Results 91 to 100 of about 305,278 (338)

Prolonged central nervous system and respiratory depression in preterm neonates after exposure to brimonidine tartrate and timolol maleate ophthalmic drops

GMS Ophthalmology Cases, 2020
Objective: We report three cases of preterm neonates who presented with central nervous system (CNS) and respiratory depression after inadvertent exposure to brimonidine tartrate 0.2% and timolol maleate 0.5% fixed-combination ophthalmic drops.Case ...
Azarcon, Corrina P., Santiago, Darby E.
doaj   +1 more source

Disorders of Respiration, Different types of APNEA, APNEA Time, Occurrence of APNEA in Different Conditions and Clinical Aspects of APNEA

, 2023
{"references": ["1.\tSemelka, M., Wilson, J., & Floyd, R. (2016). Diagnosis and treatment of obstructive sleep apnea in adults. American family physician, 94(5), 355-360.", "2.\tCenters for Medicare & Medicaid Services. (2017). National coverage determination (NCD) for continuous positive airway pressure (CPAP) therapy for obstructive sleep ...
Dr.Mohan Naidu K., Dr. Sridevi V., Dr. Muralinath E., Dr. Manjari P., Dr. Chapalamadugu C Kalyan, Dr. Sravani Pragna K., Dr. M. Guru Prasad, Nikhil J., Dr. Sony Sharlet   +8 more
openaire   +2 more sources

Caffeine for apnea in bronchiolitis [PDF]

The Journal of Pediatrics, 2017
Alansari et al1 recently have published in The Journal the results of a proof-of-concept, single-center, randomized trial evaluating the efficacy and safety of caffeine citrate in infants ≤4 months presenting to the emergency department with apnea-associated bronchiolitis during 3 bronchiolitis seasons...
Maheux, Anaïs, Pladys, Patrick, Laviolle, Bruno   +2 more
openaire   +3 more sources

Growth Hormone Treatment in Patients With KBG Syndrome: Novel Insights, Challenges and Recommendations From Six New Patients and Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT KBG syndrome is one of the most frequent neurodevelopmental disorders and is caused by ANKRD11 variants. Postnatal short stature is observed in ~50% of patients. Recombinant human growth hormone (rhGH) has become a valuable treatment for patients with growth hormone deficiency (GHD) along with Prader–Willi and Turner syndrome. Limited evidence
Sietse M. Aukema, Kim Vandenput, Emanuela Scarano, Himanshu Goel, Lily Guo, Michiel Vanneste, Koen Devriendt, Nitash Zwaveling‐Soonawala, Cordula Kiewert, Alma Kuechler, Ilaria Parenti, Eleonora Orlandini, Elke de Boer, Siddharth Banka, Elizabeth Wall, Gholson J. Lyon, Karen J. Low, Joyce M. Geelen, Yvonne G. van der Zwan, Charlotte W. Ockeloen   +19 more
wiley   +1 more source

Causes and Effects Contributing to Sudden Death in Epilepsy and the Rationale for Prevention and Intervention

Frontiers in Neurology, 2020
Sudden unexpected death in epilepsy (SUDEP) claims the lives of one in every thousand epileptic patients each year. Autonomic, cardiac, and respiratory pieces to a mechanistic puzzle have not yet been completely assembled. We propose a single sequence of
Mark Stewart, Mark Stewart, Joshua B. Silverman, Krishnamurthi Sundaram, Richard Kollmar, Richard Kollmar   +5 more
doaj   +1 more source

Contactless camera-based AHI score estimation in SAS patients

Current Directions in Biomedical Engineering, 2023
Sleep apnea syndrome (SAS) is a common sleeprelated breathing disorder characterized by recurring cessations of airflow during sleep. The gold standard for diagnosing SAS is polysomnography (PSG) which requires the patient to spend one or several nights ...
Alic Belmin, Zauber Tim, Wiede Christian, Viga Reinhard, Seidl Karsten   +4 more
doaj   +1 more source

Predicting sleep disordered breathing in outpatients with suspected OSA [PDF]

, 2014
Objective To validate the utilities of Berlin, STOP and STOP-BANG Questionnaires, other patient characteristics, comorbidities, Epworth Sleepiness Scale (ESS), fractional exhaled nitric oxide (FENO) and blood markers for the prediction of sleep ...
Allardice, Gwen, Ambler, Heather, Banham, Stephen, Carlin, Christopher, Cowan, Douglas C., Livingston, Eric, MacFarlane, Duncan, Ramsay, Darren   +7 more
core   +2 more sources

Identification and Characterization of a Novel Biallelic SLC12A2 Variant Associated With Kilquist Syndrome (OMIM #619080)

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT This study presents the case of a child with multiple congenital anomalies, severe hypotonia, and profound bilateral sensorineural hearing loss. Functional bioenergetic assessments showed no significant mitochondrial respiratory defects, and riboflavin (Rf) status evaluation excluded a deficiency in Rf transporters as a cause of hearing loss ...
Piero Leone, Alessia Nisco, Luciana de Gennaro, Maria Tolomeo, Elisa Lorefice, Giuseppe Petrosillo, Silvia Russo, Donatella De Giovanni, Claudia Rita Catacchio, Francesca Romana Lepri, Mario Ventura, Simonetta Simonetti, Albina Tummolo, Maria Barile   +13 more
wiley   +1 more source

An Oximetry Based Wireless Device for Sleep Apnea Detection

Sensors, 2020
Sleep related disorders can severely disturb the quality of sleep. Among these disorders, obstructive sleep apnea (OSA) is highly prevalent and commonly undiagnosed. Polysomnography is considered to be the gold standard exam for OSA diagnosis.
Fábio Mendonça, Sheikh Shanawaz Mostafa, Fernando Morgado-Dias, Antonio G. Ravelo-García   +3 more
doaj   +1 more source

Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Rare diseases impact approximately 1 in 10 people worldwide, and yet, less than 5% of all rare diseases currently have an approved treatment option available. This is due to many challenges unique to rare diseases, including small, diverse patient populations, the cost of drug development that is not proportionate to the number of patients who
Caleb P. Bupp, Elizabeth A. VanSickle, Julianne Michael, Chad R. Schultz, Kelly Nguyen, Melissa Hoefer, Surender Rajasekaran, André S. Bachmann   +7 more
wiley   +1 more source