Your search returned 9 results.

Results
	1.	Unconventional diagnosis of Normandy-type von Willebrand's disease in a blood donor. [electronic resource] by Kashyap, S Nesbitt, I M Makris, M Producer: 20050126 In: Transfusion medicine (Oxford, England) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	MEN 2B syndrome should be part of the working diagnosis of constipation of the newborn. [electronic resource] by Evans, C A Nesbitt, I M Walker, J Cohen, M C Producer: 20080417 In: Histopathology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	von Willebrand factor/factor VIII binding is not affected by the Arg89Gln polymorphism in von Willebrand factor. [electronic resource] by Nesbitt, I M Goodeve, A C Preston, F E Peake, I R Producer: 19970324 In: Thrombosis and haemostasis vol. 76 Availability: No items available. Save to lists Add to cart (remove)
	4.	A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutations. [electronic resource] by Nesbitt, I M Hampton, K K Preston, F E Peake, I R Goodeve, A C Producer: 19991122 In: Thrombosis and haemostasis vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	5.	Characterisation of type 2N von Willebrand disease using phenotypic and molecular techniques. [electronic resource] by Nesbitt, I M Goodeve, A C Guilliatt, A M Makris, M Preston, F E Peake, I R Producer: 19970325 In: Thrombosis and haemostasis vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	6.	The management of von Willebrand's disease-associated gastrointestinal angiodysplasia. [electronic resource] by Morris, E S Hampton, K K Nesbitt, I M Preston, F E Thomas, E G Makris, M Producer: 20010802 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Recurrent rhabdomyolysis caused by carnitine palmitoyltransferase II deficiency, common but under-recognised: Lessons to be learnt. [electronic resource] by Balasubramanian, M Jenkins, T M Kirk, R J Nesbitt, I M Olpin, S E Hill, M Gillett, G T Publication details: Molecular genetics and metabolism reports Jun 2018 In: Molecular genetics and metabolism reports vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Response to Finsterer: CPT-II deficiency needs to be detected in army personnel. [electronic resource] by Balasubramanian, M Jenkins, T M Kirk, R J Nesbitt, I M Olpin, S E Hill, M Gillett, G T Publication details: Molecular genetics and metabolism reports Sep 2018 In: Molecular genetics and metabolism reports vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor. [electronic resource] by Allen, S Abuzenadah, A M Blagg, J L Hinks, J Nesbitt, I M Goodeve, A C Gursel, T Ingerslev, J Peake, I R Daly, M E Producer: 20000407 In: Blood vol. 95 Availability: No items available. Save to lists Add to cart (remove)