Kinga Tomczak, MD, PhD

Program Director, Tic Disorders and Tourette Syndrome Program; Neurologist, Department of Neurology
Instructor of Neurology, Harvard Medical School
Kinga Tomczak, MD, PhD
Phone 617-355-6388
Fax 617-730-0284
NPI 1891962171
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Kinga Tomczak, MD, PhD

Program Director, Tic Disorders and Tourette Syndrome Program; Neurologist, Department of Neurology
Instructor of Neurology, Harvard Medical School

Medical Services

Programs & Services
Neurology Headache Program
Neurology
Languages
English
Education
Medical School
Poznan University of Medical Sciences
Poznan
Poland
Internship
Pediatrics
BaBoston Combined Residency Program (BCRP)
Boston
MA
Residency
Pediatrics
Boston Combined Residency Program (BCRP)
Boston
MA
Residency
Child Neurology
Boston Medical Center
Boston
MA
Fellowship
Post-doctoral Research Fellowship in Genetics and Genomics
Boston Children's Hospital
Boston
MA
Certifications
American Board of Psychiatry and Neurology (Child and Adolescent Neurology)

Publications

Tic-Talk: Voices on Tourette's Labelling. View Abstract
Repetitive but Not Interchangeable: Similarities and Differences in the Repetitive Behaviors of Tourette Syndrome, Obsessive-Compulsive Disorder, Tourettic Obsessive-Compulsive Disorder, and Autism Spectrum Disorder. View Abstract
Diagnostic Criteria for Primary Tic Disorders: Time for Reappraisal. View Abstract
Time is ticking for TikTok tics: A retrospective follow-up study in the post-COVID-19 isolation era. View Abstract
Benign paroxysmal vertigo of childhood. View Abstract
Tourettic OCD: Current understanding and treatment challenges of a unique endophenotype. View Abstract
Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders. View Abstract
Torticollis. View Abstract
Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscle. View Abstract
Acute appendicitis is characterized by a uniform and highly selective pattern of inflammatory gene expression. View Abstract
Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2. View Abstract
Melanoma cell adhesion molecule is a novel marker for human fetal myogenic cells and affects myoblast fusion. View Abstract
X-linked myotubular and centronuclear myopathies. View Abstract
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations. View Abstract
Expression profiling and identification of novel genes involved in myogenic differentiation. View Abstract
Production Of Artificial Antibodies Directed To Human Sperm Surface Antigens By Filamentous Phage Display Library Technique View Abstract
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