Results of search for 'au:"Hodes, M"' › مکتبة رقمیه للعلوم الطبيه catalog

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- HODES, M E
- Hodes, M
- Hodes, M E
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	201.	Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain. [electronic resource] by Bayer, S A Wills, K V Wei, J Feng, Y Dlouhy, S R Hodes, M E Verina, T Ghetti, B Producer: 19970311 In: Brain research. Developmental brain research vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	202.	cDNA approaches to isolation of the mouse mutant weaver gene. [electronic resource] by Hodes, M E Dlouhy, S R Wei, J J Wang, Y Sangameswaran, L Lazar, V Triarhou, L C Ghetti, B Producer: 19950426 In: Neurochemical research vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	203.	Diverse cell death pathways result from a single missense mutation in weaver mouse. [electronic resource] by Migheli, A Piva, R Wei, J Attanasio, A Casolino, S Hodes, M E Dlouhy, S R Bayer, S A Ghetti, B Producer: 19980102 In: The American journal of pathology vol. 151 Availability: No items available. Save to lists Add to cart (remove)
	204.	Cognitive scores in carriers of Huntington's disease gene compared to noncarriers. [electronic resource] by Foroud, T Siemers, E Kleindorfer, D Bill, D J Hodes, M E Norton, J A Conneally, P M Christian, J C Producer: 19950616 In: Annals of neurology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	205.	Hypothalamic-pituitary-gonadal axis in the mutant weaver mouse. [electronic resource] by Schwartz, N B Szabo, M Verina, T Wei, J Dlouhy, S R Won, L Heller, A Hodes, M E Ghetti, B Producer: 19990205 In: Neuroendocrinology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	206.	In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice. [electronic resource] by Wei, J Dlouhy, S R Bayer, S Piva, R Verina, T Wang, Y Feng, Y Dupree, B Hodes, M E Ghetti, B Producer: 19970807 In: Journal of neuropathology and experimental neurology vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	207.	Minimum qualifications for directors: DNA-based genetic-testing laboratories. DNA Testing Subcommittee, Quality Assurance Committee, Council of Regional Networks for Genetic Services. [electronic resource] by Murphy, P Amos, J Carpenter, N Fenwick, R Hodes, M E Kelly, T Matteson, K Seltzer, W Spence, J E Thibodeau, S Producer: 19921028 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	208.	Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15. [electronic resource] by Young, K Foroud, T Williams, P Jackson, C E Beckmann, J S Cohen, D Conneally, P M Tischfield, J Hodes, M E Producer: 19920922 In: Genomics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	209.	Transplantation for severe combined immunodeficiency with HLA-A,B,D,DR incompatible parental marrow cells fractionated by soybean agglutinin and sheep red blood cells. [electronic resource] by Reisner, Y Kapoor, N Kirkpatrick, D Pollack, M S Cunningham-Rundles, S Dupont, B Hodes, M Z Good, R A O'Reilly, R J Producer: 19830311 In: Blood vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	210.	Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. [electronic resource] by Dlouhy, S R Hsiao, K Farlow, M R Foroud, T Conneally, P M Johnson, P Prusiner, S B Hodes, M E Ghetti, B Producer: 19930610 In: Nature genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	211.	Motor changes in presymptomatic Huntington disease gene carriers. [electronic resource] by Siemers, E Foroud, T Bill, D J Sorbel, J Norton, J A Hodes, M E Niebler, G Conneally, P M Christian, J C Producer: 19960726 In: Archives of neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	212.	Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. [electronic resource] by Hsiao, K Dlouhy, S R Farlow, M R Cass, C Da Costa, M Conneally, P M Hodes, M E Ghetti, B Prusiner, S B Producer: 19930610 In: Nature genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	213.	An amylase-producing serous cystadenocarcinoma of the ovary. [electronic resource] by Hodes, M E Sisk, C J Karn, R C Ehrlich, C E Lehrner, L M Roth, L M Morley, D J Merritt, A D Producer: 19850819 In: Oncology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	214.	Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus. [electronic resource] by Allamand, V Broux, O Bourg, N Richard, I Tischfield, J A Hodes, M E Conneally, P M Fardeau, M Jackson, C E Beckmann, J S Producer: 19950803 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	215.	Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females. [electronic resource] by Inoue, Ken Osaka, Hitoshi Thurston, Virginia C Clarke, Joe T R Yoneyama, Akira Rosenbarker, Lisa Bird, Thomas D Hodes, M E Shaffer, Lisa G Lupski, James R Producer: 20021028 In: American journal of human genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	216.	Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). [electronic resource] by Hodes, M E Zimmerman, A W Aydanian, A Naidu, S Miller, N R Garcia Oller, J L Barker, B Aleck, K A Hurley, T D Dlouhy, S R Producer: 19990329 In: American journal of medical genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	217.	A brief psychological intervention for mothers of children with food allergy can change risk perception and reduce anxiety: Outcomes of a randomized controlled trial. [electronic resource] by Boyle, R J Umasunthar, T Smith, J G Hanna, H Procktor, A Phillips, K Pinto, C Gore, C Cox, H E Warner, J O Vickers, B Hodes, M Producer: 20180523 In: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	218.	Patients' ability to treat anaphylaxis using adrenaline autoinjectors: a randomized controlled trial. [electronic resource] by Umasunthar, T Procktor, A Hodes, M Smith, J G Gore, C Cox, H E Marrs, T Hanna, H Phillips, K Pinto, C Turner, P J Warner, J O Boyle, R J Producer: 20160324 In: Allergy vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	219.	Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations. [electronic resource] by Garbern, James Y Cambi, Franca Lewis, Richard Shy, Michael Sima, Anders Kraft, George Vallat, J M Bosch, E P Hodes, M E Dlouhy, Stephen Raskind, Wendy Bird, Thomas Macklin, Wendy Kamholz, John Publication details: Annals of the New York Academy of Sciences Oct 1999 In: Annals of the New York Academy of Sciences vol. 883 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	220.	Peripheral neuropathy caused by proteolipid protein gene mutations. [electronic resource] by Garbern, J Y Cambi, F Lewis, R Shy, M Sima, A Kraft, G Vallat, J M Bosch, E P Hodes, M E Dlouhy, S Raskind, W Bird, T Macklin, W Kamholz, J Producer: 19991221 In: Annals of the New York Academy of Sciences vol. 883 Availability: No items available. Save to lists Add to cart (remove)

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