly Portocarrero-Ortiz
Publikováno v:
Case Reports in Endocrinology, Vol 2020 (2020)
Introduction. Pheochromocytomas (Pheo) and paragangliomas (PGL) are rare neuroendocrine tumors arising from chromaffin cells of the adrenal medulla and from the extra-adrenal autonomic paraganglia, respectively. Only 1–3% of head and neck PGL (HNPG
Externí odkaz:
https://doaj.org/article/175e7d8909134edd90c959469584f2b7
Autor:
Tamara N. Kimball, Pamela Rivero‐García, Bernardo Pérez González, Alfredo Adolfo Reza‐Albarrán
Publikováno v:
Clinical Case Reports, Vol 11, Iss 10, Pp n/a-n/a (2023)
Key Clinical Message Diastrophic dysplasia (DTD) is caused by biallelic pathogenic variants in the SLC26A2 gene. We report the case of a 49‐year‐old female with DTD and esophageal stenosis. This broadens the phenotypic spectrum in adult patients
Externí odkaz:
https://doaj.org/article/6554cafc4a1d40a8876022932ed67be9
Autor:
Luis Geraldine Villanueva‐Rodríguez, Alfredo Adolfo Reza‐Albarrán, Enrique Cárdenas, Arturo Ángeles, Jacobo Lester
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Insulinoma may have an atypical presentation and it should be suspected in patients with neurological manifestations in spite of an atypical insulin and proinsulin levels associated with hypoglycemia. Fast test is an important tool to reach
Externí odkaz:
https://doaj.org/article/253aab9dea28452697f7624d666c9786
Autor:
Gerson Geovany Andino-Ríos, Lesly Portocarrero-Ortiz, Carlos Rojas-Guerrero, Alejandro Terrones-Lozano, Alma Ortiz-Plata, Alfredo Adolfo Reza-Albarrán
Publikováno v:
Case Reports in Endocrinology, Vol 2018 (2018)
Objective. Pituitary adenomas can be classified as clinically functional or silent. Depending on the reviewed literature, these are the first or second place in frequency of the total pituitary adenomas. Even rarer is the presence of a functional gon
Externí odkaz:
https://doaj.org/article/5a1107d894124826bd460a46f8694b83
Autor:
Óscar Alfredo Juárez-León, Miguel Ángel Gómez-Sámano, Daniel Cuevas-Ramos, Paloma Almeda-Valdés, Manuel Alejandro López-Flores A La Torre, Alfredo Adolfo Reza-Albarrán, Francisco Javier Gómez-Pérez
Publikováno v:
Case Reports in Endocrinology, Vol 2015 (2015)
Hungry Bone Syndrome refers to the severe and prolonged hypocalcemia and hypophosphatemia, following parathyroidectomy in patients with hyperparathyroidism. We present the case of an eighteen-year-old woman with a four-year history of hyporexia, poly
Externí odkaz:
https://doaj.org/article/5eeb4b67caaf4d8ba960e922ecf9b74a