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Books on the topic 'Defects classification'

Author: Grafiati

Published: 28 June 2021

Last updated: 29 July 2025

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1

Hayes, Samuel P. Color Defects: Measurement, Classification, Heredity. Creative Media Partners, LLC, 2021.

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2

Grazzi-Soncini, Giacomo. Wine: Classification, Wine Tasting, Qualities and Defects. Franklin Classics, 2018.

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Grazzi-Soncini, Giacomo. Wine: Classification, Wine Tasting, Qualities and Defects. Franklin Classics Trade Press, 2018.

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Grazzi-Soncini, Giacomo. Wine: Classification, Wine Tasting, Qualities and Defects. Franklin Classics Trade Press, 2018.

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5

Wine: Classification, Wine Tasting, Qualities and Defects. Franklin Classics, 2018.

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6

Soncini, G. Grazzi. Wine: Classification, Wine Tasting, Qualities and Defects. Creative Media Partners, LLC, 2022.

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7

ANSI/AAMI SW91:2018; Classification of defects in health software. AAMI, 2018. http://dx.doi.org/10.2345/9781570207075.

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8

Papaelias, Mayorkinos, and Fausto Pedro Garca Mrquez. Fault Detection: Classification, Techniques and Role in Industrial Systems. Nova Science Publishers, Incorporated, 2014.

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9

Lamari, Foudil, and Jean-Marie Saudubray. Disorders of Complex Lipids Synthesis and Remodeling. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0066.

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Defective lipid catabolic pathways are involved in numerous inherited metabolic diseases such as lysosomal storage diseases and peroxisome biogenesis disorders. We recently described a new classification of a rapidly growing group of inherited metabolic disorders involving biosynthesis and remodeling of complex lipids including phospholipids and sphingolipids. The remarkable progress achieved over the last decade in high throughput gene sequencing and in lipid analysis technologies have enabled the description of more than 40 diseases linked to defects in enzymes involved in these pathways. So

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10

Uffman, Joshua C. Neuronal Ceroid Lipofuscinoses (Batten Disease). Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0042.

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Neuronal ceroid lipofuscinoses (NCL) are a group of autosomal recessive genetic disorders which represent the most common form of childhood neurodegenerative disease. Classically the disease was described according to the age of diagnosis resulting in four common phenotypes: (i) infantile or Santavuori-Haltia, (ii) late infantile or Jansky-Bielschowsky, (iii) juvenile or Spielmeyer-Vogt, and (iv) adult or Kufs. With advances in genetic mutational analysis techniques and improved understanding of NCL disease as a whole, disease classification now focuses on which of the known genetic defects is

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11

Kuwabara, Satoshi. Neuromuscular junction disorders. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199658602.003.0014.

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Ten seminal papers on disorders of the neuromuscular junction are described, covering historical aspects, recent advances in immunological, biological, and genetic researches, and future perspectives. Early descriptions of myasthenia gravis (MG) date back to the seventeenth century, and MG acquired its name in the nineteenth century. The first symptomatic treatment with cholinesterase inhibitors was reported in 1934, leading to the development of modern immunological therapies. Following the discovery of anti-MuSK (muscle-specific tyrosine kinase) antibody in 2001, MG is currently classified i

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12

Karapapa, Stavroula. Defences to Copyright Infringement. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780198795636.001.0001.

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Defences to copyright infringement have gained increased significance over the past twenty years. The fourth industrial revolution emerged with the development of innovative copy-reliant services and business models, transforming the way in which copyright works can be used, from digital learning methods to mass digitization initiatives, media monitoring services, image transformation tools, and content mining technologies. The lawfulness of such innovative services and business methods, which arguably have the potential to enhance public welfare, is dubious and challenges copyright law. EU co

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13

Federico, Antonio, and Silvia Palmeri. Oligosaccharidoses. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0057.

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Oligosaccharidoses are a group of lysosomal diseases, also called glycoproteinoses, biochemically characterized by storage of protein-bound oligosaccharides within lysosomes and excretion with urine of corresponding sugars. Storage of oligosaccharides results from absence or defective function of a specific lysosomal enzyme. Classification includes α‎ and β‎ mannosidosis, fucosidosis, sialidosis types I and II, Schindler disease, and aspartylglycosaminuria. Galactosialidosis characterized by deficiency of β‎-galactosidase and α‎-neuraminidase with presence in patient urine of oligosaccharides

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14

Sprague, Stuart M., and James M. Pullman. Spectrum of bone pathologies in chronic kidney disease. Edited by David J. Goldsmith. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0122.

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Histologic bone abnormalities begin very early in the course of chronic kidney disease. The KDIGO guidelines recommend that bone disease in patients with chronic kidney disease should be diagnosed on the basis of bone biopsy examination, with bone histomorphometry. They have also proposed a new classification system (TMV), using three key features of bone histology—turnover, mineralization, and volume—to describe bone disease in these patients. However, bone biopsy is still rarely performed today, as it involves an invasive procedure and highly specialized laboratory techniques. High-turnover

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15

Öztorun, Namık Kemal, and Ezgi Öztorun Köroğlu. Steel Structures I. İstanbul University–Cerrahpaşa Press Serial Number: 88, 2025. https://doi.org/10.5152/4100.

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This book provides comprehensive information essential for both the design of new steel structures and the analysis of existing ones. It covers the fundamental principles of design, procedures, historical context, specifications, and the Turkish standard TS 498 for design loads. It also addresses probability and factor of safety, the application of steel in structures, the mechanical properties of structural steels, and an introductory comments on TS 498. The book covers fundamental concepts including the behavior of tension and compression members, methods for their analysis, and details rega

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