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1. Disease; Diseases: DISEASE; DISEASES di-zez', di-zez'-iz (chalah, choli; nosos): Palestine, from its position and physical conditions, ought to be a healthy country. That it is not so depends on the unsanitary conditions in which the people live and the ... [100%] 1915-01-01
2. Glycogen storage disease: A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by a deficiency of an enzyme or transport protein affecting glycogen synthesis, glycogen breakdown, or glucose breakdown, typically in muscles and/or liver cells. GSD has ... [87%] 2024-01-12 [Inborn errors of carbohydrate metabolism] [Hepatology]...
3. Glycogen storage disease: A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by a deficiency of an enzyme or transport protein affecting glycogen synthesis, glycogen breakdown, or glucose breakdown, typically in muscles and/or liver cells. GSD has ... (Medicine) [87%] 2023-12-24 [Hepatology] [Rare diseases]...
4. Lysosomal storage disease: Lysosomal storage diseases (LSDs; /ˌlaɪsəˈsoʊməl/) are a group of over 70 rare inherited metabolic disorders that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large molecules and pass the fragments on to other ... (Medicine) [87%] 2024-01-12 [Autosomal recessive disorders]
5. Lysosomal storage disease: Lysosomal storage diseases (LSDs; /ˌlaɪsəˈsoʊməl/) (or Lysosomal enzyme disorder ) are a group of over 70 rare inherited metabolic disorders that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large molecules and pass the ... [87%] 2024-03-27 [Lysosomal storage diseases] [Inborn errors of metabolism]...
6. Neutral lipid storage disease: Template:Wikify Articles Most recent articles on Neutral lipid storage disease Most cited articles on Neutral lipid storage disease Review articles on Neutral lipid storage disease Articles on Neutral lipid storage disease in N Eng J Med, Lancet, BMJ Media ... [76%] 2024-01-11 [Genodermatoses] [Enzyme defects]...
7. Neutral lipid storage disease: Neutral lipid storage disease (also known as Chanarin–Dorfman syndrome) is a congenital autosomal recessive disorder characterized by accumulation of triglycerides in the cytoplasm of leukocytes, (Jordan’s Anomaly) muscle, liver, fibroblasts, and other tissues. It commonly occurs as one ... [76%] 2024-01-12 [Genodermatoses] [Enzyme defects]...
8. Neutral lipid storage disease: Neutral lipid storage disease (also known as Chanarin–Dorfman syndrome) is a congenital autosomal recessive disorder characterized by accumulation of triglycerides in the cytoplasm of leukocytes, (Jordan’s Anomaly) muscle, liver, fibroblasts, and other tissues. It commonly occurs as one ... (Medicine) [76%] 2024-01-12 [Genodermatoses] [Rare diseases]...
9. Cholesteryl ester storage disease: Articles Most recent articles on Cholesteryl ester storage disease Most cited articles on Cholesteryl ester storage disease Review articles on Cholesteryl ester storage disease Articles on Cholesteryl ester storage disease in N Eng J Med, Lancet, BMJ Media Powerpoint slides ... [76%] 2024-01-11 [Hepatology] [Rare diseases]...
10. Storge: Storge is the love of community and family. Often dutiful, sometimes apparently unfeeling, or undemonstrative, but very strong nevertheless, storge love refers to natural or instinctual affection for one's own community, a natural, unforced, familial love; a primary example ... [72%] 2023-02-26 [Language] [Greece]...
11. Storge: Storge (en griego στοργή, storgē), también llamado amor familiar, es el concepto griego utilizado para el afecto natural,​ como el amor de un padre hacia sus hijos y viceversa.​ Entendido el amor como emoción o actitud, Lee​ clasifica el amor en dos ... [72%] 2024-01-09
12. Storge: Storge (en griego στοργή, storgē), también llamado amor familiar, es el concepto griego utilizado para el afecto natural,​ como el amor de un padre hacia sus hijos y viceversa.​ Entendido el amor como emoción o actitud, Lee​ clasifica el amor en dos ... [72%] 2024-03-04
13. Glycogen storage disease type II: Glycogen storage disease type II, also called Pompe disease, is an autosomal recessive metabolic disorder which damages muscle and nerve cells throughout the body. It is caused by an accumulation of glycogen in the lysosome due to deficiency of the ... [67%] 2023-10-27 [Autosomal recessive disorders] [Hepatology]...
14. Glycogen storage disease type XI: Articles Most recent articles on Glycogen storage disease type XI Most cited articles on Glycogen storage disease type XI Review articles on Glycogen storage disease type XI Articles on Glycogen storage disease type XI in N Eng J Med, Lancet ... [67%] 2023-03-09 [Inborn errors of metabolism]
15. Glycogen storage disease type I: Glycogen storage disease type I (GSD I) is an inherited disease that results in the liver being unable to properly break down stored glycogen. This impairment disrupts the liver's ability to break down stored glycogen that is necessary to ... [67%] 2023-10-28 [Autosomal recessive disorders] [Hepatology]...
16. Glycogen storage disease type I: Glycogen storage disease type I (GSD I) is an inherited disease that results in the liver being unable to properly break down stored glycogen. This impairment disrupts the liver's ability to break down stored glycogen that is necessary to ... (Medicine) [67%] 2023-01-02 [Autosomal recessive disorders] [Hepatology]...
17. Glycogen storage disease type II: For the main page on glycogen storage disease, please click here For patient information click here Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Glycogen storage disease type II from other Diseases Epidemiology and Demographics Risk Factors Screening ... [67%] 2023-11-16 [Endocrinology] [Hepatology]...
18. Glycogen storage disease type VI: Glycogen storage disease type VI (GSD VI) is a type of glycogen storage disease caused by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system. It is also known as "Hers' disease", after Henri ... [67%] 2023-11-02 [Inborn errors of carbohydrate metabolism] [Rare diseases]...
19. Glycogen storage disease type V: Glycogen storage disease type V (GSD5, GSD-V), also known as McArdle's disease, is a metabolic disorder, one of the metabolic myopathies, more specifically a muscle glycogen storage disease, caused by a deficiency of myophosphorylase. Its incidence is reported ... (Human disease caused by deficiency of a muscle enzyme) [67%] 2023-11-12 [Autosomal recessive disorders] [Inborn errors of carbohydrate metabolism]...
20. Glycogen storage disease type I: Glycogen storage disease type I (GSD I) is an inherited disease that prevents the liver from properly breaking down stored glycogen, which is necessary in maintain adequate blood sugar levels. GSD I is divided into two main types, GSD Ia ... [67%] 2023-11-08 [Autosomal recessive disorders] [Hepatology]...