Overview
Esther Maier practices practicing medicine in Munich, Germany.
Ms. Maier is highly rated in 14 conditions, according to our data. Her clinical expertise encompasses Glutaric Acidemia Type 1, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Mitochondrial Trifunctional Protein Deficiency, and Inborn Amino Acid Metabolism Disorder.
She is actively involved in clinical research, co-authoring 59 peer reviewed articles and participating in 1 clinical trial.
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.
1 Clinical Trials
Frequently Asked Questions about Esther M. Maier
Is Esther M. Maier a top-rated expert for Glutaric Acidemia Type 1?
MediFind is an objective health platform that identifies experts based on real-world data. Esther M. Maier is classified as an Distinguished expert for Glutaric Acidemia Type 1, 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 Esther M. Maier participate in research or clinical trials?
Yes. Esther M. Maier has published 59 articles and abstracts on conditions like Glutaric Acidemia Type 1. You can view a list of Esther M. Maier'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
- Glutaric Acidemia Type 1Ms. Maier isDistinguished. Learn about Glutaric Acidemia Type 1.
- Advanced
- Craniofacial-Deafness-Hand Syndrome
- HistiocytosisMs. Maier isAdvanced. Learn about Histiocytosis.
- Inborn Amino Acid Metabolism Disorder
- Isovaleric AcidemiaMs. Maier isAdvanced. Learn about Isovaleric Acidemia.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Mitochondrial Trifunctional Protein Deficiency
- Niemann-Pick DiseaseMs. Maier isAdvanced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell Histiocytosis
- Phenylketonuria (PKU)Ms. Maier isAdvanced. Learn about Phenylketonuria (PKU).
- Pyruvate Decarboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- ReticulohistiocytomaMs. Maier isAdvanced. Learn about Reticulohistiocytoma.
- RhabdomyolysisMs. Maier isAdvanced. Learn about Rhabdomyolysis.
- Experienced
- Batten DiseaseMs. Maier isExperienced. Learn about Batten Disease.
- CardiomyopathyMs. Maier isExperienced. Learn about Cardiomyopathy.
- Classic GalactosemiaMs. Maier isExperienced. Learn about Classic Galactosemia.
- CLN1 DiseaseMs. Maier isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMs. Maier isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMs. Maier isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMs. Maier isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMs. Maier isExperienced. Learn about CLN5 Disease.
- Cortical DysplasiaMs. Maier isExperienced. Learn about Cortical Dysplasia.
- Cutis LaxaMs. Maier isExperienced. Learn about Cutis Laxa.
- Deafness Craniofacial SyndromeMs. Maier isExperienced. Learn about Deafness Craniofacial Syndrome.
- Dihydrolipoamide Dehydrogenase Deficiency
- Drug Induced DyskinesiaMs. Maier isExperienced. Learn about Drug Induced Dyskinesia.
- Early Infantile Epileptic Encephalopathy
- Focal DystoniaMs. Maier isExperienced. Learn about Focal Dystonia.
- Galactokinase DeficiencyMs. Maier isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Maier isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Maier isExperienced. Learn about Galactosemia.
- Ganglion CystMs. Maier isExperienced. Learn about Ganglion Cyst.
- Glucose Phosphate Isomerase Deficiency
- HypotoniaMs. Maier isExperienced. Learn about Hypotonia.
- Increased Head CircumferenceMs. Maier isExperienced. Learn about Increased Head Circumference.
- Infantile Axonal NeuropathyMs. Maier isExperienced. Learn about Infantile Axonal Neuropathy.
- Maple Syrup Urine DiseaseMs. Maier isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaMs. Maier isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Methylmalonic AcidemiaMs. Maier isExperienced. Learn about Methylmalonic Acidemia.
- Movement DisordersMs. Maier isExperienced. Learn about Movement Disorders.
- Mucolipidosis 3Ms. Maier isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Maier isExperienced. Learn about Mucolipidosis Type 4.
- Propionic AcidemiaMs. Maier isExperienced. Learn about Propionic Acidemia.
- Severe Combined Immunodeficiency (SCID)
- SialidosisMs. Maier isExperienced. Learn about Sialidosis.
- Spinal Muscular Atrophy (SMA)Ms. Maier isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Vitamin B12 Deficiency AnemiaMs. Maier isExperienced. Learn about Vitamin B12 Deficiency Anemia.
- Von Gierke DiseaseMs. Maier isExperienced. Learn about Von Gierke Disease.