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Archives of Disease in Childhood
|
October 1, 1991
HIV-I infection in perinatally exposed siblings and twins. The Italian Register for HIV Infection in Children
M de Martino, P A Tovo, L Galli, et al.
Archives of Toxicology
|
May 15, 2013
Comparison of wood smoke PM2.5 obtained from the combustion of FIR and beech pellets on inflammation and DNA damage in A549 and THP-1 human cell lines
Emanuela Corsini, Silvia Budello, Laura Marabini, et al.
Tumori
|
January 1, 1995
The role of intraoperative therapy by electron beam and combination of adjuvant chemotherapy and external radiotherapy in carcinoma of the pancreas
V Fossati, G M Cattaneo, A Zerbi, et al.
FEBS Letters
|
October 13, 1999
Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c
L Galli, A Orrico, P Marcolongo, et al.
Human & Experimental Toxicology
|
April 1, 1996
Morphological alterations in the hippocampus following hypobaric hypoxia
B Shukitt-Hale, T Kadar, B E Marlowe, et al.
European Journal of Nuclear Medicine
|
January 1, 1992
Presurgical identification of hibernating myocardium by combined use of technetium-99m hexakis 2-methoxyisobutylisonitrile single photon emission tomography and fluorine-18 fluoro-2-deoxy-D-glucose positron emission tomography in patients with coronary artery disease
G Lucignani, G Paolini, C Landoni, et al.
Chemical Research in Toxicology
|
January 22, 2002
Facilitation of acetylcholine signaling by the dithiocarbamate fungicide propineb
Marina Marinovich, Barbara Viviani, Valerie Capra, et al.
BMC Infectious Diseases
|
January 3, 2012
Intracardiac left atrial tuberculoma in an eleven-month-old infant: case report
M Cantinotti, M De Gaudio, M de Martino, et al.
Human Molecular Genetics
|
January 1, 1994
Single base pair deletions in exons 39 and 42 of the COL4A5 gene in Alport syndrome
A Renieri, L Galli, M De Marchi, et al.
Human Mutation
|
January 1, 1994
A novel frameshift deletion in type IV collagen alpha 5 gene in a juvenile-type Alport syndrome patient: an adenine deletion (2940/2943 del A) in exon 34 of COL4A5
B Peissel, S Rossetti, A Renieri, et al.
Page
of 54
Search research articles
Search
Showing results (411-420 of 534) with videos related to
Sort By:
Page
of 54
Archives of Disease in Childhood
|
October 1, 1991
HIV-I infection in perinatally exposed siblings and twins. The Italian Register for HIV Infection in Children
M de Martino, P A Tovo, L Galli, et al.
Archives of Toxicology
|
May 15, 2013
Comparison of wood smoke PM2.5 obtained from the combustion of FIR and beech pellets on inflammation and DNA damage in A549 and THP-1 human cell lines
Emanuela Corsini, Silvia Budello, Laura Marabini, et al.
Tumori
|
January 1, 1995
The role of intraoperative therapy by electron beam and combination of adjuvant chemotherapy and external radiotherapy in carcinoma of the pancreas
V Fossati, G M Cattaneo, A Zerbi, et al.
FEBS Letters
|
October 13, 1999
Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c
L Galli, A Orrico, P Marcolongo, et al.
Human & Experimental Toxicology
|
April 1, 1996
Morphological alterations in the hippocampus following hypobaric hypoxia
B Shukitt-Hale, T Kadar, B E Marlowe, et al.
European Journal of Nuclear Medicine
|
January 1, 1992
Presurgical identification of hibernating myocardium by combined use of technetium-99m hexakis 2-methoxyisobutylisonitrile single photon emission tomography and fluorine-18 fluoro-2-deoxy-D-glucose positron emission tomography in patients with coronary artery disease
G Lucignani, G Paolini, C Landoni, et al.
Chemical Research in Toxicology
|
January 22, 2002
Facilitation of acetylcholine signaling by the dithiocarbamate fungicide propineb
Marina Marinovich, Barbara Viviani, Valerie Capra, et al.
BMC Infectious Diseases
|
January 3, 2012
Intracardiac left atrial tuberculoma in an eleven-month-old infant: case report
M Cantinotti, M De Gaudio, M de Martino, et al.
Human Molecular Genetics
|
January 1, 1994
Single base pair deletions in exons 39 and 42 of the COL4A5 gene in Alport syndrome
A Renieri, L Galli, M De Marchi, et al.
Human Mutation
|
January 1, 1994
A novel frameshift deletion in type IV collagen alpha 5 gene in a juvenile-type Alport syndrome patient: an adenine deletion (2940/2943 del A) in exon 34 of COL4A5
B Peissel, S Rossetti, A Renieri, et al.
Page
of 54