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CAROL CLERICUZIO, MD
MD
Pediatric Adolescent Medicine Physician
NPI: 1922013481Individual
Specialties, Licenses & Credentials
Pediatric Adolescent Medicine PhysicianPrimary
Pediatrics — Adolescent Medicine
Code: 2080A0000X
82-20(NM)
Research & Publications (20)
Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia.
PMID 19367194·Genet Med·2009
8-other
Serum alpha-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia.
PMID 12970646·J Pediatr·2003
5-case
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis).
PMID 19574260·J Med Genet·2010
5-case
Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.
PMID 19537283·Cutis·2009
5-case
Elements of morphology: standard terminology for the hands and feet.
PMID 19125433·Am J Med Genet A·2009
8-other
Bilateral cavernous internal carotid aneurysms in a child with juvenile paget disease and osteoprotegerin deficiency.
PMID 17947367·AJNR Am J Neuroradiol·2008
5-case
Pierre Robin sequence associated with first trimester fetal tamoxifen exposure.
PMID 18629878·Am J Med Genet A·2008
5-case
Acute lymphoblastic leukemia in a patient with Miller-Dieker syndrome.
PMID 18989166·J Pediatr Hematol Oncol·2008
5-case
Comparison of outcomes of arteriovenous grafts and fistulas at a single Veterans' Affairs medical center.
PMID 18823616·Am J Surg·2008
8-other
Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway.
PMID 18798318·Am J Med Genet A·2008
5-case
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.
PMID 18000912·Am J Med Genet A·2007
5-case
Retrospective review of forefoot amputations at a Veterans Affairs hospital and evaluation of post-amputation follow-up.
PMID 17071182·Am J Surg·2006
8-other
Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.
PMID 16770802·Am J Med Genet A·2006
8-other
Risk for leukemia in infants without Down syndrome who have transient myeloproliferative disorder.
PMID 16737888·J Pediatr·2006
5-case
Marshall-Smith syndrome: natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities.
PMID 16086394·Am J Med Genet A·2005
5-case
Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals.
PMID 14699614·Am J Med Genet A·2004
5-case
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.
PMID 15286229·Pediatrics·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
- 2211 LOMAS BLVD NE, ACC THIRD FLOOR
ALBUQUERQUE, NM 87131 - Phone
- (505) 272-5551
Quick Facts
- NPI
- 1922013481
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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