Results 191 to 200 of about 577,084 (345)
Overlapping Connective Tissue Disease-Polymyositis and Diffuse Systemic Scleroderma: A Case Report. [PDF]
Clin Med Insights Arthritis Musculoskelet DisordGreaves B, Poindexter L, Jensen H.
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Leukocyte‐connective tissue cell interaction. I. Stimulation of hyaluronate synthesis by live and dead leukocytes [PDF]
, 1969 Michael Yaron, C. William Castor
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NOTCH2NLC Repeat Expansions in Parkinsonian Disorders: Clinical and Neuroimaging Characteristics
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Neuronal intranuclear inclusion disease (NIID) is a neurodegenerative disorder caused by NOTCH2NLC GGC repeat expansions, with heterogeneous clinical manifestations, including parkinsonism. Recent studies have identified NOTCH2NLC repeat expansions in patients with Parkinson's disease (PD) and atypical parkinsonism (aPM), suggesting ...
Han‐Lin Chiang +7 more
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Dendritic cell heterogeneity and its role in connective tissue diseases. [PDF]
Inflamm RegenYamada S, Suwa Y, Fujio K.
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The chemistry of connective tissues. 5. The elastase activity of proteolytic enzymes [PDF]
, 1960 J. Thomas, S. M. Partridge
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Central Dysmyelination in SSADH‐Deficient Humans and Mice
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives Succinic semialdehyde dehydrogenase deficiency (SSADHD) is an inherited metabolic disorder characterized by an accumulation of γ‐aminobutyric (GABA). In addition to its synaptic role as an inhibitory neurotransmitter, GABA also plays an important role in myelination.
Itay Tokatly Latzer +11 more
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FLNA Mutations in Multisystem Disease: A Diagnostic Key for Unexplained Valvular and Connective Tissue Disorder. [PDF]
JACC Case RepHoffman ME +4 more
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