Dr. Douglas A Brooks PHD
Psychologist | Clinical
1531 W 32nd St Suite 201 Joplin MO, 64804About
Dr. Douglas Brooks is a psychologist practicing in Joplin, MO. Dr. Brooks specializes in the treatment of mental health problems, and helps people to cope with their mental illnesses. As a psychologist, Dr. Brooks evaluates and treats patients through a variety of methods, most typically being psychotherapy or talk therapy. Patients usually visit Dr. Brooks 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- Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): a Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network.
- Immune response to enzyme replacement therapy: single epitope control of antigen distribution from circulation.
- Alpha-L-iduronidase and enzyme replacement therapy for mucopolysaccharidosis I.
- Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy.
- Immune tolerance after long-term enzyme-replacement therapy among patients who have mucopolysaccharidosis I.
- Significance of immune response to enzyme-replacement therapy for patients with a lysosomal storage disorder.
- The alpha-L-iduronidase mutations R89Q and R89W result in an attenuated mucopolysaccharidosis type I clinical presentation.
- Iduronate-2-sulphatase protein detection in plasma from mucopolysaccharidosis type II patients.
- alpha-L-iduronidase premature stop codons and potential read-through in mucopolysaccharidosis type I patients.
- Immunoquantification of alpha-galactosidase: evaluation for the diagnosis of Fabry disease.
- Prediction of neuropathology in mucopolysaccharidosis I patients.
- Laronidase treatment of mucopolysaccharidosis I.
- Development of an assay for the detection of mucopolysaccharidosis type VI patients using dried blood-spots.
- An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum.
- Immunochemical analysis of CD107a (LAMP-1).
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