Overview
Rachelle Doody is a Neurologist in Houston, Texas. Dr. Doody is rated as an Elite provider by MediFind in the treatment of Dementia. Her top areas of expertise are Alzheimer's Disease, Dementia, Pseudobulbar Affect, and Memory Loss.
Her clinical research consists of co-authoring 112 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 99 articles in the study of Dementia.
Insurance
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Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
UT Physicians
Paul Schulz is a Psychiatrist and a Neurologist in Houston, Texas. Dr. Schulz is rated as a Distinguished provider by MediFind in the treatment of Dementia. His top areas of expertise are Dementia, Alzheimer's Disease, Neuronal Intranuclear Inclusion Disease (NIID), Normal Pressure Hydrocephalus, and Deep Brain Stimulation. Dr. Schulz is currently accepting new patients.
Baylor College Of Medicine
Recent advances have made the discovery of genetic susceptibility loci for complex human phenotypes a reality, including nervous system disorders. The critical next step will be to definitively identify the responsible genes and understand their functions in both health and disease. Our research integrates genetic investigation in human subjects and model organisms, with the goal of understanding brain function and aging, and improving the treatment of neurologic disease. We focus on Alzheimer's disease and Parkinson's disease, two incurable neurodegenerative disorders and experimental paradigms for the age-dependent failure of brain cognitive and motor control in humans. Human Genetics: The clinical manifestation of neurodegenerative disease is the culmination of a multi-tiered pathogenic cascade that evolves over decades; understanding how genetic variants impact this causal chain is essential. Although 2 percent of the population over age 65 are clinically diagnosed with Parkinson's disease, the defining pathology of disease (alpha-synuclein Lewy bodies) is discovered in 20 percent of brains from population-based autopsy studies. We are, therefore, investigating the impact of genomic variation on directly measured Lewy pathology, neuronal loss in the midbrain substantia nigra, and progressive motor impairment, leveraging human subject cohorts with detailed clinical and pathological data. In complementary investigations, we are deploying biosensor devices to improve detection of Parkinson's-related motor impairment, including the development of quantitative biometric phenotypes for genetic analyses of disease subtypes. We are also performing whole exome sequencing of individuals with familial Parkinson's disease and related disorders, and exploring potential links between inherited pediatric lysosomal and late-onset, adult neurodegenerative diseases. Drosophila Genetics: Despite the promise of current human genetic methods, such as genome-wide association studies and next generation sequencing, they often fail to definitively identify disease susceptibility genes and variants. We are, therefore, taking advantage of the rapid and powerful genetics available in the fruit fly Drosophila melanogaster in order to accelerate the validation of responsible genes and an understanding of their functions in the nervous system, including for disease pathogenesis. Expression of human amyloid-beta, Tau, or alpha-synuclein proteins in the fly nervous system recapitulates many core features of Alzheimer's disease and Parkinson's disease pathogenesis. We are testing candidate human susceptibility genes for functional genetic interactions in these fly models of neurodegeneration. Implicated molecular pathways are probed in greater depth, using both Drosophila and human genetic approaches. Current areas of interest include endolysosomal sorting, RNA metabolism/splicing, neuronal cell adhesion, and synaptic mechanisms of neurodegeneration. Dr. Shulman is rated as an Advanced provider by MediFind in the treatment of Dementia. His top areas of expertise are Parkinson's Disease, Movement Disorders, Alzheimer's Disease, and Dementia.
Hillcroft Medical Clinic Assoc
Hazem Machkhas is a Neurologist in Sugar Land, Texas. Dr. Machkhas is rated as an Advanced provider by MediFind in the treatment of Dementia. His top areas of expertise are Generalized Tonic-Clonic Seizure, Dementia, Stroke, and Seizures. Dr. Machkhas is currently accepting new patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Elite
- Alzheimer's DiseaseDr. Doody isElite. Learn about Alzheimer's Disease.
- DementiaDr. Doody isElite. Learn about Dementia.
- Distinguished
- Memory LossDr. Doody isDistinguished. Learn about Memory Loss.
- Pseudobulbar AffectDr. Doody isDistinguished. Learn about Pseudobulbar Affect.
- Advanced
- Developmental Dysphasia Familial
- Kluver Bucy SyndromeDr. Doody isAdvanced. Learn about Kluver Bucy Syndrome.
- Movement DisordersDr. Doody isAdvanced. Learn about Movement Disorders.
- Parkinson's DiseaseDr. Doody isAdvanced. Learn about Parkinson's Disease.
- Experienced
- Brown SyndromeDr. Doody isExperienced. Learn about Brown Syndrome.
- CACH SyndromeDr. Doody isExperienced. Learn about CACH Syndrome.
- Drug Induced DyskinesiaDr. Doody isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaDr. Doody isExperienced. Learn about Dysarthria.
- Frontotemporal DementiaDr. Doody isExperienced. Learn about Frontotemporal Dementia.
- Huntington DiseaseDr. Doody isExperienced. Learn about Huntington Disease.
