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	1.	Late stage care in Huntington's disease. [electronic resource] by Simpson, Sheila A Producer: 20070614 In: Brain research bulletin vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mycophenolate mofetil embryopathy may be dose and timing dependent. [electronic resource] by Ang, Ghee Soon Simpson, Sheila A Reddy, Aravind R Producer: 20080819 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	New challenges for gamete donation programmes: changes in guidelines are needed. [electronic resource] by Gazvani, Rafet Hamilton, Mark P R Simpson, Sheila A Templeton, Allan Producer: 20031001 In: Human fertility (Cambridge, England) vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	How young people find out about their family history of Huntington's disease. [electronic resource] by Forrest Keenan, Karen van Teijlingen, Edwin McKee, Lorna Miedzybrodzka, Zosia Simpson, Sheila A Producer: 20090811 In: Social science & medicine (1982) vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	How do partners find out about the risk of Huntington's disease in couple relationships? [electronic resource] by Forrest Keenan, Karen Simpson, Sheila A Miedzybrodzka, Zosia Alexander, David A Semper, June Producer: 20131209 In: Journal of genetic counseling vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Factor analysis of behavioural symptoms in Huntington's disease. [electronic resource] by Rickards, Hugh De Souza, Jenny van Walsem, Marleen van Duijn, Erik Simpson, Sheila A Squitieri, Ferdinando Landwehrmeyer, Bernhard Producer: 20110511 In: Journal of neurology, neurosurgery, and psychiatry vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Family communication about genetic risk: the little that is known. [electronic resource] by Wilson, Brenda J Forrest, Karen van Teijlingen, Edwin R McKee, Lorna Haites, Neva Matthews, Eric Simpson, Sheila A Producer: 20050208 In: Community genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Prenatal testing for Huntington's disease: a European collaborative study. [electronic resource] by Simpson, Sheila A Zoeteweij, Moniek W Nys, Kurt Harper, Peter Dürr, Alexandra Jacopini, Gioia Yapijakis, Christos Evers-Kiebooms, Gerry Producer: 20030610 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Discriminant analysis of Beck Depression Inventory and Hamilton Rating Scale for Depression in Huntington's disease. [electronic resource] by Rickards, Hugh De Souza, Jennifer Crooks, Jennifer van Walsem, Marleen R van Duijn, Erik Landwehrmeyer, Bernhard Squitieri, Ferdinando Simpson, Sheila A Producer: 20120510 In: The Journal of neuropsychiatry and clinical neurosciences vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Genetic professionals' reports of nondisclosure of genetic risk information within families. [electronic resource] by Clarke, Angus Richards, Martin Kerzin-Storrar, Lauren Halliday, Jane Young, Mary Anne Simpson, Sheila A Featherstone, Katie Forrest, Karen Lucassen, Anneke Morrison, Patrick J Quarrell, Oliver W J Stewart, Helen Producer: 20050816 In: European journal of human genetics : EJHG vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course. [electronic resource] by Squitieri, Ferdinando Gellera, Cinzia Cannella, Milena Mariotti, Caterina Cislaghi, Giuliana Rubinsztein, David C Almqvist, Elisabeth W Turner, David Bachoud-Lévi, Anne-Catherine Simpson, Sheila A Delatycki, Martin Maglione, Vittorio Hayden, Michael R Donato, Stefano Di Producer: 20030522 In: Brain : a journal of neurology vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	27 years of prenatal diagnosis for Huntington disease in the United Kingdom. [electronic resource] by Piña-Aguilar, Raul E Simpson, Sheila A Alshatti, Abdulrahman Clarke, Angus Craufurd, David Dorkins, Huw Doye, Karen Lahiri, Nayana Lashwood, Alison Lynch, Colleen Miller, Claire Morton, Sally O'Driscoll, Mary Quarrell, Oliver W Rae, Daniela Strong, Mark Tomlinson, Charlotte Turnpenny, Peter Miedzybrodzka, Zosia Producer: 20200128 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export. [electronic resource] by Legati, Andrea Giovannini, Donatella Nicolas, Gaël López-Sánchez, Uriel Quintáns, Beatriz Oliveira, João R M Sears, Renee L Ramos, Eliana Marisa Spiteri, Elizabeth Sobrido, María-Jesús Carracedo, Ángel Castro-Fernández, Cristina Cubizolle, Stéphanie Fogel, Brent L Goizet, Cyril Jen, Joanna C Kirdlarp, Suppachok Lang, Anthony E Miedzybrodzka, Zosia Mitarnun, Witoon Paucar, Martin Paulson, Henry Pariente, Jérémie Richard, Anne-Claire Salins, Naomi S Simpson, Sheila A Striano, Pasquale Svenningsson, Per Tison, François Unni, Vivek K Vanakker, Olivier Wessels, Marja W Wetchaphanphesat, Suppachok Yang, Michele Boller, Francois Campion, Dominique Hannequin, Didier Sitbon, Marc Geschwind, Daniel H Battini, Jean-Luc Coppola, Giovanni Producer: 20150807 In: Nature genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification. [electronic resource] by Hsu, Sandy Chan Sears, Renee L Lemos, Roberta R Quintáns, Beatriz Huang, Alden Spiteri, Elizabeth Nevarez, Lisette Mamah, Catherine Zatz, Mayana Pierce, Kerrie D Fullerton, Janice M Adair, John C Berner, Jon E Bower, Matthew Brodaty, Henry Carmona, Olga Dobricić, Valerija Fogel, Brent L García-Estevez, Daniel Goldman, Jill Goudreau, John L Hopfer, Suellen Janković, Milena Jaumà, Serge Jen, Joanna C Kirdlarp, Suppachok Klepper, Joerg Kostić, Vladimir Lang, Anthony E Linglart, Agnès Maisenbacher, Melissa K Manyam, Bala V Mazzoni, Pietro Miedzybrodzka, Zofia Mitarnun, Witoon Mitchell, Philip B Mueller, Jennifer Novaković, Ivana Paucar, Martin Paulson, Henry Simpson, Sheila A Svenningsson, Per Tuite, Paul Vitek, Jerrold Wetchaphanphesat, Suppachok Williams, Charles Yang, Michele Schofield, Peter R de Oliveira, João R M Sobrido, María-Jesús Geschwind, Daniel H Coppola, Giovanni Producer: 20130805 In: Neurogenetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)