Dr. Jacob Michael Hertz DC
Chiropractor
1200 W Loucks Ave Peoria IL, 61604About
Dr. Jacob Hertz is a Chiropractor practicing in Peoria, IL. Dr. Hertz 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. Hertz 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- [Hereditary neuropathy with liability to pressure palsies].
- Factors affecting de novo methylation of foreign DNA in mouse embryonic stem cells.
- X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.
- A novel splicing mutation in the V2 vasopressin receptor.
- [The molecular genetic background of hereditary craniosynostoses and chondrodysplasias].
- [Very severe spinal muscular atrophy--type 0. A cause of congenital multiple arthrogryposis].
- A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
- A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia.
- Utilization of heterologous alphavirus junction sequences as promoters by Sindbis virus.
- Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.
- Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient.
- Early onset, non-progressive, mild cerebellar ataxia co-segregating with a familial balanced translocation t(8;20)(p22;q13).
- Mutation in the alpha 5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: detection by denaturing gradient gel electrophoresis of a PCR product.
- Pericentric inversion of chromosome 12; a three family study.
- Alport syndrome in southern Sweden.
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