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THE TREATMENT OF GUANIDINOACETATE METHYLTRANSFERASE (GAMT) DEFICIENCY
2005 Leuzzi, Vincenzo; Carducci, Claudia; DE LEO, S; DI SABATO, M; Bianchi, Mc; Tosetti, M; Carducci, Carla; Antonozzi, I.
The treatment of guanidinoacetate methyltransferase (GAMT) deficiency: clinical and biochemical follow-up.
2001 Leuzzi, Vincenzo; Bianchi, Mc; Tosetti, M; Carducci, Claudia; Carducci, Carla; Antonozzi, I.
The treatment of guanidinoacetato methyltrasferase (GAMT) deficiency: clinical and biochemical follow up.
2001 Leuzzi, Vincenzo; Bianchi, Mc; Tosetti, M; Carducci, Claudia; Carducci, Carla; Antonozzi, I.
The treatment of phenylalanine hydroxylase (PAH)-deficient BH4-responsive patints with tetrahydrobiopterin (BH4): tolerance to Phe and response to BH4.
2005 Leuzzi, Vincenzo; Carducci, Claudia; DE LEO, Sabrina; Montieri, P; Carducci, Carla; Antonozzi, Italo
Transient hyperphenylalaninemia due to heterozygous mutation in pyruvoyltetrahydropterin synthase (PTS) gene
2015 Nardecchia, Francesca; Artiola, Cristiana; Carducci, Claudia; Carducci, Carla; Giovanniello, Teresa; Leuzzi, Vincenzo
Tyrosine hydroxylase (TH) deficiency improving with catechol o-methyltransferase (COMT) inhibitor treatment.
2002 Leuzzi, Vincenzo; Carducci, Claudia; C., DIONISI VICI; Antonozzi, Italo
Urine sepiapterin excretion as a new diagnostic marker for sepiapterin reductase deficiency
2015 Carducci, Claudia; Santagata, Silvia; Friedman, J; Pasquini, E; Tolve, M; Carducci, Carla; Angeloni, Antonio; Leuzzi, Vincenzo
Vulnerability and resilience to phenylalanine in PKU patients.
2016 Manti, Filippo; Nardecchia, F; Paci, S; Chiarotti, F; Carducci, Carla; Dalmazzone, S; Giordano, L; Cefalo, G; Banderali, G; Leuzzi, Vincenzo
White matter (WM) alterations and brain Phe in PKU assessed by 3 Tesla (T) magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (1-H-MRS)
2004 Leuzzi, Vincenzo; Scarabino, T; Tosetti, M; Burroni, M; Carnevale, F; Carducci, Claudia; Carducci, Carla; Antonozzi, Italo
White matter involvement and neurocognitive outcome in phenylketonuric (PKU) patients with and without BH4/sapropterin dihydrochloride supplementation
2013 Mastrangelo, Mario; Caputi, C; Berillo, Luana; Manti, Filippo; Caforio, C; Bertino, S; Carducci, Claudia; Leuzzi, Vincenzo
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
THE TREATMENT OF GUANIDINOACETATE METHYLTRANSFERASE (GAMT) DEFICIENCY | 2005 | Leuzzi, Vincenzo; Carducci, Claudia; DE LEO, S; DI SABATO, M; Bianchi, Mc; Tosetti, M; Carducci, Carla; Antonozzi, I. | |
The treatment of guanidinoacetate methyltransferase (GAMT) deficiency: clinical and biochemical follow-up. | 2001 | Leuzzi, Vincenzo; Bianchi, Mc; Tosetti, M; Carducci, Claudia; Carducci, Carla; Antonozzi, I. | |
The treatment of guanidinoacetato methyltrasferase (GAMT) deficiency: clinical and biochemical follow up. | 2001 | Leuzzi, Vincenzo; Bianchi, Mc; Tosetti, M; Carducci, Claudia; Carducci, Carla; Antonozzi, I. | |
The treatment of phenylalanine hydroxylase (PAH)-deficient BH4-responsive patints with tetrahydrobiopterin (BH4): tolerance to Phe and response to BH4. | 2005 | Leuzzi, Vincenzo; Carducci, Claudia; DE LEO, Sabrina; Montieri, P; Carducci, Carla; Antonozzi, Italo | |
Transient hyperphenylalaninemia due to heterozygous mutation in pyruvoyltetrahydropterin synthase (PTS) gene | 2015 | Nardecchia, Francesca; Artiola, Cristiana; Carducci, Claudia; Carducci, Carla; Giovanniello, Teresa; Leuzzi, Vincenzo | |
Tyrosine hydroxylase (TH) deficiency improving with catechol o-methyltransferase (COMT) inhibitor treatment. | 2002 | Leuzzi, Vincenzo; Carducci, Claudia; C., DIONISI VICI; Antonozzi, Italo | |
Urine sepiapterin excretion as a new diagnostic marker for sepiapterin reductase deficiency | 2015 | Carducci, Claudia; Santagata, Silvia; Friedman, J; Pasquini, E; Tolve, M; Carducci, Carla; Angeloni, Antonio; Leuzzi, Vincenzo | |
Vulnerability and resilience to phenylalanine in PKU patients. | 2016 | Manti, Filippo; Nardecchia, F; Paci, S; Chiarotti, F; Carducci, Carla; Dalmazzone, S; Giordano, L; Cefalo, G; Banderali, G; Leuzzi, Vincenzo | |
White matter (WM) alterations and brain Phe in PKU assessed by 3 Tesla (T) magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (1-H-MRS) | 2004 | Leuzzi, Vincenzo; Scarabino, T; Tosetti, M; Burroni, M; Carnevale, F; Carducci, Claudia; Carducci, Carla; Antonozzi, Italo | |
White matter involvement and neurocognitive outcome in phenylketonuric (PKU) patients with and without BH4/sapropterin dihydrochloride supplementation | 2013 | Mastrangelo, Mario; Caputi, C; Berillo, Luana; Manti, Filippo; Caforio, C; Bertino, S; Carducci, Claudia; Leuzzi, Vincenzo |
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Opzioni
Scopri
Tipologia
- 04 Pubblicazione in atti di convegno 70
- 04 Pubblicazione in atti di convegno::04c Atto di convegno in rivista 70
Data di pubblicazione
- 2010 - 2016 33
- 2000 - 2009 35
- 1996 - 1999 2
Editore
- Kluwer Academic Publishers:Journals Department, PO Box 322, 3300 AH Dordrecht Netherlands:011 31 78 6576050, EMAIL: frontoffice@wkap.nl, kluweronline@wkap.nl, INTERNET: http://www.kluwerlaw.com, Fax: 011 31 78 6576254 10
- Springer 3
- Blackwell Science Limited:PO Box 88, Oxford OX2 0NE United Kingdom:011 44 1865 776868, 011 44 1865 206038, EMAIL: journals.cs@blacksci.co.uk, INTERNET: http://www.blackwell-science.com, Fax: 011 44 1865 721205 1
Prodotti per rivista
- JOURNAL OF INHERITED METABOLIC DISEASE 63
- EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY 2
- JOURNAL OF SLEEP RESEARCH 2
- ANNALS OF NEUROLOGY 1
- NEUROPSYCHOLOGICAL TRENDS 1
Prodotti per parola chiave
- 6-pyruvoyl-tetrahydropterin 1
- Arginine 1
- Creatine 1
- CT1 defect 1
- history 1
- Mental retardation 1
- mental retardation 1
- natural 1
- SLC6A8 defect 1
- synthase 1
Lingua
- eng 35
- ita 1
Accesso al fulltext
- no fulltext 70