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KINGA SZIGETI, M.D.
M.D.
Neurology Physician
NPI: 1558461079IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
41483(TX)M8374(TX)
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 1994
Research & Publications (20)
Evaluation of distal symmetric polyneuropathy: the role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review).
PMID 19086069·Muscle Nerve·2009
6-review
Evaluation of distal symmetric polyneuropathy: the role of laboratory and genetic testing (an evidence-based review).
PMID 19086068·Muscle Nerve·2009
6-review
Practice Parameter: evaluation of distal symmetric polyneuropathy: role of laboratory and genetic testing (an evidence-based review). Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation.
PMID 19056666·Neurology·2009
6-review
The structure of horseradish peroxidase C characterized as a molten globule state after Ca(2+) depletion.
PMID 18805513·Biochim Biophys Acta·2008
8-other
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations.
PMID 17717711·Neurogenetics·2007
5-case
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
PMID 17572665·Nature·2007
7-preclinical
Overall survival of oropharyngeal cancer patients treated with different treatment modalities.
PMID 17251851·J Craniofac Surg·2007
8-other
[Survival prospects of mesopharyngeal carcinoma patients treated primarily with intraarterial chemotherapy. A retrospective study].
PMID 16515032·Orv Hetil·2006
8-other
Effect of human organism on the oxide layer formed on titanium osteosynthesis plates: a surface analytical study.
PMID 17119419·J Craniofac Surg·2006
8-other
Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathies.
PMID 16775379·Neuromolecular Med·2006
6-review
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.
PMID 16714318·Brain·2006
4-observational
Charcot-Marie-Tooth disease and related hereditary polyneuropathies: molecular diagnostics determine aspects of medical management.
PMID 16481890·Genet Med·2006
8-other
T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy.
PMID 16437560·Ann Neurol·2006
4-observational
Effect of induction chemotherapy on changes of laminin and syndecan expression in oral squamous cell carcinomas: a prospective, randomized, clinicopathologic and immunohistochemical study.
PMID 15750416·J Craniofac Surg·2005
3-trial
SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation.
PMID 15776429·Hum Mutat·2005
7-preclinical
[Alveolar bone regeneration stimulated by a combination of platelet-rich plasma and Cerasorb graft in Beagle dogs. Histological and histomorphometric studies].
PMID 15495539·Fogorv Sz·2004
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 100 HIGH ST.
BUFFALO, NY 14203 - Phone
- (716) 859-5600
Quick Facts
- NPI
- 1558461079
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 32
- Publications
- 20
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