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R Gatti

Showing results (201-210 of 239) with videos related to

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Translational Stroke Research|June 23, 2018
Redistribution of Mature Smooth Muscle Markers in Brain Arteries in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and LeukoencephalopathyJohn R Gatti, Xiaojie Zhang, Ejona Korcari, et al.
Clinical Nephrology|November 19, 2010
Chronic periaortitis associated with membranous nephropathy: clues to common pathogenetic mechanismsA Palmisano, D Corradi, M L Carnevali, et al.
Human Genetics|November 1, 1992
A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patientG Mosna, S Fattore, G Tubiello, et al.
European Journal of Pediatrics|January 7, 1999
Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiencyR Parini, F Menni, B Garavaglia, et al.
Pediatric Neurology|May 21, 2021
Neonatal Subpial Hemorrhage: Clinical Factors, Neuroimaging, and Outcomes in a Quaternary Care Children's CenterAnia K Dabrowski, Melisa Carrasco, John R Gatti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effectK Laake, M Telatar, G A Geitvik, et al.
Nanoscale|January 27, 2015
Pentacene on Ni(111): room-temperature molecular packing and temperature-activated conversion to grapheneL E Dinca, F De Marchi, J M MacLeod, et al.
Genomics|May 1, 1995
The CEPH consortium linkage map of human chromosome 11M Litt, P Kramer, E Kort, et al.
Cancer Chemotherapy and Pharmacology|January 27, 2007
The inhibition of glutamine synthetase sensitizes human sarcoma cells to L-asparaginaseS Tardito, J Uggeri, C Bozzetti, 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 1cL Galli, A Orrico, P Marcolongo, et al.
Pageof 24

Showing results (201-210 of 239) with videos related to

Sort By:
Pageof 24
Translational Stroke Research|June 23, 2018
Redistribution of Mature Smooth Muscle Markers in Brain Arteries in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and LeukoencephalopathyJohn R Gatti, Xiaojie Zhang, Ejona Korcari, et al.
Clinical Nephrology|November 19, 2010
Chronic periaortitis associated with membranous nephropathy: clues to common pathogenetic mechanismsA Palmisano, D Corradi, M L Carnevali, et al.
Human Genetics|November 1, 1992
A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patientG Mosna, S Fattore, G Tubiello, et al.
European Journal of Pediatrics|January 7, 1999
Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiencyR Parini, F Menni, B Garavaglia, et al.
Pediatric Neurology|May 21, 2021
Neonatal Subpial Hemorrhage: Clinical Factors, Neuroimaging, and Outcomes in a Quaternary Care Children's CenterAnia K Dabrowski, Melisa Carrasco, John R Gatti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effectK Laake, M Telatar, G A Geitvik, et al.
Nanoscale|January 27, 2015
Pentacene on Ni(111): room-temperature molecular packing and temperature-activated conversion to grapheneL E Dinca, F De Marchi, J M MacLeod, et al.
Genomics|May 1, 1995
The CEPH consortium linkage map of human chromosome 11M Litt, P Kramer, E Kort, et al.
Cancer Chemotherapy and Pharmacology|January 27, 2007
The inhibition of glutamine synthetase sensitizes human sarcoma cells to L-asparaginaseS Tardito, J Uggeri, C Bozzetti, 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 1cL Galli, A Orrico, P Marcolongo, et al.
Pageof 24