Search research articles
Contact Us
Filters
Showing results (51-60 of 98) with videos related to
Page
of 10
Sort By:
Clinical Positron Imaging : Official Journal of the Institute for Clinical P.E.T
|
October 1, 2003
Role of FDG-PET in the Pre-Operative Evaluation of Surgical Resection of Hepatic Metastases from Colorectal Cancer
R K. Halkar, J R. Toro, E H. Lim, et al.
Archives of Dermatology
|
August 5, 2000
gamma delta T-cell lymphoma of the skin: a clinical, microscopic, and molecular study
J R Toro, M Beaty, L Sorbara, et al.
Journal of the American Academy of Dermatology
|
January 11, 2003
Facial papules, spontaneous pneumothorax, and renal tumors
Jorge R Toro, Gladys Glenn, Lifang Hou, et al.
Journal of Medical Genetics
|
April 7, 2006
Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer
M Pithukpakorn, M-H Wei, O Toure, et al.
Molecular Psychiatry
|
December 24, 2009
Prenatal exposure to maternal cigarette smoking interacts with a polymorphism in the alpha6 nicotinic acetylcholine receptor gene to influence drug use and striatum volume in adolescence
S Lotfipour, G Leonard, M Perron, et al.
Journal of Medical Genetics
|
October 25, 2008
Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA
S Farasat, M-H Wei, M Herman, et al.
Archives of Dermatology
|
December 17, 2008
Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer
Laveta Stewart, Gladys M Glenn, Pamela Stratton, et al.
Placenta
|
May 31, 2016
Leptin reduces apoptosis triggered by high temperature in human placental villous explants: The role of the p53 pathway
Antonio Pérez-Pérez, Ayelén R Toro, Teresa Vilarino-Garcia, et al.
Human Mutation
|
February 26, 2009
Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis: summary of mutations (including 23 novel) and modeling of TGase-1
Matthew L Herman, Sharifeh Farasat, Peter J Steinbach, et al.
Journal of Electrocardiology
|
August 1, 2021
Electrocardiographic findings in true acute left main coronary total occlusion a subanalisys from ATOLMA registry
A Gutiérrez-Barrios, D Mialdea-Salmerón, D Cañadas-Pruaño, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 98) with videos related to
Sort By:
Page
of 10
Clinical Positron Imaging : Official Journal of the Institute for Clinical P.E.T
|
October 1, 2003
Role of FDG-PET in the Pre-Operative Evaluation of Surgical Resection of Hepatic Metastases from Colorectal Cancer
R K. Halkar, J R. Toro, E H. Lim, et al.
Archives of Dermatology
|
August 5, 2000
gamma delta T-cell lymphoma of the skin: a clinical, microscopic, and molecular study
J R Toro, M Beaty, L Sorbara, et al.
Journal of the American Academy of Dermatology
|
January 11, 2003
Facial papules, spontaneous pneumothorax, and renal tumors
Jorge R Toro, Gladys Glenn, Lifang Hou, et al.
Journal of Medical Genetics
|
April 7, 2006
Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer
M Pithukpakorn, M-H Wei, O Toure, et al.
Molecular Psychiatry
|
December 24, 2009
Prenatal exposure to maternal cigarette smoking interacts with a polymorphism in the alpha6 nicotinic acetylcholine receptor gene to influence drug use and striatum volume in adolescence
S Lotfipour, G Leonard, M Perron, et al.
Journal of Medical Genetics
|
October 25, 2008
Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA
S Farasat, M-H Wei, M Herman, et al.
Archives of Dermatology
|
December 17, 2008
Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer
Laveta Stewart, Gladys M Glenn, Pamela Stratton, et al.
Placenta
|
May 31, 2016
Leptin reduces apoptosis triggered by high temperature in human placental villous explants: The role of the p53 pathway
Antonio Pérez-Pérez, Ayelén R Toro, Teresa Vilarino-Garcia, et al.
Human Mutation
|
February 26, 2009
Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis: summary of mutations (including 23 novel) and modeling of TGase-1
Matthew L Herman, Sharifeh Farasat, Peter J Steinbach, et al.
Journal of Electrocardiology
|
August 1, 2021
Electrocardiographic findings in true acute left main coronary total occlusion a subanalisys from ATOLMA registry
A Gutiérrez-Barrios, D Mialdea-Salmerón, D Cañadas-Pruaño, et al.
Page
of 10