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FUKI HISAMA, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1780666420IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
G203183(CA)MD60076638(WA)
Neurology Physician
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD60076638(WA)
Education
UNIVERSITY OF CHICAGO, PRITZKER SCHOOL OF MEDICINE
Class of 1988
Research & Publications (20)
Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.
PMID 19151366·J Child Neurol·2009
5-case
Leukoencephalopathy in adults: is it adrenoleukodystrophy? A case report and molecular analysis.
PMID 19592040·J Neurol Sci·2009
5-case
Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia.
PMID 18976783·J Neurol Sci·2009
8-other
No association between schizophrenia and polymorphisms of the PlexinA2 gene in Chinese Han Trios.
PMID 18096369·Schizophr Res·2008
8-other
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
PMID 18536050·Am J Med Genet A·2008
8-other
Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.
PMID 19052207·J Neurosci·2008
7-preclinical
Synergistic interaction of the OCA2 and OCA3 genes in a family.
PMID 18680187·Am J Med Genet A·2008
5-case
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.
PMID 17136396·Neurogenetics·2007
8-other
Na(V)1.7 mutant A863P in erythromelalgia: effects of altered activation and steady-state inactivation on excitability of nociceptive dorsal root ganglion neurons.
PMID 17135418·J Neurosci·2006
4-observational
Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons.
PMID 15958509·Brain·2005
8-other
FXTAS, SCA10, and SCA17 in American patients with movement disorders.
PMID 15889413·Am J Med Genet A·2005
8-other
Progressive external ophthalmoplegia: a new family with tremor and peripheral neuropathy.
PMID 15800909·Am J Med Genet A·2005
5-case
Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23).
PMID 15754353·Am J Med Genet A·2005
5-case
Familial periodic paralysis and Charcot-Marie-Tooth disease in a 7-generation family.
PMID 15642860·Arch Neurol·2005
4-observational
Going deep to cut the link: cortical disconnection syndrome caused by a thalamic lesion.
PMID 12796557·Neurology·2003
5-case
Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features.
PMID 12771268·Neurology·2003
8-other
GABA and the ornithine delta-aminotransferase gene in vigabatrin-associated visual field defects.
PMID 11749107·Seizure·2001
8-other
Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous system.
PMID 11709000·Arch Neurol·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 101 THE CITY DR S
ORANGE, CA 92868 - Phone
- (714) 456-8888
Quick Facts
- NPI
- 1780666420
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 38
- Publications
- 20
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