Assessment of IL‐1β, IL‐6, TNF‐α, IL‐8, and CCL 5 levels in newly diagnosed Saudi patients with rheumatoid arthritis
W Alturaiki, A Alhamad, M Alturaiqy… - International Journal …, 2022 - Wiley Online Library
Background Rheumatoid arthritis (RA) is a chronic systemic inflammatory disorder which
mainly affects small joints, occurs most commonly in middle‐aged adults, and can be fatal in …
mainly affects small joints, occurs most commonly in middle‐aged adults, and can be fatal in …
[HTML][HTML] Non-cardiac Manifestations in Adult Patients With Mucopolysaccharidosis
KM Stepien, A Bentley, C Chen… - Frontiers in …, 2022 - frontiersin.org
Mucopolysaccharidoses (MPS) are a heterogeneous group of disorders that results in the
absence or deficiency of lysosomal enzymes, leading to an inappropriate storage of …
absence or deficiency of lysosomal enzymes, leading to an inappropriate storage of …
[HTML][HTML] Dental considerations for the treatment of patients with Morquio syndrome
A Vinod, SN Raj, A Anand, AD Shirly - International Journal of …, 2022 - ncbi.nlm.nih.gov
Aim Morquio syndrome, also called Mucopolysaccharidosis IV (MPS IV), is a rare autosomal
recessive metabolic lysosomal disorder that results in the deposition of glycosaminoglycans …
recessive metabolic lysosomal disorder that results in the deposition of glycosaminoglycans …
[HTML][HTML] RNA analysis of the GALNS transcript reveals novel pathogenic mechanisms associated with Morquio syndrome A
YB Sohn, C Rogers, J Stallworth, JAC Coleman… - Molecular genetics and …, 2022 - Elsevier
Abstract Morquio syndrome A (Mucopolysaccharidosis IVA, MPS IVA) is an autosomal
recessive lysosomal storage disorder caused by deficiency of N-acetyl-galactosamine-6 …
recessive lysosomal storage disorder caused by deficiency of N-acetyl-galactosamine-6 …
Glycosaminoglycans and Oligosaccharides Disorders: Glycosaminoglycans Synthesis Defects, Mucopolysaccharidoses, Oligosaccharidoses and Sialic Acid …
S Jones, FA Wijburg - Inborn Metabolic Diseases: Diagnosis and …, 2022 - Springer
Abstract Glycosaminoglycans,(GAGs, mucopolysaccharides) are essential constituents of
connective tissue, including cartilage and vessel walls. They are composed of long sugar …
connective tissue, including cartilage and vessel walls. They are composed of long sugar …
[HTML][HTML] Клиническая характеристика пациента с мукополисахаридозом, тип IVА (синдромом Моркио)
НД Вашакмадзе, НВ Журкова… - Вопросы …, 2022 - cyberleninka.ru
Мукополисахаридоз (МПС), тип IVА (синдром Моркио)-наследственная лизосомная
болезнь накопления, вызванная дефицитом N-ацетилглюкозамин-6-сульфатной …
болезнь накопления, вызванная дефицитом N-ацетилглюкозамин-6-сульфатной …
[HTML][HTML] Мукополисахаридоз IVА типа у детей: клинические случаи
АВ Бурлуцкая, НВ Савельева… - Кубанский научный …, 2022 - cyberleninka.ru
Введение. Мукополисахаридоз IVА типа (синдром Моркио)-это генетическое
заболевание, относящееся к редким лизосомным болезням накопления. Из-за …
заболевание, относящееся к редким лизосомным болезням накопления. Из-за …
Mucopolysaccharidosis type IVA in children: Clinical cases
AV Burlutskaya, GV Naumenko - Kuban …, 2022 - publications.openuniversitystm.com
Background. Mucopolysaccharidosis type IVA (Morquio syndrome) is a rare genetic
lysosomal storage disease. Due to rarity, the syndrome is typically diagnosed at a later stage …
lysosomal storage disease. Due to rarity, the syndrome is typically diagnosed at a later stage …