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SIDDHARTH BALE M.D
M.D
Hospitalist Physician
NPI: 1508144478IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hospitalist PhysicianPrimary
Hospitalist
Code: 208M00000X
48107(KY)
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
48107(KY)
Education
OTHER
Class of 2007
Research & Publications (20)
Tubulin encapsulation of carbon nanotubes into functional hybrid assemblies.
PMID 19148890·Small·2009
8-other
Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis: summary of mutations (including 23 novel) and modeling of TGase-1.
PMID 19241467·Hum Mutat·2009
6-review
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
PMID 19177455·Hum Mutat·2009
8-other
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome.
PMID 19282774·Genet Med·2009
8-other
Oligonucleotide array CGH studies in myeloproliferative neoplasms: comparison with JAK2V617F mutational status and conventional chromosome analysis.
PMID 18937974·Leuk Res·2009
4-observational
Observations of turbulence generated by magnetic reconnection.
PMID 19257361·Phys Rev Lett·2009
8-other
New insights into the design of inhibitors of human S-adenosylmethionine decarboxylase: studies of adenine C8 substitution in structural analogues of S-adenosylmethionine.
PMID 19209891·J Med Chem·2009
8-other
Identification of mutations in the EDA and EDAR genes in Pakistani families with hypohidrotic ectodermal dysplasia.
PMID 19438931·Clin Genet·2009
8-other
CHARGE (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness) syndrome and chromosome 22q11.2 deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features.
PMID 19403480·Pediatrics·2009
4-observational
Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA.
PMID 18948357·J Med Genet·2009
8-other
Role of the sulfonium center in determining the ligand specificity of human s-adenosylmethionine decarboxylase.
PMID 19527050·Biochemistry·2009
8-other
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
PMID 19603532·Hum Mutat·2009
8-other
Genetic testing in ectodermal dysplasia: availability, clinical utility, and the nuts and bolts of ordering a genetic test.
PMID 19681151·Am J Med Genet A·2009
8-other
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.
PMID 18414213·Genet Med·2008
8-other
Molecular genetic testing for ultra rare diseases: models for translation from the research laboratory to the CLIA-certified diagnostic laboratory.
PMID 18496031·Genet Med·2008
8-other
Structural similarities between thiamin-binding protein and thiaminase-I suggest a common ancestor.
PMID 18177053·Biochemistry·2008
8-other
Structural basis for putrescine activation of human S-adenosylmethionine decarboxylase.
PMID 19053272·Biochemistry·2008
4-observational
An intronic mutation in DKC1 in an infant with Høyeraal-Hreidarsson syndrome.
PMID 18627054·Am J Med Genet A·2008
5-case
Understanding patient experience of out-of-hours general practitioner services in South Wales: a qualitative study.
PMID 18843062·Emerg Med J·2008
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
- UK DIVISION OF HOSPITAL MEDICINE, 800 ROSE STREET, MN604
LEXINGTON, KY 40536 - Phone
- (859) 323-6047
Quick Facts
- NPI
- 1508144478
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 19
- Publications
- 20
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