Sfoglia per Autore
L-Thyroxine stored in the hair of congenital hypothyroidism newborns at time of diagnosis. An evidence of placental crossing
1996-01-01 Camilot, M.; Antoniazzi, Franco; Mengarda, F.; Radetti, G.; Tagliaro, F.; Zamboni, Giorgio; Tato', Luciano
Determination of thyroxine in the hair of newborns by radioimmunoassay with high-performance liquid chromatographic confirmation
1998-01-01 Tagliaro, Franco; Camilot, M; Valentini, R; Mengarda, F; Antoniazzi, Franco; Tato', Luciano
Incidence of inborn errors of metabolism: results of newborn screening program in North-East Italy
2001-01-01 Zaffanello, Marco; Maffeis, Claudio; Camilot, Marta; Micciolo, R; Tatò, L.
Characterizatin of phenyalanine hydroxylase alleles in North-East Italy: a preliminary investigation
2001-01-01 Zaffanello, Marco; Camilot, Marta; Maffeis, Claudio; Vella, F; Tatò, L.
Neonatal screening for congenital errors of metabolism in Northeast Italy: retrospective study of the years 1978-1997
2002-01-01 Zaffanello, Marco; Maffeis, Claudio; Camilot, Marta; Micciolo, R; Tatò, L.
Thyroxine hair content in congenital hypothyroidism and hyperthyroidism.
2003-01-01 Zamboni, Giorgio; Camilot, M; Francia, G; Lauriola, S; Arslanoglu, I; Isguven, P; Tato', Luciano
Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls
2004-01-01 Teofoli, Francesca; Camilot, Marta; Gandini, Alberto; Franceschi, Roberto; F., Pellegrini; Monti, Elena; Perlini, Silvia; A., Rapa; A., Corrias; G., Bona; L., Tatò
Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes.
2005-01-01 Camilot, Marta; Teofoli, Francesca; Gandini, Alberto; Franceschi, R; Rapa, A; Corrias, A; Bona, G; Radetti, G; Tato', Luciano
Neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: a report three years into the program.
2005-01-01 Cavarzere, Paolo; Camilot, Marta; Teofoli, Francesca; Tato', Luciano
Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern italian neonatal screening
2005-01-01 Zaffanello, Marco; Zamboni, Giorgio; Maselli, M; Gandini, Alberto; Camilot, Marta; Maffeis, Claudio; Burlina, Ab; Tato', Luciano
Osteogenesis Imperfecta: clinical, biochemical and molecular findings
2006-01-01 Venturi, Giacomo; Tedeschi, Elisa; Mottes, Monica; Valli, M.; Camilot, Marta; Viglio, S.; Antoniazzi, Franco; Tato', Luciano
Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children
2007-01-01 Teofoli, Francesca; Camilot, Marta; Tato', Luciano
Risultati del follow-up a lungo termine di pz con ipotiroidismo congenito: l'etiologia condiziona il trattamento
2007-01-01 Perlini, S.; Franceschi, R.; Gaudino, Rossella; Monti, Elena; Vanzatim, ; Camilot, M.; Antoniazzi, Franco; Lauriola, Silvana; Tatò, L.
Effect of early thyroid scanning on levothyroxine dosage and neuropsychological development in congenital hypothyroidism.
2007-01-01 Perlini, S.; Franceschi, R.; Vanzati, M.; Monti, Elena; Gaudino, Rossella; Teofoli, F.; Camilot, M.; Antoniazzi, Franco; Lauriola, Silvana; Tatò, L.
Implementation of a congenital hypothyroidism newborn screening procedure with mutation detection on genomic DNA extracted from blood spots: the experience of the Italian northeastern reference center.
2007-01-01 Camilot, Marta; Teofoli, Francesca; Monica, Vincenzi; Federici, Francesca; Perlini, Silvia; Tato', Luciano
Circulating ghrelin levels in girls with central precocious puberty are reduced during treatment with LHRH analog.
2007-01-01 Maffeis, Claudio; Franceschi, R; Moghetti, Paolo; Camilot, Marta; Lauriola, Silvana; Tato', Luciano
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis
2008-01-01 Camilot, Marta; Teofoli, Francesca; S., Longobardi; Gandini, Alberto; C., Lievore; S., Lauriola; Tato', Luciano
Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy
2008-01-01 Gaudino, Rossella; Cavarzere, Paolo; Camilot, Marta; Teofoli, Francesca; Zampieri, Nicola; Tato', Luciano
Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia
2009-01-01 De Marco, G; Agretti, P; Camilot, Marta; Teofoli, Francesca; Tato', Luciano; Vitti, P; Pinchera, A; Tonacchera, M.
L. Inibina B in bambini prepuberi con pregresso criptorchidismo: indice di disfunzione testicolare?
2009-01-01 Cavarzere, P.; Gaudino, Rossella; Marostica, A; Camilot, Marta; Teofoli, Francesca; Zuin, V.; Franceschi, R.; Vincenzi, Monica; Perlini, S.; Monti, Elena; T. a. t. o., ’.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| L-Thyroxine stored in the hair of congenital hypothyroidism newborns at time of diagnosis. An evidence of placental crossing | 1-gen-1996 | Camilot, M.; Antoniazzi, Franco; Mengarda, F.; Radetti, G.; Tagliaro, F.; Zamboni, Giorgio; Tato', Luciano | |
| Determination of thyroxine in the hair of newborns by radioimmunoassay with high-performance liquid chromatographic confirmation | 1-gen-1998 | Tagliaro, Franco; Camilot, M; Valentini, R; Mengarda, F; Antoniazzi, Franco; Tato', Luciano | |
| Incidence of inborn errors of metabolism: results of newborn screening program in North-East Italy | 1-gen-2001 | Zaffanello, Marco; Maffeis, Claudio; Camilot, Marta; Micciolo, R; Tatò, L. | |
| Characterizatin of phenyalanine hydroxylase alleles in North-East Italy: a preliminary investigation | 1-gen-2001 | Zaffanello, Marco; Camilot, Marta; Maffeis, Claudio; Vella, F; Tatò, L. | |
| Neonatal screening for congenital errors of metabolism in Northeast Italy: retrospective study of the years 1978-1997 | 1-gen-2002 | Zaffanello, Marco; Maffeis, Claudio; Camilot, Marta; Micciolo, R; Tatò, L. | |
| Thyroxine hair content in congenital hypothyroidism and hyperthyroidism. | 1-gen-2003 | Zamboni, Giorgio; Camilot, M; Francia, G; Lauriola, S; Arslanoglu, I; Isguven, P; Tato', Luciano | |
| Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls | 1-gen-2004 | Teofoli, Francesca; Camilot, Marta; Gandini, Alberto; Franceschi, Roberto; F., Pellegrini; Monti, Elena; Perlini, Silvia; A., Rapa; A., Corrias; G., Bona; L., Tatò | |
| Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. | 1-gen-2005 | Camilot, Marta; Teofoli, Francesca; Gandini, Alberto; Franceschi, R; Rapa, A; Corrias, A; Bona, G; Radetti, G; Tato', Luciano | |
| Neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: a report three years into the program. | 1-gen-2005 | Cavarzere, Paolo; Camilot, Marta; Teofoli, Francesca; Tato', Luciano | |
| Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern italian neonatal screening | 1-gen-2005 | Zaffanello, Marco; Zamboni, Giorgio; Maselli, M; Gandini, Alberto; Camilot, Marta; Maffeis, Claudio; Burlina, Ab; Tato', Luciano | |
| Osteogenesis Imperfecta: clinical, biochemical and molecular findings | 1-gen-2006 | Venturi, Giacomo; Tedeschi, Elisa; Mottes, Monica; Valli, M.; Camilot, Marta; Viglio, S.; Antoniazzi, Franco; Tato', Luciano | |
| Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children | 1-gen-2007 | Teofoli, Francesca; Camilot, Marta; Tato', Luciano | |
| Risultati del follow-up a lungo termine di pz con ipotiroidismo congenito: l'etiologia condiziona il trattamento | 1-gen-2007 | Perlini, S.; Franceschi, R.; Gaudino, Rossella; Monti, Elena; Vanzatim, ; Camilot, M.; Antoniazzi, Franco; Lauriola, Silvana; Tatò, L. | |
| Effect of early thyroid scanning on levothyroxine dosage and neuropsychological development in congenital hypothyroidism. | 1-gen-2007 | Perlini, S.; Franceschi, R.; Vanzati, M.; Monti, Elena; Gaudino, Rossella; Teofoli, F.; Camilot, M.; Antoniazzi, Franco; Lauriola, Silvana; Tatò, L. | |
| Implementation of a congenital hypothyroidism newborn screening procedure with mutation detection on genomic DNA extracted from blood spots: the experience of the Italian northeastern reference center. | 1-gen-2007 | Camilot, Marta; Teofoli, Francesca; Monica, Vincenzi; Federici, Francesca; Perlini, Silvia; Tato', Luciano | |
| Circulating ghrelin levels in girls with central precocious puberty are reduced during treatment with LHRH analog. | 1-gen-2007 | Maffeis, Claudio; Franceschi, R; Moghetti, Paolo; Camilot, Marta; Lauriola, Silvana; Tato', Luciano | |
| A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis | 1-gen-2008 | Camilot, Marta; Teofoli, Francesca; S., Longobardi; Gandini, Alberto; C., Lievore; S., Lauriola; Tato', Luciano | |
| Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy | 1-gen-2008 | Gaudino, Rossella; Cavarzere, Paolo; Camilot, Marta; Teofoli, Francesca; Zampieri, Nicola; Tato', Luciano | |
| Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia | 1-gen-2009 | De Marco, G; Agretti, P; Camilot, Marta; Teofoli, Francesca; Tato', Luciano; Vitti, P; Pinchera, A; Tonacchera, M. | |
| L. Inibina B in bambini prepuberi con pregresso criptorchidismo: indice di disfunzione testicolare? | 1-gen-2009 | Cavarzere, P.; Gaudino, Rossella; Marostica, A; Camilot, Marta; Teofoli, Francesca; Zuin, V.; Franceschi, R.; Vincenzi, Monica; Perlini, S.; Monti, Elena; T. a. t. o., ’. |
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