Optic neuritis associated with multiple sclerosis: VEPs sensitive in acute phase, OCT useful in chronic phase
2014-01-01 Di, Maggio; G., Santangelo; R. I., Guerrieri; S., Ferrari; L., Medaglini; S., Rodegher; M., Colombo; B., Moiola; Del, Carro; U., Martinelli; V., Comi; Leocani, ANNUNZIATA MARIA LETIZIA
Optical coherence tomography and multifocal visual evoked potentials can be useful in clinical practice when full-field visual evoked potentials fail in identifying visual pathway abnormalities
2015-01-01 Guerrieri, S.; Di, Maggio; G., Vitali; F., Santangelo; R., Medaglini; S., Moiola; Del, Carro; U., Martinelli; V., Comi; Leocani, ANNUNZIATA MARIA LETIZIA
A demyelinating disorder characterized by repeated episodes of optic neuritis and brainstem dysfuntions in a girl with anti-MOG positivity
2015-01-01 Moiola, L.; Sangalli, F.; Preziosa, P.; Radaelli, M.; Leocani, ANNUNZIATA MARIA LETIZIA; Di, Maggio; G., Baldoli; C., Martinellli; V., Comi
Identification and functional analysis of DUOX2 variants: biallelic mutations are associated with permanent congenital hypothyroidism
2012-01-01 Mussa, M; Zamproni, I; Persani, L; Cortinovis, F; Vigone, M; Rabbiosi, S; Beccaria, L; Visser, T; Moreno, J; Weber, Giovanna; Fugazzola, L.
Intellectual outcome at 8 years of age in a large cohort of children with congenital hypothyroidism: effect of initial LT4 dose
2012-01-01 De Martino, L; Polizzi, M; Vigone, Mc; Bruzzese, D; Bassi, L; Pozzi, L; Di Mase, R; Bravaccio, C; Weber, Giovanna; Salerno, M.
Bilateral corticospinal projections from the hand motor area in congenital mirror movements: neurophysiological evidence in a patient after stroke
2005-01-01 Leocani, ANNUNZIATA MARIA LETIZIA; Martins Silva, A; Guerriero, R; Inuggi, A; Filippi, Massimo; Comola, M; Mammi, S; Rocca, Ma; Falini, A; Comi, G.
“Juvenile lynphocytic thyroidits: 3 years follow-up in euthyroid patients non treated at disease on set
1995-01-01 Mussa, G. C.; Cacciari, E.; Chiumello, G.; De Santis, C.; Cassio, A.; Weber, Giovanna; Corrias, A.; Bona, G.; Silvestro, L.
Visuo-motor learning in multiple sclerosis: Evaluation with a virtual reality system
2006-01-01 Comi, E; Rovaris, M; Cursi, M; Annovazzi, P; Comola, M; Rossi, P; Martinelli, V; Comi, G; Leocani, ANNUNZIATA MARIA LETIZIA
"Effect of long-term glucocorticoid therapy on bone density and bone remodeling indexes in patients with congenital adrenal hyperplasia"
1995-01-01 Mora, S.; Weber, Giovanna; Saggion, F.; Russo, G.; Prinster, C.; Proverbio, M. C.; Chiumello, G.
Alternative diagnostic approach to the etiology definition of Congenital Hypothyroidism"
1995-01-01 Siragusa, V.; Vigone, M. C.; Paesano, P. L.; Dosio, F.; Mora, S.; Weber, Giovanna; Rondanini, G. F.; DEL MASCHIO, Alessandro; Fazio, F.; Chiumello, G.
Brain M.R.I. in congenital hypothyroidism in infants at diagnosis "
1993-01-01 Siragusa, V.; Triulzi, F.; Weber, Giovanna; Boffelli, S.; Scotti, G.; Chimello G. Brain M. R. I., in congenital hypothiroidism in infants at diagnosis
Neurophysiological abnormalities of CNS in congenital hypothyroid school age children
1992-01-01 Weber, Giovanna; Rondanini, G. F.; Siragusa, V.; Manzoni, P.; Garavaglia, E.; Medaglini, S.; Lia, C.; Locatelli, T.; Colombini, I.; Mora, S.; Comi, G.; Chiumello, G.
Successful human islet isolation and purification from donors aged under thirty by intraductal injection of collagenase immediately after organ removal
1992-01-01 Socci, C; Davalli, Am; Vignali, Andrea; Maffi, P; Magistretti, P; Zammarchi, O; Scaglia, L; De Nittis, P; Pozza, G; Di Carlo, V. .
Elevated endogenous ouabain and reduced wxcretion of uric acid after acute salt load in hypertensive patients.
2014-01-01 Lanzani, C; Citterio, L; Brioni, E; Simonini, M; Maggioni, C; Messaggio, E; Hamlyn, J; Manunta, Paolo
Bone mineralization in Turner syndrome: transdermic vs oral estrogen treatment
1992-01-01 Weber, Giovanna; Mora, S.; Nizzoli, G.; Pasolini, D.; Gallia, P.; Basso, S.; Chiumello, G.
Neurophysiological involvement differs between secondary and primary progressive forms of multiple sclerosis
2009-01-01 Bianco, M.; Comi, G.; Leocani, ANNUNZIATA MARIA LETIZIA; Straffi, L.; Bucello, S.; Nossa, A.; Moiola, L.; Martinelli, V.; Balnyte, R.
Neonatal screening of congenital hypothyroidism and Turner's syndrome: diagnostic and therapeutic doubts
2010-01-01 Vigone, Mc; Maina, L; Bassi, L; Passoni, A; Cortinovis, F; Rabbiosi, S; Di Frenna, M; Chiumello, G; Weber, Giovanna
Changes in attention patterns of school-aged children with Congenital Hypothyroidism
2005-01-01 Colombini, Mi; Longaretti, R; Vigone, Mc; Giovanettoni, C; Passoni, A; Saporiti, R; Groppelli, A; Weber, Giovanna
The evolution of neonatal TSH screening strategies modifies the characteristics of congenital hypothyroidism
2007-01-01 Vigone, Mc; Viganò, P; Cortinovis, F; Passoni, A; Odoni, M; Calibiro, D; Persani, L; Weber, Giovanna; Corbetta, C.
Hypercalciuria and hypocalcemia: Identification of two de novo activating mutations in the transmembrane domains of the calcium-sensing receptor
2005-01-01 Mora, S; Zamproni, I; Proverbio, Mc; Chiumello, G; Weber, Giovanna
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Optic neuritis associated with multiple sclerosis: VEPs sensitive in acute phase, OCT useful in chronic phase | 1-gen-2014 | Di, Maggio; G., Santangelo; R. I., Guerrieri; S., Ferrari; L., Medaglini; S., Rodegher; M., Colombo; B., Moiola; Del, Carro; U., Martinelli; V., Comi; Leocani, ANNUNZIATA MARIA LETIZIA | |
| Optical coherence tomography and multifocal visual evoked potentials can be useful in clinical practice when full-field visual evoked potentials fail in identifying visual pathway abnormalities | 1-gen-2015 | Guerrieri, S.; Di, Maggio; G., Vitali; F., Santangelo; R., Medaglini; S., Moiola; Del, Carro; U., Martinelli; V., Comi; Leocani, ANNUNZIATA MARIA LETIZIA | |
| A demyelinating disorder characterized by repeated episodes of optic neuritis and brainstem dysfuntions in a girl with anti-MOG positivity | 1-gen-2015 | Moiola, L.; Sangalli, F.; Preziosa, P.; Radaelli, M.; Leocani, ANNUNZIATA MARIA LETIZIA; Di, Maggio; G., Baldoli; C., Martinellli; V., Comi | |
| Identification and functional analysis of DUOX2 variants: biallelic mutations are associated with permanent congenital hypothyroidism | 1-gen-2012 | Mussa, M; Zamproni, I; Persani, L; Cortinovis, F; Vigone, M; Rabbiosi, S; Beccaria, L; Visser, T; Moreno, J; Weber, Giovanna; Fugazzola, L. | |
| Intellectual outcome at 8 years of age in a large cohort of children with congenital hypothyroidism: effect of initial LT4 dose | 1-gen-2012 | De Martino, L; Polizzi, M; Vigone, Mc; Bruzzese, D; Bassi, L; Pozzi, L; Di Mase, R; Bravaccio, C; Weber, Giovanna; Salerno, M. | |
| Bilateral corticospinal projections from the hand motor area in congenital mirror movements: neurophysiological evidence in a patient after stroke | 1-gen-2005 | Leocani, ANNUNZIATA MARIA LETIZIA; Martins Silva, A; Guerriero, R; Inuggi, A; Filippi, Massimo; Comola, M; Mammi, S; Rocca, Ma; Falini, A; Comi, G. | |
| “Juvenile lynphocytic thyroidits: 3 years follow-up in euthyroid patients non treated at disease on set | 1-gen-1995 | Mussa, G. C.; Cacciari, E.; Chiumello, G.; De Santis, C.; Cassio, A.; Weber, Giovanna; Corrias, A.; Bona, G.; Silvestro, L. | |
| Visuo-motor learning in multiple sclerosis: Evaluation with a virtual reality system | 1-gen-2006 | Comi, E; Rovaris, M; Cursi, M; Annovazzi, P; Comola, M; Rossi, P; Martinelli, V; Comi, G; Leocani, ANNUNZIATA MARIA LETIZIA | |
| "Effect of long-term glucocorticoid therapy on bone density and bone remodeling indexes in patients with congenital adrenal hyperplasia" | 1-gen-1995 | Mora, S.; Weber, Giovanna; Saggion, F.; Russo, G.; Prinster, C.; Proverbio, M. C.; Chiumello, G. | |
| Alternative diagnostic approach to the etiology definition of Congenital Hypothyroidism" | 1-gen-1995 | Siragusa, V.; Vigone, M. C.; Paesano, P. L.; Dosio, F.; Mora, S.; Weber, Giovanna; Rondanini, G. F.; DEL MASCHIO, Alessandro; Fazio, F.; Chiumello, G. | |
| Brain M.R.I. in congenital hypothyroidism in infants at diagnosis " | 1-gen-1993 | Siragusa, V.; Triulzi, F.; Weber, Giovanna; Boffelli, S.; Scotti, G.; Chimello G. Brain M. R. I., in congenital hypothiroidism in infants at diagnosis | |
| Neurophysiological abnormalities of CNS in congenital hypothyroid school age children | 1-gen-1992 | Weber, Giovanna; Rondanini, G. F.; Siragusa, V.; Manzoni, P.; Garavaglia, E.; Medaglini, S.; Lia, C.; Locatelli, T.; Colombini, I.; Mora, S.; Comi, G.; Chiumello, G. | |
| Successful human islet isolation and purification from donors aged under thirty by intraductal injection of collagenase immediately after organ removal | 1-gen-1992 | Socci, C; Davalli, Am; Vignali, Andrea; Maffi, P; Magistretti, P; Zammarchi, O; Scaglia, L; De Nittis, P; Pozza, G; Di Carlo, V. . | |
| Elevated endogenous ouabain and reduced wxcretion of uric acid after acute salt load in hypertensive patients. | 1-gen-2014 | Lanzani, C; Citterio, L; Brioni, E; Simonini, M; Maggioni, C; Messaggio, E; Hamlyn, J; Manunta, Paolo | |
| Bone mineralization in Turner syndrome: transdermic vs oral estrogen treatment | 1-gen-1992 | Weber, Giovanna; Mora, S.; Nizzoli, G.; Pasolini, D.; Gallia, P.; Basso, S.; Chiumello, G. | |
| Neurophysiological involvement differs between secondary and primary progressive forms of multiple sclerosis | 1-gen-2009 | Bianco, M.; Comi, G.; Leocani, ANNUNZIATA MARIA LETIZIA; Straffi, L.; Bucello, S.; Nossa, A.; Moiola, L.; Martinelli, V.; Balnyte, R. | |
| Neonatal screening of congenital hypothyroidism and Turner's syndrome: diagnostic and therapeutic doubts | 1-gen-2010 | Vigone, Mc; Maina, L; Bassi, L; Passoni, A; Cortinovis, F; Rabbiosi, S; Di Frenna, M; Chiumello, G; Weber, Giovanna | |
| Changes in attention patterns of school-aged children with Congenital Hypothyroidism | 1-gen-2005 | Colombini, Mi; Longaretti, R; Vigone, Mc; Giovanettoni, C; Passoni, A; Saporiti, R; Groppelli, A; Weber, Giovanna | |
| The evolution of neonatal TSH screening strategies modifies the characteristics of congenital hypothyroidism | 1-gen-2007 | Vigone, Mc; Viganò, P; Cortinovis, F; Passoni, A; Odoni, M; Calibiro, D; Persani, L; Weber, Giovanna; Corbetta, C. | |
| Hypercalciuria and hypocalcemia: Identification of two de novo activating mutations in the transmembrane domains of the calcium-sensing receptor | 1-gen-2005 | Mora, S; Zamproni, I; Proverbio, Mc; Chiumello, G; Weber, Giovanna |
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Scopri
Tipologia
- 1 Contributo su Rivista3192
Data di pubblicazione
- In corso di stampa1
- 2020 - 202596
- 2010 - 20191464
- 2000 - 20091294
- 1990 - 1999321
- 1983 - 198916
Editore
- ELSEVIER22
- LIPPINCOTT WILLIAMS & WILKINS14
- NLM (Medline)13
- URBAN & VOGEL12
- ELSEVIER SCIENCE BV11
- DR DIETRICH STEINKOPFF VERLAG10
- ELSEVIER SCIENCE INC10
- OXFORD UNIV PRESS10
- SPRINGER HEIDELBERG10
- SPRINGER9
Rivista
- EUROPEAN UROLOGY. SUPPLEMENTS174
- JOURNAL OF NEUROLOGY153
- THE JOURNAL OF UROLOGY152
- BONE MARROW TRANSPLANTATION127
- EUROPEAN NEUROPSYCHOPHARMACOLOGY126
- NEUROLOGICAL SCIENCES88
- BLOOD86
- EUROPEAN HEART JOURNAL72
- NEUROLOGY72
- GASTROENTEROLOGY71
Keyword
- systemic sclerosis12
- Children4
- fibrosis4
- JIA4
- JSLE4
- None4
- angiogenesis3
- animal model3
- Bone mass3
- IPMN3
Lingua
- eng1301
- ita202
- und13
Accesso al fulltext
- no fulltext3161
- reserved25
- open6