Back to Search

MIA MACCOLLIN, MD

MD

Pediatrics Physician

NPI: 1437149093Individual

Specialties, Licenses & Credentials

Pediatrics PhysicianPrimary

Pediatrics

Code: 208000000X

73495(MA)
Neurology with Special Qualifications in Child Neurology Physician

Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology

Code: 2084N0402X

73495(MA)

Research & Publications (20)

Familial schwannomatosis: exclusion of the NF2 locus as the germline event.
PMID 12821741·Neurology·2003
8-other
Molecular genetic aspects of the phakomatoses: tuberous sclerosis complex and neurofibromatosis 1.
PMID 11262730·Curr Opin Neurol·2001
6-review
Diagnostic criteria for schwannomatosis.
PMID 15955931·Neurology·2005
6-review
Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations.
PMID 19320657·Clin Genet·2009
8-other
A role for the p53 pathway in the pathology of meningiomas with NF2 loss.
PMID 18974932·J Neurooncol·2009
8-other
Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis.
PMID 18647326·Clin Genet·2008
8-other
Immunohistochemical analysis supports a role for INI1/SMARCB1 in hereditary forms of schwannomas, but not in solitary, sporadic schwannomas.
PMID 18422762·Brain Pathol·2008
8-other
Modeling NF2 with human arachnoidal and meningioma cell culture systems: NF2 silencing reflects the benign character of tumor growth.
PMID 17962031·Neurobiol Dis·2008
8-other
Patient and physician attitudes regarding clinical trials in neurofibromatosis 1.
PMID 19170300·J Neurosci Nurs·2008
8-other
Three-dimensional volumetrics for tracking vestibular schwannoma growth in neurofibromatosis type II.
PMID 18824998·Neurosurgery·2008
8-other
Ocular pathologic findings of neurofibromatosis type 2.
PMID 17353411·Arch Ophthalmol·2007
5-case
Mutational spectrum of the NF2 gene: a meta-analysis of 12 years of research and diagnostic laboratory findings.
PMID 16983642·Hum Mutat·2007
1-meta
Unilateral vestibular schwannoma with other neurofibromatosis type 2-related tumors: clinical and molecular study of a unique phenotype.
PMID 16509493·J Neurosurg·2006
8-other
Dopa-responsive hypersomnia and mixed movement disorder due to sepiapterin reductase deficiency.
PMID 17159114·Neurology·2006
5-case
A negative feedback signaling network underlies oncogene-induced senescence.
PMID 17157787·Cancer Cell·2006
7-preclinical
Temporal control of Rac in Schwann cell-axon interaction is disrupted in NF2-mutant schwannoma cells.
PMID 16571745·J Neurosci·2006
8-other
Glioblastoma multiforme presenting as bilateral internal auditory canal tumors.
PMID 16541215·J Neurol·2006
5-case
Inactivation patterns of NF2 and DAL-1/4.1B (EPB41L3) in sporadic meningioma.
PMID 16213361·Cancer Genet Cytogenet·2005
8-other
Multiple meningiomas in brain and lung due to acquired mutation of the NF2 gene.
PMID 15159511·Neurology·2004
5-case
Comparative pathology of nerve sheath tumors in mouse models and humans.
PMID 15150133·Cancer Res·2004
4-observational

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
149 13TH ST, 6TH FLOOR CYN 149 6
CHARLESTOWN, MA 02129

Location

Practice Location

149 13TH ST, CHARLESTOWN, MA
(617) 726-7856

Quick Facts

NPI
1437149093
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
20

Are you this provider?

Claim Your Profile