Results 141 to 150 of about 631,021 (368)

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Airway Remodeling in a Guinea Pig Model of Chronic Asthma : Its Influence on Airway Responsiveness and Pharmacological Properties of Airway Smooth Muscle, and Its Prevention by Corticosteroids

, 2003
Airway remodeling in bronchial asthma occurs as a result of continuance or repetition of eosinophilic airway inflammation. It has the potential to affect airway responsiveness to nonspecific stimuli and the pharmacological properties of airway smooth ...
Kamikawa, Yuichiro, Hiyama, Takako, Ota, Mayumi, Sagara, Hironori, Nakano, Yasuhiro   +4 more
core  

Magnesium Alloys for use as an Intraluminal Tracheal Stent [PDF]

, 2013
Tracheal stenting is used for successful management of adult airway obstructions, including tracheal stenosis, a narrowing of the tracheal lumen due to trauma or prolonged intubation.
Luffy, Sarah
core  

Evaluation of four manikins as simulators for teaching airway management procedures specified in the Difficult Airway Society guidelines, and other advanced airway skills

, 2007
Ten volunteers evaluated the performance of four currently available manikins: Airway Management Trainer, Airway Trainer, Airsim and Bill 1 as simulators for the 16 procedures described in the Difficult Airway Society Guidelines (DAS techniques) and ...
Jordan, G M, Silsby, J, Cook, T M, Difficult Airway Society, Bayley, G   +4 more
core   +1 more source

Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan, Sophia C. Pasia, Emmanouil Rampakakis, Reggie Hamdy, Frank Rauch, Lauren C. Hyer, Joel Lerman, Haluk Altiok, Krister Freese, Cary Mielke, Sarah B. Nossov, Philip F. Giampietro, Thania Ordaz‐Robles, Noémi Dahan‐Oliel   +13 more
wiley   +1 more source

Airways [PDF]

BMJ, 1963
openaire   +2 more sources

Effect of continuous positive airway pressure treatment of obstructive sleep apnea-hypopnea in multiple sclerosis: A randomized, double-blind, placebo-controlled trial (SAMS-PAP study) [PDF]

, 2021
Sulaiman Khadadah, R. John Kimoff, Pierre Duquette, Vincent Jobin, Yves Lapierre, Andrea Benedetti, Fatema Tuj Johara, Ann Robinson, Élaine Roger, Amit Bar‐Or, Gabriel Leonard, Marta Kamińska, Daria A. Trojan   +12 more
openalex   +1 more source

Associations of wheezing phenotypes in the first 6 years of life with atopy, lung function and airway responsiveness in mid-childhood

, 2008
<p>Background: Patterns of wheezing during early childhood may indicate differences in aetiology and prognosis of respiratory illnesses. Improved characterisation of wheezing phenotypes could lead to the identification of environmental influences ...
Heron, J, Sterne, J, Heron, J., Granell, R., Granell, R, Woodcock, A, Shaheen, S.O., Henderson, J., Strachan, D.P., Woodcock, A., Sherriff, AM, Simpson, A, Sherriff, A, Sterne, JA, Strachan, D. P., Sterne, J. A C, Henderson, J, Strachan, DP, Simpson, A.; id_orcid, Sherriff, A., Shaheen, S. O., Shaheen, SO, Sheriff, A., Sterne, J.A.C., Simpson, A.   +24 more
core   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source

Review for "Pulmonary function testing with tidal breath analyze technique is useful in predicting persistant small airway damage in infants with acute bronchiolitis"

, 2020

openalex   +1 more source