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13.1 Principles of hormone action 2245 Rob Fowkes,

Oxford IM SECTION 13 Endocrine disorders

13.1 Principles of hormone action 2245 Rob Fowkes, V. Krishna Chatterjee, and Mark Gurnell ESSENT...

Updated 1 month ago by Omar Ayman

12.9 Disorders of peroxisomal metabolism in adults

Oxford IM SECTION 12 Metabolic disorders

12.9 Disorders of peroxisomal metabolism in adults 2157 ESSENTIALS The peroxisome is a specialize...

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12.8 Lysosomal disease 2121

Oxford IM SECTION 12 Metabolic disorders

12.8 Lysosomal disease 2121 ESSENTIALS Lysosomal function and classification of diseases The lyso...

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12.7.2 Inherited diseases of copper metabolism Wil

Oxford IM SECTION 12 Metabolic disorders

12.7.2 Inherited diseases of copper metabolism: Wilson’s disease and Menkes’ disease 2115 12.7.2 ...

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12.7.1 Hereditary haemochromatosis 2098 William J.

Oxford IM SECTION 12 Metabolic disorders

12.7.1 Hereditary haemochromatosis 2098 William J.H. Griffiths and Timothy M. Cox CONTENTS 12.7.1...

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12.7 Trace metal disorders 2098

Oxford IM SECTION 12 Metabolic disorders

12.7 Trace metal disorders 2098

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12.6 Lipid disorders 2055

Oxford IM SECTION 12 Metabolic disorders

12.6 Lipid disorders 2055 ESSENTIALS High blood cholesterol and high blood triglycerides are caus...

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12.5 The porphyrias 2032 Timothy M. Cox

Oxford IM SECTION 12 Metabolic disorders

12.5 The porphyrias 2032 Timothy M. Cox ESSENTIALS The porphyrias are a remarkable family of meta...

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12.4 Disorders of purine and pyrimidine metabolism

Oxford IM SECTION 12 Metabolic disorders

12.4 Disorders of purine and pyrimidine metabolism 2015 ESSENTIALS These disorders are due to abn...

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12.3.3 Disorders of galactose, pentose, and pyruva

Oxford IM SECTION 12 Metabolic disorders

12.3.3 Disorders of galactose, pentose, and pyruvate metabolism 2003 12.3.3  Disorders of galacto...

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12.3.2 Inborn errors of fructose metabolism 1993 T

Oxford IM SECTION 12 Metabolic disorders

12.3.2 Inborn errors of fructose metabolism 1993 Timothy M. Cox 12.3.2  Inborn errors of fructose...

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12.3.1 Glycogen storage diseases 1985 Robin H. Lac

Oxford IM SECTION 12 Metabolic disorders

12.3.1 Glycogen storage diseases 1985 Robin H. Lachmann and Timothy M. Cox CONTENTS 12.3.1 Glyco...

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12.3 Disorders of carbohydrate metabolism 1985

Oxford IM SECTION 12 Metabolic disorders

12.3 Disorders of carbohydrate metabolism 1985

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12.2 Protein- dependent inborn errors of metabolis

Oxford IM SECTION 12 Metabolic disorders

12.2 Protein- dependent inborn errors of metabolism 1942 ESSENTIALS Protein-​dependent inborn err...

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12.13 a1- Antitrypsin deficiency and the serpinopa

Oxford IM SECTION 12 Metabolic disorders

12.13 a1- Antitrypsin deficiency and the serpinopathies 2235 ESSENTIALS α1-​Antitrypsin is an acu...

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12.12.3 Amyloidosis 2218

Oxford IM SECTION 12 Metabolic disorders

12.12.3 Amyloidosis 2218 section 12  Metabolic disorders 2218 Levy R, et  al. (2015). Phenotypic ...

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12.12.2 Hereditary periodic fever syndromes 2207

Oxford IM SECTION 12 Metabolic disorders

12.12.2 Hereditary periodic fever syndromes 2207 12.12.2  Hereditary periodic fever syndromes 220...

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12.12.1 The acute phase response and C- reactive p

Oxford IM SECTION 12 Metabolic disorders

12.12.1 The acute phase response and C- reactive protein 2199 12.12 The acute phase response, her...

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12.12 The acute phase response, hereditary periodi

Oxford IM SECTION 12 Metabolic disorders

12.12 The acute phase response, hereditary periodic fever syndromes, and amyloidosis 2199

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12.11 A physiological approach to acid– base disor

Oxford IM SECTION 12 Metabolic disorders

12.11 A physiological approach to acid– base disorders: The roles of ion transport and body fluid...

Updated 1 month ago by Omar Ayman