Results 171 to 180 of about 30,524 (205)

A recurrent ACAA2 variant causes a dominant syndrome of lipodystrophy, lipomatosis, infantile steatohepatitis, and hypoglycemia. [PDF]

J Clin Invest
Simha V, LoPiccolo MK, Platt A, Brown RJ, Johnson X, Carere DA, Donnelly C, Snyder MT, Xing C, Mathews TP, Gopal P, Ward SC, Tomchick DR, Agarwal AK, DeBerardinis RJ, Garg A.   +15 more
europepmc   +1 more source

Correction to: "The Impact of Neuregulin 4 on Metabolic Dysregulation in Lipodystrophy".

Endocrinology
europepmc   +1 more source

Health-related Quality of Life, Social, and Psychological Well-Being of 109 Adult Patients With Genetic Lipodystrophy.

J Clin Endocrinol Metab
Mosbah H, Vatier C, Andriss B, Belalem I, Delemer B, Janmaat S, Bouhnik AD, Le Collen L, Maiter D, Nobécourt E, Vantyghem MC, Vigouroux C, Dumas A.   +12 more
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Centrifugal lipodystrophy

British Journal of Dermatology, 1984
We describe a case of centrifugal lipodystrophy occurring in a young English girl, and compare the clinical and histopathological features with previous reports from Japan.
C B, Zachary, R S, Wells
openaire   +2 more sources

Lipodystrophies

The American Journal of Medicine, 2000
The lipodystrophies are rare disorders characterized by selective but variable loss of adipose tissue. Metabolic complications, such as insulin resistance, diabetes mellitus, hypertriglyceridemia, and fatty liver, increase in severity with the extent of fat loss. The lipodystrophies can be classified into two major types: familial and acquired.
openaire   +2 more sources