Theodore W AvRuskin

Summary

Affiliation: Brookdale University Hospital and Medical Center
Country: USA

Publications

  1. ncbi request reprint Transient neonatal diabetes mellitus, type 4, type 1 diabetes mellitus, or MODY: which disease is it, anyway?
    Theodore W AvRuskin
    Department of Pediatrics, The Brookdale University Hospital and Medical Center, State University of New York at Brooklyn, 11212 3198, USA
    J Pediatr Endocrinol Metab 15:629-36. 2002
  2. ncbi request reprint Familial dysalbuminemic hyperthyroxinemia: a rare example of albumin polymorphism and its rapid molecular diagnosis
    Theodore W AvRuskin
    Department of Pediatrics, The Brookdale University Hospital and Medical Center, State University of New York at Brooklyn, 11212 3198, USA
    J Pediatr Endocrinol Metab 15:801-7. 2002
  3. ncbi request reprint Monozygotic twins with congenital adrenal hyperplasia: long-term endocrine evaluation and gene analysis
    Theodore W AvRuskin
    Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, The Brookdale University Hospital and Medical Center, State University of New York at Brooklyn, NY 11212 3198, USA
    J Pediatr Endocrinol Metab 16:565-70. 2003
  4. ncbi request reprint Congenital adrenal hypoplasia and male pseudohermaphroditism due to DAX1 mutation, SF1 mutation or neither: a patient report
    Theodore W AvRuskin
    The Brookdale University Hospital and Medical Center, Department of Pediatrics, Division of Endocrinology and Metabolism and State University of New York, Health Sciences Center, Brooklyn, NY 11212 3198, USA
    J Pediatr Endocrinol Metab 17:1125-32. 2004
  5. pmc Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc
    Chan Jong Kim
    Department of Pediatrics, University of California San Francisco, San Francisco, California 94143 0978, USA
    J Clin Endocrinol Metab 93:696-702. 2008

Collaborators

Detail Information

Publications5

  1. ncbi request reprint Transient neonatal diabetes mellitus, type 4, type 1 diabetes mellitus, or MODY: which disease is it, anyway?
    Theodore W AvRuskin
    Department of Pediatrics, The Brookdale University Hospital and Medical Center, State University of New York at Brooklyn, 11212 3198, USA
    J Pediatr Endocrinol Metab 15:629-36. 2002
    ..These data suggest that, despite changing presentations of diabetes mellitus over time, the islets continued to process proinsulin, although the patient required insulin therapy...
  2. ncbi request reprint Familial dysalbuminemic hyperthyroxinemia: a rare example of albumin polymorphism and its rapid molecular diagnosis
    Theodore W AvRuskin
    Department of Pediatrics, The Brookdale University Hospital and Medical Center, State University of New York at Brooklyn, 11212 3198, USA
    J Pediatr Endocrinol Metab 15:801-7. 2002
    ..Analysis linking the FDH mutation to the Sac-1 polymorphism in this family was not informative. DNA analysis is a rapid and simple method to diagnose FDH in individuals with euthyroid hyperthyroxinemia...
  3. ncbi request reprint Monozygotic twins with congenital adrenal hyperplasia: long-term endocrine evaluation and gene analysis
    Theodore W AvRuskin
    Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, The Brookdale University Hospital and Medical Center, State University of New York at Brooklyn, NY 11212 3198, USA
    J Pediatr Endocrinol Metab 16:565-70. 2003
    ..Parental DNA samples confirmed that the mutations were on different alleles...
  4. ncbi request reprint Congenital adrenal hypoplasia and male pseudohermaphroditism due to DAX1 mutation, SF1 mutation or neither: a patient report
    Theodore W AvRuskin
    The Brookdale University Hospital and Medical Center, Department of Pediatrics, Division of Endocrinology and Metabolism and State University of New York, Health Sciences Center, Brooklyn, NY 11212 3198, USA
    J Pediatr Endocrinol Metab 17:1125-32. 2004
    ..A Wnt-4 defect was not evaluated...
  5. pmc Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc
    Chan Jong Kim
    Department of Pediatrics, University of California San Francisco, San Francisco, California 94143 0978, USA
    J Clin Endocrinol Metab 93:696-702. 2008
    ....