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CHARLES TIFFT, M.D.
M.D.
Internal Medicine Physician
NPI: 1740233063IndividualAccepts Medicare
Specialties, Licenses & Credentials
Nephrology Physician
Internal Medicine — Nephrology
Code: 207RN0300X
37348(MA)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
37348(MA)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
BOSTON UNIVERSITY SCHOOL OF MEDICINE
Class of 1972
Research & Publications (20)
Joint National Committee VI: individualized versus indiscriminate therapy for hypertension.
PMID 10981156·Curr Hypertens Rep·2000
8-other
Pharmacokinetics, safety and tolerability of miglustat in the treatment of pediatric patients with GM2 gangliosidosis.
PMID 19447653·Mol Genet Metab·2009
3-trial
Dysmorphic findings in two cases of abeta/hypobetalipoproteinemia.
PMID 19282754·Clin Dysmorphol·2009
5-case
Simultaneous quantification of GM1 and GM2 gangliosides by isotope dilution tandem mass spectrometry.
PMID 18241673·Clin Biochem·2008
8-other
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.
PMID 17277775·Nat Genet·2007
5-case
Global gene expression in a type 2 Gaucher disease brain.
PMID 15589115·Mol Genet Metab·2004
4-observational
Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.
PMID 15004558·Nat Genet·2004
7-preclinical
Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation.
PMID 14735585·Am J Med Genet A·2004
5-case
Molecular pathophysiology in Tay-Sachs and Sandhoff diseases as revealed by gene expression profiling.
PMID 12019216·Hum Mol Genet·2002
8-other
Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes.
PMID 12205104·J Med Genet·2002
6-review
Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
PMID 12116202·Am J Med Genet·2002
5-case
Enhanced survival in Sandhoff disease mice receiving a combination of substrate deprivation therapy and bone marrow transplantation.
PMID 11133779·Blood·2001
7-preclinical
Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.
PMID 11702212·Hum Genet·2001
8-other
Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation.
PMID 11005868·Proc Natl Acad Sci U S A·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 575 BOYLSTON ST, 6TH FL
BOSTON, MA 02116 - Phone
- (617) 414-9600
Quick Facts
- NPI
- 1740233063
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 54
- Publications
- 20
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