Zobrazeno 1 - 10
of 173
pro vyhledávání: '"D, Dimitrakov"'
Publikováno v:
Advances in Therapy. 25:1375-1378
Two patients with thalassemia minor and end-stage renal failure on hemodialysis were treated with epoetin zeta (Silapo®, Retacrit®; STADA, Germany), a medicinal product that was developed and registered as biosimilar to epoetin alfa. Dosing was tit
Autor:
E E, Tilkian, V D, Tzekov, S M, Pandeva, E P, Kumchev, D G, Nikolov, J D, Dimitrakov, D D, Dimitrakov
Publikováno v:
Folia medica. 42(3)
In the study a clinical assessment is made of the results of treatment of patients with renal anemia by epoetin-beta.Thirty two patients (22 women, 10 men) with chronic renal failure and anemia, ranging from 18 to 77 years of age (mean age 46.29 +/-
Publikováno v:
Akusherstvo i ginekologiia. 45(3)
[Lymphocyte populations and subpopulations in peripheral blood of pregnant women with pre-eclampsia]
Publikováno v:
Akusherstvo i ginekologiia. 44(1)
To investigate the changes of lymphocyte populations and subpopulations in peripheral blood of pregnant women suffering preeclampsia.By means of flowcytometry the following lymphocyte populations and subpopulations were determined in peripheral blood
Autor:
Elena D, Dimitrakova, Jordan D, Dimitrakov, S A, Karumanchi, S G, Karumanchi, Blagovest K, Pehlivanov, Nikola P, Milchev, Dimitar I, Dimitrakov
Publikováno v:
Folia medica. 46(1)
The pathophysiology of preeclampsia remains largely unknown. A number of circulating placenta-produced factors have been implicated in causing the endothelial dysfunction and the clinical phenotype characteristic of preeclampsia.Determination of seru
Publikováno v:
Folia medica. 45(1)
Autosomal recessive polycystic kidney disease (ARPKD) is a genetic disorder inherited in a recessive manner. The ARPKD gene is located on chromosome 6. The disease is characterised by specific changes in the kidney and liver.To make a review of moder
Publikováno v:
Folia medica. 44(4)
We conducted a ten-year clinical and ultrasound follow-up study of 120 siblings with ADPKD (68 men and 52 women, aged 19-40). 40 subjects had polycystic kidney disease. During the study period, the number and size of the cysts increased. Symptoms and
Autor:
G K, Kuvandzhiev, J D, Dimitrakov
Publikováno v:
Folia medica. 42(1)
The authors draw attention to the possibility that some of the equivocal cases of internal diseases diagnosed variously and treated in various hospitals may actually be caused by Chlamydia trachomatis or other species of the genus Chlamydia. We repor
Autor:
N, Bogdanova, M, McCluskey, K, Sikmann, A, Markoff, V, Todorov, D, Dimitrakov, T, Schiavello, M, Thomas, L, Kalaydjieva, B, Dworniczak, J, Horst
Publikováno v:
Human mutation. 16(2)
Screening for disease-causing mutations in the unique region of the polycystic kidney disease 1 (PKD1) gene was performed in 41 unrelated individuals with autosomal dominant polycystic kidney disease. Exons 34-41 and 43-46 were assayed using PCR ampl
Publikováno v:
Folia medica. 41(4)
Using a highly sensitive and specific polymerase chain reaction (PCR) protocol, we studied 36 renal allograft recipients and 30 healthy controls. Midstream urine samples were analyzed using routine microbiological methods and the Mycoplasma IST (BioM