Physician

Neurology

Dr. Mia M. Maccollin, MD

Doctor Mia M. Maccollin, MD works in the field of Neurology. She studied medicine at Washington University School of Medicine in St. Louis. Maccollin is a published MD. She has 26 publications published. The most current publication "Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities."

Publications

Patient and physician attitudes regarding clinical trials in neurofibromatosis 1.
A role for the p53 pathway in the pathology of meningiomas with NF2 loss.
Three-dimensional volumetrics for tracking vestibular schwannoma growth in neurofibromatosis type II.
Immunohistochemical analysis supports a role for INI1/SMARCB1 in hereditary forms of schwannomas, but not in solitary, sporadic schwannomas.
Modeling NF2 with human arachnoidal and meningioma cell culture systems: NF2 silencing reflects the benign character of tumor growth.
Ocular pathologic findings of neurofibromatosis type 2.
Dopa-responsive hypersomnia and mixed movement disorder due to sepiapterin reductase deficiency.
A negative feedback signaling network underlies oncogene-induced senescence.
Mutational spectrum of the NF2 gene: a meta-analysis of 12 years of research and diagnostic laboratory findings.
Temporal control of Rac in Schwann cell-axon interaction is disrupted in NF2-mutant schwannoma cells.
Unilateral vestibular schwannoma with other neurofibromatosis type 2-related tumors: clinical and molecular study of a unique phenotype.
Inactivation patterns of NF2 and DAL-1/4.1B (EPB41L3) in sporadic meningioma.
Comparative pathology of nerve sheath tumors in mouse models and humans.
Neurofibromatosis 2 in the pediatric population.
Somatic instability of the NF2 gene in schwannomatosis.
Multiple meningiomas: Investigating the molecular basis of sporadic and familial forms.
The neurofibromatosis type 2 gene product, merlin, reverses the F-actin cytoskeletal defects in primary human Schwannoma cells.
Spinal ependymomas in neurofibromatosis Type 2: a retrospective analysis of 55 patients.
Superficial neurofibromas in the setting of schwannomatosis: nosologic implications.
Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations.
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.
Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas.
Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas.
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1).

Schools

Washington Center School of Medicine
Ny and Presby Hp Columbia Campus
Presbytern Hsp NyBabies H

Doctors Specialties

Pediatric Neurology
Pediatrics
Neurology

Accepted Insurances

Education

New York Presbyterian Hospital - Columbia Campus
Washington University School of Medicine in St. Louis

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