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FRANCESCO DE LUCA, M.D.
M.D.
Pediatric Endocrinology Physician
NPI: 1649228040Individual
Specialties, Licenses & Credentials
Pediatric Endocrinology PhysicianPrimary
Pediatrics — Pediatric Endocrinology
Code: 2080P0205X
2017040671(MO)
Research & Publications (20)
Severe SHOX gene haploinsufficiency in a girl with a novel mutation (M1T) involving the first codon of coding region.
PMID 19636220·J Endocrinol Invest·2010
5-case
Graves' disease prevalence in a young population with Turner syndrome.
PMID 19542755·J Endocrinol Invest·2010
8-other
Association of five autoimmune diseases in a young woman with Down's syndrome.
PMID 19574731·J Endocrinol Invest·2010
5-case
Recovery of acanthosis nigricans under prolonged metformin treatment in an adolescent with normal weight.
PMID 19494716·J Endocrinol Invest·2009
5-case
P450 oxidoreductase expressed in rat chondrocytes modulates chondrogenesis via cholesterol- and Indian Hedgehog-dependent mechanisms.
PMID 19264869·Endocrinology·2009
7-preclinical
Menarcheal timing in intensively treated girls with type 1 diabetes mellitus.
PMID 18554878·Nutr Metab Cardiovasc Dis·2009
8-other
Effects of moderate-severe exercise on blood glucose in Type 1 diabetic adolescents treated with insulin pump or glargine insulin.
PMID 19474521·J Endocrinol Invest·2009
8-other
Characterization of the heat shock protein 90 gene in the plant parasitic nematode Meloidogyne artiellia and its expression as related to different developmental stages and temperature.
PMID 19348876·Gene·2009
7-preclinical
Pulmonary autoimmunity as a feature of autoimmune polyendocrine syndrome type 1 and identification of KCNRG as a bronchial autoantigen.
PMID 19251657·Proc Natl Acad Sci U S A·2009
8-other
Crystal structure of the OXA-48 beta-lactamase reveals mechanistic diversity among class D carbapenemases.
PMID 19477418·Chem Biol·2009
8-other
Novel mutation of CYP21A2 gene (N387K) affecting a non-conserved amino acid residue in exon 9.
PMID 19474522·J Endocrinol Invest·2009
5-case
Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives.
PMID 18616706·Clin Endocrinol (Oxf)·2009
8-other
11-Hydroxylase deficiency as a cause of pre-pubertal gynecomastia.
PMID 19636210·J Endocrinol Invest·2009
5-case
Chronic inflammatory demyelinating polyneuropathy as a possible novel component of autoimmune poly-endocrine-candidiasis-ectodermal dystrophy.
PMID 18461357·Eur J Pediatr·2009
5-case
IND-6, a highly divergent IND-type metallo-beta-lactamase from Chryseobacterium indologenes strain 597 isolated in Burkina Faso.
PMID 19651915·Antimicrob Agents Chemother·2009
8-other
Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescence.
PMID 19074464·Eur J Endocrinol·2009
8-other
Bifid T waves in leads V2 and V3 in children: a normal variant.
PMID 19558653·Ital J Pediatr·2009
8-other
Stimulatory effects of insulin-like growth factor-I on growth plate chondrogenesis are mediated by nuclear factor-kappaB p65.
PMID 18922796·J Biol Chem·2008
7-preclinical
PPNEMA: A resource of plant-parasitic nematodes multialigned ribosomal cistrons.
PMID 18818776·Int J Plant Genomics·2008
8-other
Morphological and molecular characterization of Pratylenchus lentis n. sp. (Nematoda: Pratylenchidae) from Sicily.
PMID 19440258·J Nematol·2008
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
- 2401 GILLHAM RD
KANSAS CITY, MO 64108 - Phone
- (816) 234-3000
Quick Facts
- NPI
- 1649228040
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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