Pages that link to "Q15051322"
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The following pages link to inborn error of lipid metabolism (Q15051322):
Displaying 50 items.
- sitosterolemia (Q1336034) (← links)
- Fatty-acid metabolism disorder (Q5437988) (← links)
- mitochondrial trifunctional protein deficiency (Q6881883) (← links)
- A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation (Q26699142) (← links)
- Bent spine syndrome as an initial manifestation of late-onset multiple acyl-CoA dehydrogenase deficiency: a case report and literature review (Q26800084) (← links)
- Unique features of high-density lipoproteins in the Japanese: in population and in genetic factors (Q28085611) (← links)
- Kanuma (Q29006069) (← links)
- Anderson-Fabry Dyslipidosis (Q35143041) (← links)
- SERUM LIPIDS (Q35488168) (← links)
- Fatty acid oxidation disorders: A new class of metabolic diseases (Q36297561) (← links)
- The Lipid Storage Diseases: New Concepts and Control (Q36345202) (← links)
- Heritable catabolic and anabolic disorders of lipid metabolism (Q39132617) (← links)
- Refsum's disease (heredopathia atactica polyneuritiformis). An inborn error of lipid metabolism with storage of 3,7,11,15 tetramethyl hexadecanoic acid. A review of the clinical findings (Q39876080) (← links)
- Hereditary Diseases?Causes, Cures, and Problems (Q39956684) (← links)
- Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations (Q41691162) (← links)
- Familial plasma cholesterol ester deficiency. Clinical studies of a family (Q43534534) (← links)
- Cytogenetic study of a kinship with Fabry-Anderson syndrome (angiokeratoma corporis diffusion universale) (Q43702534) (← links)
- β-Galactosidase in Tissue Culture Derived from Human Skin and Bone Marrow: Enzyme defect in GM1 Gangliosidosis (Q43827643) (← links)
- GM1- and GM2-gangliosidosis. First cases in Finland (Q44256310) (← links)
- The Enzyme Defect in Fabry's Disease (Q44808743) (← links)
- Syndrome of the sea blue histiocyte (a case report) (Q45075757) (← links)
- Sphingolipidosis in childhood (Q45122974) (← links)
- Metachromatic leukodystrophy in the adult: A biochemical study (Q45175592) (← links)
- Wolman Disease in a Pakistani Infant (Q45793858) (← links)
- Carnitine-acylcarnitine translocase deficiency with c.199-10 T>G and novel c.1A>G mutation: Two case reports and brief literature review (Q47136044) (← links)
- Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys. (Q47281654) (← links)
- Perioperative measures in very long chain acyl-CoA dehydrogenase deficiency (Q48285183) (← links)
- Abnormality in sphingolipid fatty acids from sciatic nerve and brain of Quaking mice1 (Q48809863) (← links)
- Lactosyl Ceramidosis: Catabolic Enzyme Defect of Glycosphingolipid Metabolism (Q48888724) (← links)
- Propionicacidemia, a New Inborn Error of Metabolism (Q49129201) (← links)
- Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland) (Q50674487) (← links)
- Juvenile GM1 gangliosidosis: Clinical, pathological, chemical and enzymatic studies (Q51111107) (← links)
- GENERALIZED GANGLIOSIDOSIS: ANOTHER INBORN ERROR OF GANGLIOSIDE METABOLISM? (Q51253791) (← links)
- Anesthetic management in a patient with trifunctional protein deficiency (Q51372678) (← links)
- REFSUM'S DISEASE (HEREDOPATHIA ATACTICA POLYNEURITIFORMIS): AN INBORN ERROR OF LIPID METABOLISM WITH STORAGE OF 3,7,11,15-TETRAMETHYL HEXADECANOIC ACID. I. REPORT OF A CASE. (Q52132779) (← links)
- An inborn error of lipid metabolism. (Q52163136) (← links)
- Recent findings in lipidoses (Q53848469) (← links)
- Congenital lipid metabolism disorders (Q53998805) (← links)
- Refsum's disease (heredopathia atactica polyneuritiformis). An inborn error of lipid metabolism with storage of 3,7,11,15 tetramethyl hexadecanoic acid formal genetics. (Q54397621) (← links)
- Study of an unusual disorder of post-heparin lipoprotein lipase activity in a child with fat-dependent hyperglyceridemia (Q54422295) (← links)
- Renal Transplantation in Fabry’s Disease (Q54516405) (← links)
- sterol metabolism disorder (Q55788571) (← links)
- Sitosterolemia, Hypercholesterolemia, and Coronary Artery Disease (Q57164484) (← links)
- Neutral-lipid storage disease: a new disorder of lipid metabolism (Q57971906) (← links)
- Enzymatic Defect in Fabry's Disease (Q59383540) (← links)
- Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet Function (Q64118342) (← links)
- Clinical features and genetic analysis of childhood sitosterolemia: Two case reports and literature review (Q64235862) (← links)
- "Odor of sweaty feet" syndrome (Q67071113) (← links)
- Ocular manifestations of inborn errors of carbohydrate and lipid metabolism (Q67509559) (← links)
- Lipoprotein and lecithin: cholesterol acyltransferase changes in galactosamine-induced rat liver injury (Q67514944) (← links)