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FREDERICK POPE, M.D.
M.D.
Psychiatry Physician
NPI: 1093874992Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
NV 3146(NV)
Research & Publications (20)
Paediatric surgical complications of Ehlers-Danlos syndrome.
PMID 19585409·Eur J Pediatr Surg·2014
5-case
An atypical cutaneous presentation of vasculitis with features of Churg-Strauss syndrome, associated with anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane antibodies.
PMID 19558532·Clin Exp Dermatol·2009
5-case
Molecular genetic and clinical review of Ehlers-Danlos Type VIIA: implications for management by the plastic surgeon in a multidisciplinary setting.
PMID 19233756·J Plast Reconstr Aesthet Surg·2009
5-case
Ultraviolet photolysis of HCHO: absolute HCO quantum yields by direct detection of the HCO radical photoproduct.
PMID 18998660·J Phys Chem A·2008
8-other
Ultraviolet absorption spectrum of chlorine peroxide, ClOOCl.
PMID 17474723·J Phys Chem A·2007
8-other
Absorption cross sections of formaldehyde at wavelengths from 300 to 340 nm at 294 and 245 K.
PMID 17034158·J Phys Chem A·2006
4-observational
Kinetics, mechanism, and thermochemistry of the gas phase reaction of atomic chlorine with dimethyl sulfoxide.
PMID 16722703·J Phys Chem A·2006
8-other
Photochemistry of formaldehyde under tropospheric conditions.
PMID 16161778·Faraday Discuss·2005
8-other
Unexpected ultrastructral changes in bone osteiod collagens in osteogenesis imperfecta.
PMID 16182545·Micron·2005
8-other
Autosomal dominant cutis laxa with severe lung disease: synthesis and matrix deposition of mutant tropoelastin.
PMID 15955094·J Invest Dermatol·2005
5-case
Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13.
PMID 12776252·Am J Hum Genet·2003
8-other
Connective tissue naevus (collagenoma) in a patient with benign joint hypermobility syndrome (Ehlers-Danlos syndrome type III).
PMID 12780726·Clin Exp Dermatol·2003
5-case
A glycine to aspartic acid substitution of COL2A1 in a family with the Strudwick variant of spondyloepimetaphyseal dysplasia.
PMID 12925722·QJM·2003
8-other
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.
PMID 14508707·Am J Hum Genet·2003
7-preclinical
Severe panniculitis caused by homozygous ZZ alpha1-antitrypsin deficiency treated successfully with human purified enzyme (Prolastin).
PMID 12452881·Br J Dermatol·2002
5-case
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.
PMID 12214284·Am J Hum Genet·2002
8-other
Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule.
PMID 12205109·J Med Genet·2002
5-case
Pulmonary valvuloplasty in a case of vascular Ehlers-Danlos syndrome.
PMID 12203938·Catheter Cardiovasc Interv·2002
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2980 S RAINBOW BLVD, SUITE 210 G
LAS VEGAS, NV 89146 - Phone
- (702) 401-5471
Quick Facts
- NPI
- 1093874992
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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