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	701.	Chemical, experimental, and clinical studies on endogenous ouabain-like substance in hypertension. [electronic resource] by Cloix, J F Crabos, M Devynck, M A Elghozi, J L Henning, G Kamal, L A Lacerda-Jacomini, L C Meyer, P Pernollet, M G Rosenfeld, J B Producer: 19850322 In: Advances in nephrology from the Necker Hospital vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	702.	A preliminary evaluation of a prospective study of pulmonary function studies and symptoms of hypoventilation in ALS/MND patients. [electronic resource] by Jackson, C E Rosenfeld, J Moore, D H Bryan, W W Barohn, R J Wrench, M Myers, D Heberlin, L King, R Smith, J Gelinas, D Miller, R G Producer: 20020130 In: Journal of the neurological sciences vol. 191 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	703.	Dipyridamole preserved platelets and reduced blood loss after cardiopulmonary bypass. [electronic resource] by Teoh, K H Christakis, G T Weisel, R D Wong, P Y Mee, A V Ivanov, J Madonik, M M Levitt, D S Reilly, P A Rosenfeld, J M Producer: 19880908 In: The Journal of thoracic and cardiovascular surgery vol. 96 Availability: No items available. Save to lists Add to cart (remove)
	704.	Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. [electronic resource] by Miller, R G Jackson, C E Kasarskis, E J England, J D Forshew, D Johnston, W Kalra, S Katz, J S Mitsumoto, H Rosenfeld, J Shoesmith, C Strong, M J Woolley, S C Producer: 20091104 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	705.	Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. [electronic resource] by Miller, R G Jackson, C E Kasarskis, E J England, J D Forshew, D Johnston, W Kalra, S Katz, J S Mitsumoto, H Rosenfeld, J Shoesmith, C Strong, M J Woolley, S C Producer: 20091104 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	706.	The international database of self-recorded blood pressures in normotensive and untreated hypertensive subjects. [electronic resource] by Thijs, L Staessen, J A Celis, H Fagard, R De Cort, P de Gaudemaris, R Enström, I Imai, Y Julius, S Ménard, J Mion, D Palatini, P Rosenfeld, J Shapiro, D Spence, D Stergiou, G Producer: 19991012 In: Blood pressure monitoring vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	707.	Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions. [electronic resource] by Traylor, R N Dobyns, W B Rosenfeld, J A Wheeler, P Spence, J E Bandholz, A M Bawle, E V Carmany, E P Powell, C M Hudson, B Schultz, R A Shaffer, L G Ballif, B C Publication details: Molecular syndromology Sep 2012 In: Molecular syndromology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	708.	Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype. [electronic resource] by Balasubramanian, M Smith, K Basel-Vanagaite, L Feingold, M F Brock, P Gowans, G C Vasudevan, P C Cresswell, L Taylor, E J Harris, C J Friedman, N Moran, R Feret, H Zackai, E H Theisen, A Rosenfeld, J A Parker, M J Producer: 20110826 In: Journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	709.	Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly. [electronic resource] by Rosenfeld, J A Kim, K H Angle, B Troxell, R Gorski, J L Westemeyer, M Frydman, M Senturias, Y Earl, D Torchia, B Schultz, R A Ellison, J W Tsuchiya, K Zimmerman, S Smolarek, T A Ballif, B C Shaffer, L G Producer: 20130422 In: Molecular syndromology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	710.	Randomised double-blind comparison of placebo and active treatment for older patients with isolated systolic hypertension. The Systolic Hypertension in Europe (Syst-Eur) Trial Investigators. [electronic resource] by Staessen, J A Fagard, R Thijs, L Celis, H Arabidze, G G Birkenhäger, W H Bulpitt, C J de Leeuw, P W Dollery, C T Fletcher, A E Forette, F Leonetti, G Nachev, C O'Brien, E T Rosenfeld, J Rodicio, J L Tuomilehto, J Zanchetti, A Producer: 19971014 In: Lancet (London, England) vol. 350 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	711.	De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations. [electronic resource] by Probst, F J James, R A Burrage, L C Rosenfeld, J A Bohan, T P Ward Melver, C H Magoulas, P Austin, E Franklin, A I A Azamian, M Xia, F Patel, A Bi, W Bacino, C Belmont, J W Ware, S M Shaw, C Cheung, S W Lalani, S R Producer: 20160229 In: Orphanet journal of rare diseases vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	712.	The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. [electronic resource] by Gillentine, M A Berry, L N Goin-Kochel, R P Ali, M A Ge, J Guffey, D Rosenfeld, J A Hannig, V Bader, P Proud, M Shinawi, M Graham, B H Lin, A Lalani, S R Reynolds, J Chen, M Grebe, T Minard, C G Stankiewicz, P Beaudet, A L Schaaf, C P Producer: 20170925 In: Journal of autism and developmental disorders vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	713.	Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. [electronic resource] by Gillentine, M A Berry, L N Goin-Kochel, R P Ali, M A Ge, J Guffey, D Rosenfeld, J A Hannig, V Bader, P Proud, M Shinawi, M Graham, B H Lin, A Lalani, S R Reynolds, J Chen, M Grebe, T Minard, C G Stankiewicz, P Beaudet, A L Schaaf, C P Publication details: Journal of autism and developmental disorders 03 2017 In: Journal of autism and developmental disorders vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	714.	Systolic Hypertension in Europe (Syst-Eur) trial phase 2: objectives, protocol, and initial progress. Systolic Hypertension in Europe Investigators. [electronic resource] by Gasowski, J Staessen, J A Celis, H Fagard, R H Thijs, L Birkenhäger, W H Bulpitt, C J Fletcher, A E Arabidze, G G de Leeuw, P Dollery, C T Duggan, J Kawecka-Jaszcz, K Leonetti, G Nachev, C Safar, M Rodico, J L Rosenfeld, J Seux, M L Tuomilehto, J Webster, J Yodfat, Y Producer: 19990520 In: Journal of human hypertension vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	715.	A randomized, placebo-controlled trial of topiramate in amyotrophic lateral sclerosis. [electronic resource] by Cudkowicz, M E Shefner, J M Schoenfeld, D A Brown, R H Johnson, H Qureshi, M Jacobs, M Rothstein, J D Appel, S H Pascuzzi, R M Heiman-Patterson, T D Donofrio, P D David, W S Russell, J A Tandan, R Pioro, E P Felice, K J Rosenfeld, J Mandler, R N Sachs, G M Bradley, W G Raynor, E M Baquis, G D Belsh, J M Novella, S Goldstein, J Hulihan, J Producer: 20040129 In: Neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	716.	Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes. [electronic resource] by Loviglio, M N Leleu, M Männik, K Passeggeri, M Giannuzzi, G van der Werf, I Waszak, S M Zazhytska, M Roberts-Caldeira, I Gheldof, N Migliavacca, E Alfaiz, A A Hippolyte, L Maillard, A M Van Dijck, A Kooy, R F Sanlaville, D Rosenfeld, J A Shaffer, L G Andrieux, J Marshall, C Scherer, S W Shen, Y Gusella, J F Thorsteinsdottir, U Thorleifsson, G Dermitzakis, E T Deplancke, B Beckmann, J S Rougemont, J Jacquemont, S Reymond, A Producer: 20171017 In: Molecular psychiatry vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	717.	ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome. [electronic resource] by Zak, J Vives, V Szumska, D Vernet, A Schneider, J E Miller, P Slee, E A Joss, S Lacassie, Y Chen, E Escobar, L F Tucker, M Aylsworth, A S Dubbs, H A Collins, A T Andrieux, J Dieux-Coeslier, A Haberlandt, E Kotzot, D Scott, D A Parker, M J Zakaria, Z Choy, Y S Wieczorek, D Innes, A M Jun, K R Zinner, S Prin, F Lygate, C A Pretorius, P Rosenfeld, J A Mohun, T J Lu, X Producer: 20171219 In: Cell death and differentiation vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	718.	Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1. [electronic resource] by Theisen, A Rosenfeld, J A Shane, K McBride, K L Atkin, J F Gaba, C Hoo, J Kurczynski, T W Schnur, R E Coffey, L B Zackai, E H Schimmenti, L Friedman, N Zabukovec, M Ball, S Pagon, R Lucas, A Brasington, C K Spence, J E Sparks, S Banks, V Smith, W Friedberg, T Wyatt, P R Aust, M Tervo, R Crowley, A Skidmore, D Lamb, A N Ravnan, B Sahoo, T Schultz, R Torchia, B S Sgro, M Chitayat, D Shaffer, L G Publication details: Molecular syndromology 2010 In: Molecular syndromology vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	719.	De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. [electronic resource] by Palmer, E E Stuhlmann, T Weinert, S Haan, E Van Esch, H Holvoet, M Boyle, J Leffler, M Raynaud, M Moraine, C van Bokhoven, H Kleefstra, T Kahrizi, K Najmabadi, H Ropers, H-H Delgado, M R Sirsi, D Golla, S Sommer, A Pietryga, M P Chung, W K Wynn, J Rohena, L Bernardo, E Hamlin, D Faux, B M Grange, D K Manwaring, L Tolmie, J Joss, S Cobben, J M Duijkers, F A M Goehringer, J M Challman, T D Hennig, F Fischer, U Grimme, A Suckow, V Musante, L Nicholl, J Shaw, M Lodh, S P Niu, Z Rosenfeld, J A Stankiewicz, P Jentsch, T J Gecz, J Field, M Kalscheuer, V M Producer: 20190215 In: Molecular psychiatry vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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