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UnknownLong-term survival advantage and prognostic factors associated with intraperitoneal chemotherapy treatment in advanced ovarian cancer: a gynecologic oncology group study.
Not available
S-EPMC4404424 | biostudies-literature
UnknownNegative drift of sedation depth in critically ill patients receiving constant minimum alveolar concentration of isoflurane, sevoflurane, or desflurane: a randomized controlled trial.
Not available
S-EPMC8042630 | biostudies-literature
UnknownInfluence of Absorption, Distribution, Metabolism, and Excretion Genomic Variants on Tacrolimus/Sirolimus Blood Levels and Graft-versus-Host Disease after Allogeneic Hematopoietic Cell Transplantation.
Not available
S-EPMC4716887 | biostudies-literature
UnknownRandomized, placebo-controlled trial of propranolol added to topiramate in chronic migraine.
Not available
S-EPMC3310312 | biostudies-literature
UnknownImpact of elexacaftor/tezacaftor/ivacaftor on lung function, nutritional status, pulmonary exacerbation frequency and sweat chloride in people with cystic fibrosis: real-world evidence from the German CF Registry.
Not available
S-EPMC10405057 | biostudies-literature
UnknownNeuropeptide Y1 receptor antagonism protects β-cells and improves glycemic control in type 2 diabetes.
Not available
S-EPMC8733231 | biostudies-literature
UnknownSerotonin type 3 receptor subunit gene polymorphisms associated with psychosomatic symptoms in irritable bowel syndrome: A multicenter retrospective study.
Not available
S-EPMC9185212 | biostudies-literature
UnknownA POETIC Phase II study of continuous oral everolimus in recurrent, radiographically progressive pediatric low-grade glioma.
Not available
S-EPMC9161236 | biostudies-literature
UnknownATHENA (GOG-3020/ENGOT-ov45): a randomized, phase III trial to evaluate rucaparib as monotherapy (ATHENA-MONO) and rucaparib in combination with nivolumab (ATHENA-COMBO) as maintenance treatment following frontline platinum-based chemotherapy in ovarian cancer.
Not available
S-EPMC8666815 | biostudies-literature
UnknownBiallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
Not available
S-EPMC6117612 | biostudies-literature
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