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LARRY HUDGINS, MD
MD
Geriatric Medicine (Internal Medicine) Physician
NPI: 1386698843Individual
Specialties, Licenses & Credentials
Geriatric Medicine (Internal Medicine) PhysicianPrimary
Internal Medicine — Geriatric Medicine
Code: 207RG0300X
MD 7295(TN)
Research & Publications (20)
Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog.
PMID 19277064·Eur J Hum Genet·2009
8-other
Preaxial hallucal polydactyly as a marker for diabetic embryopathy.
PMID 18798547·Birth Defects Res A Clin Mol Teratol·2009
8-other
Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay.
PMID 19187739·J Pediatr·2009
5-case
Surgical portosystemic shunts and the Rex bypass in children: a single-centre experience.
PMID 19590656·HPB (Oxford)·2009
8-other
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.
PMID 19668217·Nat Genet·2009
8-other
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood.
PMID 18838674·Proc Natl Acad Sci U S A·2008
8-other
Long-term safety and efficacy of low-density lipoprotein apheresis in childhood for homozygous familial hypercholesterolemia.
PMID 18940291·Am J Cardiol·2008
8-other
The effect of dietary carbohydrate on genes for fatty acid synthase and inflammatory cytokines in adipose tissues from lean and obese subjects.
PMID 17618104·J Nutr Biochem·2008
8-other
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
PMID 18245432·Pediatrics·2008
8-other
Use of array-based technology in the practice of medical genetics.
PMID 17873654·Genet Med·2007
6-review
Lofgren's syndrome presenting as a case of fever of unknown origin.
PMID 17682699·Tenn Med·2007
5-case
The diagnostic utility of a genetics evaluation in children with pervasive developmental disorders.
PMID 16418599·Genet Med·2006
8-other
Genitopatellar syndrome: expanding the phenotype and excluding mutations in LMX1B and TBX4.
PMID 16761293·Am J Med Genet A·2006
5-case
Triplication of 8p22-8p23 in a patient with features similar to Kabuki syndrome.
PMID 16353235·Am J Med Genet A·2006
5-case
Clinical features and management issues in Mowat-Wilson syndrome.
PMID 17103451·Am J Med Genet A·2006
8-other
Autosomal dominant microtia and ocular coloboma: new syndrome or an extension of the oculo-auriculo-vertebral spectrum?
PMID 15800906·Am J Med Genet A·2005
5-case
Detection of sonographic markers of fetal aneuploidy depends on maternal and fetal characteristics.
PMID 15914685·J Ultrasound Med·2005
8-other
Terminal deletion of 6p results in a recognizable phenotype.
PMID 15940702·Am J Med Genet A·2005
5-case
Gatifloxacin-induced cholestatic hepatitis--a challenging diagnosis.
PMID 15974103·Tenn Med·2005
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 715 RAMBLING RD
JOHNSON CITY, TN 37604 - Phone
- (423) 434-0922
Quick Facts
- NPI
- 1386698843
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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