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SHELDON HOLDER, MD
MD
Hematology & Oncology Physician
NPI: 1952509127IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hematology & Oncology PhysicianPrimary
Internal Medicine — Hematology & Oncology
Code: 207RH0003X
MD448690(PA)MD17540(RI)
CMS Specialties
PrimaryHEMATOLOGY/ONCOLOGY
Education
LOMA LINDA UNIVERSITY SCHOOL OF MEDICINE
Class of 2007
Research & Publications (20)
Increasing molecular weight parameters of a helical polymer through polymerization in a chiral solvent.
PMID 16984183·J Am Chem Soc·2006
8-other
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.
PMID 19582487·Neurogenetics·2010
5-case
The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.
PMID 19481195·Am J Hum Genet·2009
8-other
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
PMID 19498035·Hum Mol Genet·2009
5-case
Macrocephaly-cutis marmorata telangiectatica congenita: a report on the natural history of a mild case.
PMID 18978660·Clin Dysmorphol·2008
5-case
Cryo electron tomography reveals confined complex morphologies of tripeptide-containing amphiphilic double-comb diblock copolymers.
PMID 18785667·Angew Chem Int Ed Engl·2008
8-other
Keipert syndrome: two further cases and review of the literature.
PMID 18541962·Clin Dysmorphol·2008
5-case
Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.
PMID 18474587·J Med Genet·2008
5-case
Addition polymerization of 1,1-dimesitylneopentylgermene: synthesis of a polygermene.
PMID 18473065·Chem Commun (Camb)·2008
8-other
Caudal appendage in focal dermal hypoplasia (Goltz syndrome).
PMID 18388786·Clin Dysmorphol·2008
5-case
Comparative molecular field analysis of flavonoid inhibitors of the PIM-1 kinase.
PMID 17637507·Bioorg Med Chem·2007
4-observational
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
PMID 17236139·Am J Hum Genet·2007
8-other
Characterization of a potent and selective small-molecule inhibitor of the PIM1 kinase.
PMID 17218638·Mol Cancer Ther·2007
8-other
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.
PMID 16582908·Nat Genet·2006
8-other
Indian boarding schools and the Therapeutic Residential Model project.
PMID 17602399·Am Indian Alsk Native Ment Health Res·2006
4-observational
Shaping amorphous calcium carbonate films into 2D model substrates for bone cell culture.
PMID 16475224·Angew Chem Int Ed Engl·2006
7-preclinical
Chondrodysplasia punctata: case report and review of audiological and ENT features.
PMID 16359148·J Laryngol Otol·2006
5-case
De novo t(7;10)(q33;q23) translocation and closely juxtaposed microdeletion in a patient with macrocephaly and developmental delay.
PMID 15834588·Hum Genet·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
- 593 EDDY STREET, APC MAIN
PROVIDENCE, RI 02903 - Phone
- (401) 444-5435
Quick Facts
- NPI
- 1952509127
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 19
- Publications
- 20
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