Aleksandra Vladimirovna Kezhaykina
Research Subjects
Research Interests
Aleksandra Vladimirovna Kezhaykina has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Ella Ivanovna Polozova
National Research Ogarev Mordovia State University
1 shared publication - Irina Evgenievna Trokhina
National Research Mordovia State University
1 shared publication - Olga Georgievna Radaikina
N.P. Ogarev Mordovia State University
1 shared publication - Vsevolod Vladimirovich Skvortsov
Volgograd State Medical University of the Ministry of Health of the Russian Federation, Volgograd
1 shared publication
Latest Publications
- 27 September 2020
- Published by PANORAMA Publishing House in Spravočnik vrača obŝej praktiki (Journal of Family Medicine)
- No. 10,p. 35-41
Rare Clinical Masks of Amyloidosis
Amyloidosis is a group of diseases characterized by the deposition of a protein having a fibrillar structure in the organs and tissues of the body. The main difference between amyloid is a high ordering of the structure, which manifests itself in the ability to birefringence in combination with dichroism, i.e. a change in the red colour of amyloid deposits to apple green in polarized light. Today, the disease has stopped to be a rare one, but the similarity of clinical data with well-known diseases increases the timing of diagnosis, affects the prognosis and survival of patients. Rare forms of amyloidosis, the description of which is reflected in this article, deserve special attention.
- 27 September 2020
- Published by PANORAMA Publishing House in Spravočnik vrača obŝej praktiki (Journal of Family Medicine)
- No. 10,p. 35-41
Rare Clinical Masks of Amyloidosis
Amyloidosis is a group of diseases characterized by the deposition of a protein having a fibrillar structure in the organs and tissues of the body. The main difference between amyloid is a high ordering of the structure, which manifests itself in the ability to birefringence in combination with dichroism, i.e. a change in the red colour of amyloid deposits to apple green in polarized light. Today, the disease has stopped to be a rare one, but the similarity of clinical data with well-known diseases increases the timing of diagnosis, affects the prognosis and survival of patients. Rare forms of amyloidosis, the description of which is reflected in this article, deserve special attention.