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effects of dust formulations of three entomophatogenic fungal
effects of dust formulations of three entomophatogenic fungal

- Wiley Online Library
- Wiley Online Library

... aberrations in diabetes development, there is currently no molecular probe that allows measurement of hepatic gluconeogenic pathways in vivo and in a noninvasive manner. In this study, we used hyperpolarized carbon 13 (13C)-labeled pyruvate magnetic resonance spectroscopy (MRS) to determine changes ...
Principal elements
Principal elements

... Iron is present in the following compounds: Hemoglobin (70% of iron). Myoglobin (5% of iron). Respiratory enzymes (5%): Cytochrome a, b and c, catalase and peroxidase. Transferrin and ferritin. ...
Hypercholesterolaemia
Hypercholesterolaemia

... While heredity may be a factor for some people, the main culprits are lack of exercise and diets high in saturated fat. High cholesterol can be prevented, sometimes with lifestyle changes (diet and exercise) alone. If not, drug treatment has to be taken. Signs and Symptoms There usually aren't any s ...
Biomarkers of Oxidative Stress i
Biomarkers of Oxidative Stress i

... central nervous system disorders all characterized by the progressive loss of neuronal tissues. 5 Tremendous efforts have been made in the past years to identify neuropathological, biochemical, and genetic biomarkers of neurodegcncrative diseases for a diagnosis at earlier stages, which presumably w ...
Alcohol
Alcohol

... • Chronic ethanol consumption induces cytochrome P450 2E1, w leads to ! generation of ROS & RNS + a deficiency of oxygen in ! tissues (hypoxia). • Chronic ethanol use: NAD & of NADH by ! liver. • All of these biochemical changes have been proposed to contribute to DNA damage, hepatocyte injury & li ...
Candidate Gene Polymorphisms in Patients with Acetaminophen
Candidate Gene Polymorphisms in Patients with Acetaminophen

... used pain-relieving and fever-reducing drugs. Unfortunately, this drug is also one of the leading causes of acute liver failure (ALF) in this country, accounting for approximately half of all ALF cases identified by the Acute Liver Failure Study Group in the United States (Larson et al., 2005). In m ...
Influence of hepatic ammonia removal on ureagenesis, amino acid
Influence of hepatic ammonia removal on ureagenesis, amino acid

... The mass transfers of O 2, glucose, NH 3, urea and amino acids across the portal-drained viscera (PDV) and the liver were quantified, by arterio–venous techniques, during the last 4 h of a 100 h infusion of 0 (basal), 150 or 400 mmol NH 4HCO 3/min into the mesenteric vein of three sheep given 800 g ...
23-Peritoneum2007-12-29 04:534.1 MB
23-Peritoneum2007-12-29 04:534.1 MB

... Prof. Saeed Abuel Makarem ...
Liver Enlargement - STP Regulatory Policy Papers
Liver Enlargement - STP Regulatory Policy Papers

The peritoneum
The peritoneum

...  Intestinal border-folded, 6-7 m long  Root of mesentery • 15 cm long • Directed obliquely from ...
Nutritional Disorders of Skin
Nutritional Disorders of Skin

... Metallothioneines regulates the transport of zinc into the circulation and then to the liver and ...
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)

physiologicoanatomical features of the digestive system in children
physiologicoanatomical features of the digestive system in children

... PROFESSIONAL MOTIVATION: Every period of childhood has the inherent peculiarities of anatomic structure, physiological functions and metabolism. For children of early age, first of all infants, there is relative immaturity of the digestive system. At the ...
Porphyrins (Structure of Porphyrins)
Porphyrins (Structure of Porphyrins)

... Most urobilinogen is oxidized to sterbilin( brown color & excreted in feces). (b) Some is reabsorbed from the gut and enter portal blood to participate in the enterohepatic urobilinogen cycle. © The remainder urobilinogen is transported by the blood to the kidney where it is converted to yellow urob ...
Chapter 17 Abdomen Abdominal examination is performed: As part
Chapter 17 Abdomen Abdominal examination is performed: As part

... Usually heard as clicks and gurgles that occur irregularly and range from 5 to 35 per minute Generalized so most often they can be assessed adequately by listening in one place Loud prolonged gurgles are called borborygmi (stomach growling) Auscultation (Cont.) Bowel sounds Increased bowel sounds ma ...
Alexander Disease: Diagnosis with MR Imaging
Alexander Disease: Diagnosis with MR Imaging

... MR studies of three patients with a histopathologically confirmed diagnosis of Alexander disease were available and formed the basis of the defined MR imaging criteria. These criteria were then applied to 217 children with leukoencephalopathy of unknown origin whose MR studies we had received for re ...
Oxidation of C`4-labeled Carbohydrate
Oxidation of C`4-labeled Carbohydrate

... relatively high rates of aerobic glycolysis shown by tumor slices as evidence for a defect in respiration which distinguished them from normal tissues. Dickens and Simer (10) then pointed out that tu mors, in contradistinction to normal tissues (brain, retina, embryo) having a high anaerobic glycoly ...
All About Fat and Cholesterol
All About Fat and Cholesterol

... Cholesterol acts as an antioxidant and antiinflammatory. This may be the explanation for the fact that cholesterol levels go up with age. As an antioxidant, cholesterol protects us against free radical damage that leads to heart disease and cancer. It is needed for proper function of serotonin recep ...
S1 File.
S1 File.

... mice can survive for a longer period of time, allowing more time for lesion development. Additionally, because it is possible that the tested compound induces an acute phase response and subsequent cytokine storm, analysis of serum TNFa levels are recommended. Clinical signs prior to death did not s ...
True - Food and Health Communications
True - Food and Health Communications

... • Only 1-2% of those people have the gene activated. ...
An Enderleinian approach to the problem of
An Enderleinian approach to the problem of

... not appropriate for all people in which case a raw food diet or brown rice fast is prefarable. Drainage It is important to ensure that liver and kidney function is optimal which can be supported with the use of herbal and homeopathic drainage remedies. In the treatment of Candida the anti-fungal pro ...
Kevin Schuer
Kevin Schuer

Carbohydrate intake and nonalcoholic fatty liver disease: fructose as
Carbohydrate intake and nonalcoholic fatty liver disease: fructose as

... hepatic de novo lipogenesis (DNL) and are more likely to directly contribute to NAFLD than dietary fat. Substrates used for the synthesis of newly made fatty acids by DNL are primarily glucose, fructose, and amino acids. Epidemiological studies linked HFCS consumption to the severity of fibrosis in ...
Lesson 9 Readings
Lesson 9 Readings

... fats in the duodenum. It breaks apart large fat globules so that enzymes from the pancreas can digest the fats. This is called emulsification. Without bile, most of the fat taken into the body would remain undigested. Besides producing bile, the liver has several other vital and important functions ...
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Wilson's disease



Wilson's disease or hepatolenticular degeneration is an autosomal recessive genetic disorder in which copper accumulates in tissues; this manifests as neurological or psychiatric symptoms and liver disease. It is treated with medication that reduces copper absorption or removes the excess copper from the body, but occasionally a liver transplant is required.The condition is due to mutations in the Wilson disease protein (ATP7B) gene. A single abnormal copy of the gene is present in 1 in 100 people, who do not develop any symptoms (they are carriers). If a child inherits the gene from both parents, the child may develop Wilson's disease. Symptoms usually appear between the ages of 6 and 20 years, but cases in much older people have been described. Wilson's disease occurs in 1 to 4 per 100,000 people. It is named after Samuel Alexander Kinnier Wilson (1878–1937), the British neurologist who first described the condition in 1912.
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