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Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|June 26, 2019
Comparison of Quantitative Analysis of Methylated Alleles Real-Time PCR and Methylation-Specific MLPA for Molecular Diagnosis of Beckwith-Wiedemann SyndromeMassimiliano Bergallo, Ilaria Galliano, Paola Montanari, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 28, 2007
Bone alterations in children and young adults with renal transplant assessed by phalangeal quantitative ultrasoundAlessandro Mussa, Francesco Porta, Bruno Gianoglio, et al.
Current Issues in Molecular Biology|March 28, 2026
Human Endogenous Retroviruses and Epigenetic Regulators Are Dysregulated in Beckwith-Wiedemann SyndromeIlaria Galliano, Pier-Angelo Tovo, Cristina Calvi, et al.
European Journal of Endocrinology|September 17, 2015
Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiologyMalgorzata Wasniewska, Tommaso Aversa, Mariacarolina Salerno, et al.
Hormone Research in Paediatrics|June 16, 2012
Comparative evaluation of therapy with L-thyroxine versus no treatment in children with idiopathic and mild subclinical hypothyroidismMalgorzata Wasniewska, Andrea Corrias, Tommaso Aversa, et al.
European Journal of Pediatrics|June 19, 2009
A heritable cause of cleft lip and palate--Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosisGiovanni Battista Ferrero, Giuseppina Baldassarre, Emanuele Panza, et al.
European Journal of Pediatrics|July 21, 2009
Remittent hyperammonemia in congenital portosystemic shuntGiovanni Battista Ferrero, Francesco Porta, Elisa Biamino, et al.
Pediatric Gastroenterology, Hepatology & Nutrition|January 15, 2015
The complex surgical management of the first case of severe combined immunodeficiency and multiple intestinal atresias surviving after the fourth year of lifeRiccardo Guanà, Salvatore Garofano, Elisabetta Teruzzi, et al.
Pediatric Gastroenterology, Hepatology & Nutrition|April 14, 2015
Correction: the complex surgical management of the first case of severe combined immunodeficiency and multiple intestinal atresias surviving after the fourth year of lifeRiccardo Guanà, Salvatore Garofalo, Elisabetta Teruzzi, et al.
European Journal of Pediatrics|March 31, 2011
Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndromeAlessandro Mussa, Giovanni Battista Ferrero, Barbara Ceoloni, et al.
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