Suchergebnisse - Marco Cappa

Profile of mecasermin for the long-term treatment of growth failure in children and adolescents with severe primary IGF-1 deficiency von Danilo Fintini, Claudia Brufani, Marco Cappa

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Metreleptin for the treatment of progressive encephalopathy with/without lipodystrophy (PELD) in a child with progressive myoclonic epilepsy: a case report von Stefania Pedicelli, Luca de Palma, Caterina Pelosini, Marco Cappa

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Chronic Kidney Disease and Growth Failure in Children von Tommaso Todisco, Grazia Maria Ubertini, Carla Bizzarri, Sandro Loche, Marco Cappa

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"Impact of COVID-19 pandemic lockdown on early onset of puberty: experience of an Italian tertiary center" von Martina Verzani, Carla Bizzarri, Laura Chioma, Giorgia Bottaro, Stefania Pedicelli, Marco Cappa

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Lipoid congenital adrenal hyperplasia by steroidogenic acute regulatory protein (STAR) gene mutation in an Italian infant: an uncommon cause of adrenal insufficiency von Carla Bizzarri, Elisa Pisaneschi, Mafalda Mucciolo, Stefania Pedicelli, Daniela Galeazzi, Antonio Novelli, Marco Cappa

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The impact of IGF-I, puberty and obesity on early retinopathy in children: a cross-sectional study von Carla Bizzarri, Stefania Pedicelli, Antonino Romanzo, Sarah Bocchini, Giorgia Bottaro, Stefano Cianfarani, Marco Cappa

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Antioxidant Response in Human X-Linked Adrenoleukodystrophy Fibroblasts von Sara Petrillo, Jessica D'Amico, Francesco Nicita, Caterina Torda, Gessica Vasco, Enrico S. Bertini, Marco Cappa, Fiorella Piemonte

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Prenatal hydrocolpos in a male von Antonio Zaccara, Massimiliano Silveri, Maria Luisa Capitanucci, Giovanni Mosiello, Mario De Gennaro, Carla Bizzarri, Marco Cappa, Cinzia Orazi

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Longitudinal Neuropsychological Profile in a Patient with Triple A Syndrome von Luigi Mazzone, Valentina Postorino, Lavinia De Peppo, Lia Vassena, Laura Fatta, Marco Armando, Giuseppe Scirè, Marco Cappa, Stefano Vicari

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Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin von Carla Bizzarri, Germana Antonella Giannone, Jacopo Gervasoni, Sabina Benedetti, Federica Albanese, Luca Dello Strologo, Isabella Guzzo, Mafalda Mucciolo, Francesca Diomedi Camassei, Francesco Emma, Marco Cappa, Ottavia Porzio

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Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review von Marcello Niceta, Maria Lisa Dentici, Andrea Ciolfi, Romana Marini, Sabina Barresi, Francesca Romana Lepri, Antonio Novelli, Enrico Bertini, Marco Cappa, Maria Cristina Digilio, Bruno Dallapiccola, Marco Tartaglia

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