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    Free Full-Text Nutritional and Metabolic Diseases Articles

    FREE FULL-TEXT NUTRITIONAL AND METABOLIC DISEASES ARTICLES

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    Abetalipoproteinemia

    Acatalasia

    Acidosis, Renal Tubular

    Adiposis Dolorosa

    Adrenal Hyperplasia, Congenital

    Adrenoleukodystrophy

    Adrenoleukodystrophy

    alpha-Mannosidosis

    alpha-Mannosidosis

    Aminoaciduria, Renal

    Arthritis, Gouty

    beta-Mannosidosis

    beta-Mannosidosis

    Biotinidase Deficiency

    Carbohydrate Metabolism, Inborn Errors

    Carbohydrate-Deficient Glycoprotein Syndrome

    Cholesterol Ester Storage Disease

    Cholesterol Ester Storage Disease

    Chondrodysplasia Punctata, Rhizomelic

    Crigler-Najjar Syndrome

    Cystinosis

    Cystinuria

    Cytochrome-c Oxidase Deficiency

    Cytochrome-c Oxidase Deficiency

    Fabry Disease

    Fabry Disease

    Fabry Disease

    Fabry Disease

    Fabry Disease

    Fanconi Syndrome

    Friedreich Ataxia

    Fructose Intolerance

    Fructose Metabolism, Inborn Errors

    Fructose-1,6-Diphosphatase Deficiency

    Fucosidosis

    Fucosidosis

    Fucosidosis

    Galactosemias

    Gangliosidoses

    Gangliosidoses

    Gangliosidoses

    Gangliosidoses

    Gangliosidoses

    Gangliosidoses GM2

    Gangliosidoses GM2

    Gangliosidoses GM2

    Gangliosidoses GM2

    Gangliosidoses GM2

    Gangliosidosis GM1

    Gangliosidosis GM1

    Gangliosidosis GM1

    Gangliosidosis GM1

    Gaucher Disease

    Gaucher Disease

    Gaucher Disease

    Gaucher Disease

    Gaucher Disease

    Gilbert Disease

    Glucosephosphate Dehydrogenase Deficiency

    Glycogen Storage Disease

    Glycogen Storage Disease Type I

    Glycogen Storage Disease Type II

    Glycogen Storage Disease Type II

    Glycogen Storage Disease Type II

    Glycogen Storage Disease Type III

    Glycogen Storage Disease Type IV

    Glycogen Storage Disease Type V

    Glycogen Storage Disease Type VI

    Glycogen Storage Disease Type VII

    Glycogen Storage Disease Type VIII

    Glycosuria, Renal

    Gout

    Hartnup Disease

    Hemochromatosis

    Hepatolenticular Degeneration

    Holocarboxylase Synthetase Deficiency

    Hyperbilirubinemia, Hereditary

    Hypercholesterolemia, Familial

    Hypercholesterolemia, Familial

    Hyperlipidemia, Familial Combined

    Hyperlipoproteinemia Type III

    Hyperlipoproteinemia Type IV

    Hyperlipoproteinemia Type IV

    Hyperlipoproteinemia Type V

    Hyperoxaluria, Primary

    Hypobetalipoproteinemia

    Hypokalemic Periodic Paralysis

    Hypolipoproteinemia

    Hypophosphatasia

    Hypophosphatemia

    Hypophosphatemia, Familial

    Hypophosphatemia, Familial

    Ichthyosis, X-Linked

    Jaundice, Chronic Idiopathic

    Kearns Syndrome

    Lactose Intolerance

    Lecithin Acyltransferase Deficiency

    Leigh Disease

    Leigh Disease

    Lesch-Nyhan Syndrome

    Leukodystrophy, Globoid Cell

    Leukodystrophy, Globoid Cell

    Leukodystrophy, Globoid Cell

    Leukodystrophy, Globoid Cell

    Leukodystrophy, Globoid Cell

    Leukodystrophy, Metachromatic

    Leukodystrophy, Metachromatic

    Leukodystrophy, Metachromatic

    Leukodystrophy, Metachromatic

    Leukodystrophy, Metachromatic

    Lipid Metabolism, Inborn Errors

    Lipoidosis

    Lipoidproteinosis

    Lipoprotein Lipase Deficiency, Familial

    Lysosomal Storage Diseases

    Lysosomal Storage Diseases, Nervous System

    Mannosidase Deficiency Diseases

    Mannosidase Deficiency Diseases

    Maple Syrup Urine Disease

    MELAS Syndrome

    MELAS Syndrome

    Menkes Kinky Hair Syndrome

    Menkes Kinky Hair Syndrome

    MERRF Syndrome

    MERRF Syndrome

    Metal Metabolism, Inborn Errors

    Mineralocorticoid Excess Syndrome, Apparent

    Mitochondrial Diseases

    Mitochondrial Encephalomyopathies

    Mitochondrial Myopathies

    Mucolipidoses

    Mucolipidoses

    Mucolipidoses

    Mucolipidoses

    Mucopolysaccharidoses

    Mucopolysaccharidoses

    Mucopolysaccharidosis I

    Mucopolysaccharidosis I

    Mucopolysaccharidosis II

    Mucopolysaccharidosis II

    Mucopolysaccharidosis III

    Mucopolysaccharidosis III

    Mucopolysaccharidosis IV

    Mucopolysaccharidosis IV

    Mucopolysaccharidosis VI

    Mucopolysaccharidosis VI

    Mucopolysaccharidosis VII

    Mucopolysaccharidosis VII

    Multiple Carboxylase Deficiency

    Neuronal Ceroid-Lipofuscinosis

    Niemann-Pick Diseases

    Niemann-Pick Diseases

    Niemann-Pick Diseases

    Niemann-Pick Diseases

    Niemann-Pick Diseases

    Ochronosis

    Oculocerebrorenal Syndrome

    Oculocerebrorenal Syndrome

    Ophthalmoplegia, Chronic Progressive External

    Optic Atrophy, Autosomal Dominant

    Optic Atrophy, Hereditary, Leber

    Ornithine Carbamoyltransferase Deficiency Disease

    Paralyses, Familial Periodic

    Paralysis, Hyperkalemic Periodic

    Peroxisomal Disorders

    Peroxisomal Disorders

    Phenylketonuria, Maternal

    Phenylketonurias

    Phosphorus Metabolism Disorders

    Porphyria

    Porphyria Cutanea Tarda

    Porphyria Cutanea Tarda

    Porphyria, Acute Intermittent

    Porphyria, Acute Intermittent

    Porphyria, Erythrohepatic

    Porphyria, Erythrohepatic

    Porphyria, Erythropoietic

    Porphyria, Erythropoietic

    Porphyria, Hepatic

    Porphyria, Hepatic

    Progeria

    Pseudohypoaldosteronism

    Pseudohypoparathyroidism

    Pseudopseudohypoparathyroidism

    Purine-Pyrimidine Metabolism, Inborn Errors

    Pyruvate Carboxylase Deficiency Disease

    Pyruvate Carboxylase Deficiency Disease

    Pyruvate Carboxylase Deficiency Disease

    Pyruvate Dehydrogenase Complex Deficiency Disease

    Pyruvate Dehydrogenase Complex Deficiency Disease

    Pyruvate Dehydrogenase Complex Deficiency Disease

    Pyruvate Metabolism, Inborn Errors

    Refsum Disease

    Refsum Disease

    Refsum Disease

    Renal Tubular Transport, Inborn Errors

    Sandhoff Disease

    Sandhoff Disease

    Sandhoff Disease

    Sandhoff Disease

    Sandhoff Disease

    Sea-Blue Histiocyte Syndrome

    Sea-Blue Histiocyte Syndrome

    Sialic Acid Storage Disease

    Sialic Acid Storage Disease

    Sjogren-Larsson Syndrome

    Skin Diseases, Metabolic

    Smith-Lemli-Opitz Syndrome

    Smith-Lemli-Opitz Syndrome

    Sphingolipidoses

    Sphingolipidoses

    Sphingolipidoses

    Sphingolipidoses

    Sphingolipidoses

    Steroid Metabolism, Inborn Errors

    Tangier Disease

    Tay-Sachs Disease

    Tay-Sachs Disease

    Tay-Sachs Disease

    Tay-Sachs Disease

    Tay-Sachs Disease

    Tyrosinemias

    Wasting Syndrome

    Wolman Disease

    Wolman Disease

    Wolman Disease

    Xanthogranuloma, Juvenile

    Xanthomatosis

    Xanthomatosis, Cerebrotendinous

    Xanthomatosis, Cerebrotendinous

    Zellweger Syndrome

    Zellweger Syndrome

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