Overview
Henna Tyynismaa practices practicing medicine in Helsinki, Finland.
Ms. Tyynismaa is highly rated in 8 conditions, according to our data. Her clinical expertise encompasses Glycogen Storage Disease Type 7, Charcot-Marie-Tooth Disease, Mitochondrial Complex V Deficiency, and Hereditary Sensory Neuropathy Type 1 (HSN1).
She is actively involved in clinical research, co-authoring 78 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 Henna Tyynismaa
Is Henna Tyynismaa a top-rated expert for Glycogen Storage Disease Type 7?
MediFind is an objective health platform that identifies experts based on real-world data. Henna Tyynismaa is classified as an Advanced expert for Glycogen Storage Disease Type 7, 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 Henna Tyynismaa participate in research or clinical trials?
Yes. Henna Tyynismaa has published 78 articles and abstracts on conditions like Glycogen Storage Disease Type 7. You can view a list of Henna Tyynismaa'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
- AnhidrosisMs. Tyynismaa isAdvanced. Learn about Anhidrosis.
- Charcot-Marie-Tooth DiseaseMs. Tyynismaa isAdvanced. Learn about Charcot-Marie-Tooth Disease.
- Glycogen Storage Disease Type 7Ms. Tyynismaa isAdvanced. Learn about Glycogen Storage Disease Type 7.
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- Mitochondrial Complex V DeficiencyMs. Tyynismaa isAdvanced. Learn about Mitochondrial Complex V Deficiency.
- PEHO SyndromeMs. Tyynismaa isAdvanced. Learn about PEHO Syndrome.
- Pyruvate Carboxylase DeficiencyMs. Tyynismaa isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Spastic ParaparesisMs. Tyynismaa isAdvanced. Learn about Spastic Paraparesis.
- Experienced
- Adrenoleukodystrophy (ALD)Ms. Tyynismaa isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Autonomic NeuropathyMs. Tyynismaa isExperienced. Learn about Autonomic Neuropathy.
- CACH SyndromeMs. Tyynismaa isExperienced. Learn about CACH Syndrome.
- CardiomyopathyMs. Tyynismaa isExperienced. Learn about Cardiomyopathy.
- Cerebellar Multiple System AtrophyMs. Tyynismaa isExperienced. Learn about Cerebellar Multiple System Atrophy.
- Congenital Fiber-Type DisproportionMs. Tyynismaa isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Early Infantile Epileptic EncephalopathyMs. Tyynismaa isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- Hairy Cell Leukemia (HCL)Ms. Tyynismaa isExperienced. Learn about Hairy Cell Leukemia (HCL).
- Hajdu-Cheney SyndromeMs. Tyynismaa isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- HypotoniaMs. Tyynismaa isExperienced. Learn about Hypotonia.
- Infantile Axonal NeuropathyMs. Tyynismaa isExperienced. Learn about Infantile Axonal Neuropathy.
- Infantile-Onset Spinocerebellar Ataxia (IOSCA)
- Limb-Girdle Muscular DystrophyMs. Tyynismaa isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- MELAS SyndromeMs. Tyynismaa isExperienced. Learn about MELAS Syndrome.
- Muscle AtrophyMs. Tyynismaa isExperienced. Learn about Muscle Atrophy.
- Nemaline MyopathyMs. Tyynismaa isExperienced. Learn about Nemaline Myopathy.
- Optic Nerve AtrophyMs. Tyynismaa isExperienced. Learn about Optic Nerve Atrophy.
- Pontocerebellar HypoplasiaMs. Tyynismaa isExperienced. Learn about Pontocerebellar Hypoplasia.
- Primary Lateral SclerosisMs. Tyynismaa isExperienced. Learn about Primary Lateral Sclerosis.
- RhabdomyolysisMs. Tyynismaa isExperienced. Learn about Rhabdomyolysis.
- Spastic Paraplegia Type 2Ms. Tyynismaa isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Ms. Tyynismaa isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityMs. Tyynismaa isExperienced. Learn about Spasticity.
- Spinal Muscular Atrophy (SMA)Ms. Tyynismaa isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Spinal Muscular Atrophy Type 2Ms. Tyynismaa isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Ms. Tyynismaa isExperienced. Learn about Spinal Muscular Atrophy Type 3.
- Spinocerebellar AtaxiaMs. Tyynismaa isExperienced. Learn about Spinocerebellar Ataxia.
- Tubular Aggregate MyopathyMs. Tyynismaa isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular MyopathyMs. Tyynismaa isExperienced. Learn about X-Linked Myotubular Myopathy.