Overview
Dorothea Haas practices practicing medicine in Heidelberg, Germany.
Ms. Haas is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses Smith-Lemli-Opitz Syndrome, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Mitochondrial Trifunctional Protein Deficiency, and Von Gierke Disease.
She is actively involved in clinical research, co-authoring 61 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 Dorothea Haas
Is Dorothea Haas a top-rated expert for Smith-Lemli-Opitz Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Dorothea Haas is classified as an Elite expert for Smith-Lemli-Opitz Syndrome, 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 Dorothea Haas participate in research or clinical trials?
Yes. Dorothea Haas has published 61 articles and abstracts on conditions like Smith-Lemli-Opitz Syndrome. You can view a list of Dorothea Haas'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
- Elite
- Smith-Lemli-Opitz Syndrome
- Distinguished
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Advanced
- Keratosis Follicularis Spinulosa Decalvans
- Mitochondrial Trifunctional Protein Deficiency
- Phenylketonuria (PKU)Ms. Haas isAdvanced. Learn about Phenylketonuria (PKU).
- RhabdomyolysisMs. Haas isAdvanced. Learn about Rhabdomyolysis.
- Vitamin B12 DeficiencyMs. Haas isAdvanced. Learn about Vitamin B12 Deficiency.
- Vitamin B12 Deficiency AnemiaMs. Haas isAdvanced. Learn about Vitamin B12 Deficiency Anemia.
- Von Gierke DiseaseMs. Haas isAdvanced. Learn about Von Gierke Disease.
- Experienced
- ADULT SyndromeMs. Haas isExperienced. Learn about ADULT Syndrome.
- AgranulocytosisMs. Haas isExperienced. Learn about Agranulocytosis.
- Argininosuccinic AciduriaMs. Haas isExperienced. Learn about Argininosuccinic Aciduria.
- Atrioventricular Septal DefectMs. Haas isExperienced. Learn about Atrioventricular Septal Defect.
- CACH SyndromeMs. Haas isExperienced. Learn about CACH Syndrome.
- CardiomyopathyMs. Haas isExperienced. Learn about Cardiomyopathy.
- Carnitine Palmitoyltransferase 1 Deficiency
- Darier DiseaseMs. Haas isExperienced. Learn about Darier Disease.
- Dihydropyrimidine Dehydrogenase Deficiency
- Dilated Cardiomyopathy (DCM)Ms. Haas isExperienced. Learn about Dilated Cardiomyopathy (DCM).
- Drug Induced DyskinesiaMs. Haas isExperienced. Learn about Drug Induced Dyskinesia.
- Hallervorden-Spatz DiseaseMs. Haas isExperienced. Learn about Hallervorden-Spatz Disease.
- HomocystinuriaMs. Haas isExperienced. Learn about Homocystinuria.
- Infantile Axonal NeuropathyMs. Haas isExperienced. Learn about Infantile Axonal Neuropathy.
- Infantile NeutropeniaMs. Haas isExperienced. Learn about Infantile Neutropenia.
- LeukodystrophyMs. Haas isExperienced. Learn about Leukodystrophy.
- Low Blood SugarMs. Haas isExperienced. Learn about Low Blood Sugar.
- MalnutritionMs. Haas isExperienced. Learn about Malnutrition.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Metachromatic LeukodystrophyMs. Haas isExperienced. Learn about Metachromatic Leukodystrophy.
- Methylmalonic AcidemiaMs. Haas isExperienced. Learn about Methylmalonic Acidemia.
- Mevalonate Kinase DeficiencyMs. Haas isExperienced. Learn about Mevalonate Kinase Deficiency.
- Multiple Sulfatase DeficiencyMs. Haas isExperienced. Learn about Multiple Sulfatase Deficiency.
- Nephrotic SyndromeMs. Haas isExperienced. Learn about Nephrotic Syndrome.
- Newborn Low Blood SugarMs. Haas isExperienced. Learn about Newborn Low Blood Sugar.
- Propionic AcidemiaMs. Haas isExperienced. Learn about Propionic Acidemia.
- Retinopathy Pigmentary Mental Retardation
- Urea Cycle Disorders (UCD)Ms. Haas isExperienced. Learn about Urea Cycle Disorders (UCD).
- Ventricular Septal DefectsMs. Haas isExperienced. Learn about Ventricular Septal Defects.