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2024
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Deep intronic deletion in intron 3 of PLP1 is associated with a severe phenotype of Pelizaeus-Merzbacher disease.
Not available
S-EPMC8016919
|
biostudies-literature
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Age- and height-adjusted total kidney volume growth rate in autosomal dominant polycystic kidney diseases.
Not available
S-EPMC6344392
|
biostudies-literature
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Phase 1b/2 study of the liposomal formulation of eribulin (E7389-LF) in combination with nivolumab: Results from the phase 2 esophageal cancer cohort.
Not available
S-EPMC11523933
|
biostudies-literature
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Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome.
Not available
S-EPMC2227933
|
biostudies-literature
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Phase II Study of the Liposomal Formulation of Eribulin (E7389-LF) in Combination with Nivolumab: Results from the Gastric Cancer Cohort.
Not available
S-EPMC10982638
|
biostudies-literature
Cite
Phase II Study of the Liposomal Formulation of Eribulin (E7389-LF) in Combination with Nivolumab: Results from the Small Cell Lung Cancer Cohort.
Not available
S-EPMC10823908
|
biostudies-literature
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Urate-lowering therapy for CKD patients with asymptomatic hyperuricemia without proteinuria elucidated by attribute-based research in the FEATHER Study.
Not available
S-EPMC8904814
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biostudies-literature
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Cancer diagnosis and prognosis after initiation of hemodialysis: multicenter Japan CANcer and DialYsis (J-CANDY) study.
Not available
S-EPMC11826057
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biostudies-literature
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Impact of Blood Pressure Visit-to-Visit Variability on Adverse Events in Patients With Nonvalvular Atrial Fibrillation: Subanalysis of the J-RHYTHM Registry.
Not available
S-EPMC7955501
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biostudies-literature
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