Sort   by:  
 Page size 
UnknownARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
Not available
S-EPMC2441586 | biostudies-literature
UnknownGlut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group.
Not available
S-EPMC7469861 | biostudies-literature
UnknownGenome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis.
Not available
S-EPMC4169706 | biostudies-literature
UnknownUnresectable Intermediate-Size (3-5 cm) Colorectal Liver Metastases: Stereotactic Ablative Body Radiotherapy Versus Microwave Ablation (COLLISION-XL): Protocol of a Phase II/III Multicentre Randomized Controlled Trial.
Not available
S-EPMC10382334 | biostudies-literature
UnknownDisruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.
Not available
S-EPMC6794285 | biostudies-literature
UnknownDe Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Not available
S-EPMC6216110 | biostudies-literature
UnknownGenome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.
Not available
S-EPMC4388784 | biostudies-literature
UnknownA syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Not available
S-EPMC10806447 | biostudies-literature
UnknownAnalysis of shared heritability in common disorders of the brain.
Not available
S-EPMC6097237 | biostudies-literature
UnknownSpectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.
Not available
S-EPMC6452443 | biostudies-literature
Sort   by:  
 Page size