Dr. Fuki Marie Hisama MD
Neurologist | Neurology
1959 Ne Pacific St Box 357720 Seattle WA, 98195Rating
2/5
About
Dr. Hisama joined the University of Washington in 2009 as the medical director of the Genetic Medicine Clinic. She is a UW associate professor in the Department of Medicine in the Division of Genetics, ...
Education and Training
U Of Chgo Div Of Bio Sci Pritzker Sch Of Med 1988
Univ. of Chicago 1988
University of Chicago Division of the Biological Sciences The Pritzker School of Medicine 1988
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Psychiatry and NeurologyAmerican Board of Psychiatry and NeurologyABPN
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous system.
- Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features.
- Familial periodic paralysis and Charcot-Marie-Tooth disease in a 7-generation family.
- Progressive external ophthalmoplegia: a new family with tremor and peripheral neuropathy.
- FXTAS, SCA10, and SCA17 in American patients with movement disorders.
- WRN's tenth anniversary.
- Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.
- Synergistic interaction of the OCA2 and OCA3 genes in a family.
- Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations
- A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features.
- Diagnostic yield of array comparative genomic hybridization in adults with autism spectrum disorders.
- Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.
- The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations.
- CORRIGENDUM: The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations.
- A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Treatments
- Birth Defects
Fellowships
- Yale Univ. School of Medicine
Dr. Fuki Marie Hisama MD's Practice location
Practice At 1959 Ne Pacific St Box 357720
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Nearest Hospitals
SEATTLE CHILDREN'S HOSPITALl
4800 SAND POINT WAY NE, PO BOX C-5371 SEATTLE WA 98105GROUP HEALTH CENTRAL HOSPITALl
201 - 16TH AVENUE EAST SEATTLE WA 98112VIRGINIA MASON MEDICAL CENTERl
925 SENECA ST SEATTLE WA 98101