Publication Type:

Journal Article

Authors:

Kumar, S.

Source:

Pediatric Diabetes, Volume 11, Number 1, p.28-37 (2010)

URL:

http://www.scopus.com/inward/record.url?eid=2-s2.0-77954435633&partnerID=40&md5=4db07e0bcd816207d6cde25f8c76c75b

Keywords:

adolescent, adult, anemia, behavior disorder, bladder dysfunction, child, cholinergic receptor blocking agent, clinical feature, congenital heart disease, congenital rubella syndrome, diabetes insipidus, diabetes mellitus, Diagnosis, Differential, differential diagnosis, endoplasmic reticulum, endoplasmic reticulum intermembrane small protein, female, gene mutation, growth hormone deficiency, hearing impairment, Helicobacter infection, heterozygote, HLA antigen, human, Humans, hypogonadism, infant, insulin, insulin dependent diabetes mellitus, intermittent catheterization, joint limitation, Leber hereditary optic neuropathy, male, membrane protein, Membrane Proteins, mental disease, mitochondrial DNA, neurological complication, newborn, optic nerve atrophy, pediatrician, peptic ulcer, perception deafness, Preschool, prevalence, priority journal, protein localization, review, short stature, Type 1, unclassified drug, urinary tract disease, vasopressin, WFS1 protein, WFS2 protein, Wolfram syndrome, wolframin, Young Adult, ZCD2 protein

Abstract:

Kumar S. Wolfram syndrome: important implications for pediatricians and pediatric endocrinologists. © 2009 John Wiley & Sons A/S.

Notes:

cited By (since 1996)16

Cite this Research Publication

S. Kumar, “Wolfram syndrome: Important implications for pediatricians and pediatric endocrinologists”, Pediatric Diabetes, vol. 11, pp. 28-37, 2010.