Results 11 to 20 of about 635,330 (264)
Phenylketonuria (PKU) is an inherited metabolic disorder derived from a deficiency in the enzyme phenylalanine hydroxylase, which converts the amino acid phenylalanine (Phe) into tyrosine (Tyr).
Roseani Andrade MSc +5 more
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ЛАБОРАТОРНАЯ МЕДИЦИНА — ФУНДАМЕНТ СОВРЕМЕННОЙ ТЕРАПЕВТИЧЕСКОЙ КЛИНИКИ
Analytical reliability and clinical significance of laboratory data allows to consider them as a basis for diagnosis and treatment monitoring in therapeutic clinic.
Л. П. Ефимова
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THE NAVAL LABORATORY.-ERROR CORRECTED. [PDF]
ABSTRACT 1932 Chestnut St., Philadelphia, Aug. 29, 1883.Editor of the Journal of the American Medical Association: In No. 6, August 18, p. 192, of The Journal of the American Medical Association, received the 27th, is a brief obituary notice of Dr. Benjamin Franklin Bache.It is stated in it that "he established the Naval Laboratory," etc.
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Variation in Laboratory Reports: Causes other than Laboratory Error
When a sample of an individual is measured at different times at the same or different clinical laboratory, the results are always different, even the state of health of an individual is the same. This disparity in the results from clinical laboratories might confuse diagnosing, treating, and monitoring disease.
Santosh Pradhan +2 more
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Ocular changes in premature infants [PDF]
Introduction: This article aimed to review the literatures on visual impairments and ocular changes in premature infants with low birth weight and gestational age.Methods: Five electronic databases including: PubMed, Web of Science, Science direct, Ovid,
Negareh Yazdani +6 more
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Error evaluation in the laboratory testing process and laboratory information systems
Background: The laboratory testing process consist of five analysis phases featuring the total testing process framework. Activities in laboratory process, including those of testing are error-prone and affect the use of laboratory information systems. This study seeks to identify error factors related to system use and the first and last phases of the
Azila Arifin, Maryati Mohd Yusof
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The use of specialized centers has been the main alternative for an appropriate diagnosis, management and follow up of patients affected by inborn errors of metabolism (IEM).
Olga Y. Echeverri +8 more
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Short-chain enoyl-CoA hydratase (ECHS1) is a mitochondrial beta-oxidation enzyme involved in the metabolism of acyl-CoA fatty acid esters, as well as in valine metabolism.
S. Pajares +13 more
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Error tracking in a clinical biochemistry laboratory [PDF]
We report our results for the systematic recording of all errors in a standard clinical laboratory over a 1-year period.Recording was performed using a commercial database program. All individuals in the laboratory were allowed to report errors. The testing processes were classified according to function, and errors were classified as pre-analytical ...
Szecsi, Pal Bela, Ødum, Lars
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Background and objectives: Laboratory medicine is equally challenged by economic and new technological pressures. Clinical laboratories have undergone major change due to advancement of technology, which has improved the decision making of clinicians but
KAPILA GAIKWAD, SOHAN SELKAR
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