Overview
Joana Jacinto practices practicing medicine in Bern, Switzerland.
Jacinto is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Familial Porencephaly, Porencephaly, Achondrogenesis, and Deafness Craniofacial Syndrome.
They are actively involved in clinical research, co-authoring 45 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 Joana P. Jacinto
Is Joana P. Jacinto a top-rated expert for Familial Porencephaly?
MediFind is an objective health platform that identifies experts based on real-world data. Joana P. Jacinto is classified as an Advanced expert for Familial Porencephaly, 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 Joana P. Jacinto participate in research or clinical trials?
Yes. Joana P. Jacinto has published 45 articles and abstracts on conditions like Familial Porencephaly. You can view a list of Joana P. Jacinto'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
- Advanced
- Familial PorencephalyJacinto isAdvanced. Learn about Familial Porencephaly.
- PorencephalyJacinto isAdvanced. Learn about Porencephaly.
- Experienced
- Acanthosis NigricansJacinto isExperienced. Learn about Acanthosis Nigricans.
- AchondrogenesisJacinto isExperienced. Learn about Achondrogenesis.
- AchondroplasiaJacinto isExperienced. Learn about Achondroplasia.
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- Acromicric DysplasiaJacinto isExperienced. Learn about Acromicric Dysplasia.
- AlbinismJacinto isExperienced. Learn about Albinism.
- Amyotonia CongenitaJacinto isExperienced. Learn about Amyotonia Congenita.
- Aplasia Cutis CongenitaJacinto isExperienced. Learn about Aplasia Cutis Congenita.
- Arthrogryposis Multiplex Congenita
- Autosomal Recessive HypotrichosisJacinto isExperienced. Learn about Autosomal Recessive Hypotrichosis.
- Brachydactyly Mononen TypeJacinto isExperienced. Learn about Brachydactyly Mononen Type.
- Cerebellar HypoplasiaJacinto isExperienced. Learn about Cerebellar Hypoplasia.
- Chiari MalformationJacinto isExperienced. Learn about Chiari Malformation.
- Chiari Malformation Type 2Jacinto isExperienced. Learn about Chiari Malformation Type 2.
- ChondrodystrophyJacinto isExperienced. Learn about Chondrodystrophy.
- Clouston SyndromeJacinto isExperienced. Learn about Clouston Syndrome.
- Color BlindnessJacinto isExperienced. Learn about Color Blindness.
- Congenital ContracturesJacinto isExperienced. Learn about Congenital Contractures.
- Congenital Fiber-Type Disproportion
- Cortical DysplasiaJacinto isExperienced. Learn about Cortical Dysplasia.
- Crouzon SyndromeJacinto isExperienced. Learn about Crouzon Syndrome.
- Deafness Craniofacial SyndromeJacinto isExperienced. Learn about Deafness Craniofacial Syndrome.
- Dominant Dystrophic Epidermolysis Bullosa
- Dowling-Meara Epidermolysis Bullosa Simplex
- Ectodermal DysplasiasJacinto isExperienced. Learn about Ectodermal Dysplasias.
- Ehlers-Danlos Syndrome (EDS)Jacinto isExperienced. Learn about Ehlers-Danlos Syndrome (EDS).
- Epidermolysis BullosaJacinto isExperienced. Learn about Epidermolysis Bullosa.
- Familial HypertriglyceridemiaJacinto isExperienced. Learn about Familial Hypertriglyceridemia.
- Goldenhar DiseaseJacinto isExperienced. Learn about Goldenhar Disease.
- Hereditary XanthinuriaJacinto isExperienced. Learn about Hereditary Xanthinuria.
- Hypermobile JointsJacinto isExperienced. Learn about Hypermobile Joints.
- Hypohidrotic Ectodermal DysplasiaJacinto isExperienced. Learn about Hypohidrotic Ectodermal Dysplasia.
- Hypomelanotic DisorderJacinto isExperienced. Learn about Hypomelanotic Disorder.
- HypospadiasJacinto isExperienced. Learn about Hypospadias.
- Lamellar IchthyosisJacinto isExperienced. Learn about Lamellar Ichthyosis.
- MosaicismJacinto isExperienced. Learn about Mosaicism.
- Myotonia CongenitaJacinto isExperienced. Learn about Myotonia Congenita.
- Nonbullous Congenital Ichthyosiform Erythroderma
- Osteogenesis ImperfectaJacinto isExperienced. Learn about Osteogenesis Imperfecta.
- Paramyotonia CongenitaJacinto isExperienced. Learn about Paramyotonia Congenita.
- Patent Foramen OvaleJacinto isExperienced. Learn about Patent Foramen Ovale.
- Schwartz-Jampel SyndromeJacinto isExperienced. Learn about Schwartz-Jampel Syndrome.
- Short Stature (Growth Disorders)Jacinto isExperienced. Learn about Short Stature (Growth Disorders).
- SpasticityJacinto isExperienced. Learn about Spasticity.
- SyndactylyJacinto isExperienced. Learn about Syndactyly.
- ToxoplasmosisJacinto isExperienced. Learn about Toxoplasmosis.
- Transposition of the Great Arteries
- Treacher Collins SyndromeJacinto isExperienced. Learn about Treacher Collins Syndrome.
- Tubular Aggregate MyopathyJacinto isExperienced. Learn about Tubular Aggregate Myopathy.
- Usher SyndromeJacinto isExperienced. Learn about Usher Syndrome.
- X-Linked Myotubular MyopathyJacinto isExperienced. Learn about X-Linked Myotubular Myopathy.
- X-Linked Spondyloepiphyseal Dysplasia Tarda