E Spellacy
Overview
Explore the profile of E Spellacy including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
18
Citations
238
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0
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Recent Articles
1.
Spellacy E
J Obstet Gynecol Neonatal Nurs
. 2001 Nov;
30(6):634-41.
PMID: 11724199
Objective: To describe the incidence of urinary incontinence (UI) during pregnancy and the puerperium and to identify potential contributing factors. Design: A descriptive correlational design, using participant interviews and reviews...
2.
Watts R, HARKNESS R, Spellacy E, Taylor N
J Inherit Metab Dis
. 1987 Jan;
10(3):210-23.
PMID: 2828760
There is a failure of growth in hypoxanthine guanine phosphoribosyltransferase deficiency; slow weight gain is marked after the second year of age but is apparent in the birth weights of...
3.
Watts R, Spellacy E, Adams J
J Inherit Metab Dis
. 1986 Jan;
9(3):261-72.
PMID: 3099070
We report studies on two patients (1 and 2) with Hurler disease. They both had all of the non-neurological features of Hurler disease to a similar and extreme degree and...
4.
Histopathological studies of the temporal bones in Hurler's disease [mucopolysaccharidosis (MPS) IH]
FRIEDMANN I, Spellacy E, CROW J, Watts R
J Laryngol Otol
. 1985 Jan;
99(1):29-41.
PMID: 3918131
The structural basis of the combined conductive and sensorineural deafness has been described in two patients with Hurler's disease. All parts of the ear contained numerous large vacuolated Hurler cells,...
5.
Shull R, Helman R, Spellacy E, CONSTANTOPOULOS G, Munger R, Neufeld E
Am J Pathol
. 1984 Mar;
114(3):487-95.
PMID: 6320652
This report presents the necropsy and biochemical findings on the first dog to die with alpha-L-iduronidase deficiency (mucopolysaccharidosis I, MPS I). Gross pathologic features, light- and electron-microscopic findings, and tissue...
6.
Spellacy E, Shull R, CONSTANTOPOULOS G, Neufeld E
Proc Natl Acad Sci U S A
. 1983 Oct;
80(19):6091-5.
PMID: 6412235
A disease discovered in three Plott Hound littermates was found to be associated with a profound and specific deficiency of alpha-L-iduronidase (mucopolysaccharide alpha-L-iduronohydrolase; EC 3.2.1.76) in fibroblasts and leukocytes. The...
7.
CROW J, Gibbs D, Cozens W, Spellacy E, Watts R
J Clin Pathol
. 1983 Apr;
36(4):415-30.
PMID: 6403596
Biochemical and pathological observations on tissues from two patients with Hurler disease (mucopolysaccharidosis IH; alpha-L-iduronidase deficiency) who had been treated by fibroblast transplants as a means of enzyme replacement treatment...
8.
Gibbs D, Spellacy E, Tompkins R, Watts R, Mowbray J
J Inherit Metab Dis
. 1983 Jan;
6(2):62-81.
PMID: 6410119
This paper reports the clinical and biochemical results in six patients with Hurler disease (Mucopolysaccharidosis IH; McKusick 25280), two patients with Hunter disease (Mucopolysaccharidosis II; McKusick 25285) and one patient...
9.
Shull R, Munger R, Spellacy E, Hall C, CONSTANTOPOULOS G, Neufeld E
Am J Pathol
. 1982 Nov;
109(2):244-8.
PMID: 6215865
No abstract available.
10.
Watts R, Spellacy E, Gibbs D, Allsop J, McKeran R, Slavin G
Q J Med
. 1982 Jan;
51(201):43-78.
PMID: 7111674
No abstract available.