Results 101 to 110 of about 4,917 (213)

Hereditary Angioedema: Novel Molecules for Treatment of Acute Attacks and Long-Term Prophylaxis

open access: yesFuture Pharmacology
Hereditary angioedema (HAE) is a rare disease caused by a genetic alteration of the SERPING1 gene and characterized by recurrent attacks of angioedema that involve the skin, and the mucosae of the gastrointestinal tract and upper airways, which ...
Bianca Covella   +4 more
doaj   +1 more source

Role of Gastric Colonization in Nosocomial Infections and Endotoxemia: A Prospective Study in Neurosurgical Patients on Mechanical Ventilation [PDF]

open access: yes, 2017
The role of gastric microbial colonization in nosocomial infections and endotoxemia was investigated prospectively in 40 neurosurgical patients requiring mechanical ventilation for >48 h. Each was studied up to 7 d.
Buser, Mauro   +5 more
core  

Proteolysis-induced pathomechanisms in acute inflammation and related therapeutic approaches [PDF]

open access: yes, 1991
A Billing   +30 more
core   +1 more source

Phagocyte proteinases in multiple trauma and sepsis [PDF]

open access: yes, 1993
Fritz, Hans   +4 more
core   +1 more source

Recombinant Activated Factor VII (rFVIIa/ NovoSeven®) In The Management Of Massive Bleeding In Hospital Universiti Sains Malaysia [PDF]

open access: yes, 2017
Pendarahan yang teruk adalah salah satu faktor penyumbang kematian di dunia. Rawatan dalam keadaan pendarahan teruk adalah penting bagi mengembalikan hemostasis pesakit Massive bleeding has been a one of the contributing causes of death in the world ...
Mohd Shah, Nurfatin
core  

NEW POSSIBILITIES OF ATROPHIC CHANGES PREDICTING IN VAGINAL TISSUE AT WOMEN IN POST REPRODUCTIVE PERIOD

open access: yesКубанский научный медицинский вестник, 2016
With the aim of increasing the effectiveness of early diagnostics and medical therapy of atrophic colpitis the valuation analysis of the kallikrein-kinin system and the activity of inducible NO-synthase in peripheral blood is carried out.
O. G. Sarkisan
doaj  

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies

open access: yesClinical and Applied Thrombosis/Hemostasis, 2021
Antonio Girolami MD, Silvia Ferrari PhD
doaj   +1 more source

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