Results 91 to 100 of about 1,553 (193)
A case report of lipoid proteinosis with brain and laryngeal presentation [PDF]
Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis. Genetic mutation leads to deposition of abnormal amounts of hyaline like material in the skin and viscera, which is the cause of clinical manifestations.
Hemmati, S. +4 more
core
Amygdalae Enlargement and Activation are Associated with Social Network Complexity in Individuals with Human Immunodeficiency Virus (HIV) [PDF]
Brain volumetric studies reveal that human immunodeficiency virus (HIV) infection is associated with significant changes in several neural regions, including enlargements in the amygdalae, which are small subcortical structures located deep within the ...
Jasper, Christina
core +1 more source
Proceedings from the 2\u3csup\u3end\u3c/sup\u3eNext Gen Therapies for Systemic Juvenile Idiopathic Arthritis and Macrophage Activation Syndrome symposium held on October 3-4, 2019 [PDF]
© 2020 The Author(s). For reasons poorly understood, and despite the availability of biological medications blocking IL-1 and IL-6 that have markedly improved overall disease control, children with Systemic Juvenile Idiopathic Arthritis (SJIA) are now ...
+20 additional authors +10 more
core +1 more source
Lipoid proteinosis in a six-year-old child
Lipoid proteinosis (LiP) (OMIM 247100) is a rare autosomal recessive disease caused by loss of function mutations in the extracellular matrix protein 1 gene, ECM1, on chromosome 1q21.
Surajit Nayak, Basanti Acharjya
doaj +1 more source
Preferential attention to animals and people is independent of the amygdala [PDF]
The amygdala is thought to play a critical role in detecting salient stimuli. Several studies have taken ecological approaches to investigating such saliency, and argue for domain-specific effects for processing certain natural stimulus categories, in ...
Adolphs, Ralph +4 more
core +2 more sources
Lipoid Proteinosis of the Pharynx and Larynx: A Case Report
Lipoid proteinosis (LP) is a rare inherited multisystem disease. Classical clinical features include beaded eyelid papules, laryngeal infiltration, and neurological symptoms.
Zhuojun Li BS +7 more
doaj +1 more source
A 20-year old male presented with hoarseness of voice since birth, beaded papular lesions on both eyelids, multiple hypopigmented atrophic scars on trunk and extremities and yellowish infiltrated plaques on tongue, palate and buccal mucosae. Patient was diagnosed clinically as a case of lipoid proteinosis. It was confirmed by mucosal biopsy.
M K, Shah +3 more
openaire +1 more source

