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Seminars in Arthritis and Rheumatism
|
June 1, 1997
Lymphoma in patients with rheumatoid arthritis: association with the disease state or methotrexate treatment
L Georgescu, G C Quinn, S Schwartzman, et al.
Clinical and Experimental Immunology
|
April 1, 1988
Interaction between fibronectin and C1q in rheumatoid synovial fluid and normal plasma
S E Carsons, S Schwartzman, H S Diamond, et al.
Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)
|
June 23, 2006
[Non-autistic pervasive developmental disorders: Rett syndrome, disintegrative disorder and pervasive developmental disorder not otherwise specified]
Marcos T Mercadante, Rutger J Van der Gaag, Jose S Schwartzman
Arthritis and Rheumatism
|
March 23, 2000
Ovulation induction and in vitro fertilization in systemic lupus erythematosus and antiphospholipid syndrome
N Guballa, L Sammaritano, S Schwartzman, et al.
Journal of Biological Response Modifiers
|
December 1, 1984
Protective effect of muramyl dipeptide analogs in combination with trehalose dimycolate against aerogenic influenza virus and Mycobacterium tuberculosis infections in mice
K N Masihi, W Brehmer, W Lange, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis
|
January 1, 1991
Disposal of CAPD waste in the community
G R Bailie, S F Kowalsky, G Eisele, et al.
Arquivos De Neuro-Psiquiatria
|
February 25, 1999
[Rett phenotype in patient with XXY karyotype: case report]
J S Schwartzman, A M De Souza, G Faiwichow, et al.
Journal of Intellectual Disability Research : JIDR
|
August 12, 2006
Cognitive performance in Rett syndrome girls: a pilot study using eyetracking technology
P M Baptista, M T Mercadante, E C Macedo, et al.
Computers in Biology and Medicine
|
March 13, 2018
Mechano-electric finite element model of the left atrium
Alessandro Satriano, Edward J Vigmond, David S Schwartzman, et al.
Neuropediatrics
|
August 25, 2001
Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene
J S Schwartzman, A Bernardino, A Nishimura, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 80) with videos related to
Sort By:
Page
of 8
Seminars in Arthritis and Rheumatism
|
June 1, 1997
Lymphoma in patients with rheumatoid arthritis: association with the disease state or methotrexate treatment
L Georgescu, G C Quinn, S Schwartzman, et al.
Clinical and Experimental Immunology
|
April 1, 1988
Interaction between fibronectin and C1q in rheumatoid synovial fluid and normal plasma
S E Carsons, S Schwartzman, H S Diamond, et al.
Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)
|
June 23, 2006
[Non-autistic pervasive developmental disorders: Rett syndrome, disintegrative disorder and pervasive developmental disorder not otherwise specified]
Marcos T Mercadante, Rutger J Van der Gaag, Jose S Schwartzman
Arthritis and Rheumatism
|
March 23, 2000
Ovulation induction and in vitro fertilization in systemic lupus erythematosus and antiphospholipid syndrome
N Guballa, L Sammaritano, S Schwartzman, et al.
Journal of Biological Response Modifiers
|
December 1, 1984
Protective effect of muramyl dipeptide analogs in combination with trehalose dimycolate against aerogenic influenza virus and Mycobacterium tuberculosis infections in mice
K N Masihi, W Brehmer, W Lange, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis
|
January 1, 1991
Disposal of CAPD waste in the community
G R Bailie, S F Kowalsky, G Eisele, et al.
Arquivos De Neuro-Psiquiatria
|
February 25, 1999
[Rett phenotype in patient with XXY karyotype: case report]
J S Schwartzman, A M De Souza, G Faiwichow, et al.
Journal of Intellectual Disability Research : JIDR
|
August 12, 2006
Cognitive performance in Rett syndrome girls: a pilot study using eyetracking technology
P M Baptista, M T Mercadante, E C Macedo, et al.
Computers in Biology and Medicine
|
March 13, 2018
Mechano-electric finite element model of the left atrium
Alessandro Satriano, Edward J Vigmond, David S Schwartzman, et al.
Neuropediatrics
|
August 25, 2001
Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene
J S Schwartzman, A Bernardino, A Nishimura, et al.
Page
of 8