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LEFKOTHEA KARAVITI, MD
MD
Pediatric Endocrinology Physician
NPI: 1609956960Individual
Specialties, Licenses & Credentials
Pediatric Endocrinology PhysicianPrimary
Pediatrics — Pediatric Endocrinology
Code: 2080P0205X
J0548(TX)
Research & Publications (13)
Pituitary and systemic autoimmunity in a case of intrasellar germinoma.
PMID 19466616·Pituitary·2011
5-case
X-linked hypophosphatemic rickets associated with respiratory failure.
PMID 18057152·Clin Pediatr (Phila)·2008
5-case
Rapid resolution of consumptive hypothyroidism in a child with hepatic hemangioendothelioma following liver transplantation.
PMID 17709695·Ann Clin Lab Sci·2007
5-case
Ethical and legal implications of genetic testing in androgen insensitivity syndrome.
PMID 17382127·J Pediatr·2007
5-case
Osteopenic effects of MgSO4 in multiple pregnancies.
PMID 17172083·J Pediatr Endocrinol Metab·2006
8-other
Variable presentation of precocious puberty associated with the D564G mutation of the LHCGR gene in children with testotoxicosis.
PMID 16887451·J Pediatr·2006
5-case
Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults.
PMID 16611713·J Am Soc Nephrol·2006
8-other
Neonatal diabetes mellitus: patient reports and review of current knowledge and clinical practice.
PMID 16459456·J Pediatr Endocrinol Metab·2005
6-review
Insulin pump therapy in preschool children with type 1 diabetes mellitus improves glycemic control and decreases glucose excursions and the risk of hypoglycemia.
PMID 16386093·Diabetes Technol Ther·2005
3-trial
Continuous glucose monitoring and the reality of metabolic control in preschool children with type 1 diabetes.
PMID 15562201·Diabetes Care·2004
8-other
von Voss-Cherstvoy syndrome with transient thrombocytopenia and normal psychomotor development.
PMID 15054846·Am J Med Genet A·2004
5-case
Concordance of phenotypic expression and gender identity in a large kindred with a mutation in the androgen receptor.
PMID 14756668·Clin Genet·2004
5-case
Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene.
PMID 11701710·J Clin Endocrinol Metab·2001
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6701 FANNIN ST
HOUSTON, TX 77030 - Phone
- (832) 822-2778
Quick Facts
- NPI
- 1609956960
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 13
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