Overview
Sabine Schroder practices practicing medicine in Koeln, Germany.
Ms. Schroder is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses Fumarase Deficiency, Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, and Pyruvate Carboxylase Deficiency.
She is actively involved in clinical research, co-authoring 25 peer reviewed articles.
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Frequently Asked Questions about Sabine Schroder
Is Sabine Schroder a top-rated expert for Fumarase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Sabine Schroder is classified as an Distinguished expert for Fumarase 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.
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
- Fumarase DeficiencyMs. Schroder isDistinguished. Learn about Fumarase Deficiency.
- Advanced
- Pyruvate Carboxylase DeficiencyMs. Schroder isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Pyruvate Decarboxylase DeficiencyMs. Schroder isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMs. Schroder isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Experienced
- Achalasia Microcephaly SyndromeMs. Schroder isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Adrenal Insufficiency PediatricMs. Schroder isExperienced. Learn about Adrenal Insufficiency Pediatric.
- Alport SyndromeMs. Schroder isExperienced. Learn about Alport Syndrome.
- Apolipoprotein C2 DeficiencyMs. Schroder isExperienced. Learn about Apolipoprotein C2 Deficiency.
- Cortical DysplasiaMs. Schroder isExperienced. Learn about Cortical Dysplasia.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Schroder isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Early Infantile Epileptic EncephalopathyMs. Schroder isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- Fabry DiseaseMs. Schroder isExperienced. Learn about Fabry Disease.
- Familial Lipoprotein Lipase DeficiencyMs. Schroder isExperienced. Learn about Familial Lipoprotein Lipase Deficiency.
- GangliosidosisMs. Schroder isExperienced. Learn about Gangliosidosis.
- HypotoniaMs. Schroder isExperienced. Learn about Hypotonia.
- Isolated ACTH DeficiencyMs. Schroder isExperienced. Learn about Isolated ACTH Deficiency.
- Metabolic AcidosisMs. Schroder isExperienced. Learn about Metabolic Acidosis.
- MicrocephalyMs. Schroder isExperienced. Learn about Microcephaly.
- MicrognathiaMs. Schroder isExperienced. Learn about Micrognathia.
- Niemann-Pick DiseaseMs. Schroder isExperienced. Learn about Niemann-Pick Disease.
- Sandhoff DiseaseMs. Schroder isExperienced. Learn about Sandhoff Disease.
- Sideroblastic AnemiaMs. Schroder isExperienced. Learn about Sideroblastic Anemia.
- Tay-Sachs DiseaseMs. Schroder isExperienced. Learn about Tay-Sachs Disease.