In the field of obstetrics:
Modern assisted reproductive technology (ART).
Methods of treating severe, combined forms of infertility in the case of impossibility of natural conception, including in vitro fertilization and embryo transfer into the uterine cavity, sperm injected into the cytoplasm of the oocyte, sperm donation, oocyte donation, surrogacy, pre-implantation diagnosis of genetic diseases, artificial insemination with a husband (donor) .
Medical-diagnostic Fetoscopy fetus in the course of pregnancy.
The method of studying the fetus in the uterus for the diagnosis of hereditary and congenital malformations. Only for medical reasons after 16 weeks of pregnancy, under local anesthesia, laparoscopy and controlled by ultrasound.
In the field of neonatology and pediatrics:
Treatment method lazerokoagulyatsii retinopathy of prematurity.
Providing eye care preterm infants having symptoms of retinopathy by applying lazerokoagulyatsii method trasskleralnym exposure.
Early neurosurgical correction of severe intraventricular hemorrhage.
Method normalize intracranial pressure in the treatment of intraventricular hemorrhage, hydrocephalus become complicated.
Conducting audiological screening of newborns for early detection and treatment of disorders of the auditory analyzer function .
The survey includes the registration of risk factors for hearing loss in the newborn, the study of otoacoustic emissions for the early detection of hearing loss.
Early surgical correction of persistent fetal Communications (patent ductus arteriosus) in very preterm infants .
Ligation of patent ductus arteriosus reduces the stiffness parameters and duration of mechanical ventilation, which reduces the risk of developing bronchopulmonary dysplasia, intraventricular hemorrhage, encephalopathy in children with extremely low birth weight.
In the field of medical genetics:
Mass spectrometric diagnosis of inherited metabolic diseases .
Mass spectrometry, liquid chromatography method opens up new possibilities diagnosis of inherited metabolic diseases.Early diagnosis of hereditary metabolic disorders associated with accumulation in the body of amino acids, organic and fatty acids or shortage of energy substrates, allow time to properly manage and ensure optimal psychological development of the child.
Diagnosis of hereditary and acquired thrombophilia.
Diagnosis of hereditary and acquired thrombophilic states conducted to establish the cause of recurrent miscarriage, clarify the causes of complicated pregnancy and the postpartum period. Comprehensive diagnosis of inherited and acquired thrombophilic state is most effective during the examination of patients with venous thrombosis and thromboembolism.
Diagnosis of genetic disorders in patients with various forms of hereditary diseases based on high performance liquid chromatography.
Denaturing high performance liquid chromatography allows to determine the changes in the nucleotide sequence of DNA molecules in size from 150 to 1500 base pairs. To date, the technology is used to identify gene mutations that cause the development of cystic fibrosis, phenylketonuria, neuropathy, Charcot-Marie-Tooth type 1X.