Neurobiology. Most of the senses begin to make some sense

Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2017

A role for TENM1 mutations in congenital general anosmia.

Clinical genetics·2016

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Clinical genetics·2015

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2009

Further evidence for association of the RGS2 gene with antipsychotic-induced parkinsonism: protective role of a functional polymorphism in the 3'-untranslated region.

The pharmacogenomics journal·2008

Search for hand osteoarthritis susceptibility locus on chromosome 6p12.3-p12.1.

Human biology·2007

Salivary Excretion Of Torque Teno Virus And Sars-Cov-2 In Children Who Underwent Kidney Transplantation.

Revista brasileira de enfermagem·2026

Sensing in Sacral Neuromodulation: Objective, Individualized Stimulation Response Thresholds Directly From the Lead.

Neurourology and urodynamics·2026

National Medicare trends in navigation-assisted spine surgery: A temporal and geographic analysis.

Journal of craniovertebral junction & spine·2026

Pulsed Radiofrequency of the Stellate Ganglion for Tinnitus: A Two-Case Series Suggesting a Novel Approach.

Case reports in anesthesiology·2026

Acupuncture for chronic tinnitus: study protocol for a clinical trial with auditory brainstem response outcomes.

Frontiers in neurology·2026

Spinal Cord Injury Severity Influences Microstructural Alterations in the Supraspinal Somatosensory Pathways.

Academic radiology·2026

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Neurobiology. Most of the senses begin to make some sense

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Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.

A role for TENM1 mutations in congenital general anosmia.

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

Further evidence for association of the RGS2 gene with antipsychotic-induced parkinsonism: protective role of a functional polymorphism in the 3'-untranslated region.

Search for hand osteoarthritis susceptibility locus on chromosome 6p12.3-p12.1.

Salivary Excretion Of Torque Teno Virus And Sars-Cov-2 In Children Who Underwent Kidney Transplantation.

Sensing in Sacral Neuromodulation: Objective, Individualized Stimulation Response Thresholds Directly From the Lead.

National Medicare trends in navigation-assisted spine surgery: A temporal and geographic analysis.

Pulsed Radiofrequency of the Stellate Ganglion for Tinnitus: A Two-Case Series Suggesting a Novel Approach.

Acupuncture for chronic tinnitus: study protocol for a clinical trial with auditory brainstem response outcomes.

Spinal Cord Injury Severity Influences Microstructural Alterations in the Supraspinal Somatosensory Pathways.

Related Experiment Videos

Neurobiology. Most of the senses begin to make some sense

Related Concept Videos

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