Search Results - "Heinemann, Gabriela"

Validation of the Argentine version of the Montreal Cognitive Assessment Test (MOCA): A screening tool for Mild Cognitive Impairment and Mild Dementia in Elderly by Serrano, Cecilia M, Sorbara, Marcos, Minond, Alexander, Finlay, John B, Arizaga, Raul L, Iturry, Monica, Martinez, Patricia, Heinemann, Gabriela, Gagliardi, Celina, Serra, Andrea, Magliano, Florencia Ces, Yacovino, Darío, Rojas, María Martha Esnaola Y, Ruiz, Adelaida Susana, Graviotto, Héctor Gastón

“…The MoCA is a brief useful test to diagnose mild cognitive impairment (MCI) and mild dementia (MD). To date, no Argentine cross-cultural adapted validations of…”
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Mutation screening of the medium-chain acyl-CoA dehydrogenase (MCAD) and the ornithine transcarbamylase (OTC) genes by multiplex PCR amplification and sequencing by Horn, Michael P, Mäder-Heinemann, Gabriela, Andrey, Gisela, Largiadèr, Carlo R

“…Sequencing based mutation screening assays of genes encompassing large numbers of exons could be substantially optimized by multiplex PCR, which enables…”
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Cloning and expression of carbonyl reductase from rat testis by Wermuth, B, Mäder-Heinemann, G, Ernst, E

“…Carbonyl reductase is a cytosolic, monomeric, NADPH-dependent oxidoreductase with broad specificity for carbonyl compounds and a general distribution in human…”
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A new substitution, gamma 358 Ser-->Cys, in fibrinogen Milano VII causes defective fibrin polymerization by Steinmann, C, Bogli, C, Jungo, M, Lammle, B, Heinemann, G, Wermuth, B, Redaelli, R, Baudo, F, Furlan, M

“…Fibrinogen Milano VII is a hereditary fibrinogen variant detected in a woman with no clinical symptoms of bleeding or thrombosis. Thrombin and reptilase…”
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Cloning and Expression of Carbonyl Reductase from Rat Testis by Wermuth, Bendicht, Mäder‐Heinemann, Gabriela, Ernst, Elsbeth

“…Carbonyl reductase is a cytosolic, monomeric, NADPH‐dependent oxidoreductase with broad specificity for carbonyl compounds and a general distribution in human…”
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Fibrinogen Bern I: Substitution y 337 Asn → Lys Is Responsible for Defective Fibrin Monomer Polymerization by Steinmann, Colette, Reber, Peter, Jungo, Myriam, Lammle, Bernhard, Heinemann, Gabriela, Wermuth, Bendicht, Furlan, Miha

“…An inherited fibrinogen variant, fibrinogen Bern I, was isolated from plasma of an asymptomatic woman. Routine coagulation studies showed prolonged thrombin…”
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Fibrinogen Bern I : substitution γ 337 Asn → Lys is responsible for defective fibrin monomer polymerization by STEINMANN, C, REBER, P, JUNGO, M, LÄMMLE, B, HEINEMANN, G, WERMUTH, B, FURLAN, M

“…An inherited fibrinogen variant, fibrinogen Bern I, was isolated from plasma of an asymptomatic woman. Routine coagulation studies showed prolonged thrombin…”
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