Svetlana Yaremchuk
A5070644130- Adrenal and Paraganglionic Tumors
- Voice and Speech Disorders
- Dysphagia Assessment and Management
- Pituitary Gland Disorders and Treatments
- Obstructive Sleep Apnea Research
- Tracheal and airway disorders
- Hormonal Regulation and Hypertension
- Neuroscience of respiration and sleep
- Cancer, Hypoxia, and Metabolism
- Intelligent Tutoring Systems and Adaptive Learning
- Phonetics and Phonology Research
- Nasal Surgery and Airway Studies
- Cardiovascular and Diving-Related Complications
- Neuroendocrine Tumor Research Advances
- Asthma and respiratory diseases
- Lung Cancer Research Studies
- Cardiovascular Syncope and Autonomic Disorders
- Ear Surgery and Otitis Media
- Neuroblastoma Research and Treatments
- Respiratory and Cough-Related Research
- Otitis Media and Relapsing Polychondritis
- Sleep and Wakefulness Research
- Sleep and related disorders
Institute of Otolaryngology named after Prof. A.I. Kolomiychenko of the National Academy of Medical Sciences of Ukraine
2018-2024
Institute of Urology of the National Academy of Medical Sciences of Ukraine
2019
V.P. Komisarenko Institute of Endocrinology and Metabolism
2018
Institute of Neurology, Psychiatry and Narcology
2017
Institute of Cardiology
2009
Cleveland Clinic
2009
Multiple genes and their variants that lend susceptibility to many diseases will play a major role in clinical routine. Genetics-based cost reduction strategies diagnostic processes are important the setting of multiple for single disease. Head neck paraganglioma (HNP) is caused by germline mutations at least three succinate dehydrogenase subunit (SDHx). Mutation analysis all 3 costs approximately US$2,700 per patient. Genetic classification essential downstream management patient preemptive...
Abstract Purpose: Six pheochromocytoma susceptibility genes causing distinct syndromes have been identified; approximately one of three all patients carry a predisposing germline mutation. When four major (VHL, RET, SDHB, SDHD) are analyzed in clinical laboratory, costs ∼$3,400 per patient. The aim the study is to systematically obtain robust algorithm identify who should be genetically tested, and determine order which tested. Experimental Design: DNA from 989 apparently nonsyndromic were...
A third of patients with paraganglial tumors, pheochromocytoma, and paraganglioma, carry germline mutations in one the susceptibility genes, RET, VHL, NF1, SDHAF2, SDHA, SDHB, SDHC, SDHD, TMEM127 , MAX . Despite increasing importance, data for long-term prognosis are scarce pediatric presentations. The European-American-Pheochromocytoma–Paraganglioma-Registry, a total 2001 confirmed was platform this study. Molecular genetic phenotypic classification assessment gene-specific outcome second...
Pancreatic neuroendocrine tumors (PanNETs) are rare in von Hippel-Lindau disease (VHL) but cause serious morbidity and mortality. Management guidelines for VHL-PanNETs continue to be based on limited evidence, survival data guide surgical management lacking. We established the European-American-Asian-VHL-PanNET-Registry assess risks metastases, long-term outcomes provide best recommendations. Of 2330 VHL patients, 273 had a total of 484 PanNETs. Median age at diagnosis PanNET was 35 years...
According to the literature, post-traumatic stress disorder (PTSD) is often associated with obstructive sleep apnea syndrome (OSAS). These conditions have a bidirectional relationship and negatively influence each other’s course. Unfortunately, in Ukraine, due martial law, number of patients PTSD increasing, many them may also OSAS. Therefore, aim this study was determine cause-and-effect between OSAS progression PTSD. The research conducted as cohort using Berlin Questionnaire. A total 84...
To collect data on diagnosis, treatment, patient's management, and quality of life in patient with bilateral vocal fold paralysis (BVFP). A retrospective, observational, multicenter registry study was performed. Medical records 326 adults permanent BVFP (median age: 61 years; 70% female, 60% after thyroid surgery) generated between 2010 2017. Median time onset inclusion 1.2 years. post-treatment follow-up 2 months (range: 0-42). Surgery treatment choice 61.7% the cases, a 2-year revision...
Snoring and obstructive sleep apnea syndrome (OSAS) are common pathologies. Sleep disorders cause a daytime sleepiness, impaired concentration, other cognitive impairments. All this can lead to fatal consequences. Unfortunately, only about 20 % of patients suffering from pathology identified. As rule, do not know the presence OSAS, on one hand, they which specialist need seek help from. Given fact that upper airway patency is main causes most should be treated by an otolaryngologist. This...
Diese internationale Registry zur beidseitigen Stimmlippenlähmung (bilateral vocal fold palsy; BVFP) wurde 2015 initiiert, um die Eigenschaften der BVFP Population und eingesetzten diagnostischen Verfahren, Behandlungsmöglichkeiten Nachsorge zu untersuchen.
<div>Abstract<p>Multiple genes and their variants that lend susceptibility to many diseases will play a major role in clinical routine. Genetics-based cost reduction strategies diagnostic processes are important the setting of multiple for single disease. Head neck paraganglioma (HNP) is caused by germline mutations at least three succinate dehydrogenase subunit (<i>SDHx</i>). Mutation analysis all 3 costs ∼US$2,700 per patient. Genetic classification essential...
Other Supporting Colleagues from Clinical Predictors for Germline Mutations in Head and Neck Paraganglioma Patients: Cost Reduction Strategy Genetic Diagnostic Process as Fall-Out
Other Supporting Colleagues from Clinical Predictors for Germline Mutations in Head and Neck Paraganglioma Patients: Cost Reduction Strategy Genetic Diagnostic Process as Fall-Out
<div>Abstract<p>Multiple genes and their variants that lend susceptibility to many diseases will play a major role in clinical routine. Genetics-based cost reduction strategies diagnostic processes are important the setting of multiple for single disease. Head neck paraganglioma (HNP) is caused by germline mutations at least three succinate dehydrogenase subunit (<i>SDHx</i>). Mutation analysis all 3 costs ∼US$2,700 per patient. Genetic classification essential...
Im Rahmen der 2015 initiierten multinationalen Registry werden Informationen über Patienten mit beidseitiger Stimmlippenlähmung (BVFP) und die bei dieser Krankheit übliche Diagnostik, Behandlung Nachsorge gesammelt.
The international BVFP registry started in 2015 is collecting data on the characteristics of population as well standard diagnostic, treatment and follow-up methods.