Xem 1-20 trên 149 kết quả Metabolic disease
  • Since the publication of the first edition sixteen years ago, Inborn Metabolic Diseases – Diagnosis and Treatment has become a classic textbook, indispensable for those involved in the care of children and adults with inborn errors of metabolism, including pediatricians, biochemists, dieticians, neurologists, internists, geneticists, psychologists, nurses, and social workers. This new 4th edition has been extensively revised.

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  • Diseases of the Tongue See Table 32-4.

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  • (BQ) Part 2 book "Textbook of biochemistry" presents the following contents: Electrolyte and water balance, metabolic diseases, free radicals and antioxidants, mineral metabolism and abnormalities, energy metabolism and nutrition, nucleotides chemistry and metabolism,... Invite you to consult.

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  • Obesity and related metabolic diseases, such as type 2 diabetes, hyperten-sion and hyperlipidemia are an increasingly prevalent medical and social problem in developed and developing countries. These conditions are asso-ciated with increased risk of cardiovascular disease, the leading cause of death.

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  • Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí sinh học Journal of Biology đề tài: AAV-mediated gene therapy for metabolic diseases: dosage and reapplication studies in the molybdenum cofactor deficiency model

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  • (BQ) Part 1 book "Goldman's cecil medicine" presents the following contents: Oncology, metabolic diseases, endocrine diseases, nutritional diseases, diseases of allergy and clinical immunology, infectious diseases, neurology, skin diseases, medical consultation, infectious diseases,...

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  • (BQ) Part 2 book "Clinical chemistry (organ function tests, laboratory investigation)" presents the following contents: Laboratory investigations, miscellaneous, inborn metabolic diseases (inborn errors of metabolism).

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  • (BQ) Part 2 book "Escourolle & poirier’s manual of basic neuropathology" presentation of content: Acquired metabolic disorders, hereditary metabolic diseases, congenital malformations and perinatal diseases, pathology of skeletal muscle, pathology of peripheral nerve, diseases of the pituitary gland.

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  • A global research community of scientists is teasing out the biochemical mechanisms that regulate normal cellular physiology in a variety of organisms. Much of current research aims to understand the network of molecular reactions that regulate cellular homeostasis, and to learn what allows cells to sense stress and activate appropriate biochemical responses.

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  • Non-alcoholic fatty liver disease (NAFLD), like hepatitis C and HIV, is a disease of our generation. Mostly unrecognized prior to 1980 and seldom taken seriously until the past few years, NAFLD has seemingly been thrust upon us unexpectantly like an orphaned child left at our clinical bedside. In fact, NAFLD was conceived during the industrial revolution, which caused food to be processed differently, provided that food more abundantly and made physical work less demanding.

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  • Liver Metabolism and Fatty Liver Disease addresses the current understanding of the development of nonalcoholic fatty liver disease as well as the clinical aspects of the disease by examining the current knowledge surrounding metabolism in the liver. The book discusses various topics including the involvement of oxidative stress, metabolic effects, and inflammation as well as the effect of nutrition on the development and progression of the disease.

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  • This book began as a collection of articles on neuropsychiatric disease, but with a clear focus on Schizophrenia, which is a poorly understood but very disabling group of brain disorders. We now recognize schizophrenia as a disorder of the brain, but despite advances in treatment options we are still a long way from having effective treatments, particularly for cognitive symptoms, and lack effective interventions and ways to prevent this disease.

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  • Dr. Sharon Rounds, the editor for this series who invited us to write a book on rare lung diseases, developed the idea after attending the 2004 Lymphangioleiomyomatosis (LAM) Foundation annual research meeting. She was a keynote speaker at that event (during her tenure as the president of the American Thoracic Society) and was witness to the power of patient advocacy and the mission-based scientific effort that had brought this rare disease of women from obscurity to clinical trials with targeted molecular therapies in under a decade.

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  • Table 54-12 Causes of Vesicles/Bullae I. Primary cutaneous diseases A. Primary blistering diseases (autoimmune) 1. Pemphigusa 2. Bullous pemphigoidb 3. Gestational pemphigoidb 4. Cicatricial pemphigoidb 5. Dermatitis herpetiformisb,c 6. Linear IgA bullous dermatosisb 7. Epidermolysis bullosa acquisitab,d B. Secondary blistering diseases 1. Contact dermatitisa 2. Erythema multiformea,b 3. Stevens-Johnson syndrome 4. Toxic epidermal necrolysisb C. Infections 1. Varicella/zoster virusa,e 2. Herpes simplex virusa,e 3. Enteroviruses, e.g., hand-foot-and-mouth disease 4.

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  • In the diffuse forms of hyperpigmentation, the darkening of the skin may be of equal intensity over the entire body or may be accentuated in sun-exposed areas. The causes of diffuse hyperpigmentation can be divided into four major groups—endocrine, metabolic, autoimmune, and drugs. The endocrinopathies that frequently have associated hyperpigmentation include Addison's disease, Nelson syndrome, and ectopic ACTH syndrome. In these diseases, the increased pigmentation is diffuse but is accentuated in the palmar creases, sites of friction, scars, and the oral mucosa.

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  • Several metabolic disorders are associated with blister formation, including diabetes mellitus, renal failure, and porphyria. Local hypoxia secondary to decreased cutaneous blood flow can also produce blisters, which explains the presence of bullae over pressure points in comatose patients (coma bullae). In diabetes mellitus, tense bullae with clear viscous fluid arise on normal skin. The lesions can be as large as 6 cm in diameter and are located on the distal extremities. There are several types of porphyria, but the most common form with cutaneous findings is PCT.

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  • Tham khảo sách 'diseases and disorders diabetes', y tế - sức khoẻ, y học thường thức phục vụ nhu cầu học tập, nghiên cứu và làm việc hiệu quả

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  • The metabolic disease 3-methylglutaconic aciduria type I (MGA1) is char-acterized by an abnormal organic acid profile in which there is excessive urinary excretion of 3-methylglutaconic acid, 3-methylglutaric acid and 3-hydroxyisovaleric acid. Affected individuals display variable clinical manifestations ranging from mildly delayed speech development to severe psychomotor retardation with neurological handicap.

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  • Congenital heart disease in newborns is associated with global impairment in development. We characterized brain metabolism and microstructure, as measures of brain maturation, in newborns with congenital heart disease before they underwent heart surgery. Methods We studied 41 term newborns with congenital heart disease — 29 who had transposition of the great arteries and 12 who had single-ventricle physiology — with the use of magnetic resonance imaging (MRI), magnetic resonance spectroscopy (MRS), and diffusion tensor imaging (DTI) before cardiac surgery....

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  • Nutritional counseling and management are becoming important in health care, particularly in the management of a number of chronic conditions and diseases. The publication of this book is timely, because it aims to help physicians and their staffs identify conditions and diseases that can be treated effectively with nutritional intervention, and provides specifics on appropriate counseling and management. The first of the 13 chapters discusses nutritional support for children, with emphasis on premature infants, cystic fibrosis, and bronchopulmonary dysplasia....

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