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Chapters: Phenylketonuria, Sly Syndrome, Myoadenylate Deaminase Deficiency, Glycogen Storage Disease Type V, Lesch-nyhan Syndrome, Newborn Screening, Succinic Semialdehyde Dehydrogenase Deficiency, Glycogen Storage Disease Type I, Carnitine Palmitoyltransferase Ii Deficiency, Niemann-Pick Disease, Type C, Glutaric Aciduria Type 1, Glycogen Storage Disease Type Ii, Inborn Error of Metabolism, X-Linked Ichthyosis, Trimethylaminuria, Lysosomal Storage Disease, Urea Cycle Disorder, Crigler-Najjar Syndrome, Galactosemia, Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency, Adenylosuccinate Lyase Deficiency, Maple Syrup Urine Disease, Menkes Disease, Fumarase Deficiency, Krabbe Disease, Methylmalonic Acidemia, Propionic Acidemia, Refsum's Disease, Mitochondrial Trifunctional Protein Deficiency, Congenital Disorder of Glycosylation, Metab-L, Schindler Disease, Argininosuccinic Aciduria, Lysinuric Protein Intolerance, Citrullinemia, Ornithine Translocase Deficiency, Glucose-Galactose Malabsorption, Adenosine Deaminase Deficiency, Ornithine Transcarbamylase Deficiency, Hyperprolinemia, Isovaleric Acidemia, D-Glyceric Acidemia, Tetrahydrobiopterin Deficiency, Aspartylglucosaminuria, Short-Chain Acyl-Coenzyme a Dehydrogenase Deficiency, Fucosidosis, Pyruvate Carboxylase Deficiency, Wolman Disease, Idiosyncrasy, Guanidinoacetate Methyltransferase Deficiency, Smith-Lemli-Opitz Syndrome, Tangier Disease, Zellweger Syndrome, Argininemia, Pyruvate Kinase Deficiency, Organic Acidemia, N-Acetylglutamate Synthase Deficiency, Galactose-1-Phosphate Uridylyltransferase Galactosemia, Dihydropyrimidine Dehydrogenase Deficiency, Hereditary Fructose Intolerance, Primary Carnitine Deficiency, Hypermethioninemia, Lipid Storage Disorder, Carnitine-Acylcarnitine Translocase Deficiency, Malonyl-Coa Decarboxylase Deficiency, Prolidase Deficiency, Carnitine Palmitoyltransferase I Deficiency, 3-Hydroxyacyl-Coenzyme a Dehydrogenase Deficiency, 3-Hydroxy-3-...More: http://booksllc.net/?id=1115749 ... Read more

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This up-to-date and comprehensive set of two CD-ROM discs provides a superb collection of authoritative documents on the subject of Phenylketonuria (PKU). Phenylketonuria (PKU) is a genetic disorder in which the body can't process part of a protein called phenylalanine (Phe). Phe is in almost all foods. If the Phe level gets too high, it can damage the brain and cause severe mental retardation. All babies born in U.S. hospitals must now have a screening test for PKU. This makes it easier to diagnose and treat the problem early. The best treatment for PKU is a diet of low-protein foods. There are special formulas for newborns. For older children and adults, the diet includes many fruits and vegetables. It also includes some low-protein breads, pastas and cereals. Nutritional formulas provide the vitamins and minerals they can't get from their food.For patients, practical information is provided in clearly written patient education documents. For medical professionals, doctor reference tools and texts have detailed technical information and clinical background material. There is no other reference that is as fast, convenient, and portable - everything you need to know, from the federal sources you trust. This thoroughly researched collection presents vital information from many authoritative sources: Food and Drug Administration (FDA), Centers for Disease Control (CDC), National Institutes of Health (NIH) and the relevant institute for this disease, and others.In addition to the comprehensive disease-specific coverage, this disc set also includes our Medical Encyclopedia, a $19.95 value! The Encyclopedia presents a collection of official documents about a wide range of medical topics, diseases, illnesses, health and wellness. There is vital information from the National Institutes of Health (NIH), the Centers for Disease Control (CDC), National Cancer Institute, and more. Topics covered include: major diseases, including cancer, heart and vascular disease, stroke, blood diseases and disorders, lung diseases, and neurological disorders such as dementia and epilepsy * CDC Health Topics A to Z, Foodborne Illnesses, Infants and Children, Injuries, Occupational Health, Older Adults, Women * CDC Travelers' Health - Destinations, Vaccinations, Diseases, Mosquito, Tick, Food, Water, Clinics, Yellow Book, Children, Airplanes, Cruise Ships, Special Needs, Relief Workers * Dietary Guidelines * NIH A to Z from abnormalities to X-rays.Since navigating the Internet to find additional non-governmental medical information can be confusing, we've also provided our exclusive "Guide to Leading Medical Websites" with updated links to 67 of the best sites for medical information! Built-in weblinks let you quickly check for the latest clinical updates directly from the government and the best commercial portals, news sites, reference/textbook/non-commercial portals, and health organizations. ... Read more

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Chapters: Tay-Sachs disease, Phenylketonuria, Cystic fibrosis, Canavan disease, Wilson's disease, Lafora disease, Alkaptonuria, Abetalipoproteinemia, Sly syndrome, Cenani Lenz syndactylism, Acheiropodia, Glycogen storage disease type V, Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, Sickle-cell disease, Usher syndrome, Neuronal ceroid lipofuscinosis, Succinic semialdehyde dehydrogenase deficiency, Mucopolysaccharidosis, Glycogen storage disease type II, Iminoglycinuria, Carnitine palmitoyltransferase II deficiency, Niemann-Pick disease, type C, Fanconi anemia, Johanson-Blizzard syndrome, Urbach-Wiethe disease, Sandhoff disease, Glutaric aciduria type 1, Gaucher's disease, Thalassemia, Familial dysautonomia, Lipoid congenital adrenal hyperplasia, Acute fatty liver of pregnancy, Primary ciliary dyskinesia, Pseudoxanthoma elasticum, Shwachman-Bodian-Diamond syndrome, Survival motor neuron spinal muscular atrophy, Situs inversus, Metachromatic leukodystrophy, Finnish heritage disease, Friedreich's ataxia, Gerodermia osteodysplastica, Niemann-Pick disease, Carpenter syndrome, Fibrochondrogenesis, Sickle cell trait, Methemoglobinemia, Trimethylaminuria, Mucolipidosis, Hermansky-Pudlak syndrome, Hypertryptophanemia, Chondrodystrophy, Harlequin type ichthyosis, Donohue syndrome, Carnosinemia, Familial Mediterranean fever, Compound heterozygosity, Batten disease, Dubowitz syndrome, Gastroschisis, Nemaline myopathy, Bloom syndrome, Lamellar ichthyosis, Xeroderma pigmentosum, Medium-chain acyl-coenzyme A dehydrogenase deficiency, Adenylosuccinate lyase deficiency, Hemophagocytic lymphohistiocytosis, Maple syrup urine disease, Fumarase deficiency, Microvillous inclusion disease, Biotinidase deficiency, Cystinosis, Cystinuria, Ellis-van Creveld syndrome, Chédiak-Higashi syndrome, Pendred syndrome, Hurler syndrome, Persistent Mullerian duct syndrome, Krabbe disease, Methylmalonic acidemia, Meckel syndrome, Hartnup disease, GM2-gangliosidosis, AB variant, C... ... Read more

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Avoiding hard-to-understand medical jargon, the four-volume “Gale Encyclopedia of Children’s Health” uses language that parents can understand, while still providing enough depth to benefit today's health science students. The set provides in-depth coverage of pediatric diseases and disorders, along with issues related to physical and cognitive/behavioral development.

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This volume features original contributions from international groups involved in the prevention, diagnosis and treatment of phenylketonuria. ... Read more

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The Phenylketonuria Medical Guide is a publication which has been designed to better help readers understand Phenylketonuria. This Qontro Medical Guide has been designed with the reader in mind, and is a useful information source for readers at all levels looking to learn more about Phenylketonuria. The Phenylketonuria Medical Guide is highly recommended for those interested in understanding and learning more about Phenylketonuria. ... Read more

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The “Gale Encyclopedia of Science” is written at a level somewhere between the introductory sources and the highly technical texts currently available. This six-volume set covers all major areas of science and engineering, as well as mathematics and the medical and health sciences, while providing a comprehensive overview of current scientific knowledge and technology. Alphabetically arranged entries provide a user-friendly format that makes the broad scope of information easy to access and decipher. Entries typically describe scientific concepts, provide overviews of scientific areas and, in some cases, define terms.

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Chapters: Phenylketonuria, Adrenoleukodystrophy, Gout, Porphyria, Lafora Disease, Alkaptonuria, Sly Syndrome, Lesch-nyhan Syndrome, Urbach-wiethe Disease, Hunter Syndrome, Gaucher's Disease, Porphyria Cutanea Tarda, Carotenosis, Amyloidosis, Niemann-pick Disease, Erythropoietic Protoporphyria, Verruciform Xanthoma, Acute Intermittent Porphyria, Fabry Disease, Variegate Porphyria, Cadasil Syndrome, Hurler Syndrome, Hartnup Disease, Hereditary Coproporphyria, Pseudoporphyria, Sanfilippo Syndrome, Sitosterolemia, Citrullinemia, Myxedema, Fucosidosis, Morquio Syndrome, Tangier Disease, Farber Disease, Sialidosis, Prolidase Deficiency, Ochronosis, Gunther Disease, Combined Hyperlipidemia, Erythropoietic Porphyria, Cerebrotendineous Xanthomatosis, Amyloid Purpura, Xanthelasma, Necrobiosis Lipoidica, Hepatoerythropoietic Porphyria, Calcinosis Cutis, Primary Cutaneous Amyloidosis, Diabetic Bulla, Familial Dysbetalipoproteinemia, Apolipoprotein B Deficiency, Lipoprotein Lipase Deficiency, Diabetic Dermadrome, Palmar Xanthoma, Tuberoeruptive Xanthoma, Subepidermal Calcified Nodule, Tumoral Calcinosis, Diabetic Dermopathy, Xanthoma Tendinosum, Secondary Systemic Amyloidosis, Idiopathic Scrotal Calcinosis, Secondary Cutaneous Amyloidosis, Lichen Amyloidosis, Xanthoma Planum, Transient Erythroporphyria of Infancy, Traumatic Calcinosis Cutis, Dystrophic Calcinosis Cutis, Familial Hypertriglyceridemia, Diabetic Cheiroarthropathy, Hyaluronidase Deficiency, Medication-Induced Hyperlipoproteinemia, Iatrogenic Calcinosis Cutis, Metastatic Calcinosis Cutis, Normolipoproteinemic Xanthomatosis, Xanthoma Tuberosum, Macular Amyloidosis, Osteoma Cutis, Heredofamilial Amyloidosis, Xanthoma Striatum Palmare, Xanthomatous Biliary Cirrhosis, Primary Systemic Amyloidosis, Limited Joint Mobility, Waxy Skin, Familial Apoprotein Cii Deficiency, Nodular Xanthoma, B-Mannosidase Deficiency, Nodular Amyloidosis, Xanthoma Diabeticorum, Scheie Syndrome, Broad Beta...More: http://booksllc.net/?id=55584 ... Read more

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This up-to-date and comprehensive set of two CD-ROM discs provides a superb collection of authoritative documents on the subject of Phenylketonuria (PKU). Phenylketonuria (PKU) is a genetic disorder in which the body can't process part of a protein called phenylalanine (Phe). Phe is in almost all foods. If the Phe level gets too high, it can damage the brain and cause severe mental retardation. All babies born in U.S. hospitals must now have a screening test for PKU. This makes it easier to diagnose and treat the problem early. The best treatment for PKU is a diet of low-protein foods. There are special formulas for newborns. For older children and adults, the diet includes many fruits and vegetables. It also includes some low-protein breads, pastas and cereals. Nutritional formulas provide the vitamins and minerals they can't get from their food.For patients, practical information is provided in clearly written patient education documents. For medical professionals, doctor reference tools and texts have detailed technical information and clinical background material. There is no other reference that is as fast, convenient, and portable - everything you need to know, from the federal sources you trust. This thoroughly researched collection presents vital information from many authoritative sources: Food and Drug Administration (FDA), Centers for Disease Control (CDC), National Institutes of Health (NIH) and the relevant institute for this disease, and others.In addition to the comprehensive disease-specific coverage, this disc set also includes our Medical Encyclopedia, a $19.95 value! The Encyclopedia presents a collection of official documents about a wide range of medical topics, diseases, illnesses, health and wellness. There is vital information from the National Institutes of Health (NIH), the Centers for Disease Control (CDC), National Cancer Institute, and more. Topics covered include: major diseases, including cancer, heart and vascular disease, stroke, blood diseases and disorders, lung diseases, and neurological disorders such as dementia and epilepsy * CDC Health Topics A to Z, Foodborne Illnesses, Infants and Children, Injuries, Occupational Health, Older Adults, Women * CDC Travelers' Health - Destinations, Vaccinations, Diseases, Mosquito, Tick, Food, Water, Clinics, Yellow Book, Children, Airplanes, Cruise Ships, Special Needs, Relief Workers * Dietary Guidelines * NIH A to Z from abnormalities to X-rays.Since navigating the Internet to find additional non-governmental medical information can be confusing, we've also provided our exclusive "Guide to Leading Medical Websites" with updated links to 67 of the best sites for medical information! Built-in weblinks let you quickly check for the latest clinical updates directly from the government and the best commercial portals, news sites, reference/textbook/non-commercial portals, and health organizations. ... Read more

Product Description
This up-to-date and comprehensive set of two CD-ROM discs provides a superb collection of authoritative documents on the subject of Phenylketonuria (PKU). Phenylketonuria (PKU) is a genetic disorder in which the body can't process part of a protein called phenylalanine (Phe). Phe is in almost all foods. If the Phe level gets too high, it can damage the brain and cause severe mental retardation. All babies born in U.S. hospitals must now have a screening test for PKU. This makes it easier to diagnose and treat the problem early. The best treatment for PKU is a diet of low-protein foods. There are special formulas for newborns. For older children and adults, the diet includes many fruits and vegetables. It also includes some low-protein breads, pastas and cereals. Nutritional formulas provide the vitamins and minerals they can't get from their food.For patients, practical information is provided in clearly written patient education documents. For medical professionals, doctor reference tools and texts have detailed technical information and clinical background material. There is no other reference that is as fast, convenient, and portable - everything you need to know, from the federal sources you trust. This thoroughly researched collection presents vital information from many authoritative sources: Food and Drug Administration (FDA), Centers for Disease Control (CDC), National Institutes of Health (NIH) and the relevant institute for this disease, and others.In addition to the comprehensive disease-specific coverage, this disc set also includes our Medical Encyclopedia, a $19.95 value! The Encyclopedia presents a collection of official documents about a wide range of medical topics, diseases, illnesses, health and wellness. There is vital information from the National Institutes of Health (NIH), the Centers for Disease Control (CDC), National Cancer Institute, and more. Topics covered include: major diseases, including cancer, heart and vascular disease, stroke, blood diseases and disorders, lung diseases, and neurological disorders such as dementia and epilepsy * CDC Health Topics A to Z, Foodborne Illnesses, Infants and Children, Injuries, Occupational Health, Older Adults, Women * CDC Travelers' Health - Destinations, Vaccinations, Diseases, Mosquito, Tick, Food, Water, Clinics, Yellow Book, Children, Airplanes, Cruise Ships, Special Needs, Relief Workers * Dietary Guidelines * NIH A to Z from abnormalities to X-rays.Since navigating the Internet to find additional non-governmental medical information can be confusing, we've also provided our exclusive "Guide to Leading Medical Websites" with updated links to 67 of the best sites for medical information! Built-in weblinks let you quickly check for the latest clinical updates directly from the government and the best commercial portals, news sites, reference/textbook/non-commercial portals, and health organizations. ... Read more

Product Description
This volume is produced from digital images created through the University of Michigan University Library's large-scale digitization efforts. The Library seeks to preserve the intellectual content of items in a manner that facilitates and promotes a variety of uses. The digital reformatting process results in an electronic version of the original text that can be both accessed online and used to create new print copies. The Library also understands and values the usefulness of print and makes reprints available to the public whenever possible. This book and hundreds of thousands of others can be found in the HathiTrust, an archive of the digitized collections of many great research libraries. For access to the University of Michigan Library's digital collections, please see http://www.lib.umich.edu and for information about the HathiTrust, please visit http://www.hathitrust.org ... Read more

Product Description
This volume is produced from digital images created through the University of Michigan University Library's large-scale digitization efforts. The Library seeks to preserve the intellectual content of items in a manner that facilitates and promotes a variety of uses. The digital reformatting process results in an electronic version of the original text that can be both accessed online and used to create new print copies. The Library also understands and values the usefulness of print and makes reprints available to the public whenever possible. This book and hundreds of thousands of others can be found in the HathiTrust, an archive of the digitized collections of many great research libraries. For access to the University of Michigan Library's digital collections, please see http://www.lib.umich.edu and for information about the HathiTrust, please visit http://www.hathitrust.org ... Read more