MediFind found 6 doctor with experience in Carnitine Palmitoyltransferase 1 Deficiency near Portugal. Of these, 6 are Experienced.
Patricia Janeiro practices in Santa Maria, Portugal. Ms. Janeiro is rated as an Experienced expert by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, Glutaric Acidemia Type 2, and Classic Galactosemia.
Cristina Florindo practices in Lisbon, Portugal. Ms. Florindo is rated as an Experienced expert by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, Dihydrolipoamide Dehydrogenase Deficiency, and Malnutrition.
Ruben Ramos practices in Lisbon, Portugal. Mr. Ramos is rated as an Experienced expert by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. His top areas of expertise are Carnitine Palmitoyltransferase 1 Deficiency, Aortic Valve Stenosis, Coronary Heart Disease, Transcatheter Aortic Valve Replacement (TAVR), and Heart Bypass Surgery.
Isabel Almeida-De practices in Lisbon, Portugal. Ms. Almeida-De is rated as an Experienced expert by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, Classic Galactosemia, and Dihydrolipoamide Dehydrogenase Deficiency.
Laura Vilarinho practices in Porto, Portugal. Ms. Vilarinho is rated as an Experienced expert by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are Glutaric Acidemia Type 2, Leigh Syndrome, Homocystinuria, and Tyrosinemia Type 3.
Fatima Ventura practices in Lisbon, Portugal. Ms. Ventura is rated as an Experienced expert by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, Glutaric Acidemia Type 2, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
Last Updated: 01/09/2026