Urine catecholamine levels as diagnostic markers for neuroblastoma in a defined population: implications for ophthalmic practice

Author:

Smith S J,Diehl N N,Smith B D,Mohney B G

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Reference26 articles.

1. Smith S, Diehl N, Smith B, Mohney B . Incidence, Ocular Manifestations, and Survival in Children with Neuroblastoma: A Population-Based Study. Am J Ophthalmol 2010; 149 (4): 677–682.e2.

2. Castleberry RP . Biology and Treatment of Neuroblastoma. Pediatr Clin North Am 1997; 44: 919–937.

3. Laug WE, Siegel SE, Shaw KNF, Landing B, Baptista J, Gutenstein M . Initial Urinary Catecholamine Metabolite Concentrations and Prognosis in Neuroblastoma. Pediatrics 1978; 62: 77–83.

4. LaBrosse EH, Com-Nougue C, Zucker JM, Comoy E, Bohuon C, Lemerle J et al. Urinary excretion of 3-methoxy-4-hydroxymandelic acid and 3-methoxy-4-hydroxyphenylacetic acid by 288 patients with neuroblastoma and related neural crest tumors. Cancer Res 1980; 40: 1995–2001.

5. Mahoney NR, Liu GT, Menacker SJ, Wilson MC, Hogarty MD, Maris JM . Pediatric Horner Syndrome: Etiologies and Roles of Imaging and Urine Studies to Detect Neuroblastoma and Other Responsible Mass Lesions. Am J Ophthalmol 2006; 142: 651–659.

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