MAGHNIE, MOHAMAD
MAGHNIE, MOHAMAD
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
"Do no harm": workshop on the management of craniopharyngioma.
2008-01-01 Gleeson, H; Amin, R; Maghnie, Mohamad
"Pesto" Mutation: Phenotypic and Genotypic Characteristics of Eight GCK/MODY Ligurian Patients
2023-01-01 Salina, Alessandro; Bassi, Marta; Aloi, Concetta; Strati, Marina Francesca; Bocciardi, Renata; D'Annunzio, Giuseppe; Maghnie, Mohamad; Minuto, Nicola
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias.
2012-01-01 Gana, S; Veggiotti, P; Sciacca, G; Fedeli, C; Bersano, A; Micieli, G; Maghnie, Mohamad; Ciccone, R; Rossi, E; Plunkett, K; Bi, W; Sutton, Vr; Zuffardi, O.
[Effects of chorionic gonadotropin (hCG) therapy on the immune system].
1990-01-01 Maghnie, Mohamad; Valtorta, A; Moretta, A; Priora, C; Preti, P.
[Evaluation of humoral immunity in children with growth hormone deficiency].
1988-01-01 Moretta, A; Valtorta, A; Maghnie, Mohamad; Biscaldi, I; Girani, Ma; Cerbo, Rm
A "hot spot" in the Pit-1 gene responsible for combined pituitary hormone deficiency: clinical and molecular correlates.
1995-01-01 Cohen, Le; Wondisford, Fe; Salvatoni, A; Maghnie, Mohamad; Brucker Davis, F; Weintraub, Bd; Radovick, S.
A case of interference in testosterone, DHEA-S and progesterone measurements by second generation immunoassays
2021-01-01 Cresta, F.; Arcuri, L.; Bianchin, S.; Castellani, C.; Casciaro, R.; Cavedagna, T. M.; Maghnie, M.; Barco, S.; Cangemi, G.
A case of multiple intestinal atresias, brain anomalies, mental retardation, growth hormone deficiency and clitoris hypertrophy.
1998-01-01 Guala, A; Licardi, G; Maghnie, Mohamad; Minniti, S; Danesino, C.
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure.
2009-01-01 Corre, T; Schuettler, J; Bione, S; Marozzi, A; Persani, L; Rossetti, R; Torricelli, F; Giotti, I; Vogt, P; Toniolo, D; Maghnie, Mohamad
A longitudinal printo study on growth and puberty in juvenile systemic lupus erythematosus.
2012-01-01 Rygg, M; Pistorio, A; Ravelli, Angelo; Maghnie, Mohamad; DI IORGI, Natascia; Bader Meunier, B; Da Silva, C; Roldan Molina, R; Barash, J; Dracou, C; Gandom Laloum, S; Jarosova, K; Job Deslandre, C; Kone Paut, I; Garofalo, F; Press, J; Sengler, C; Tauber, T; Martini, Alberto; Ruperto, N.
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes
2016-01-01 Russo, S; Calzari, L; Mussa, A; Mainini, E; Cassina, M; Di Candia, S; Clementi, M; Guzzetti, Sara; Tabano, S; Miozzo, M; Sirchia, S; Finelli, P; Prontera, P; Maitz, S; Sorge, G; Calcagno, A; Maghnie, M; Divizia, Mt; Melis, D; Manfredini, E; Ferrero, Gb; Pecile, V; Larizza, L.
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype
2023-01-01 Palumbo, S; Cirillo, G; Sanchez, G; Aiello, F; Fachin, A; Baldo, F; Pellegrin, M C; Cassio, A; Salerno, M; Maghnie, M; Faienza, M F; Wasniewska, M; Fintini, D; Giacomozzi, C; Ciccone, S; Miraglia Del Giudice, E; Tornese, G; Grandone, A
A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusion
2019-01-01 Scala, M.; Accogli, A.; De Grandis, E.; Allegri, A.; Bagowski, C.; Shoukier, M.; Maghnie, M.; Capra, V.
A novel pathogenic MYH3 mutation in a child with SheldonâHall syndrome and vertebral fusions
2018-01-01 Scala, Marcello; Accogli, Andrea; De Grandis, Elisa; Allegri, Anna; Bagowski, Christoph P.; Shoukier, Moneef; Maghnie, Mohamad; Capra, Valeria
Abnormalities of pubertal development and gonadal function in Noonan syndrome
2023-01-01 Patti, Giuseppa; Scaglione, Marco; Maiorano, Nadia Gabriella; Rosti, Giulia; Divizia, Maria Teresa; Camia, Tiziana; De Rose, Elena Lucia; Zucconi, Alice; Casalini, Emilio; Napoli, Flavia; Di Iorgi, Natascia; Maghnie, Mohamad
Accuracy and limitations of the growth hormone (GH) releasing hormone-arginine retesting in young adults with childhood-onset GH deficiency
2019-01-01 Patti, G.; Noli, S.; Capalbo, D.; Allegri, A. M. E.; Napoli, F.; Cappa, M.; Ubertini, G. M.; Gallizia, A.; Notarnicola, S.; Ibba, A.; Crocco, M.; Parodi, S.; Salerno, M.; Loche, S.; Garre, M. L.; Tornari, E.; Maghnie, M.; Iorgi, N. D.
Accuracy of Glucagon Testing Across Transition in Young Adults with Childhood-Onset Growth Hormone Deficiency
2024-01-01 Fava, Daniela; Guglielmi, Davide; Pepino, Carlotta; Angelelli, Alessia; Casalini, Emilio; Varotto, Carolina; Panciroli, Marta; Tedesco, Caterina; Camia, Tiziana; Naim, Alessandro; Allegri, Anna Elsa Maria; Patti, Giuseppa; Napoli, Flavia; Gastaldi, Roberto; Parodi, Stefano; Salerno, Maria Carolina; Maghnie, Mohamad; Di Iorgi, Natascia
Addressing gaps in care of people with conditions affecting sex development and maturation
2019-01-01 Hiort, O.; Cools, M.; Springer, A.; Mcelreavey, K.; Greenfield, A.; Wudy, S. A.; Kulle, A.; Ahmed, S. F.; Dessens, A.; Balsamo, A.; Maghnie, M.; Bonomi, M.; Dattani, M.; Persani, L.; Audi, L.
Adenosine Blood Level: A Biomarker of White Matter Damage in Very Low Birth Weight Infants
2022-01-01 Colella, Marina; Panfoli, Isabella; Doglio, Matteo; Cassanello, Michela; Bruschi, Maurizio; Angelis, Laura C De; Candiano, Giovanni; Parodi, Alessandro; Malova, Mariya; Petretto, Andrea; Morana, Giovanni; Tortora, Domenico; Severino, Mariasavina; Maghnie, Mohamad; Buonocore, Giuseppe; Rossi, Andrea; Baud, Oliver; Ramenghi, Luca A
Adherence in children with growth hormone deficiency treated with r-hGH and the easypod™ device
2016-01-01 Loche, S.; Salerno, M.; Garofalo, P.; Cardinale, G. M.; Licenziati, Mr; Citro, G.; Caruso Nicoletti, M.; Cappa, M.; Longobardi, S.; Maghnie, Mohamad; Perrone, R.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
"Do no harm": workshop on the management of craniopharyngioma. | 1-gen-2008 | Gleeson, H; Amin, R; Maghnie, Mohamad | |
"Pesto" Mutation: Phenotypic and Genotypic Characteristics of Eight GCK/MODY Ligurian Patients | 1-gen-2023 | Salina, Alessandro; Bassi, Marta; Aloi, Concetta; Strati, Marina Francesca; Bocciardi, Renata; D'Annunzio, Giuseppe; Maghnie, Mohamad; Minuto, Nicola | |
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias. | 1-gen-2012 | Gana, S; Veggiotti, P; Sciacca, G; Fedeli, C; Bersano, A; Micieli, G; Maghnie, Mohamad; Ciccone, R; Rossi, E; Plunkett, K; Bi, W; Sutton, Vr; Zuffardi, O. | |
[Effects of chorionic gonadotropin (hCG) therapy on the immune system]. | 1-gen-1990 | Maghnie, Mohamad; Valtorta, A; Moretta, A; Priora, C; Preti, P. | |
[Evaluation of humoral immunity in children with growth hormone deficiency]. | 1-gen-1988 | Moretta, A; Valtorta, A; Maghnie, Mohamad; Biscaldi, I; Girani, Ma; Cerbo, Rm | |
A "hot spot" in the Pit-1 gene responsible for combined pituitary hormone deficiency: clinical and molecular correlates. | 1-gen-1995 | Cohen, Le; Wondisford, Fe; Salvatoni, A; Maghnie, Mohamad; Brucker Davis, F; Weintraub, Bd; Radovick, S. | |
A case of interference in testosterone, DHEA-S and progesterone measurements by second generation immunoassays | 1-gen-2021 | Cresta, F.; Arcuri, L.; Bianchin, S.; Castellani, C.; Casciaro, R.; Cavedagna, T. M.; Maghnie, M.; Barco, S.; Cangemi, G. | |
A case of multiple intestinal atresias, brain anomalies, mental retardation, growth hormone deficiency and clitoris hypertrophy. | 1-gen-1998 | Guala, A; Licardi, G; Maghnie, Mohamad; Minniti, S; Danesino, C. | |
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. | 1-gen-2009 | Corre, T; Schuettler, J; Bione, S; Marozzi, A; Persani, L; Rossetti, R; Torricelli, F; Giotti, I; Vogt, P; Toniolo, D; Maghnie, Mohamad | |
A longitudinal printo study on growth and puberty in juvenile systemic lupus erythematosus. | 1-gen-2012 | Rygg, M; Pistorio, A; Ravelli, Angelo; Maghnie, Mohamad; DI IORGI, Natascia; Bader Meunier, B; Da Silva, C; Roldan Molina, R; Barash, J; Dracou, C; Gandom Laloum, S; Jarosova, K; Job Deslandre, C; Kone Paut, I; Garofalo, F; Press, J; Sengler, C; Tauber, T; Martini, Alberto; Ruperto, N. | |
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes | 1-gen-2016 | Russo, S; Calzari, L; Mussa, A; Mainini, E; Cassina, M; Di Candia, S; Clementi, M; Guzzetti, Sara; Tabano, S; Miozzo, M; Sirchia, S; Finelli, P; Prontera, P; Maitz, S; Sorge, G; Calcagno, A; Maghnie, M; Divizia, Mt; Melis, D; Manfredini, E; Ferrero, Gb; Pecile, V; Larizza, L. | |
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype | 1-gen-2023 | Palumbo, S; Cirillo, G; Sanchez, G; Aiello, F; Fachin, A; Baldo, F; Pellegrin, M C; Cassio, A; Salerno, M; Maghnie, M; Faienza, M F; Wasniewska, M; Fintini, D; Giacomozzi, C; Ciccone, S; Miraglia Del Giudice, E; Tornese, G; Grandone, A | |
A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusion | 1-gen-2019 | Scala, M.; Accogli, A.; De Grandis, E.; Allegri, A.; Bagowski, C.; Shoukier, M.; Maghnie, M.; Capra, V. | |
A novel pathogenic MYH3 mutation in a child with SheldonâHall syndrome and vertebral fusions | 1-gen-2018 | Scala, Marcello; Accogli, Andrea; De Grandis, Elisa; Allegri, Anna; Bagowski, Christoph P.; Shoukier, Moneef; Maghnie, Mohamad; Capra, Valeria | |
Abnormalities of pubertal development and gonadal function in Noonan syndrome | 1-gen-2023 | Patti, Giuseppa; Scaglione, Marco; Maiorano, Nadia Gabriella; Rosti, Giulia; Divizia, Maria Teresa; Camia, Tiziana; De Rose, Elena Lucia; Zucconi, Alice; Casalini, Emilio; Napoli, Flavia; Di Iorgi, Natascia; Maghnie, Mohamad | |
Accuracy and limitations of the growth hormone (GH) releasing hormone-arginine retesting in young adults with childhood-onset GH deficiency | 1-gen-2019 | Patti, G.; Noli, S.; Capalbo, D.; Allegri, A. M. E.; Napoli, F.; Cappa, M.; Ubertini, G. M.; Gallizia, A.; Notarnicola, S.; Ibba, A.; Crocco, M.; Parodi, S.; Salerno, M.; Loche, S.; Garre, M. L.; Tornari, E.; Maghnie, M.; Iorgi, N. D. | |
Accuracy of Glucagon Testing Across Transition in Young Adults with Childhood-Onset Growth Hormone Deficiency | 1-gen-2024 | Fava, Daniela; Guglielmi, Davide; Pepino, Carlotta; Angelelli, Alessia; Casalini, Emilio; Varotto, Carolina; Panciroli, Marta; Tedesco, Caterina; Camia, Tiziana; Naim, Alessandro; Allegri, Anna Elsa Maria; Patti, Giuseppa; Napoli, Flavia; Gastaldi, Roberto; Parodi, Stefano; Salerno, Maria Carolina; Maghnie, Mohamad; Di Iorgi, Natascia | |
Addressing gaps in care of people with conditions affecting sex development and maturation | 1-gen-2019 | Hiort, O.; Cools, M.; Springer, A.; Mcelreavey, K.; Greenfield, A.; Wudy, S. A.; Kulle, A.; Ahmed, S. F.; Dessens, A.; Balsamo, A.; Maghnie, M.; Bonomi, M.; Dattani, M.; Persani, L.; Audi, L. | |
Adenosine Blood Level: A Biomarker of White Matter Damage in Very Low Birth Weight Infants | 1-gen-2022 | Colella, Marina; Panfoli, Isabella; Doglio, Matteo; Cassanello, Michela; Bruschi, Maurizio; Angelis, Laura C De; Candiano, Giovanni; Parodi, Alessandro; Malova, Mariya; Petretto, Andrea; Morana, Giovanni; Tortora, Domenico; Severino, Mariasavina; Maghnie, Mohamad; Buonocore, Giuseppe; Rossi, Andrea; Baud, Oliver; Ramenghi, Luca A | |
Adherence in children with growth hormone deficiency treated with r-hGH and the easypod™ device | 1-gen-2016 | Loche, S.; Salerno, M.; Garofalo, P.; Cardinale, G. M.; Licenziati, Mr; Citro, G.; Caruso Nicoletti, M.; Cappa, M.; Longobardi, S.; Maghnie, Mohamad; Perrone, R. |