81. Reactome: Galactosemia Title, galactosemia. Publication year, 2001. Journal, The Metabolic and Molecular Bases of Inherited Disease, 8th ed (Scriver CR, et al., editors) http://www.reactome.org/cgi-bin/eventbrowser?DB=gk_current&FOCUS_SPECIES=Homo sa

82. Living With Classical Galactosemia: Health-Related Quality Of Life Consequences Classical galactosemia (McKusick 230400) is an autosomal recessive However, longterm follow-up of patients with classical galactosemia has shown that, http://pediatrics.aappublications.org/cgi/content/full/113/5/e423

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract Full Text (PDF) P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Bosch, A. M. Articles by Last, B. F. Related Collections PEDIATRICS Vol. 113 No. 5 May 2004, pp. e423-e428 ELECTRONIC ARTICLE Living With Classical Galactosemia: Health-Related Quality of Life Consequences Annet M. Bosch, MD Martha A. Grootenhuis, PhD Henk D. Bakker, MD, PhD Hugo S.A. Heijmans, MD, PhD Frits A. Wijburg, MD, PhD and Bob F. Last, PhD Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands Department of Pediatrics, Gooi-Noord Hospital Blaricum, Blaricum, The Netherlands Pediatric Psychosocial Department, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands ABSTRACT TOP ABSTRACT METHODS RESULTS DISCUSSION REFERENCES Objective.

83. Phenylketonuria And Galactosemia (from Disease, Human) --  Britannica Student E Phenylketonuria and galactosemia (from disease, human) Phenylketonuria (PKU) and galactosemia also are genetically inherited metabolic diseases. http://www.britannica.com/ebi/article-234386

Home Browse Newsletters Store ... Subscribe Already a member? Log in This Article's Table of Contents Expand all Collapse all Introduction How Disease Is Classified ... Upper Respiratory Diseases Infectious Lower Respiratory Diseases Pneumonia Inflammatory diseases Fungal diseases Lung abscess ... Tuberculosis Noninfectious Respiratory Diseases Emphysema Pulmonary edema Occupational lung diseases Respiratory distress syndrome ... Nervous System Infections Noninfectious Nerve Disorders Neuritis and neuralgia Inflammation Vertigo Parkinson's disease ... Diabetes mellitus Metabolic Diseases Gout Cystic fibrosis changeTocNode('toc199687','img199687'); Phenylketonuria and galactosemia Malnutrition and Deficiency Diseases Autoimmune Diseases Bone and Muscle Diseases ... Kidney and Genital Diseases Kidney Disorders Inflammatory diseases Calculi Other kidney disorders Reproductive System Disorders ... Print this Table of Contents Shopping Price: USD $1495 Revised, updated, and still unrivaled. The Official Scrabble Players Dictionary (Hardcover) Price: USD $15.95 The Scrabble player's bible on sale! Save 30%.

84. THE MERCK MANUAL--SECOND HOME EDITION, Carbohydrate Metabolism In Ch. 282, Hered galactosemia (a high blood level of galactose) is caused by lack of one of the enzymes galactosemia is treated by completely eliminating milk and milk http://www.merck.com/mmhe/sec23/ch282/ch282b.html

var externalLinkWarning = "The link you have selected will take you to a site outside Merck and The Merck Manuals.*n*nThe Merck Manuals do not review or control the content of any non-Merck site. The Merck Manuals do not endorse and are not responsible for the accuracy, content, practices, or standards of any non-Merck sources."; Search The Second Home Edition , Online Version Search Index A B C D ... Z Sections Accidents and Injuries Blood Disorders Bone, Joint, and Muscle Disorders Brain, Spinal Cord, and Nerve Disorders ... Women's Health Issues Resources Anatomical Drawings Multimedia Pronunciations Weights and Measures ... , Online Version Section Children's Health Issues Chapter Hereditary Metabolic Disorders Topics Introduction Amino Acid Metabolism Carbohydrate Metabolism Lipid Metabolism Pyruvate Metabolism Carbohydrate Metabolism Buy The Book Print This Topic Email This Topic Pronunciations cirrhosis galactosemia hemolysis pyruvate ... von Gierke's disease Carbohydrates are sugars. Some sugars are simple, and others are more complex. Sucrose (table sugar) is made of two simpler sugars called glucose and fructose. Lactose (milk sugar) is made of glucose and galactose. Both sucrose and lactose must be broken down into their component sugars by enzymes before the body can absorb and make use of them. The carbohydrates in bread, pasta, rice, and other carbohydrate-containing foods are long chains of simple sugar molecules. These longer molecules must also be broken down by the body. If an enzyme needed to process a certain sugar is missing, the sugar can accumulate in the body, causing problems.

85. Inborn Errors Of Metabolism Endocrinology Metabolism galactosemia. galactosemia; Erythrocyte Galactose1-Phosphate uridyl transferase. Activity diminished. Urine exam http://www.fpnotebook.com/END91.htm

Home About Links Index ... Editor's Choice document.write(code); Advertisement Endocrinology Metabolism Assorted Pages Inborn Errors of Metabolism Disorders of Energy Metabolism Lysosomal storage disease Inborn Error of Small Molecule Metabolism ... Tay-Sachs Disease Inborn Errors of Metabolism Book Home Page Cardiovascular Medicine Dentistry Dermatology Emergency Medicine Endocrinology Gastroenterology Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Practice Management Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Endocrinology Index Adrenal Disease Dermatology Diabetes Mellitus Examination Ophthalmology Geriatric Medicine Growth Hematology and Oncology Hypoglycemia Laboratory General Metabolism Neurology Neonatology Obesity Obstetrics Parathyroid Disease Pediatrics Pharmacology Pituitary Disease Prevention Radiology Nephrology Sex Sports Medicine Surgery Symptom Evaluation Thyroid Disease Page Metabolism Index Background Class Energy Class Lysosomal Storage Class Small Molecules Fructose Intolerance Galactosemia Gauchers Disease Homocystinuria Tay-Sachs Metabolic disorders testable on Newborn Screen Congenital Hypothyroidism Phenylketonuria (PKU) Galactosemia Galactokinase deficiency Maple syrup urine disease Homocystinuria Biotinidase deficiency Classification Inborn Errors of Small Mole cule Metabolism Example: Galactosemia Lysosomal storage disease s Example:

86. Short Description Of Cell Lines. Pathology: Asymptomatic Galactosemia Version 4.200205. Short description of cell lines. Pathology asymptomatic galactosemia OMIM Home. By selecting the cell line name, you will receive the http://www.biotech.ist.unige.it/cldb/pat233.html

Version Short description of cell lines. Pathology: asymptomatic galactosemia OMIM Home By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser CHP 4 human, Black skin, fibroblast IZSBS ... By Beatrice...

87. Short Description Of Cell Lines. Pathology: Galactosemia *230400 Pathology galactosemia *230400 OMIM record. By selecting the cell line name, you will receive the detailed description of the cell line http://www.biotech.ist.unige.it/cldb/pat14.html

Version Short description of cell lines. Pathology: galactosemia OMIM record By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser CHP 3 human, Black skin, fibroblast IZSBS ... By Beatrice...

88. Galactosemia galactosemia is the inability of the body to use (metabolize) the simple sugar galactosemia is an inherited disorder (transmitted as an autosomal http://www.shands.org/health/information/article/000366.htm

Disease Injury Nutrition Poison ... Galactosemia Galactosemia Definition: Galactosemia is the inability of the body to use ( metabolize ) the simple sugar galactose (causing the accumulation of galactose 1-phosphate), which then reaches high levels in the body, causing damage to the liver, central nervous system, and various other body systems. Alternative Names: Galactose-1-phosphate uridyl transferase deficiency; Galactokinase deficiency; Galactose-6-phosphate epimerase deficiency Causes, incidence, and risk factors: Galactosemia is an inherited disorder (transmitted as an autosomal recessive trait). It occurs at a rate of approximately 1 out of 60,000 births. There are 3 forms of the disease galactose-1 phosphate uridyl transferase deficiency (classic galactosemia) and deficiency of galactose kinase or galactose-6-phosphate epimerase. Of these, the galactose-1-phosphate transferase deficiency is the most severe (and more common). People with galactosemia are unable to fully metabolize the simple sugar galactose. Galactose makes up half of the sugar, called lactose, that is found in milk. Lactose is called a disaccharide (di meaning 2 and saccharide meaning sugar) since lactose is made up of two sugars, galactose and glucose, bound together. If an infant with galactosemia is given milk, derivatives of galactose builds up in the infants system causing damage to the liver, brain, kidneys, and eyes. Individuals with galactosemia cannot tolerate any form of milk (human or animal), or must carefully watch intake of other galactose-containing foods. Exposure to milk products may result in liver damage, mental retardation

89. Galactosemia Google Directory Health Conditions and Diseases Neurological Parents of Galactosemic Children, Inc. - http//www.galactosemia.org/ Presented is a case study of galactosemia in a four month old female child. http://www.websters-online-dictionary.org/definition/english/Ga/Galactosemia.htm

Philip M. Parker, INSEAD. Galactosemia Definition: Galactosemia Galactosemia Noun . A genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent; typically develops shortly after birth. Source: WordNet 1.7.1 Specialty Definitions: Galactosemia Domain Definitions Health Buildup of galactose in the blood. Caused by lack of one of the enzymes needed to break down galactose into glucose. ( references Source: compiled by the editor from various references ; see credits. Top Crosswords: Galactosemia Specialty definitions using "galactosemia" Galactitol Galactokinase UDPglucose-Hexose-1-Phosphate Uridylyltransferase references ... Top Non-Fiction Usage: Galactosemia Subject Topic Quote Health Galactosemia , a rare genetic disorder, hampers the body's ability to process the sugar galactose. ( references Alpha-1 antitrypsin deficiency, hemochromatosis, Wilson's disease, galactosemia , and glycogen storage diseases are among the inherited diseases that interfere with the way the liver produces, processes, and stores enzymes, proteins, metals, and other substances the body needs to function properly. ( references Source: compiled by the editor from ICON Group International, Inc.

90. Galactosemia galactosemia is the inability of the body to use (metabolize) the simple sugar galactose (causing the accumulation of galactose 1phosphate), http://www.pennhealth.com/ency/article/000366.htm

Appointments Medical Services Health Information Find a Doctor Search: Search Encyclopedia: List of Topics Print This Page  Endocrinology, Pediatrics Galactosemia Galactosemia Definition: Galactosemia is the inability of the body to use ( metabolize ) the simple sugar galactose (causing the accumulation of galactose 1-phosphate), which then reaches high levels in the body, causing damage to the liver, central nervous system, and various other body systems. Alternative Names: Galactose-1-phosphate uridyl transferase deficiency; Galactokinase deficiency; Galactose-6-phosphate epimerase deficiency Causes, incidence, and risk factors: Galactosemia is an inherited disorder (transmitted as an autosomal recessive trait). It occurs at a rate of approximately 1 out of 60,000 births. There are 3 forms of the disease: galactose-1 phosphate uridyl transferase deficiency (classic galactosemia, the most common and most severe form), deficiency of galactose kinase, and deficiency of galactose-6-phosphate epimerase. People with galactosemia are unable to fully break down the simple sugar galactose. Galactose makes up half of lactose, the sugar found in milk. Lactose is called a disaccharide (di meaning 2 and saccharide meaning sugar) because it is made up of two sugars, galactose and glucose, bound together.

91. Galactosemia Clásica Translate this page galactosemia clásica. Esta condición es un desorden metabólico raro y heredirario. Para que un niño herede esta condición se necesita que ambos padres http://www.paraqueestesbien.com.mx/hombre/torax/sistemadigestivo/sistdige78.htm

Sistema Digestivo Galactosemia clásica Esta condición es un desorden metabólico raro y heredirario. Para que un niño herede esta condición se necesita que ambos padres tengan el gen de la galactosemia. Se caracteriza por la acumulación del disacárido galactosa en la sangre y los tejidos, por la ausencia de la enzima necesaria para que la galactosa se transforme en glucosa. Generalmente cuando una persona consume un producto que contiene lactosa, el organismo la rompe o metaboliza en  galactosa y glucosa. La glucosa es el azúcar que el organismo usa como energía. El organismo al no poder romper esta enzima se va acumulando en el organismo volviéndose una especie de veneno y puede provocar ciertos desórdenes como: Crecimiento del hígado Falla renal Cataratas Daño cerebral Por lo general este tipo de condiciones se detectan al momento de nacer a través de los estudios realizados a los recién nacidos.

92. Health Library - Wisconsin Newborn Screening LaboratoryGeneral information on galactosemia. Although detection of classical galactosemia using the GALT enzyme test is not dependent on the feeding status, http://12.42.224.150/library/healthguide/en-us/illnessconditions/topic.asp?hwid=

93. Liver Disease In Saudi Arabia - Liver Diseases - Galactosemia liver diseases in middle east, riyadh, saudi arabia, bahrain, qatar, kuwait, United arab emirates, oman. http://www.liverme.org/liver_diseases/galactosemia.htm

About us About Liver Liver Diseases Livery Surgery ... Liver Abcesses Liver Diseases - Galactosemia Under Construction Signs and Symptoms: Diagnosis: Treatment: Site search Web search Tips for Healthy Liver Discussion Forum Alternative Treatment Lifestyle Changes ... Liver Diseases Liver Surgery Liver Transplant Procedures Contact Us Site Map

94. Disease - Galactosemia - Detroit, Michigan Disease galactosemia - courtesy of Henry Ford Health System of Detroit, Michigan. http://www.henryfordhealth.org/14465.cfm

3D Tour of the Vattikuti Institute About the Institute The Vattikuti Institute Prostatectomy Prostate Cancer ... Health Encyclopedia Health Encyclopedia Back to main Health Information page Disease - Galactosemia Galactosemia Definition: Galactosemia is the inability of the body to use ( metabolize ) the simple sugar galactose (causing the accumulation of galactose 1-phosphate), which then reaches high levels in the body, causing damage to the liver, central nervous system, and various other body systems. Alternative Names: Galactose-1-phosphate uridyl transferase deficiency; Galactokinase deficiency; Galactose-6-phosphate epimerase deficiency Causes And Risk: Galactosemia is an inherited disorder (transmitted as an autosomal recessive trait). It occurs at a rate of approximately 1 out of 60,000 births. There are 3 forms of the disease galactose-1 phosphate uridyl transferase deficiency (classic galactosemia) and deficiency of galactose kinase or galactose-6-phosphate epimerase. Of these, the galactose-1-phosphate transferase deficiency is the most severe (and more common). People with galactosemia are unable to fully metabolize the simple sugar galactose. Galactose makes up half of the sugar, called lactose, that is found in milk. Lactose is called a disaccharide (di meaning 2 and saccharide meaning sugar) since lactose is made up of two sugars, galactose and glucose, bound together.

95. Welcome To Intertops.com! http://www.galactosemia.ca/galactosemia/default.asp

96. Resource Library Find Information On Galactosemia At MerckSource Find information on galactosemia at MerckSource. Learn more about galactosemia, galactosemia is the inability of the body to use (metabolize) the simple http://www.mercksource.com/pp/us/cns/cns_hc_children_content_adam.jspzQzpgzEzzSz

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