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RASILA LALA, M.D
M.D
Specialist
NPI: 1669532586Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
1195901-1(NY)
Research & Publications (20)
Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot study.
PMID 18313203·Ultrasound Med Biol·2008
8-other
Multiple bone fractures in an 8-year-old child with cow's milk allergy and inappropriate calcium supplementation.
PMID 17587794·Ann Nutr Metab·2007
5-case
Persistent hyperestrogenism after precocious puberty in young females with McCune-Albright syndrome.
PMID 17982390·Pediatr Endocrinol Rev·2007
6-review
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family.
PMID 16567474·J Clin Pathol·2006
5-case
Laparoscopic management of ovarian cysts in peripheral precocious puberty of McCune-Albright syndrome.
PMID 16789619·J Pediatr Endocrinol Metab·2006
5-case
McCune-Albright syndrome: persistence of autonomous ovarian hyperfunction during adolescence and early adult age.
PMID 16789624·J Pediatr Endocrinol Metab·2006
8-other
Bisphosphonate treatment of bone fibrous dysplasia in McCune-Albright syndrome.
PMID 16789621·J Pediatr Endocrinol Metab·2006
3-trial
Endocrine function and water metabolism in children and adolescents with surgically treated intra/parasellar tumors.
PMID 15570985·J Pediatr Endocrinol Metab·2004
8-other
Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males.
PMID 15520771·J Pediatr·2004
8-other
Homeobox HOXA10 gene analysis in cryptorchidism.
PMID 14960020·J Pediatr Endocrinol Metab·2004
8-other
Bone mass and metabolism in thalassemic children and adolescents treated with different iron-chelating drugs.
PMID 14691688·J Bone Miner Metab·2004
3-trial
Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society.
PMID 12703030·J Pediatr Orthop B·2003
4-observational
Pubertal development in patients with McCune-Albright syndrome or pseudohypoparathyroidism.
PMID 12729407·J Pediatr Endocrinol Metab·2003
6-review
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
PMID 12621129·Pediatr Res·2003
8-other
Impact of endocrine hyperfunction and phosphate wasting on bone in McCune-Albright syndrome.
PMID 12199350·J Pediatr Endocrinol Metab·2002
6-review
Pamidronate treatment in bone fibrous dysplasia in children and adolescents with McCune-Albright syndrome.
PMID 12199352·J Pediatr Endocrinol Metab·2002
3-trial
Searching for Arg201 mutations in the GNAS1 gene in Italian patients with McCune-Albright syndrome.
PMID 12199346·J Pediatr Endocrinol Metab·2002
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
- 234 E 149TH ST, ROOM 232
BRONX, NY 10451 - Phone
- (718) 579-5360
Quick Facts
- NPI
- 1669532586
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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