Nanobiomaterials for Preclinical Studies and Clinical Diagnostic

2016 ◽  
pp. 667-690
Keyword(s):  
Preclinical Studies ◽  
Clinical Diagnostic

Preclinical studies on the radioprotective efficacy and pharmacokinetics of subcutaneously administered amifostine

2002 ◽  
Vol 29 (6 Suppl 19) ◽  
pp. 2-8 ◽  
Author(s):  
David R. Cassatt ◽  
Christine A. Fazenbaker ◽  
Gizachew Kifle ◽  
Christine M. Bachy
Keyword(s):  
Preclinical Studies

New statistical ways for analyzing sleep data in clinical and preclinical studies

2009 ◽  
Vol 42 (05) ◽  
Author(s):  
T Möller ◽  
A Steiger ◽  
L Fahrmeir ◽  
A Yassouridis
Keyword(s):  
Preclinical Studies

Preclinical studies on Myrcludex B, a novel Hepatitis B virus (HBV)-envelope protein derived entry inhibitor

2010 ◽  
Vol 48 (01) ◽  
Author(s):  
A Schulze ◽  
A Schieck ◽  
C Gähler ◽  
A Meier ◽  
T Müller ◽  
...  
Keyword(s):  
Hepatitis B Virus ◽  
Hepatitis B ◽  
Envelope Protein ◽  
Entry Inhibitor ◽  
Preclinical Studies ◽  
B Virus

Genetics in Ophthalmology

2020 ◽  
pp. 44-45
Author(s):  
А.Ю. Рудник ◽  
М.А. Федяков ◽  
О.С. Глотов
Keyword(s):  
Genetic Basis ◽  
Genetic Diseases ◽  
Mendelian Inheritance ◽  
Diagnostic Screening ◽  
Online Mendelian Inheritance ◽  
Clinical Diagnostic ◽  
Omim Database

На сегодняшний день в базе данных Online Mendelian Inheritance in Man (OMIM) описано более 6613 заболеваний и фенотипов, 4241 имеют доказанную генетическую основу, не менее 45% вкючают офтальмологические проявления. В статье приведен ряд клинический примеров пациентов с офтальмологическими симптомами различных генетических заболеваний (алкаптонурия, болезнь Штаргардта, синдром микроцефалии с или без хориоретинопатии; астроцитарная гамартома) с целью демонстрации эффективного клинико-диагностического скрининга генетической патологии у пациентов. So far, the Online Mendelian Inheritance in Man (OMIM) database describes more than 6613 diseases and phenotypes, 4241 have a proven genetic basis, 45% of which are combined with ophthalmological manifestations. The article provides a number of clinical examples of patients with ophthalmological manifestations of various genetic diseases (alcaptonuria, Stadgart ‘s disease, microcephaly syndrome with or without choriretinopathy; Astrocytic gamartoma) to demonstrate effective clinical-diagnostic screening of genetic pathology in patients.

Clinical diagnostic algorithm for determining subtype of ischemic stroke in patientsof integrated stroke block

2020 ◽  
Vol 0 (1—2) ◽  
pp. 20-27
Author(s):  
Y. V. Flomin ◽  
G. S. Trepet ◽  
V. G. Guryanov ◽  
L. I. Sokolova
Keyword(s):  
Ischemic Stroke ◽  
Diagnostic Algorithm ◽  
Clinical Diagnostic
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