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PAUL LATOUR, M.D.
M.D.
Dermatology Physician
NPI: 1619976412Individual
Specialties, Licenses & Credentials
Dermatology PhysicianPrimary
Dermatology
Code: 207N00000X
MD11106(TN)
Research & Publications (20)
[Multiple phenotypic manifestations of X-linked spinobulbar muscular atrophy].
PMID 18667219·Rev Neurol (Paris)·2009
5-case
Relapsing demyelinating disease affecting both the central and peripheral nervous systems.
PMID 18208860·J Neurol Neurosurg Psychiatry·2008
5-case
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findings.
PMID 18394888·Neuromuscul Disord·2008
5-case
Human dendritic cells pulsed with specific lipopeptides stimulate autologous antigen-specific T cells without the addition of exogenous maturation factors.
PMID 18637077·J Viral Hepat·2008
8-other
Clinical, electrophysiological and genetic studies of two families with mutations in the GDAP1 gene.
PMID 18991200·Neuropediatrics·2008
5-case
Trichobilharzia spp. in natural conditions in Annecy Lake, France.
PMID 18320223·Parasitol Res·2008
7-preclinical
A new MPZ mutation associated with a mild CMT1 phenotype presenting with recurrent nerve compression.
PMID 18663734·Muscle Nerve·2008
5-case
NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement.
PMID 17142040·Neuromuscul Disord·2007
5-case
Hereditary hemochromatosis and movement disorders: the still controversial relationship. Response to Russo et al. in J Neurol (2004) 251:849-852.
PMID 16096812·J Neurol·2006
8-other
Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.
PMID 16373087·Neuromuscul Disord·2006
4-observational
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations.
PMID 16787513·J Peripher Nerv Syst·2006
4-observational
A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies.
PMID 15955700·Neuromuscul Disord·2005
4-observational
Charcot-Marie-Tooth disease type 1A: clinicopathological correlations in 24 patients.
PMID 15703022·J Peripher Nerv Syst·2005
8-other
Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthase.
PMID 16021469·Hum Genet·2005
8-other
[Encephalopathy and acute renal failure during acyclovir treatment].
PMID 15247861·Rev Neurol (Paris)·2004
5-case
Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene.
PMID 15019704·Neuromuscul Disord·2004
4-observational
Drug induced encephalopathy in six epileptic patients: topiramate? valproate? or both?
PMID 15079854·Hum Psychopharmacol·2004
5-case
Peripheral nerve biopsy study in 19 cases with 17p11.2 deletion.
PMID 15581184·J Neuropathol Exp Neurol·2004
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 740 COOL SPRINGS BLVD, SUITE 200
FRANKLIN, TN 37067 - Phone
- (615) 771-1881
Quick Facts
- NPI
- 1619976412
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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