Genetic heterogeneity in hereditary sensory and autonomic neuropathies: The need for improved ascertainment

Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set.

Nature communications·2015

SLC6A4 variation and citalopram response.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2008

Genetic diversity and function in the human cytosolic sulfotransferases.

The pharmacogenomics journal·2006

Estimation and tests of haplotype-environment interaction when linkage phase is ambiguous.

Human heredity·2003

Validity of family history data on PD: evidence for a family information bias.

Neurology·2003

Progression of familial and non-familial dilated cardiomyopathy: long term follow up.

Heart (British Cardiac Society)·2003

Using High-Field Magnetic Resonance Spectroscopy to Measure Muscle Glycogen in Patients With McArdle Disease.

Muscle & nerve·2026

One-Year Clinical Course of Patients With Amyotrophic Lateral Sclerosis Admitted to a Home Palliative Care Program: An Extension Study.

Muscle & nerve·2026

Systematic Review of Patient- and Observer-Reported Outcomes of Fatigue in Pediatric Neuromuscular Disorders.

Muscle & nerve·2026

Muscle Imaging Patterns and Variant-Specific Progression in DNM2-Related Centronuclear Myopathy.

Muscle & nerve·2026

Quantitative Ultrasound Analysis of Muscle Reinnervation Following Anterior Interosseous Nerve-To-Ulnar Motor Branch Supercharged End-To-Side Transfer Surgery: A Preliminary Study.

Muscle & nerve·2026

Predictors for Successful Non-Invasive Ventilation in Patients With Neuralgic Amyotrophy and Phrenic Nerve Involvement.

Muscle & nerve·2026

Related Experiment Videos

Genetic heterogeneity in hereditary sensory and autonomic neuropathies: The need for improved ascertainment

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Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set.

SLC6A4 variation and citalopram response.

Genetic diversity and function in the human cytosolic sulfotransferases.

Estimation and tests of haplotype-environment interaction when linkage phase is ambiguous.

Validity of family history data on PD: evidence for a family information bias.

Progression of familial and non-familial dilated cardiomyopathy: long term follow up.

Using High-Field Magnetic Resonance Spectroscopy to Measure Muscle Glycogen in Patients With McArdle Disease.

One-Year Clinical Course of Patients With Amyotrophic Lateral Sclerosis Admitted to a Home Palliative Care Program: An Extension Study.

Systematic Review of Patient- and Observer-Reported Outcomes of Fatigue in Pediatric Neuromuscular Disorders.

Muscle Imaging Patterns and Variant-Specific Progression in DNM2-Related Centronuclear Myopathy.

Quantitative Ultrasound Analysis of Muscle Reinnervation Following Anterior Interosseous Nerve-To-Ulnar Motor Branch Supercharged End-To-Side Transfer Surgery: A Preliminary Study.

Predictors for Successful Non-Invasive Ventilation in Patients With Neuralgic Amyotrophy and Phrenic Nerve Involvement.

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Genetic heterogeneity in hereditary sensory and autonomic neuropathies: The need for improved ascertainment

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