Ειδοποίηση Μελετητή:[ Laryngomalacia ]
A study on paediatric stridor causes and management: case series
DK Selvam, VJ Vikram, M Saktheeswaran, MI MP - International Journal of …, 2017
... Results: Laryngomalacia was the most common cause of infant stridor in less than
one year of age in 348 cases, while Foreign body aspiration is the most common
cause of stridor in age group one to 12 years in 122 cases. ...
one year of age in 348 cases, while Foreign body aspiration is the most common
cause of stridor in age group one to 12 years in 122 cases. ...
Robotic epiglottopexy for severe epiglottic prolapse limiting decannulation
CA Colaianni, SN Bowe, HA Osborn, DT Lin… - International Journal of …, 2017
... Postoperatively the patient is tolerating capping during waking hours. Keywords.
Robot-assisted surgery; Laryngomalacia; Suprastomal collapse; Petiole prolapse. 1.
Introduction. ... Epiglottopexy for the treatment of severe laryngomalacia. Eur. Arch. ...
Robot-assisted surgery; Laryngomalacia; Suprastomal collapse; Petiole prolapse. 1.
Introduction. ... Epiglottopexy for the treatment of severe laryngomalacia. Eur. Arch. ...
Clinical variables determining the success of adenotonsillectomy in children with Down syndrome
M da Rocha, RCM Ferraz, VG Chen, GA Moreira… - International Journal of …, 2017
... followed by postoperative PSG. We excluded patient who lack pre- or post-operative
PSG, or who had upper airway comorbidities (subglottic stenosis, laryngomalacia),
and sleep period <180 min. The complaints reported by ...
PSG, or who had upper airway comorbidities (subglottic stenosis, laryngomalacia),
and sleep period <180 min. The complaints reported by ...
[PDF] Access to Dental Services for Children with Special Health Care Needs: A Pilot Study at the Dental Department of BC Children's Hospital
N Vertel, RL Harrison, KM Campbell - J Can Dent Assoc, 2017
... Other† 12 24.0 *The number of medical conditions exceeds the number of participants because
some had multiple comorbidities. †Includes cerebral palsy, craniofacial disorders, cancer,
prematurity, delayed tooth development, Kawasaki disease, laryngomalacia. Page 4. ...
some had multiple comorbidities. †Includes cerebral palsy, craniofacial disorders, cancer,
prematurity, delayed tooth development, Kawasaki disease, laryngomalacia. Page 4. ...
[HTML] A Vallecular Thyroglossal Duct Cyst Presenting with Persistent Unexplained Cough in a Toddler. Inter J Otorhinolaryngology. 2014; 1 (1): 3. Copyright© 2014 Bitar et …
MA Bitar, M Kamal, C Rameh - International Journal of Otorhinolaryngology| ISSN
... Vallecular masses, in general, have been associated with laryngomalacia [4,7] but that was
not encountered in our case. When large enough, they can also displace the epiglottis and
obscure the airway [4], and thus require extra care during intubation. ...
not encountered in our case. When large enough, they can also displace the epiglottis and
obscure the airway [4], and thus require extra care during intubation. ...
Diagnostic accuracy of current glossoptosis classification systems: A nested cohort cross‐sectional study
D Manica, C Schweiger, L Sekine, SC Fagondes… - The Laryngoscope, 2017
... Comorbid lesions were pharyngomalacia (10 patients), laryngomalacia (five patients),
layngopharyngomalacia (two patients), tracheo- malacia (one patient), nasal synechiae (one
patient), maxillary atresia (one patient), maxillary atresia and sub- mucosal palatine cleft (one ...
layngopharyngomalacia (two patients), tracheo- malacia (one patient), nasal synechiae (one
patient), maxillary atresia (one patient), maxillary atresia and sub- mucosal palatine cleft (one ...
Phenotype comparison confirms ZMYND11 as a critical gene for 10p15. 3 microdeletion syndrome
B Tumiene, Ž Čiuladaitė, E Preikšaitienė… - Journal of Applied Genetics, 2017
Page 1. HUMAN GENETICS • ORIGINAL PAPER Phenotype comparison confirms ZMYND11
as a critical gene for 10p15.3 microdeletion syndrome Birute Tumiene1,2 & Ž. Čiuladaitė1,2 &
E. Preikšaitienė1,2 & R. Mameniškienė3 & A. Utkus1,2 & V. Kučinskas1,2 ...
as a critical gene for 10p15.3 microdeletion syndrome Birute Tumiene1,2 & Ž. Čiuladaitė1,2 &
E. Preikšaitienė1,2 & R. Mameniškienė3 & A. Utkus1,2 & V. Kučinskas1,2 ...
The spectrum of DNMT3A variants in Tatton–Brown–Rahman syndrome overlaps with that in hematologic malignancies
W Shen, JM Heeley, CM Carlston, R Acuna‐Hidalgo… - … Journal of Medical Genetics Part A
... 1.2 SD). Medical problems included a history of laryngomalacia, nystagmus,
astigmatism, ptosis, inguinal and umbilical hernias, and hydronephrosis with
vesicoureteral reflux that required ureteral reimplantation. The patient ...
astigmatism, ptosis, inguinal and umbilical hernias, and hydronephrosis with
vesicoureteral reflux that required ureteral reimplantation. The patient ...
Airway ciliary dysfunction: Association with adverse postoperative outcomes in non-heterotaxy congenital heart disease patients
E Stewart, PS Adams, X Tian, O Khalifa, P Wearden… - The Journal of Thoracic and …, 2017
Page 1. Accepted Manuscript Airway ciliary dysfunction: Association with adverse
postoperative outcomes in non- heterotaxy congenital heart disease patients Eileen
Stewart, MD, Phillip S. Adams, DO, Xin Tian, PhD, Omar ...
postoperative outcomes in non- heterotaxy congenital heart disease patients Eileen
Stewart, MD, Phillip S. Adams, DO, Xin Tian, PhD, Omar ...
[PDF] Estridor congénito crónico:¿ qué hacer, cuándo y por quién?
AG Martínez, PR Iglesias, CG San Román, FM Serrano…
... Endosco- py revealed laryngomalacia, tracheomalacia and extrinsic tracheal compression, which
was due to innominate artery as angioCT revealed. Aortopexy, recommended by a multi-
disciplinary team, was curative. Key words: Innominate artery; Stridor; Aortopexy. ...
was due to innominate artery as angioCT revealed. Aortopexy, recommended by a multi-
disciplinary team, was curative. Key words: Innominate artery; Stridor; Aortopexy. ...
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