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MARIE MONTFORT, MD
MD
Family Medicine Physician
NPI: 1215015128Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
A73753(CA)
Research & Publications (17)
Expression and functional characterization of human mutant sulfamidase in insect cells.
PMID 15542396·Mol Genet Metab·2004
4-observational
Functional analysis of 13 GBA mutant alleles identified in Gaucher disease patients: Pathogenic changes and "modifier" polymorphisms.
PMID 15146461·Hum Mutat·2004
7-preclinical
Adult blood vessels restore host hematopoiesis following lethal irradiation.
PMID 12160847·Exp Hematol·2002
7-preclinical
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred.
PMID 19153782·Neurogenetics·2009
8-other
Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlation.
PMID 17324573·Neuromuscul Disord·2007
8-other
Directed antigen delivery as a vaccine strategy for an intracellular bacterial pathogen.
PMID 16549792·Proc Natl Acad Sci U S A·2006
7-preclinical
[Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene].
PMID 15885549·Arch Pediatr·2005
5-case
The development of functional CD8 T cell memory after Listeria monocytogenes infection is not dependent on CD40.
PMID 15356158·J Immunol·2004
7-preclinical
A signal through OX40 (CD134) allows anergic, autoreactive T cells to acquire effector cell functions.
PMID 15153490·J Immunol·2004
7-preclinical
Clinical features and neuroradiological findings of mitochondrial pathology in six neonates.
PMID 12420122·Childs Nerv Syst·2002
5-case
Mutation and haplotype analyses in 26 Spanish Sanfilippo syndrome type A patients: possible single origin for 1091delC mutation.
PMID 11343308·Am J Med Genet·2001
8-other
Differential healing response of bone adjacent to porous implants coated with hydroxyapatite and 45S5 bioactive glass.
PMID 11288089·J Biomed Mater Res·2001
4-observational
Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expression.
PMID 10967146·Mamm Genome·2000
8-other
On the age of the most prevalent Gaucher disease-causing mutation, N370S.
PMID 10801390·Am J Hum Genet·2000
8-other
Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failure.
PMID 10731063·Pediatr Transplant·2000
5-case
Mechanical strength of fracture callus in osteopenic bone at different phases of healing.
PMID 10716378·J Orthop Trauma·2000
4-observational
Assessment of resorbable bioactive material for grafting of critical-size cancellous defects.
PMID 10716290·J Orthop Res·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
- 4601 DALE RD
MODESTO, CA 95356 - Phone
- (209) 557-1000
Quick Facts
- NPI
- 1215015128
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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