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AddTerveys ja Talous
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AddVeterinary clinics of North America. Equine practice
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AddVeterinary clinics of North America. Small animal practice
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Genetic risk for Alzheimer disease affects the brain throughout the lifespan.Neurology Genetics359 dayssaveRefWorksSFX Info
D-DEMO, a distinct phenotype caused by ATP1A3 mutations.Neurology Genetics359 dayssaveRefWorksSFX Info
Genetic risk scores and hallucinations in patients with Parkinson disease.Neurology Genetics359 dayssaveRefWorksSFX Info
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathy.Neurology Genetics359 dayssaveRefWorksSFX Info
Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease.Neurology Genetics359 dayssaveRefWorksSFX Info
LINS1-associated neurodevelopmental disorder: Family with novel mutation expands the phenotypic spectrum.Neurology Genetics359 dayssaveRefWorksSFX Info
Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1.Neurology Genetics359 dayssaveRefWorksSFX Info
Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy.Neurology Genetics359 dayssaveRefWorksSFX Info
Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan.Neurology Genetics359 dayssaveRefWorksSFX Info
Disease duration in autosomal dominant familial Alzheimer disease: A survival analysis.Neurology Genetics359 dayssaveRefWorksSFX Info
Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia.Neurology Genetics359 dayssaveRefWorksSFX Info
Integrative analysis identifies the association between CASZ1 methylation and ischemic stroke.Neurology Genetics359 dayssaveRefWorksSFX Info
Manifesting carriers of X-linked myotubular myopathy: Genetic modifiers modulating the phenotype.Neurology Genetics359 dayssaveRefWorksSFX Info
Identification of a novel mutation in ATP13A2 associated with a complicated form of hereditary spastic paraplegia.Neurology Genetics359 dayssaveRefWorksSFX Info
Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability.Neurology Genetics359 dayssaveRefWorksSFX Info
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations.Neurology Genetics359 dayssaveRefWorksSFX Info
Childhood-onset epileptic encephalopathy due to FGF12 exon 1-4 tandem duplication.Neurology Genetics359 dayssaveRefWorksSFX Info
Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation.Neurology Genetics359 dayssaveRefWorksSFX Info
KCNQ2 encephalopathy manifesting with Rett-like features: A follow-up into adulthood.Neurology Genetics359 dayssaveRefWorksSFX Info
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene.Neurology Genetics359 dayssaveRefWorksSFX Info
Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference?.Neurology Genetics359 dayssaveRefWorksSFX Info
Neuraxial dysraphism in EPAS1-associated syndrome due to improper mesenchymal transition.Neurology Genetics359 dayssaveRefWorksSFX Info
Genetic risk for Alzheimer disease affects the brain throughout the lifespan.Neurology Genetics361 dayssaveRefWorksSFX Info
D-DEMO, a distinct phenotype caused by ATP1A3 mutations.Neurology Genetics361 dayssaveRefWorksSFX Info
Genetic risk scores and hallucinations in patients with Parkinson disease.Neurology Genetics361 dayssaveRefWorksSFX Info
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathy.Neurology Genetics361 dayssaveRefWorksSFX Info
Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease.Neurology Genetics361 dayssaveRefWorksSFX Info
LINS1-associated neurodevelopmental disorder: Family with novel mutation expands the phenotypic spectrum.Neurology Genetics361 dayssaveRefWorksSFX Info
Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1.Neurology Genetics361 dayssaveRefWorksSFX Info
Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy.Neurology Genetics361 dayssaveRefWorksSFX Info
Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan.Neurology Genetics361 dayssaveRefWorksSFX Info
Disease duration in autosomal dominant familial Alzheimer disease: A survival analysis.Neurology Genetics361 dayssaveRefWorksSFX Info
Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia.Neurology Genetics361 dayssaveRefWorksSFX Info
Integrative analysis identifies the association between CASZ1 methylation and ischemic stroke.Neurology Genetics361 dayssaveRefWorksSFX Info
Manifesting carriers of X-linked myotubular myopathy: Genetic modifiers modulating the phenotype.Neurology Genetics361 dayssaveRefWorksSFX Info
Identification of a novel mutation in ATP13A2 associated with a complicated form of hereditary spastic paraplegia.Neurology Genetics361 dayssaveRefWorksSFX Info
Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability.Neurology Genetics361 dayssaveRefWorksSFX Info
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations.Neurology Genetics361 dayssaveRefWorksSFX Info
Childhood-onset epileptic encephalopathy due to FGF12 exon 1-4 tandem duplication.Neurology Genetics361 dayssaveRefWorksSFX Info
Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation.Neurology Genetics361 dayssaveRefWorksSFX Info
KCNQ2 encephalopathy manifesting with Rett-like features: A follow-up into adulthood.Neurology Genetics361 dayssaveRefWorksSFX Info
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene.Neurology Genetics361 dayssaveRefWorksSFX Info
Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference?.Neurology Genetics361 dayssaveRefWorksSFX Info
Neuraxial dysraphism in EPAS1-associated syndrome due to improper mesenchymal transition.Neurology Genetics361 dayssaveRefWorksSFX Info
What does a defect in N-glycosylation mean for neuronal migration and function?.Neurology Genetics413 dayssaveRefWorksSFX Info
Genetic background of ataxia in children younger than 5 years in Finland.Neurology Genetics413 dayssaveRefWorksSFX Info
Brainstem ischemic syndrome in juvenile NF2.Neurology Genetics413 dayssaveRefWorksSFX Info
Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene.Neurology Genetics413 dayssaveRefWorksSFX Info
Synonymous variants associated with Alzheimer disease in multiplex families.Neurology Genetics413 dayssaveRefWorksSFX Info
Expanded genetic insight and clinical experience of DNMT1-complex disorder.Neurology Genetics413 dayssaveRefWorksSFX Info
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