Overview
Temis Felix practices practicing medicine in Porto Alegre, Brazil.
Felix is highly rated in 11 conditions, according to our data. Their clinical expertise encompasses Osteogenesis Imperfecta, Deafness Craniofacial Syndrome, Craniofacial-Deafness-Hand Syndrome, and Cartilage-Hair Hypoplasia.
They are actively involved in clinical research, co-authoring 73 peer reviewed articles.
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 Temis M. Felix
Is Temis M. Felix a top-rated expert for Osteogenesis Imperfecta?
MediFind is an objective health platform that identifies experts based on real-world data. Temis M. Felix is classified as an Distinguished expert for Osteogenesis Imperfecta, 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 Temis M. Felix participate in research or clinical trials?
Yes. Temis M. Felix has published 73 articles and abstracts on conditions like Osteogenesis Imperfecta. You can view a list of Temis M. Felix'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
- Craniofacial-Deafness-Hand Syndrome
- Deafness Craniofacial SyndromeFelix isDistinguished. Learn about Deafness Craniofacial Syndrome.
- Osteogenesis ImperfectaFelix isDistinguished. Learn about Osteogenesis Imperfecta.
- Advanced
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- Biotinidase DeficiencyFelix isAdvanced. Learn about Biotinidase Deficiency.
- Cartilage-Hair Hypoplasia
- Cleft Lip and PalateFelix isAdvanced. Learn about Cleft Lip and Palate.
- Goldenhar DiseaseFelix isAdvanced. Learn about Goldenhar Disease.
- Multiple Carboxylase Deficiency
- Treacher Collins Syndrome
- Experienced
- Absence SeizureFelix isExperienced. Learn about Absence Seizure.
- Acanthosis NigricansFelix isExperienced. Learn about Acanthosis Nigricans.
- AchondroplasiaFelix isExperienced. Learn about Achondroplasia.
- Autosomal Recessive Hypotrichosis
- Brachydactyly Mononen TypeFelix isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyFelix isExperienced. Learn about Chondrodystrophy.
- Cockayne SyndromeFelix isExperienced. Learn about Cockayne Syndrome.
- Cockayne Syndrome Type 1Felix isExperienced. Learn about Cockayne Syndrome Type 1.
- Cockayne Syndrome Type 2Felix isExperienced. Learn about Cockayne Syndrome Type 2.
- Crouzon SyndromeFelix isExperienced. Learn about Crouzon Syndrome.
- DiGeorge SyndromeFelix isExperienced. Learn about DiGeorge Syndrome.
- Epilepsy in ChildrenFelix isExperienced. Learn about Epilepsy in Children.
- Generalized Tonic-Clonic Seizure
- Glucose Phosphate Isomerase Deficiency
- Hearing LossFelix isExperienced. Learn about Hearing Loss.
- HoloprosencephalyFelix isExperienced. Learn about Holoprosencephaly.
- HypoparathyroidismFelix isExperienced. Learn about Hypoparathyroidism.
- Immune Defect due to Absence of Thymus
- Infant Hearing LossFelix isExperienced. Learn about Infant Hearing Loss.
- Microcephaly Deafness Syndrome
- MicrognathiaFelix isExperienced. Learn about Micrognathia.
- Muenke SyndromeFelix isExperienced. Learn about Muenke Syndrome.
- Schwartz-Jampel SyndromeFelix isExperienced. Learn about Schwartz-Jampel Syndrome.
- Williams SyndromeFelix isExperienced. Learn about Williams Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia Tarda
- Xeroderma PigmentosumFelix isExperienced. Learn about Xeroderma Pigmentosum.