Andrews DF - Search Results

1

Relation between apolipoprotein E genotype, hepatitis B virus status, and thyroid status in a sample of older persons with Down syndrome.

Percy ME, Potyomkina Z, Dalton AJ, Fedor B, Mehta P, Andrews DF, Mazzulli T, Murk L, Warren AC, Wallace RA, Chau H, Jeng W, Moalem S, O'Brien L, Schellenberger S, Tran H, Wu L. Percy ME, et al. Among authors: andrews df. Am J Med Genet A. 2003 Jul 15;120A(2):191-8. doi: 10.1002/ajmg.a.20099. Am J Med Genet A. 2003. PMID: 12833399

2

Autoimmune thyroiditis associated with mild "subclinical" hypothyroidism in adults with Down syndrome: a comparison of patients with and without manifestations of Alzheimer disease.

Percy ME, Dalton AJ, Markovic VD, Crapper McLachlan DR, Gera E, Hummel JT, Rusk AC, Somerville MJ, Andrews DF, Walfish PG. Percy ME, et al. Among authors: andrews df. Am J Med Genet. 1990 Jun;36(2):148-54. doi: 10.1002/ajmg.1320360205. Am J Med Genet. 1990. PMID: 2142381

3

Age-associated chromosome 21 loss in Down syndrome: possible relevance to mosaicism and Alzheimer disease.

Percy ME, Markovic VD, Dalton AJ, McLachlan DR, Berg JM, Rusk AC, Somerville MJ, Chodakowski B, Andrews DF. Percy ME, et al. Among authors: andrews df. Am J Med Genet. 1993 Mar 1;45(5):584-8. doi: 10.1002/ajmg.1320450513. Am J Med Genet. 1993. PMID: 8456829

4

Are hereditary hemochromatosis mutations involved in Alzheimer disease?

Moalem S, Percy ME, Andrews DF, Kruck TP, Wong S, Dalton AJ, Mehta P, Fedor B, Warren AC. Moalem S, et al. Among authors: andrews df. Am J Med Genet. 2000 Jul 3;93(1):58-66. doi: 10.1002/1096-8628(20000703)93:1<58::aid-ajmg10>3.0.co;2-l. Am J Med Genet. 2000. PMID: 10861683

5

Red cell superoxide dismutase, glutathione peroxidase and catalase in Down syndrome patients with and without manifestations of Alzheimer disease.

Percy ME, Dalton AJ, Markovic VD, McLachlan DR, Hummel JT, Rusk AC, Andrews DF. Percy ME, et al. Among authors: andrews df. Am J Med Genet. 1990 Apr;35(4):459-67. doi: 10.1002/ajmg.1320350403. Am J Med Genet. 1990. PMID: 2139757

6

Involvement of ApoE E4 and H63D in sporadic Alzheimer's disease in a folate-supplemented Ontario population.

Percy M, Moalem S, Garcia A, Somerville MJ, Hicks M, Andrews D, Azad A, Schwarz P, Beheshti Zavareh R, Birkan R, Choo C, Chow V, Dhaliwal S, Duda V, Kupferschmidt AL, Lam K, Lightman D, Machalek K, Mar W, Nguyen F, Rytwinski PJ, Svara E, Tran M, Wheeler K, Yeung L, Zanibbi K, Zener R, Ziraldo M, Freedman M. Percy M, et al. J Alzheimers Dis. 2008 May;14(1):69-84. doi: 10.3233/jad-2008-14107. J Alzheimers Dis. 2008. PMID: 18525129

7

Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: I. Application of a new model for estimation of the risk of disease associated with the marker.

Percy ME, Markovic VD, Crapper McLachlan DR, Berg JM, Hummel JT, Laing ME, Dearie TG, Andrews DF. Percy ME, et al. Among authors: andrews df. Am J Med Genet. 1991 Jun 1;39(3):307-13. doi: 10.1002/ajmg.1320390312. Am J Med Genet. 1991. PMID: 1867282

8

Monozygotic twins concordant for late-onset probable Alzheimer disease with suspected Alzheimer disease in four sibs.

Karlinsky H, Berg JM, Lennox A, Ray PN, St George-Hyslop P, Farrer LA, Percy ME, Andrews DF, Atack EA. Karlinsky H, et al. Among authors: andrews df. Am J Med Genet. 1992 Nov 15;44(5):591-7. doi: 10.1002/ajmg.1320440512. Am J Med Genet. 1992. PMID: 1481815

9

Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase and hemopexin in combination.

Percy ME, Andrews DF, Thompson MW. Percy ME, et al. Among authors: andrews df. Am J Med Genet. 1981;8(4):397-409. doi: 10.1002/ajmg.1320080406. Am J Med Genet. 1981. PMID: 7246612

10

Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase, hemopexin, pyruvate kinase, and lactate dehydrogenase in combination.

Percy ME, Andrews DF, Thompson MW. Percy ME, et al. Among authors: andrews df. Am J Med Genet. 1982 Sep;13(1):27-38. doi: 10.1002/ajmg.1320130107. Am J Med Genet. 1982. PMID: 7137219

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