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BMJ Open Gastroenterology
|
November 20, 2025
Non-invasive liver fibrosis scores and mortality in a cohort of World Trade Center rescue/recovery workers
Ankura Singh, Rachel Zeig-Owens, Nikolina Icitovic, et al.
Brain Research. Brain Research Reviews
|
January 11, 1991
Regulation and genetic control of brain amyloid. FESN Study Group
D C Gajdusek, K Beyreuther, P Brown, et al.
Neurology
|
February 11, 1992
Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene
P Brown, L G Goldfarb, W R McCombie, et al.
Experimental Neurology
|
June 1, 1990
Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome
L G Goldfarb, P Brown, D Goldgaber, et al.
Neurology
|
March 1, 1991
Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndrome
P Brown, L G Goldfarb, W T Brown, et al.
Neuromuscular Disorders : NMD
|
July 8, 2010
Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation
Zagaa Odgerel, Anna Sarkozy, Hee-Suk Lee, et al.
Experimental Neurology
|
November 1, 1989
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome
D Goldgaber, L G Goldfarb, P Brown, et al.
Nature Genetics
|
August 11, 1998
Missense mutations in desmin associated with familial cardiac and skeletal myopathy
L G Goldfarb, K Y Park, L Cervenáková, et al.
British Journal of Anaesthesia
|
October 5, 2007
Sevoflurane preconditioning at 1 MAC only provides limited protection in patients undergoing coronary artery bypass surgery: a randomized bi-centre trial
V Piriou, J Mantz, G Goldfarb, et al.
Neurology
|
June 1, 1995
Clinical and genetic studies of fatal familial insomnia
A T Reder, A S Mednick, P Brown, et al.
Page
of 25
Search research articles
Search
Showing results (181-190 of 244) with videos related to
Sort By:
Page
of 25
BMJ Open Gastroenterology
|
November 20, 2025
Non-invasive liver fibrosis scores and mortality in a cohort of World Trade Center rescue/recovery workers
Ankura Singh, Rachel Zeig-Owens, Nikolina Icitovic, et al.
Brain Research. Brain Research Reviews
|
January 11, 1991
Regulation and genetic control of brain amyloid. FESN Study Group
D C Gajdusek, K Beyreuther, P Brown, et al.
Neurology
|
February 11, 1992
Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene
P Brown, L G Goldfarb, W R McCombie, et al.
Experimental Neurology
|
June 1, 1990
Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome
L G Goldfarb, P Brown, D Goldgaber, et al.
Neurology
|
March 1, 1991
Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndrome
P Brown, L G Goldfarb, W T Brown, et al.
Neuromuscular Disorders : NMD
|
July 8, 2010
Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation
Zagaa Odgerel, Anna Sarkozy, Hee-Suk Lee, et al.
Experimental Neurology
|
November 1, 1989
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome
D Goldgaber, L G Goldfarb, P Brown, et al.
Nature Genetics
|
August 11, 1998
Missense mutations in desmin associated with familial cardiac and skeletal myopathy
L G Goldfarb, K Y Park, L Cervenáková, et al.
British Journal of Anaesthesia
|
October 5, 2007
Sevoflurane preconditioning at 1 MAC only provides limited protection in patients undergoing coronary artery bypass surgery: a randomized bi-centre trial
V Piriou, J Mantz, G Goldfarb, et al.
Neurology
|
June 1, 1995
Clinical and genetic studies of fatal familial insomnia
A T Reder, A S Mednick, P Brown, et al.
Page
of 25