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DANIEL FELDMANN, M.D.
M.D.
Orthopaedic Surgery Physician
NPI: 1558338632IndividualAccepts Medicare
Specialties, Licenses & Credentials
Sports Medicine (Orthopaedic Surgery) Physician
Orthopaedic Surgery — Sports Medicine
Code: 207XX0005X
MD066306L(PA)
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
MD066306L(PA)
CMS Specialties
PrimaryORTHOPEDIC SURGERY
Education
JEFFERSON MEDICAL COLLEGE OF THOMAS JEFFERSON UNIVERSITY
Class of 1996
Research & Publications (20)
Development of a synovial cyst following anterior cruciate ligament reconstruction.
PMID 11172251·Arthroscopy·2001
5-case
Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysis.
PMID 15150777·Am J Med Genet A·2004
8-other
Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene.
PMID 14694360·Eur J Hum Genet·2004
8-other
CFTR genotypes in patients with normal or borderline sweat chloride levels.
PMID 12955726·Hum Mutat·2003
8-other
A novel nonsense mutation (Q1291X) in exon 20 of CFTR (ABCC7) gene.
PMID 11295849·Hum Mutat·2001
8-other
Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.
PMID 10906158·J Am Soc Nephrol·2000
8-other
A new case of alpha-1-antitrypsin frameshift mutation (1123insT) causing severe deficiency and emphysema.
PMID 11058908·Hum Mutat·2000
5-case
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.
PMID 18985073·Eur J Hum Genet·2009
8-other
Familial interstitial disease with I73T mutation: A mid- and long-term study.
PMID 19148933·Pediatr Pulmonol·2009
8-other
New surfactant protein C gene mutations associated with diffuse lung disease.
PMID 19443464·J Med Genet·2009
8-other
New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.
PMID 18462486·BMC Med Genet·2008
4-observational
[Lung diseases associated with inherited disorders of surfactant metabolism].
PMID 18804975·Arch Pediatr·2008
8-other
Perrault syndrome: report of four new cases, review and exclusion of candidate genes.
PMID 18241061·Am J Med Genet A·2008
5-case
Occurrence, fate and assessment of polar metamizole (dipyrone) residues in hospital and municipal wastewater.
PMID 18164746·Chemosphere·2008
8-other
Epitaxial ternary nitride thin films prepared by a chemical solution method.
PMID 18939844·J Am Chem Soc·2008
8-other
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
PMID 17637808·Eur J Hum Genet·2007
5-case
[The mutation 35delG of the gene of the connexin 26 is a frequent cause of autosomal-recessive non-syndromic hearing loss in Morocco].
PMID 17229560·Arch Pediatr·2007
8-other
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
PMID 16570074·Eur J Hum Genet·2006
8-other
Association between two distinct executive tasks in schizophrenia: a functional transcranial Doppler sonography study.
PMID 16723019·BMC Psychiatry·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 16 WOODBINE LANE
DANVILLE, PA 17822 - Phone
- (570) 271-6700
Quick Facts
- NPI
- 1558338632
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 30
- Publications
- 20
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