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Items: 1 to 20 of 25

1.

How does type 1 diabetes develop?: the notion of homicide or β-cell suicide revisited.

Atkinson MA, Bluestone JA, Eisenbarth GS, Hebrok M, Herold KC, Accili D, Pietropaolo M, Arvan PR, Von Herrath M, Markel DS, Rhodes CJ.

Diabetes. 2011 May;60(5):1370-9. doi: 10.2337/db10-1797. No abstract available.

2.

The CTSA mandate: are we there yet?

Sampselle CM, Pienta KJ, Markel DS.

Res Theory Nurs Pract. 2010;24(1):64-73.

PMID:
20333913
4.

Recommendations for standardized human pedigree nomenclature.

Bennett RL, Steinhaus KA, Uhrich SB, O'Sullivan CK, Resta RG, Lochner-Doyle D, Markel DS, Vincent V, Hamanishi J.

J Genet Couns. 1995 Dec;4(4):267-79. doi: 10.1007/BF01408073.

5.

A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.

Johnson DW, Berg JN, Gallione CJ, McAllister KA, Warner JP, Helmbold EA, Markel DS, Jackson CE, Porteous ME, Marchuk DA.

Genome Res. 1995 Aug;5(1):21-8.

6.

Inconsistencies in pedigree symbols in human genetics publications: a need for standardization.

Steinhaus KA, Bennett RL, Resta RG, Uhrich SB, Doyle DL, Markel DS, Vincent VA.

Am J Med Genet. 1995 Apr 10;56(3):291-5. Review.

PMID:
7778593
7.

Recommendations for standardized human pedigree nomenclature. Pedigree Standardization Task Force of the National Society of Genetic Counselors.

Bennett RL, Steinhaus KA, Uhrich SB, O'Sullivan CK, Resta RG, Lochner-Doyle D, Markel DS, Vincent V, Hamanishi J.

Am J Hum Genet. 1995 Mar;56(3):745-52.

8.

A gene for familial venous malformations maps to chromosome 9p in a second large kindred.

Gallione CJ, Pasyk KA, Boon LM, Lennon F, Johnson DW, Helmbold EA, Markel DS, Vikkula M, Mulliken JB, Warman ML, et al.

J Med Genet. 1995 Mar;32(3):197-9.

9.

Longitudinal neuropsychological and genetic linkage analysis of persons at risk for Huntington's disease.

Giordani B, Berent S, Boivin MJ, Penney JB, Lehtinen S, Markel DS, Hollingsworth Z, Butterbaugh G, Hichwa RD, Gusella JF, et al.

Arch Neurol. 1995 Jan;52(1):59-64.

PMID:
7826277
10.

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.

McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, Helmbold EA, Markel DS, McKinnon WC, Murrell J, et al.

Nat Genet. 1994 Dec;8(4):345-51.

PMID:
7894484
11.

Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.

McAllister KA, Lennon F, Bowles-Biesecker B, McKinnon WC, Helmbold EA, Markel DS, Jackson CE, Guttmacher AE, Pericak-Vance MA, Marchuk DA.

J Med Genet. 1994 Dec;31(12):927-32.

12.

Structural and functional brain imaging in Friedreich's ataxia.

Junck L, Gilman S, Gebarski SS, Koeppe RA, Kluin KJ, Markel DS.

Arch Neurol. 1994 Apr;51(4):349-55.

PMID:
8155012
13.

A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34.

McDonald MT, Papenberg KA, Ghosh S, Glatfelter AA, Biesecker BB, Helmbold EA, Markel DS, Zolotor A, McKinnon WC, Vanderstoep JL, et al.

Nat Genet. 1994 Feb;6(2):197-204.

PMID:
8162075
14.

Positron emission tomography measures of benzodiazepine receptors in Huntington's disease.

Holthoff VA, Koeppe RA, Frey KA, Penney JB, Markel DS, Kuhl DE, Young AB.

Ann Neurol. 1993 Jul;34(1):76-81.

15.

Genetic counseling for families with inherited susceptibility to breast and ovarian cancer.

Biesecker BB, Boehnke M, Calzone K, Markel DS, Garber JE, Collins FS, Weber BL.

JAMA. 1993 Apr 21;269(15):1970-4. Erratum in: JAMA 1993 Aug 18;270(7):832.

PMID:
8352830
16.

BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.

Chamberlain JS, Boehnke M, Frank TS, Kiousis S, Xu J, Guo SW, Hauser ER, Norum RA, Helmbold EA, Markel DS, et al.

Am J Hum Genet. 1993 Apr;52(4):792-8.

17.

Cerebral glucose hypermetabolism in Friedreich's ataxia detected with positron emission tomography.

Gilman S, Junck L, Markel DS, Koeppe RA, Kluin KJ.

Ann Neurol. 1990 Dec;28(6):750-7.

18.

Neuropsychological changes in olivopontocerebellar atrophy.

Berent S, Giordani B, Gilman S, Junck L, Lehtinen S, Markel DS, Boivin M, Kluin KJ, Parks R, Koeppe RA.

Arch Neurol. 1990 Sep;47(9):997-1001.

PMID:
2396941
19.

Abnormalities of striatal projection neurons and N-methyl-D-aspartate receptors in presymptomatic Huntington's disease.

Albin RL, Young AB, Penney JB, Handelin B, Balfour R, Anderson KD, Markel DS, Tourtellotte WW, Reiner A.

N Engl J Med. 1990 May 3;322(18):1293-8. No abstract available.

20.

Motor dysfunction in olivopontocerebellar atrophy is related to cerebral metabolic rate studied with positron emission tomography.

Rosenthal G, Gilman S, Koeppe RA, Kluin KJ, Markel DS, Junck L, Gebarski SS.

Ann Neurol. 1988 Sep;24(3):414-9.

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