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Journal of Pediatric Ophthalmology and Strabismus|January 1, 1988
Congenital glaucoma associated with cutis marmorata telangiectatica congenita: two case reportsS E Sato, J Herschler, P J Lynch, et al.Journal of Medical Genetics|April 1, 1997
Detection of a novel mutation in the ryanodine receptor gene in an Irish malignant hyperthermia pedigree: correlation of the IVCT response with the affected and unaffected haplotypesK E Keating, L Giblin, P J Lynch, et al.BMC Pediatrics|February 4, 2016
Prediction of congenital hypothyroidism based on initial screening thyroid-stimulating-hormoneDavid S Saleh, Sarah Lawrence, Michael T Geraghty, et al.Pediatric Diabetes|March 26, 2011
Microvascular complications assessment in adolescents with 2- to 5-yr duration of type 1 diabetes from 1990 to 2006Yoon Hi Cho, Maria E Craig, Stephen Hing, et al.Pediatric Diabetes|November 19, 2016
Reduced prevalence of impaired awareness of hypoglycemia in a population-based clinic sample of youth with type 1 diabetesMary B Abraham, Patricia H Gallego, Wade M Brownlee, et al.Diabetes Care|March 12, 2008
Plantar fascia thickness, a measure of tissue glycation, predicts the development of complications in adolescents with type 1 diabetesMaria E Craig, Anthony C Duffin, Patricia H Gallego, et al.Anesthesiology|March 1, 1997
Identification of heterozygous and homozygous individuals with the novel RYR1 mutation Cys35Arg in a large kindredP J Lynch, R Krivosic-Horber, H Reyford, et al.Human Pathology|May 1, 1985
The immunoarchitecture of cutaneous pseudolymphomaD P Wirt, T M Grogan, C S Jolley, et al.Archives of Dermatology|September 2, 1998
The pathophysiological significance of nondesmoglein targets of pemphigus autoimmunity. Development of antibodies against keratinocyte cholinergic receptors in patients with pemphigus vulgaris and pemphigus foliaceusT N Vu, T X Lee, A Ndoye, et al.Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core diseaseP J Lynch, J Tong, M Lehane, et al.Pageof 8