Results 161 to 170 of about 3,299,699 (357)

آیا تصمیم ‌سازی بالینی ما مبتنی بر بهترین شواهد علمی است؟

open access: yesمجله دانشکده پزشکی اصفهان, 2011
• مقـدمـه: پزشكی مبتنی برشواهد فرآیند دریافت، نقد و به‌ کارگیری نتایج تحقیقات بر بالین بیماران می‌باشد. با وجود انتشار مقالات متعدد پیرامون میزان تطابق عملکرد پزشکان با شواهد علمی در سایر کشورها، هنوز مطالعه‌ای در ایران صورت نگرفته است.
Tahereh Changiz   +7 more
doaj  

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco   +18 more
wiley   +1 more source

Clinical Practice Guidelines for Auricular Fibrillation.

open access: yesMedisur, 2009
Clinical Practice Guidelines for Auricular Fibrillation. This is the most common cardiac arrhythmia and can bring about deleterious consequences on the cardiac function and risk of systemic embolism. It includes important aspects as aetiology and trigger
Jorge Luis Ulloa Capestany   +4 more
doaj   +2 more sources

Strengthening primary care: The role of clinical practice guidelines [PDF]

open access: yes, 2010
published_or_final_versio
Baker, R   +5 more
core  

The quality of clinical practice guidelines for chronic respiratory diseases and the reliability of the AGREE II: an observational study [PDF]

open access: bronze, 2016
Juliana Souza Uzeloto   +6 more
openalex   +1 more source

Antithrombotic therapy for VTE disease: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines.

open access: yesChest, 2012
C. Kearon   +11 more
semanticscholar   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas   +18 more
wiley   +1 more source

2016 European Guidelines on cardiovascular disease prevention in clinical practice.

open access: yesRevista Española de Cardiología, 2016
M. Piepoli   +25 more
semanticscholar   +1 more source

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