Overview
Sylvia Stockler-Ipsiroglu practices practicing medicine in Vancouver, Canada.
Ms. Stockler-Ipsiroglu is highly rated in 10 conditions, according to our data. Her clinical expertise encompasses Guanidinoacetate Methyltransferase Deficiency, Pyruvate Carboxylase Deficiency, X-Linked Creatine Deficiency, and Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome).
She is actively involved in clinical research, co-authoring 66 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 Sylvia G. Stockler-Ipsiroglu
Is Sylvia G. Stockler-Ipsiroglu a top-rated expert for Guanidinoacetate Methyltransferase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Sylvia G. Stockler-Ipsiroglu is classified as an Distinguished expert for Guanidinoacetate Methyltransferase 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 Sylvia G. Stockler-Ipsiroglu participate in research or clinical trials?
Yes. Sylvia G. Stockler-Ipsiroglu has published 65 articles and abstracts on conditions like Guanidinoacetate Methyltransferase Deficiency. You can view a list of Sylvia G. Stockler-Ipsiroglu'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
- Distinguished
- Guanidinoacetate Methyltransferase DeficiencyMs. Stockler-Ipsiroglu isDistinguished. Learn about Guanidinoacetate Methyltransferase Deficiency.
- Pyruvate Carboxylase DeficiencyMs. Stockler-Ipsiroglu isDistinguished. Learn about Pyruvate Carboxylase Deficiency.
- Advanced
- Brachydactyly Mononen TypeMs. Stockler-Ipsiroglu isAdvanced. Learn about Brachydactyly Mononen Type.
- GangliosidosisMs. Stockler-Ipsiroglu isAdvanced. Learn about Gangliosidosis.
- GM1 GangliosidosisMs. Stockler-Ipsiroglu isAdvanced. Learn about GM1 Gangliosidosis.
- Lactic AcidosisMs. Stockler-Ipsiroglu isAdvanced. Learn about Lactic Acidosis.
- Mitochondrial Complex 1 DeficiencyMs. Stockler-Ipsiroglu isAdvanced. Learn about Mitochondrial Complex 1 Deficiency.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)Ms. Stockler-Ipsiroglu isAdvanced. Learn about Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome).
- Phenylketonuria (PKU)Ms. Stockler-Ipsiroglu isAdvanced. Learn about Phenylketonuria (PKU).
- X-Linked Creatine DeficiencyMs. Stockler-Ipsiroglu isAdvanced. Learn about X-Linked Creatine Deficiency.
- Experienced
- AnhidrosisMs. Stockler-Ipsiroglu isExperienced. Learn about Anhidrosis.
- Aromatic L-Amino Acid Decarboxylase (AADC) DeficiencyMs. Stockler-Ipsiroglu isExperienced. Learn about Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency.
- Autonomic NeuropathyMs. Stockler-Ipsiroglu isExperienced. Learn about Autonomic Neuropathy.
- ColobomaMs. Stockler-Ipsiroglu isExperienced. Learn about Coloboma.
- Drug Induced DyskinesiaMs. Stockler-Ipsiroglu isExperienced. Learn about Drug Induced Dyskinesia.
- EpilepsyMs. Stockler-Ipsiroglu isExperienced. Learn about Epilepsy.
- Hajdu-Cheney SyndromeMs. Stockler-Ipsiroglu isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hereditary Sensory and Autonomic Neuropathy Type 2Ms. Stockler-Ipsiroglu isExperienced. Learn about Hereditary Sensory and Autonomic Neuropathy Type 2.
- Hereditary Sensory Neuropathy Type 1 (HSN1)Ms. Stockler-Ipsiroglu isExperienced. Learn about Hereditary Sensory Neuropathy Type 1 (HSN1).
- High Blood Pressure in InfantsMs. Stockler-Ipsiroglu isExperienced. Learn about High Blood Pressure in Infants.
- HypotoniaMs. Stockler-Ipsiroglu isExperienced. Learn about Hypotonia.
- LeukodystrophyMs. Stockler-Ipsiroglu isExperienced. Learn about Leukodystrophy.
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyMs. Stockler-Ipsiroglu isExperienced. Learn about Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
- Movement DisordersMs. Stockler-Ipsiroglu isExperienced. Learn about Movement Disorders.
- ParaplegiaMs. Stockler-Ipsiroglu isExperienced. Learn about Paraplegia.
- Primary Carnitine DeficiencyMs. Stockler-Ipsiroglu isExperienced. Learn about Primary Carnitine Deficiency.
- Propionic AcidemiaMs. Stockler-Ipsiroglu isExperienced. Learn about Propionic Acidemia.
- RhabdomyolysisMs. Stockler-Ipsiroglu isExperienced. Learn about Rhabdomyolysis.
- SeizuresMs. Stockler-Ipsiroglu isExperienced. Learn about Seizures.
- SplenomegalyMs. Stockler-Ipsiroglu isExperienced. Learn about Splenomegaly.
- Von Gierke DiseaseMs. Stockler-Ipsiroglu isExperienced. Learn about Von Gierke Disease.