Dr. Wendy Ying wan Hung D.C.
Chiropractor
5810 Oakwood Dr 3g Lisle IL, 60532About
Dr. Wendy Hung is a Chiropractor practicing in Lisle, IL. Dr. Hung specializes in preventing, diagnosing, and treating conditions associated with the neuromusculoskeletal system, while improving each patients functionality and quality of life. Conditions treated include sciatica, neck pain, and arthritis pain, among many others. Dr. Hung seeks to reduce pain and discomfort through manipulation and adjustment of the spine.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis.
- Multiple transcripts of the human Cu,Zn superoxide dismutase gene.
- Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22.
- The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
- A molecular genetic approach to amyotrophic lateral sclerosis.
- Baseline BMD and bone loss at distal radius measured by peripheral quantitative computed tomography in peri- and postmenopausal Hong Kong Chinese women.
- Membrane abnormalities of Huntington's chorea fibroblasts in culture.
- Membrane abnormalities of Huntington's chorea fibroblasts in culture.
- Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.
- RsaI RFLP for electron transport flavoprotein-beta(ETFB).
- Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.
- North Carolina macular dystrophy: exclusion map using RFLPs and microsatellites.
- Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA.
- MspI RFLP for microtubule associated protein-2 (MAP2).
- Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms.
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