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J Lachmann

Showing results (271-280 of 426) with videos related to

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Scientific Reports|October 28, 2020
Cardiovascular disease risk assessment in patients with familial Mediterranean fever related renal amyloidosisMicol Romano, David Piskin, Roberta A Berard, et al.
Immunology Letters|December 23, 2003
Determination of CD59 protein in normal human serum by enzyme immunoassay, using octyl-glucoside detergent to release glycosyl-phosphatidylinositol-CD59 from lipid complexA P G Landi, A B Wilson, A Davies, et al.
Rheumatology (Oxford, England)|August 7, 2019
British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literatureDorota M Rowczenio, Taryn Youngstein, Hadija Trojer, et al.
Rheumatology (Oxford, England)|December 20, 2013
Efficacy and safety of canakinumab therapy in paediatric patients with cryopyrin-associated periodic syndrome: a single-centre, real-world experienceRicardo A G Russo, Sonia Melo-Gomes, Helen J Lachmann, et al.
American Heart Journal|September 29, 1999
Protruding aortic arch atheromas: risk of stroke during heart surgery with and without aortic arch endarterectomyA Stern, P A Tunick, A T Culliford, et al.
Arthritis and Rheumatism|May 30, 2006
AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two casesHelen J Lachmann, Hugh J B Goodman, Peter A Andrews, et al.
Journal of the American Society of Nephrology : JASN|December 17, 2008
Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosisJulian D Gillmore, Helen J Lachmann, Dorota Rowczenio, et al.
Immunology|July 1, 1996
How partial C7 deficiency with chronic and recurrent bacterial infections can mimic total C7 deficiency: temporary restoration of host C7 levels following plasma transfusionR Würzner, A E Platonov, V B Beloborodov, et al.
Human Mutation|July 22, 2014
Online registry for mutations in hereditary amyloidosis including nomenclature recommendationsDorota M Rowczenio, Islam Noor, Julian D Gillmore, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 29, 2014
A novel transthyretin variant p.H110D (H90D) as a cause of familial amyloid polyneuropathy in a large Irish kindredVictor H Jimenez-Zepeda, Nizar J Bahlis, Janet Gilbertson, et al.
Pageof 43

Showing results (271-280 of 426) with videos related to

Sort By:
Pageof 43
Scientific Reports|October 28, 2020
Cardiovascular disease risk assessment in patients with familial Mediterranean fever related renal amyloidosisMicol Romano, David Piskin, Roberta A Berard, et al.
Immunology Letters|December 23, 2003
Determination of CD59 protein in normal human serum by enzyme immunoassay, using octyl-glucoside detergent to release glycosyl-phosphatidylinositol-CD59 from lipid complexA P G Landi, A B Wilson, A Davies, et al.
Rheumatology (Oxford, England)|August 7, 2019
British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literatureDorota M Rowczenio, Taryn Youngstein, Hadija Trojer, et al.
Rheumatology (Oxford, England)|December 20, 2013
Efficacy and safety of canakinumab therapy in paediatric patients with cryopyrin-associated periodic syndrome: a single-centre, real-world experienceRicardo A G Russo, Sonia Melo-Gomes, Helen J Lachmann, et al.
American Heart Journal|September 29, 1999
Protruding aortic arch atheromas: risk of stroke during heart surgery with and without aortic arch endarterectomyA Stern, P A Tunick, A T Culliford, et al.
Arthritis and Rheumatism|May 30, 2006
AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two casesHelen J Lachmann, Hugh J B Goodman, Peter A Andrews, et al.
Journal of the American Society of Nephrology : JASN|December 17, 2008
Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosisJulian D Gillmore, Helen J Lachmann, Dorota Rowczenio, et al.
Immunology|July 1, 1996
How partial C7 deficiency with chronic and recurrent bacterial infections can mimic total C7 deficiency: temporary restoration of host C7 levels following plasma transfusionR Würzner, A E Platonov, V B Beloborodov, et al.
Human Mutation|July 22, 2014
Online registry for mutations in hereditary amyloidosis including nomenclature recommendationsDorota M Rowczenio, Islam Noor, Julian D Gillmore, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 29, 2014
A novel transthyretin variant p.H110D (H90D) as a cause of familial amyloid polyneuropathy in a large Irish kindredVictor H Jimenez-Zepeda, Nizar J Bahlis, Janet Gilbertson, et al.
Pageof 43