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JOSEPH PRUD'HOMME, M.D.
M.D.
Specialist
NPI: 1275571861Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
D0261(TX)
Research & Publications (20)
An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders.
PMID 19554025·J Invest Dermatol·2009
8-other
Biomechanical analysis of medial collateral ligament reconstruction grafts of the elbow.
PMID 18182653·Am J Sports Med·2008
8-other
Confirmation of psoriasis susceptibility loci on chromosome 6p21 and 20p13 in French families.
PMID 17344932·J Invest Dermatol·2007
8-other
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.
PMID 17515546·Neurology·2007
5-case
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
PMID 16822249·Epilepsia·2006
4-observational
Exploration of the genetic architecture of idiopathic generalized epilepsies.
PMID 17054691·Epilepsia·2006
8-other
Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3.
PMID 16436457·Hum Mol Genet·2006
8-other
FIAT represses ATF4-mediated transcription to regulate bone mass in transgenic mice.
PMID 15911876·J Cell Biol·2005
7-preclinical
Infantile convulsions and paroxysmal choreoathetosis in a consanguineous family.
PMID 15165638·Pediatr Neurol·2004
5-case
Rescue of the phenotype of CYP27B1 (1alpha-hydroxylase)-deficient mice.
PMID 15225794·J Steroid Biochem Mol Biol·2004
7-preclinical
CGI-58/ABHD5 gene is mutated in Dorfman-Chanarin syndrome.
PMID 15316960·Am J Med Genet A·2004
8-other
L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1.
PMID 15385440·Hum Mol Genet·2004
8-other
GSK3 beta-dependent phosphorylation of the alpha NAC coactivator regulates its nuclear translocation and proteasome-mediated degradation.
PMID 15005626·Biochemistry·2004
7-preclinical
Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis.
PMID 15317751·Hum Mol Genet·2004
8-other
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome.
PMID 12668616·Hum Mol Genet·2003
8-other
Correction of the abnormal mineral ion homeostasis with a high-calcium, high-phosphorus, high-lactose diet rescues the PDDR phenotype of mice deficient for the 25-hydroxyvitamin D-1alpha-hydroxylase (CYP27B1).
PMID 12689675·Bone·2003
4-observational
Reduced chondrocyte proliferation and chondrodysplasia in mice lacking the integrin-linked kinase in chondrocytes.
PMID 12835312·J Cell Biol·2003
7-preclinical
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
PMID 12915478·Hum Mol Genet·2003
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
- 1015 E IDEL ST
TYLER, TX 75701 - Phone
- (903) 592-8301
Quick Facts
- NPI
- 1275571861
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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