Overview
Sinead Murphy practices practicing medicine in London, United Kingdom.
Ms. Murphy is highly rated in 11 conditions, according to our data. Her clinical expertise encompasses Hereditary Sensory Neuropathy Type 1 (HSN1), Charcot-Marie-Tooth Disease, Anhidrosis, and Hereditary Ataxia.
She is actively involved in clinical research, co-authoring 93 peer reviewed articles.
Gender
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. 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 Sinead M. Murphy
Is Sinead M. Murphy a top-rated expert for Hereditary Sensory Neuropathy Type 1 (HSN1)?
MediFind is an objective health platform that identifies experts based on real-world data. Sinead M. Murphy is classified as an Advanced expert for Hereditary Sensory Neuropathy Type 1 (HSN1), 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 Sinead M. Murphy participate in research or clinical trials?
Yes. Sinead M. Murphy has published 93 articles and abstracts on conditions like Hereditary Sensory Neuropathy Type 1 (HSN1). You can view a list of Sinead M. Murphy'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
- Acute Cerebellar AtaxiaMs. Murphy isAdvanced. Learn about Acute Cerebellar Ataxia.
- AnhidrosisMs. Murphy isAdvanced. Learn about Anhidrosis.
- Charcot-Marie-Tooth DiseaseMs. Murphy isAdvanced. Learn about Charcot-Marie-Tooth Disease.
- Drug Induced DyskinesiaMs. Murphy isAdvanced. Learn about Drug Induced Dyskinesia.
- Friedreich AtaxiaMs. Murphy isAdvanced. Learn about Friedreich Ataxia.
- Hajdu-Cheney SyndromeMs. Murphy isAdvanced. Learn about Hajdu-Cheney Syndrome.
- Hereditary AtaxiaMs. Murphy isAdvanced. Learn about Hereditary Ataxia.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- Primary Lateral SclerosisMs. Murphy isAdvanced. Learn about Primary Lateral Sclerosis.
- Spinocerebellar AtaxiaMs. Murphy isAdvanced. Learn about Spinocerebellar Ataxia.
- Experienced
- ApraxiaMs. Murphy isExperienced. Learn about Apraxia.
- Arachnoid CystsMs. Murphy isExperienced. Learn about Arachnoid Cysts.
- Autonomic NeuropathyMs. Murphy isExperienced. Learn about Autonomic Neuropathy.
- Blue Cone MonochromatismMs. Murphy isExperienced. Learn about Blue Cone Monochromatism.
- Brachial PlexopathyMs. Murphy isExperienced. Learn about Brachial Plexopathy.
- Brown SyndromeMs. Murphy isExperienced. Learn about Brown Syndrome.
- Carotid Artery DiseaseMs. Murphy isExperienced. Learn about Carotid Artery Disease.
- Color BlindnessMs. Murphy isExperienced. Learn about Color Blindness.
- Congenital Myasthenic SyndromeMs. Murphy isExperienced. Learn about Congenital Myasthenic Syndrome.
- Corpus Callosum AgenesisMs. Murphy isExperienced. Learn about Corpus Callosum Agenesis.
- Cytochrome C Oxidase DeficiencyMs. Murphy isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- DysarthriaMs. Murphy isExperienced. Learn about Dysarthria.
- EpilepsyMs. Murphy isExperienced. Learn about Epilepsy.
- GangliosidosisMs. Murphy isExperienced. Learn about Gangliosidosis.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- HeadacheMs. Murphy isExperienced. Learn about Headache.
- Hearing LossMs. Murphy isExperienced. Learn about Hearing Loss.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- MigraineMs. Murphy isExperienced. Learn about Migraine.
- Mitochondrial Trifunctional Protein Deficiency
- Oculomotor Apraxia Cogan TypeMs. Murphy isExperienced. Learn about Oculomotor Apraxia Cogan Type.
- Olivopontocerebellar AtrophyMs. Murphy isExperienced. Learn about Olivopontocerebellar Atrophy.
- Pigmented Purpuric DermatosisMs. Murphy isExperienced. Learn about Pigmented Purpuric Dermatosis.
- Primary AmyloidosisMs. Murphy isExperienced. Learn about Primary Amyloidosis.
- Progressive External OphthalmoplegiaMs. Murphy isExperienced. Learn about Progressive External Ophthalmoplegia.
- Protein DeficiencyMs. Murphy isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisMs. Murphy isExperienced. Learn about Rhabdomyolysis.
- Sensorimotor PolyneuropathyMs. Murphy isExperienced. Learn about Sensorimotor Polyneuropathy.
- Spastic Paraplegia Type 2Ms. Murphy isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 5AMs. Murphy isExperienced. Learn about Spastic Paraplegia Type 5A.
- Spastic Paraplegia Type 7Ms. Murphy isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityMs. Murphy isExperienced. Learn about Spasticity.
- Spinal Muscular Atrophy (SMA)Ms. Murphy isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Spinal Muscular Atrophy Type 2Ms. Murphy isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Ms. Murphy isExperienced. Learn about Spinal Muscular Atrophy Type 3.
- Spinocerebellar Ataxia Type 17Ms. Murphy isExperienced. Learn about Spinocerebellar Ataxia Type 17.
- Spinocerebellar Ataxia Type 4Ms. Murphy isExperienced. Learn about Spinocerebellar Ataxia Type 4.
- Spinocerebellar Ataxia Type 5Ms. Murphy isExperienced. Learn about Spinocerebellar Ataxia Type 5.
- StrokeMs. Murphy isExperienced. Learn about Stroke.
- Subacute Combined DegenerationMs. Murphy isExperienced. Learn about Subacute Combined Degeneration.
- Tay-Sachs DiseaseMs. Murphy isExperienced. Learn about Tay-Sachs Disease.
- Transient Ischemic Attack (TIA)Ms. Murphy isExperienced. Learn about Transient Ischemic Attack (TIA).
- Vitamin B12 Deficiency AnemiaMs. Murphy isExperienced. Learn about Vitamin B12 Deficiency Anemia.
- Waardenburg SyndromeMs. Murphy isExperienced. Learn about Waardenburg Syndrome.
- Waardenburg Syndrome Type 1Ms. Murphy isExperienced. Learn about Waardenburg Syndrome Type 1.