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Your search keyword '"Grechanina IuB"' showing total 5 results
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5 results on '"Grechanina IuB"'

1. [Impairments of gastrointestinal tract in autism].

Author

Grechanina IuB, Grechanina EIa, and Beletskaia SV

Subjects
Autistic Disorder diagnosis, Autistic Disorder therapy, Central Nervous System drug effects, Child, Child, Preschool, Combined Modality Therapy, Constipation physiopathology, Diarrhea physiopathology, Diet methods, Dietary Supplements, Dyspepsia physiopathology, Enzyme Replacement Therapy, Female, Food Hypersensitivity physiopathology, Gastrointestinal Tract drug effects, Helicobacter Infections diagnosis, Helicobacter Infections therapy, Helicobacter pylori isolation & purification, Humans, Male, Treatment Outcome, Autistic Disorder physiopathology, Central Nervous System physiopathology, Gastrointestinal Tract physiopathology, Helicobacter Infections physiopathology, Vitamins administration & dosage
Abstract

In the article the peculiarities of the gastrointestinal tract in children with autism. Presents the algorithm for evaluation of children with autism in KhSMGC, the statistical data about the frequency of lesions of the gastrointestinal tract. The main directions of correction of digestive disorders and its results.

Published
2014

2. [Mitochondrial neurogastrointestinal encephalopathy syndrome].

Author

Grechanina IuB

Subjects
Adult, Female, Ferredoxin-NADP Reductase deficiency, Humans, Intestinal Pseudo-Obstruction enzymology, Intestinal Pseudo-Obstruction physiopathology, Mitochondrial Encephalomyopathies enzymology, Mitochondrial Encephalomyopathies physiopathology, Muscular Dystrophy, Oculopharyngeal, Ophthalmoplegia congenital, Ferredoxin-NADP Reductase genetics, Intestinal Pseudo-Obstruction diagnosis, Intestinal Pseudo-Obstruction genetics, Mitochondrial Encephalomyopathies diagnosis, Mitochondrial Encephalomyopathies genetics, Mutation
Abstract

The article presents a case report of clinical observations of syndrome mitochondrial neurogastroenterology encephalomyopathy (MNGIE syndrome).

Published
2014

3. [Gastrointestinal and metabolic impairments in cystic fibrosis].

Author

Grechanina EIa, Grechanina IuB, and Ianovskaia AA

Subjects
Adolescent, Adult, Amino Acids metabolism, Child, Child, Preschool, Cystic Fibrosis pathology, Female, Gallbladder pathology, Humans, Infant, Intestines pathology, Lipid Metabolism, Liver pathology, Lung pathology, Male, Pancreas pathology, Purines metabolism, Cystic Fibrosis metabolism, Gallbladder metabolism, Intestinal Mucosa metabolism, Liver metabolism, Lung metabolism, Pancreas metabolism
Abstract

This article is about the peculiarities of gastrointestinal lesions, and the nature of metabolic disorders in patients with cystic fibrosis. Presented statistical data abouth the frequency of various gastrointestinal disorders in cystic fibrosis, studied the spectrum of ultrasound changes and changes in the biochemical status of patients with cystic fibrosis.

Published
2014

4. [A clinical case of Li syndrome caused by a mitochondrial DNA mutation].

Author

Zhadanov SI, Grechanina EIa, Grechanina IuB, Gusar VA, Fedoseeva NP, and Shurr TG

Subjects
Brain diagnostic imaging, Child, Diagnosis, Differential, Disease Progression, Fatal Outcome, Female, Follow-Up Studies, Humans, Leigh Disease diagnosis, Tomography, X-Ray Computed, DNA, Mitochondrial genetics, Leigh Disease genetics, Mutation
Published
2008

5. [Programs of mass and selective screening of pregnant women in prenatal studies. Screening of alpha fetoprotein in the blood serum of the mother].

Author

Grechanina OIa, Stepanets' AP, Nevedrova NV, Grechanina IuB, and Malanchuk LM

Subjects
Amniotic Fluid metabolism, Biomarkers blood, Echocardiography, Embryonic and Fetal Development physiology, Female, Humans, Nervous System Malformations, Placenta diagnostic imaging, Polymorphism, Genetic genetics, Predictive Value of Tests, Syndrome, Umbilical Cord abnormalities, Genetic Testing methods, Pregnancy blood, Ultrasonography, Prenatal, alpha-Fetoproteins metabolism
Abstract

The total of 38479 echography studies and 25147 alpha-fetoprotein estimations in mother blood serum have been performed upon prenatal screening. 445 congenital developmental defects are revealed. AFP base and limiting values (2.5 MoM and 0.5 MoM) are found. AFP values and echocardiography results in the nor and in genetic syndromes of multiple congenital developmental defects are compared. It is found that AFP values are higher than MoM or only slightly higher than Me in the same syndromes. The different level of AFP for the same syndromes appeared to be associated with the phenomenon of overlapping due to the clinical polymorphism and type of injury of the nervous system and with the extent of changes in placenta, amniotic fluid and umbilical cord were revealed in 99% of syndromes. The increased AFP level can be considered as a marker to detect signs of the genetic syndromes. Low AFP level peculiar to aneuploidy appeared to be normal or increased. The AFP test can be used as a marker of changed embryogenesis.

Published
1992

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