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LOUIS VIOLLET, MD, PHD
MD, PHD
Pediatrics Physician
NPI: 1881097947Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
10118502-1205(UT)
Research & Publications (20)
Utility of cystatin C to monitor renal function in Duchenne muscular dystrophy.
PMID 19623638·Muscle Nerve·2009
8-other
Death of CD4+ T cells from lymph nodes during primary SIVmac251 infection predicts the rate of AIDS progression.
PMID 17082581·J Immunol·2006
7-preclinical
Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.
PMID 12112104·Ann Neurol·2002
5-case
The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy.
PMID 19129172·Hum Mol Genet·2009
7-preclinical
Re-examination of the electrocardiogram in boys with Duchenne muscular dystrophy and correlation with its dilated cardiomyopathy.
PMID 19121448·Am J Cardiol·2009
8-other
Early divergence in lymphoid tissue apoptosis between pathogenic and nonpathogenic simian immunodeficiency virus infections of nonhuman primates.
PMID 18032487·J Virol·2008
4-observational
CD4+ CCR5+ T-cell dynamics during simian immunodeficiency virus infection of Chinese rhesus macaques.
PMID 17898067·J Virol·2007
7-preclinical
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
PMID 17634419·Neurology·2007
8-other
TGF-beta in intestinal lymphoid organs contributes to the death of armed effector CD8 T cells and is associated with the absence of virus containment in rhesus macaques infected with the simian immunodeficiency virus.
PMID 17612589·Cell Death Differ·2007
7-preclinical
A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy.
PMID 17609673·Eur J Hum Genet·2007
8-other
The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset.
PMID 17564964·Am J Hum Genet·2007
7-preclinical
A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.
PMID 16728649·Neurology·2006
4-observational
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene.
PMID 17190947·Neurology·2006
8-other
Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells.
PMID 16449324·J Cell Sci·2006
7-preclinical
Brain MRI abnormalities in muscular dystrophy due to FKRP mutations.
PMID 16368217·Brain Dev·2006
8-other
CD8+ T cell dynamics during primary simian immunodeficiency virus infection in macaques: relationship of effector cell differentiation with the extent of viral replication.
PMID 15905532·J Immunol·2005
4-observational
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus.
PMID 16550918·Acta Myol·2005
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 295 S CHIPETA WAY
SALT LAKE CITY, UT 84108 - Phone
- (801) 585-6600
Quick Facts
- NPI
- 1881097947
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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