Leonard CO - Search Results

1

Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiency.

Spence JE, Maddalena A, O'Brien WE, Fernbach SD, Batshaw ML, Leonard CO, Beaudet AL. Spence JE, et al. Among authors: leonard co. J Pediatr. 1989 Apr;114(4 Pt 1):582-8. doi: 10.1016/s0022-3476(89)80697-3. J Pediatr. 1989. PMID: 2564432 Free article.

2

Late-onset ornithine transcarbamylase deficiency in male patients.

Finkelstein JE, Hauser ER, Leonard CO, Brusilow SW. Finkelstein JE, et al. Among authors: leonard co. J Pediatr. 1990 Dec;117(6):897-902. doi: 10.1016/s0022-3476(05)80129-5. J Pediatr. 1990. PMID: 2246687 Free article.

3

Ornithine transcarbamylase deficiency: neuropathologic changes acquired in utero.

Filloux F, Townsend JJ, Leonard C. Filloux F, et al. J Pediatr. 1986 Jun;108(6):942-5. doi: 10.1016/s0022-3476(86)80935-0. J Pediatr. 1986. PMID: 3712162 No abstract available.

4

Spina bifida: a new disease.

Leonard CO, Freeman JM. Leonard CO, et al. Pediatrics. 1981 Jul;68(1):136-7. Pediatrics. 1981. PMID: 7017581 No abstract available.

5

Letter: Late sequelae of aberrant intrauterine bands.

Leonard CO, Riccardi VM. Leonard CO, et al. J Pediatr. 1974 Sep;85(3):434-5. doi: 10.1016/s0022-3476(74)80137-x. J Pediatr. 1974. PMID: 4431505 No abstract available.

6

Living with phenylketonuria: perspectives of patients and their families.

Bilginsoy C, Waitzman N, Leonard CO, Ernst SL. Bilginsoy C, et al. Among authors: leonard co. J Inherit Metab Dis. 2005;28(5):639-49. doi: 10.1007/s10545-005-4478-8. J Inherit Metab Dis. 2005. PMID: 16151894

7

Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndrome.

Rauch A, Feindt KA, Leonard CO, Thompson JA, Hoffman RO, Creel DJ, Opitz JM. Rauch A, et al. Among authors: leonard co. Am J Med Genet. 1999 Jan 15;82(2):194-8. doi: 10.1002/(sici)1096-8628(19990115)82:2<194::aid-ajmg18>3.0.co;2-7. Am J Med Genet. 1999. PMID: 9934988

8

Pituitary macroadenoma and cranial osteoma in a manifesting heterozygote with the Opitz G/BBB syndrome.

Brooks JK, Leonard CO, Zawadzki JK, Ommaya AK, Levy BA, Orenstein JM. Brooks JK, et al. Among authors: leonard co. Am J Med Genet. 1998 Nov 16;80(3):291-3. doi: 10.1002/(sici)1096-8628(19981116)80:3<291::aid-ajmg23>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9843057 No abstract available.

9

Testing for inborn errors of metabolism in the acutely ill newborn.

Leonard CO, Nuttall KL. Leonard CO, et al. Ann Clin Lab Sci. 1997 Jan-Feb;27(1):34-40. Ann Clin Lab Sci. 1997. PMID: 8997455

10

Children and adolescents with neurofibromatosis 1: a behavioral phenotype.

Dilts CV, Carey JC, Kircher JC, Hoffman RO, Creel D, Ward K, Clark E, Leonard CO. Dilts CV, et al. Among authors: leonard co. J Dev Behav Pediatr. 1996 Aug;17(4):229-39. J Dev Behav Pediatr. 1996. PMID: 8856518

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

36 results

Search Page

Filters