Proud VK - Search Results

1

Students online: learning medical genetics.

Proud VK, Johnson ED, Mitchell JA. Proud VK, et al. Am J Hum Genet. 1993 Mar;52(3):637-42. Am J Hum Genet. 1993. PMID: 8447329 Free PMC article.

2

Medical students using Grateful Med: analysis of failed searches and a six-month follow-up study.

Mitchell JA, Johnson ED, Hewett JE, Proud VK. Mitchell JA, et al. Among authors: proud vk. Comput Biomed Res. 1992 Feb;25(1):43-55. doi: 10.1016/0010-4809(92)90034-8. Comput Biomed Res. 1992. PMID: 1547626

3

Teaching human genetics in biochemistry by computer literature searching.

Proud VK, Schmidt FJ, Johnson ED, Mitchell JA. Proud VK, et al. Am J Hum Genet. 1989 Apr;44(4):597-604. Am J Hum Genet. 1989. PMID: 2648820 Free PMC article.

4

New thoughts about medical students as effective searchers of MEDLINE.

Mitchell JA, Johnson ED, Proud VK. Mitchell JA, et al. Among authors: proud vk. Acad Med. 1990 Jul;65(7):434-7. doi: 10.1097/00001888-199007000-00003. Acad Med. 1990. PMID: 2242194 No abstract available.

5

Updating McKusick: an educational exercise for medical students.

Bodurtha JN, Townsend JI, Proud VK, Nance WE. Bodurtha JN, et al. Among authors: proud vk. Am J Med Genet. 1986 Jul;24(3):505-11. doi: 10.1002/ajmg.1320240313. Am J Med Genet. 1986. PMID: 3728569

6

New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum.

Proud VK, Levine C, Carpenter NJ. Proud VK, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):458-66. doi: 10.1002/ajmg.1320430169. Am J Med Genet. 1992. PMID: 1605226

7

Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene.

Kernohan KD, Dyment DA, Pupavac M, Cramer Z, McBride A, Bernard G, Straub I, Tetreault M, Hartley T, Huang L, Sell E, Majewski J, Rosenblatt DS, Shoubridge E, Mhanni A, Myers T, Proud V, Vergano S, Spangler B, Farrow E, Kussman J, Safina N; Care4Rare Consortium; Saunders C, Boycott KM, Thiffault I. Kernohan KD, et al. Hum Mutat. 2017 May;38(5):511-516. doi: 10.1002/humu.23196. Epub 2017 Mar 6. Hum Mutat. 2017. PMID: 28185376

8

Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical Genetics.

Alford RL, Friedman TB, Keats BJ, Kimberling WJ, Proud VK, Smith RJ, Arnos KS, Korf BR, Rehm HL, Toriello HV. Alford RL, et al. Among authors: proud vk. Genet Med. 2003 Jul-Aug;5(4):338-41. doi: 10.1097/01.GIM.0000077415.19887.08. Genet Med. 2003. PMID: 12865764

9

Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus.

Kaler SG, Gallo LK, Proud VK, Percy AK, Mark Y, Segal NA, Goldstein DS, Holmes CS, Gahl WA. Kaler SG, et al. Among authors: proud vk. Nat Genet. 1994 Oct;8(2):195-202. doi: 10.1038/ng1094-195. Nat Genet. 1994. PMID: 7842019

10

Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program.

Wolf B, Heard GS, Jefferson LG, Proud VK, Nance WE, Weissbecker KA. Wolf B, et al. Among authors: proud vk. N Engl J Med. 1985 Jul 4;313(1):16-9. doi: 10.1056/NEJM198507043130104. N Engl J Med. 1985. PMID: 4000223 Free article.

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