Overview
Aline Cano practices in Marseille, France. Ms. Cano is rated as an Experienced expert by MediFind in the treatment of Fructose-1,6-Bisphosphatase Deficiency. Her top areas of expertise are Chanarin-Dorfman Syndrome, Methylmalonic Acidemia, Rhabdomyolysis, Delayed Growth, and Liver Transplant.
Her clinical research consists of co-authoring 67 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Fructose-1,6-Bisphosphatase Deficiency.
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.
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
- Chanarin-Dorfman SyndromeMs. Cano isAdvanced. Learn about Chanarin-Dorfman Syndrome.
- Delayed GrowthMs. Cano isAdvanced. Learn about Delayed Growth.
- Inborn Renal AminoaciduriaMs. Cano isAdvanced. Learn about Inborn Renal Aminoaciduria.
- Methylmalonic AcidemiaMs. Cano isAdvanced. Learn about Methylmalonic Acidemia.
- RhabdomyolysisMs. Cano isAdvanced. Learn about Rhabdomyolysis.
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)
- Arginase DeficiencyMs. Cano isExperienced. Learn about Arginase Deficiency.
- Batten DiseaseMs. Cano isExperienced. Learn about Batten Disease.
- Brachydactyly Mononen TypeMs. Cano isExperienced. Learn about Brachydactyly Mononen Type.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CLN1 DiseaseMs. Cano isExperienced. Learn about CLN1 Disease.