Establishment of an immortalized human subglottic epithelial cell line
The Laryngoscope, Volume 129, Issue 11, Page 2640-2645, November 2019., 2019 Objective Translational research into subglottic disease is restricted by the availability of primary human tissue originating from this subsite. Primary epithelial cells are also limited by their inability to survive beyond several divisions in culture outside of the body.
Jason Powell +5 more
wiley +1 more source
Identificación de potenciales biomarcadores de calcificación vascular en pacientes con diabetes mellitus tipo 2 mediante el uso de herramientas bioinformáticas de libre acceso [PDF]
, 2018 Identificación de potenciales biomarcadores implicados en procesos de calcificación vascular para avanzar en el diagnóstico y tratamiento de esta patología en sus estadíos subclínicos.
Andujar Vera, Francisco +5 more
core +4 more sources
Brazilian Journal of Otorhinolaryngology, 2011 O manejo da estenose subglótica (ESG) em crianças continua sendo um desafio para os otorrinolaringologistas. A laringoplastia com balão (LPB) consiste num procedimento endoscópico, descrito inicialmente em 1984, para tratamento de estenoses da via aérea ...
Claudia Schweiger +4 more
doaj +1 more source
Caracterización de la estenosis laringotraqueal [PDF]
, 2020 Background: the increase in the number of cases with laryngeal-tracheal stenosis is a concern in the present and future of medical practice. Objective: to characterize laryngeal-tracheal stenosis.
Estrada-Brizuela, Yarima +4 more
core +1 more source
Surgical treatment of median laryngostenosis of paralitic ethiology [PDF]
, 2010 The article gives the information about 44 patients with laterofixation of true vocal cord. The research includes 41 patients with median laryngostenosis diagnosis with paralitic ethiology and tracheostoma, and 3 patients with transaction of both ...
Ginzburg, A. G. +1 more
core
Pediatric Gastroesophageal Reflux Disease [PDF]
, 2016 Gastroesophageal reflux is the return of stomach contents into the esophagus. It is normal in the newborn due to an immature gastroesophageal sphincter.
Prusinski, Regina F
core +1 more source
NLM at ImageCLEF 2017 caption task [PDF]
, 2017 This paper describes the participation of the U.S. National Library of Medicine (NLM) in the ImageCLEF 2017 caption task. We proposed different machine learning methods using training subsets that we selected from the provided data as well as retrieval ...
Abacha, AB +4 more
core
Granulomatoza s poliangiitisom (GPA) i lokaliziranim zahvaćanjem gornjega dišnog sustava – prikaz bolesnice [Granulomatosis with polyangiitis (GPA) limited to upper respiratory tract - a case report] [PDF]
, 2016 Granulomatosis with polyangiitis (Wegener's granulomatosis) is one of the anti-neutrophil cytoplasmic anti-body-associated small vessel vasculitides. Upper and lower respiratory system and kidneys are most commonly affected.
Gudelj-Gračanin, Ana +6 more
core
GRANULOMATOSIS WITH POLYANGIITIS (GPA) LIMITED TO UPPER RESPIRATORY TRACT – A CASE REPORT [PDF]
, 2016 Granulomatoza s poliangiitisom (Wegenerova granulomatoza) ubraja se u vaskulitise malih krvnih žila povezane s antineutrofilnim citoplazmatskim protutijelima. Najčešće su zahvaćeni gornji i donji dišni sustav te bubrezi.
Ana Gudelj-Gračanin +6 more
core +1 more source
DECRIPTION OF A HEREDITARY ANGIONEUROTIC EDEMA FORM IN A CHILD [PDF]
, 2020 Congenital deficiency of the C1-component inhibitor of the complement cascade, or hereditary angioneurotic edema, is a rare autosomal dominant disease due to a mutation in the human C1-esterase inhibitor.
Luiza M. Karzakova +5 more
core +1 more source