Dr. Gabriela M Mancini PSY.D.
Psychologist | Clinical
5201 Raymond St 116 Orlando FL, 32803About
Dr. Gabriela Mancini is a psychologist practicing in Orlando, FL. Dr. Mancini specializes in the treatment of mental health problems, and helps people to cope with their mental illnesses. As a psychologist, Dr. Mancini evaluates and treats patients through a variety of methods, most typically being psychotherapy or talk therapy. Patients usually visit Dr. Mancini because they have been experiencing depression, anxiety, stress or anger for a significant period of time and are seeking help. Psychologists may perform a variety of exams and assessments to diagnose a mental condition.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Juvenile hyaline fibromatosis: clinical heterogeneity in three patients.
- Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage disease.
- A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases.
- Lysosomal transport disorders.
- A new simple enzyme assay for pre- and postnatal diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and its variants.
- Pitfalls in the diagnosis of multiple sulfatase deficiency.
- An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease.
- Studies on the pathogenesis of Costello syndrome.
- Hereditary porencephaly: clinical and MRI findings in two Dutch families.
- Salla disease variant in a Dutch patient. Potential value of polymorphonuclear leucocytes for heterozygote detection.
- [From gene to disease; Krabbe disease and galactosylceramidase deficiency].
- NPT4, a new microsomal phosphate transporter: mutation analysis in glycogen storage disease type Ic.
- Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families.
- Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly.
- Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla disease.
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10101 FOREST HILL BLVD WELLINGTON FL 33414