Overview
Michael Geraghty practices practicing medicine in Ottawa, Canada.
Mr. Geraghty is highly rated in 6 conditions, according to our data. His clinical expertise encompasses Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Sialic Acid Storage Disease, Sialuria, and Spinocerebellar Ataxia Type 29.
He is actively involved in clinical research, co-authoring 66 peer reviewed articles.
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Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts 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.
Frequently Asked Questions about Michael T. Geraghty
Is Michael T. Geraghty a top-rated expert for Medium-Chain Acyl-CoA Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Michael T. Geraghty is classified as an Advanced expert for Medium-Chain Acyl-CoA Dehydrogenase Deficiency, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Michael T. Geraghty participate in research or clinical trials?
Yes. Michael T. Geraghty has published 65 articles and abstracts on conditions like Medium-Chain Acyl-CoA Dehydrogenase Deficiency. You can view a list of Michael T. Geraghty's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Advanced
- Glutaric Acidemia Type 2Mr. Geraghty isAdvanced. Learn about Glutaric Acidemia Type 2.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Ornithine Translocase DeficiencyMr. Geraghty isAdvanced. Learn about Ornithine Translocase Deficiency.
- Sialic Acid Storage DiseaseMr. Geraghty isAdvanced. Learn about Sialic Acid Storage Disease.
- SialuriaMr. Geraghty isAdvanced. Learn about Sialuria.
- Spinocerebellar Ataxia Type 29Mr. Geraghty isAdvanced. Learn about Spinocerebellar Ataxia Type 29.
- Experienced
- Absence SeizureMr. Geraghty isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeMr. Geraghty isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acute Cerebellar AtaxiaMr. Geraghty isExperienced. Learn about Acute Cerebellar Ataxia.
- Childhood VolvulusMr. Geraghty isExperienced. Learn about Childhood Volvulus.
- Ciliary Dyskinesia-BronchiectasisMr. Geraghty isExperienced. Learn about Ciliary Dyskinesia-Bronchiectasis.
- Cortical DysplasiaMr. Geraghty isExperienced. Learn about Cortical Dysplasia.
- DextrocardiaMr. Geraghty isExperienced. Learn about Dextrocardia.
- Dextrocardia with Situs InversusMr. Geraghty isExperienced. Learn about Dextrocardia with Situs Inversus.
- Drug Induced DyskinesiaMr. Geraghty isExperienced. Learn about Drug Induced Dyskinesia.
- Familial Benign Copper DeficiencyMr. Geraghty isExperienced. Learn about Familial Benign Copper Deficiency.
- Generalized Tonic-Clonic SeizureMr. Geraghty isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- HypotoniaMr. Geraghty isExperienced. Learn about Hypotonia.
- Infant Respiratory Distress SyndromeMr. Geraghty isExperienced. Learn about Infant Respiratory Distress Syndrome.
- Kartagener SyndromeMr. Geraghty isExperienced. Learn about Kartagener Syndrome.
- Lennox-Gastaut Syndrome (LGS)Mr. Geraghty isExperienced. Learn about Lennox-Gastaut Syndrome (LGS).
- MicrocephalyMr. Geraghty isExperienced. Learn about Microcephaly.
- Mitochondrial Complex V DeficiencyMr. Geraghty isExperienced. Learn about Mitochondrial Complex V Deficiency.
- Movement DisordersMr. Geraghty isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidoses (MPS)Mr. Geraghty isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Ornithine Transcarbamylase DeficiencyMr. Geraghty isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Phenylketonuria (PKU)Mr. Geraghty isExperienced. Learn about Phenylketonuria (PKU).
- Primary Carnitine DeficiencyMr. Geraghty isExperienced. Learn about Primary Carnitine Deficiency.
- SeizuresMr. Geraghty isExperienced. Learn about Seizures.
- Sideroblastic AnemiaMr. Geraghty isExperienced. Learn about Sideroblastic Anemia.
- Situs InversusMr. Geraghty isExperienced. Learn about Situs Inversus.
- Spastic Paraplegia Type 11Mr. Geraghty isExperienced. Learn about Spastic Paraplegia Type 11.
- Spastic Paraplegia Type 2Mr. Geraghty isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Mr. Geraghty isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityMr. Geraghty isExperienced. Learn about Spasticity.
- Urea Cycle Disorders (UCD)Mr. Geraghty isExperienced. Learn about Urea Cycle Disorders (UCD).