A I Arbisser
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Explore the profile of A I Arbisser including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
41
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Recent Articles
1.
Howell R, Arbisser A, PARSONS D, Scott C, Fraustadt U, Collie W, et al.
Am J Hum Genet
. 1981 Nov;
33(6):957-67.
PMID: 7325159
We have defined a new autosomal recessive disorder in patients stemming from a small community in northern Mexico. Diagnosable at birth, its major symptoms include brittle hair, mental retardation, and...
2.
Drouilhet J, Arbisser A, Mazow M
J Pediatr Ophthalmol
. 1977 Nov;
14(6):368-72.
PMID: 604444
A family is described with hypoplasia of the anterior iris stroma, no angle anomalies, and no glaucoma. The pedigree is suggestive of an autosomal dominant mode of inheritance. This is...
3.
Arbisser A, Donnelly K, Scott Jr C, DIFERRANTE N, Singh J, Stevenson R, et al.
Am J Med Genet
. 1977 Jan;
1(2):195-205.
PMID: 416714
A 14-year-old white girl with mild dysostosis multiplex, odontoid hypoplasia, short stature, cloudy corneas, keratansulfaturia, but without detectable central nervous system abnormalities was referred with the diagnosis of Morquio syndrome....
4.
Arbisser A, Murphree A, Garcia C, Howell R
Am J Ophthalmol
. 1976 Sep;
82(3):465-71.
PMID: 961797
Three patients with typical features of mannosidosis and deficiency of alpha-mannosidase activity, who were examined ophthalmologically, had similar lenticular opacities. Corneal opacities were absent. Chamber angle and striking ophthalmoscopic anomalies...
5.
Arbisser A, Scott Jr C, Howell B
Lancet
. 1976 Feb;
1(7954):312-3.
PMID: 55632
No abstract available.
6.
Arbisser A, Scott Jr C, Howell R, Ong P, Cox Jr H
Birth Defects Orig Artic Ser
. 1976 Jan;
12(5):219-28.
PMID: 953226
We have presented 2 affected sibs-a male and female-with unaffected parents and sib from a small remote northern Mexican village. The syndrome includes mental deficit, brittle hair with decreased cuticular...