Results 161 to 170 of about 1,588,563 (356)
THE CHEMISTRY OF THE LIPIDS OF TUBERCLE BACILLI
, 1936 M. A. Spielman, R. J. Anderson
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Moyamoya Disease and the Risk of Parkinson's Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives Moyamoya disease (MMD) is a rare cerebrovascular disorder characterized by the progressive narrowing of arteries at the base of the brain, forming abnormal collateral vascular networks. While vascular parkinsonism is noted in MMD, its link to Parkinson's disease (PD) has not been explored.
Dallah Yoo +9 more
wiley +1 more source
Change in Cognition Following Ischaemic Stroke
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Cognitive decline can occur following ischaemic stroke. How cognition changes over time and associations with cognitive change are poorly understood. This study aimed to explore these issues over 2 years following ischaemic stroke.
Wenci Yan +8 more
wiley +1 more source
Study of methods for chemical synthesis of edible fatty acids and lipids - Final summary [PDF]
Chemical feasibility and nutrional value in synthesis of edible fatty acids and lipids from metabolic wastes for space flight ...
Frankenfeld, J. W.
core +2 more sources
The Diverse Neuromuscular Spectrum of VPS13A Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective VPS13A disease (chorea‐acanthocytosis) is a rare neurodegenerative disorder caused by biallelic variants in VPS13A, typically presenting with hyperkinetic movement disorders, while neuromuscular signs are often mild. The aim of the project was to investigate the frequency and severity of neuromuscular impairment in VPS13A disease ...
Anne Buchberger +16 more
wiley +1 more source
THE STUDY OF SERUM PROTEINS AND LIPIDS WITH THE AID OF THE QUANTITY ULTRACENTRIFUGE. I. PROCEDURE AND PRINCIPAL FEATURES OF THE CENTRIFUGATE OF UNTREATED NORMAL SERUM AS DETERMINED BY QUANTITATIVE ANALYSIS OF SAMPLES FROM TEN LEVELS 12 [PDF]
, 1951 Roy H. Turner +5 more
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
wiley +1 more source
THE RESPONSE OF LIPID METABOLISM TO ALTERATIONS IN NUTRITIONAL STATE
, 1942 C. Entenman, I.L. Chaikoff
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SPECIES VARIATIONS IN THE RESPONSE OF SERUM PROTEINS, LIPIDS AND LIPOPROTEINS TO THE CORTISONES*† [PDF]
, 1956 Elaine T. Bossak +2 more
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