Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maria del Carmen Moleon"'
Autor:
Marisa Flook, Maria-Del-Carmen Moleon, Maria Alharilla Montilla-Ibañez, Juan Antonio Gallego, Andreina Peralta-Leal, Emilio Domínguez-Durán, Jose A. Lopez-Escamez, Estrella Martínez-Gómez, Andrés Soto-Varela, Ismael Aran, Lidia Frejo, Hortensia Sánchez-Gómez
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Journal of Clinical Medicine
Volume 10
Issue 18
Journal of Clinical Medicine, Vol 10, Iss 4052, p 4052 (2021)
instname
Journal of Clinical Medicine
Volume 10
Issue 18
Journal of Clinical Medicine, Vol 10, Iss 4052, p 4052 (2021)
Background: Meniere disease (MD) is an inner ear disorder associated with comorbidities such as autoimmune diseases or migraine. This study describes clinical and cytokine profiles in MD according to the age of onset of the condition. Methods: A cros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd882cfbc4e29d06a5205b4301c3d2d
https://doi.org/10.20944/preprints202108.0162.v1
https://doi.org/10.20944/preprints202108.0162.v1
Autor:
Paz Pérez-Vázquez, Pablo Roman-Naranjo, Angel Batuecas-Caletrio, Maria del Carmen Moleon, Jose A. Lopez-Escamez, Alvaro Gallego-Martinez, Juan Manuel Espinosa-Sanchez, Andrés Soto-Varela, Ismael Aran, Juan Carlos Amor-Dorado
Publikováno v:
Ear and hearing. 41(6)
OBJECTIVES Meniere's disease (MD) is a rare inner ear disorder characterized by sensorineural hearing loss, episodic vertigo, and tinnitus. Familial MD has been reported in 6 to 9% of sporadic cases, and few genes including FAM136A, DTNA, PRKCB, SEMA
Autor:
Paz Pérez-Vázquez, Jose A. Lopez-Escamez, Pablo Roman-Naranjo, Juan Manuel Espinosa-Sanchez, Andrés Soto-Varela, Ismael Aran, Juan Carlos Amor-Dorado, Alvaro Gallego-Martinez, Maria del Carmen Moleon, Angel Batuecas-Caletrio
ObjectivesMeniere’s disease (MD) is a rare inner ear disorder characterized by sensorineural hearing loss, episodic vertigo and tinnitus. Familial MD has been reported in 6-9% of sporadic cases, and few genes includingFAM136A, DTNA, PRKCB, SEMA3Dan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe91e5b1a157cc196b8031ddf6e2a538