Microstructure and corrosion resistance of AZ91- Hydroxyapatite composites processed via deformation-driven metallurgy. [PDF]
Jamshidi K, Jamaati R, Jamshidi Aval H.
europepmc +1 more source
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
SGLT2 Inhibitors as a Therapeutic Option for Both Acute and Chronic Refractory Hypomagnesemia in Diabetic and Nondiabetic Patients: A Multicenter Case Series. [PDF]
Ayub F +7 more
europepmc +1 more source
The Availability of Magnesium from Organic Carriers in Artificial Substrates. [PDF]
Stuart Dunn, Suzanne S. Roberts
openalex +1 more source
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini +13 more
wiley +1 more source
Influence of Tempeh, Daidzein, Probiotics, and Their Combination on Magnesium Status and Hematological Ratios in a Postmenopausal Osteoporotic Animal Model. [PDF]
Harahap IA +5 more
europepmc +1 more source
Widersprüche und Irrtümer in der analytischen Chemie. III. Die Trennung des Zinks von Magnesium, Calcium, Aluminium durch Phosphatfällung. IV. Die Überführung von Alkalisulfaten in Chloride [PDF]
Friedrich L. Hahn +2 more
openalex +1 more source
Somsri Wiwanitkit, Viroj Wiwanitkit
openaire +3 more sources
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source

