In vitro study of uptake and synthesis of creatine and its precursors by cerebellar granule cells and astrocytes suggests some hypotheses on the physiopathology of the inherited di... von Carducci, Claudia, Carducci, Carla, Santagata, Silvia, Adriano, Enrico, Artiola, Cristiana, Thellung, Stefano, Gatta, Elena, Robello, Mauro, Florio, Tullio, Antonozzi, Italo, Leuzzi, Vincenzo, Balestrino, Maurizio

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Quantitative determination of guanidinoacetate and creatine in dried blood spot by flow injection analysis-electrospray tandem mass spectrometry von Carducci, Claudia, Santagata, Silvia, Leuzzi, Vincenzo, Carducci, Carla, Artiola, Cristiana, Giovanniello, Teresa, Battini, Roberta, Antonozzi, Italo

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Guanidinoacetate and Creatine plus Creatinine Assessment in Physiologic Fluids: An Effective Diagnostic Tool for the Biochemical Diagnosis of Arginine:Glycine Amidinotransferase an... von Carducci, Claudia, Birarelli, Maurizio, Leuzzi, Vincenzo, Carducci, Carla, Battini, Roberta, Cioni, Giovanni, Antonozzi, Italo

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Enhanced interpretation of newborn screening results without analyte cutoff values von Marquardt, Gregg, Currier, Robert, McHugh, David M.S., Gavrilov, Dimitar, Magera, Mark J., Matern, Dietrich, Oglesbee, Devin, Raymond, Kimiyo, Rinaldo, Piero, Smith, Emily H., Tortorelli, Silvia, Turgeon, Coleman T., Lorey, Fred, Wilcken, Bridget, Greed, Lawrence C., Lewis, Barry, Schoos, Roland, Domingos, Mouseline Torquado, Sinclair, Graham, Al-Dirbashi, Osama Y., Chakraborty, Pranesh, Dymerski, Mark, Porter, Cory, Manning, Adrienne, Seashore, Margretta R., Quesada, Jonessy, Reuben, Alejandra, Hornik, Petr, Mandour, Iman Atef, Bodamer, Olaf, Dy, Bonifacio, Torres, Jasmin, Zori, Roberto, Cheillan, David, Ludvigson, David, Stembridge, Adrya, Bonham, Jim, Dotsikas, Yannis, Loukas, Yannis L., Papakonstantinou, Vagelis, Zacharioudakis, Georgios S.A., Baráth, Ákos, Karg, Eszter, Franzson, Leifur, Breen, Nancy N., Lesko, Barbara G., Berberich, Stanton L., Scolamiero, Emanuela, Antonozzi, Italo, Carducci, Claudia, Caruso, Ubaldo, Marca, Giancarlo la, Pasquini, Elisabetta, Di Gangi, Iole Maria, Giordano, Giuseppe, Teofoli, Francesca, Manos, Shawn M., Peterson, Colleen K., Mayfield Gibson, Stephanie K., Sevier, Darrin W., Park, Hyung-Doo, Khneisser, Issam, Browning, Phaidra, Gulamali-Majid, Fizza, Watson, Michael S., Eaton, Roger B., Sahai, Inderneel, Ruiz, Consuelo, Torres, Rosario, Seeterlin, Mary A., Stanley, Eleanor L., Hietala, Amy, McCann, Mark, Campbell, Carlene, Hopkins, Patrick V., de Sain–Van der Velden, Monique G., Elvers, Bert, Morrissey, Mark A., Sunny, Sherlykutty, Knoll, Detlef, Webster, Dianne, Frazier, Dianne M., McClure, Julie D., Sesser, David E., Rocha, Hugo, Vilarinho, Laura, John, Catharine, Lim, James, Caldwell, S. Graham, Castiñeiras Ramos, Daisy E., Fernández, Inmaculada Rueda, Egea-Mellado, José María, González-Gallego, Inmaculada, Pecellin, Carmen Delgado, Childs, Thomas, McKeever, Christine D., Abdulrahman, Mahera, Queijo, Cecilia, Lemes, Aída, Hoffman, Gary L.

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Methylenetetrahydrofolate reductase homozygous mutation in a young boy with cerebellar infarction von Spalice, Alberto, Del Balzo, Francesca, Perla, Francesco Massimo, Properzi, Enrico, Carducci, Carla, Antonozzi, Italo, Iannetti, Paola

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A New Tyrosine Hydroxylase Genotype Associated With Early-Onset Severe Encephalopathy von Giovanniello, Teresa, Claps, Dianella, Carducci, Carla, Carducci, Claudia, Blau, Nenad, Vigevano, Federico, Antonozzi, Italo, Leuzzi, Vincenzo

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Urinary Neopterin and Phenylalanine Loading Test as Tools for the Biochemical Diagnosis of Segawa Disease von Leuzzi, Vincenzo, Carducci, Claudia, Chiarotti, Flavia, D’Agnano, Daniela, Giannini, Maria Teresa, Antonozzi, Italo, Carducci, Carla

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A mutation on exon 6 of guanidinoacetate methyltransferase (GAMT) gene supports a different function for isoform a and b of GAMT enzyme von Leuzzi, Vincenzo, Carducci, Carla, Carducci, Claudia, Matricardi, Maria, Bianchi, Maria Cristina, Di Sabato, Maria Lucia, Artiola, Cristiana, Antonozzi, Italo

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The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acid von Marescau, Bart, De Deyn, Peter P., Qureshi, Ijaz A., De Broe, Marc E., Antonozzi, Italo, Cederbaum, Stephen D., Cerone, Roberto, Chamoles, Nestor, Gatti, Rosa, Kang, Soo-Sang, Lambert, Marie, Possemiers, Ilse, Snyderman, Selma E., Yoshino, Makoto

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A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia von De Rosa, Anna, Carducci, Carla, Antonozzi, Italo, Giovanniello, Teresa, Xhoxhi, Evgjeni, Criscuolo, Chiara, Menchise, Valeria, Striano, Salvatore, Filla, Alessandro, De Michele, Giuseppe

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Screening for eating disorders : false negatives and eating disorders not otherwise specified von VETRONE, Giuseppe, CUZZOLARO, Massimo, ANTONOZZI, Italo, GARFINKEL, Paul E

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Two New Severe Mutations Causing Guanidinoacetate Methyltransferase Deficiency von Carducci, Carla, Leuzzi, Vincenzo, Carducci, Claudia, Prudente, Sabrina, Mercuri, Luana, Antonozzi, Italo

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Automated high-performance liquid chromatographic method for the determination of guanidinoacetic acid in dried blood spots: a tool for early diagnosis of guanidinoacetate methyltr... von Carducci, Claudia, Birarelli, Maurizio, Santagata, Pino, Leuzzi, Vincenzo, Carducci, Carla, Antonozzi, Italo

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Automated method for the measurement of amino acids in urine by high-performance liquid chromatography von Carducci, Claudia, Birarelli, Maurizio, Leuzzi, Vincenzo, Santagata, Giuseppe, Serafini, Paola, Antonozzi, Italo

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Neuropsychological and Neuroradiological (MRI) Variations During Phenylalanine Load: Protective Effect of Valine, Leucine, and Isoleucine Supplementation von Leuzzi, Vincenzo, Fois, Daniela, Carducci, Claudia, Antonozzi, Italo, Trasimeni, Guido

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Reduced natural killer cell activity in major depression: neuroendocrine implications von Nerozzi, Dina, Santoni, Angela, Bersani, Giuseppe, Magnani, Armando, Bressan, Annamaria, Pasini, Augusto, Antonozzi, Italo, Frajese, Gaetano

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Dexamethasone Suppression Test in Childhood Headache von Guidetti, Vincenzo, Antonozzi, Italo, Fabiano, Antonella, Seri, Stefano

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Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy von CARDUCCI, C, LEUZZI, V, SCUDERI, M, DE NEGRI, A. M, BALACCO GABRIELI, C, ANTONOZZI, I, PONTECORVI, A

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Prolactin responses to domperidone in chronic schizophrenia von Nerozzi, Dina, Magnani, Armando, Dastoli, Corrado, Ferri, Edoardo, Capesciotti, Giampiero, Antonozzi, Italo, Frajese, Gaetano, Meltzer, Herbert Y.

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Plasma prolactin response to domperidone in acute schizophrenia and schizophreniform illness von Nerozzi, Dina, Magnani, Armando, Sforza, Vincenzo, Scaramucci, Elena, Cerilli, Marco, Moretti, Costanzo, Frajese, Gaetano, Antonozzi, Italo, Meltzer, Herbert Y.

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