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pro vyhledávání: '"E F, Andreeva"'
Autor:
E. F. Andreeva, N. D. Savenkova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 1, Pp 47-51 (2021)
For the first time in 1946 E.L. Potter (1901–1993) described the characteristic appearance of stillborns and deceased newborns with bilateral renal agenesis. Due to the further observations Potter distinguished the syndrome (Q60.6) – a set of cha
Autor:
N. D. Savenkova, E. F. Andreeva
Publikováno v:
Nephrology (Saint-Petersburg). 24:54-63
The review provides historical information on the study of renal cystosis that occurs with glomerular cysts, discusses terminology issues and classification of diseases that occur with glomerulocystic kidney. The course features, diagnostic methods,
Autor:
E. F. Andreeva, N. D. Savenkova
Publikováno v:
Nephrology (Saint-Petersburg). 23:77-87
THE AIM:to characterize the features of the course of autosomal dominant (ADPKD) and autosomal recessive (ARPKD) polycystic kidney disease detected in the prenatal, neonatal and thoracic periods.PATIENTS AND METHODS:ADP was diagnosed in 28 and ARPP i
Autor:
E. F. Andreeva, N. D. Savenkova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 64, Iss 2, Pp 22-29 (2019)
The article reflects the genetic variants of polycystic kidney disease, describes the modern strategy for the treatment of polycystic kidney disease in children and adults. The authors present the results of clinical trials of vasopressin V2 receptor
Autor:
E. F. Andreeva
Publikováno v:
Nephrology (Saint-Petersburg). 22:95-100
Deletion 12p (del12p; synonyms: рartial deletion of the short arm of chromosome 12; рartial monosomy of chromosome 12p; рartial monosomy of the short arm of chromosome 12) relates to orphan diseases (ORPHA: 316244; ICD-X: Q93.5) and is characteriz
Autor:
E. F. Andreeva, N. D. Savenkova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 63, Iss 1, Pp 100-105 (2018)
The tuberous sclerosis is a systemic orphan disease. According to the literature data, the article summarizes the clinical and genetic features, presents the large and small criteria for the tuberous sclerosis diagnostics in children. The authors pro
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 62, Iss 3, Pp 79-84 (2017)
The article presents literature data and a clinical case on the rare Imerslund-Grasbeck syndrome. The pathogenetic foundations, the features of the clinical picture, course and treatment of this syndrome in children are discussed. Own clinical observ
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 75(1)
Publikováno v:
Vestnik dermatologii i venerologii. (10)