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2023
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Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities.
Not available
S-EPMC6906308
|
biostudies-literature
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Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures.
Not available
S-EPMC7118584
|
biostudies-literature
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Estimated GFR Variability and Risk of Cardiovascular Events and Mortality in SPRINT (Systolic Blood Pressure Intervention Trial).
Not available
S-EPMC8200370
|
biostudies-literature
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De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures.
Not available
S-EPMC6821231
|
biostudies-literature
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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.
Not available
S-EPMC8045518
|
biostudies-literature
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The Phosphate Binder Ferric Citrate and Mineral Metabolism and Inflammatory Markers in Maintenance Dialysis Patients: Results From Prespecified Analyses of a Randomized Clinical Trial.
Not available
S-EPMC4868355
|
biostudies-literature
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Ferric citrate controls phosphorus and delivers iron in patients on dialysis.
Not available
S-EPMC4310662
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biostudies-literature
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Encorafenib, Cetuximab, and mFOLFOX6 in <i>BRAF</i>-Mutated Colorectal Cancer.
Not available
S-EPMC12197837
|
biostudies-literature
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Final Report of a Trial of Intensive versus Standard Blood-Pressure Control.
Not available
S-EPMC9907774
|
biostudies-literature
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Chronic kidney disease, cerebral blood flow, and white matter volume in hypertensive adults.
Not available
S-EPMC4818564
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biostudies-literature
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