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ALI TOPALOGLU, M.D.
M.D.
Pediatric Endocrinology Physician
NPI: 1265896807Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
292230(MA)
Pediatric Endocrinology PhysicianPrimary
Pediatrics — Pediatric Endocrinology
Code: 2080P0205X
292230(MA)965-L(MS)
Research & Publications (20)
Influence of metabolic control on growth in homocystinuria due to cystathionine B-synthase deficiency.
PMID 11385140·Pediatr Res·2001
8-other
Metabolic acidosis in a patient with type 1 diabetes mellitus complicated by methanol and amitriptyline intoxication.
PMID 19106720·Eur J Emerg Med·2009
5-case
TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction.
PMID 19079066·Nat Genet·2009
5-case
Ambulatory blood pressure monitoring and serum nitric oxide concentration in type 1 diabetic children.
PMID 19225212·Endocr J·2009
8-other
P450c17 deficiency: clinical and molecular characterization of six patients.
PMID 17192295·J Clin Endocrinol Metab·2007
5-case
Athyreosis, dysgenesis, and dyshormonogenesis in congenital hypothyroidism.
PMID 17551472·Pediatr Endocrinol Rev·2006
6-review
Molecular genetic analysis of normosmic hypogonadotropic hypogonadism in a Turkish population: identification and detailed functional characterization of a novel mutation in the gonadotropin-releasing hormone receptor gene.
PMID 17179725·Neuroendocrinology·2006
7-preclinical
Crigler-Najjar syndrome type II caused by a homozygous triple mutation [T-3279G, A(TA)7TAA, and H39D] of UGT1A1.
PMID 16456422·J Pediatr Gastroenterol Nutr·2006
5-case
Bone calcium changes during diabetic ketoacidosis: a comparison with lactic acidosis due to volume depletion.
PMID 15869925·Bone·2005
4-observational
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.
PMID 15220213·Diabetes·2004
8-other
Bone mineral changes in acute metabolic acidosis due to acute gastroenteritis.
PMID 15592794·Calcif Tissue Int·2004
4-observational
Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.
PMID 15292359·J Clin Endocrinol Metab·2004
5-case
Growth hormone and insulin-like growth factor 1 levels and their relation to survival in children with bacterial sepsis and septic shock.
PMID 15009554·J Paediatr Child Health·2004
8-other
Three children with triple A syndrome due to a mutation (R478X) in the AAAS gene.
PMID 14646395·Horm Res·2004
5-case
Extremely immature infant who developed clitoromegaly during the second month of her postnatal life probably due to frequent whole blood transfusion from an adult male.
PMID 12828595·Pediatr Int·2003
5-case
Urinary N-acetyl-beta-D-glucosaminidase activity in type I diabetes mellitus.
PMID 12768043·Indian Pediatr·2003
8-other
Serum IL-1, IL-2, TNFalpha and INFgamma levels of patients with type 1 diabetes mellitus and their siblings.
PMID 12713258·J Pediatr Endocrinol Metab·2003
3-trial
Evaluation of cerebral maturation by visual and quantitative analysis of resting electroencephalography in children with primary nocturnal enuresis.
PMID 11669343·J Child Neurol·2001
8-other
Chronic mercury intoxication simulating pheochromocytoma: effect of captopril on urinary mercury excretion.
PMID 11472594·Pediatr Int·2001
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
- 55 FRUIT ST
BOSTON, MA 02114 - Phone
- (617) 724-1655
Quick Facts
- NPI
- 1265896807
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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