LG-11 ENDOCRINE LONG TERM FOLLOW-UP OF CHILDREN WITH NEUROFIBROMATOSIS TYPE 1(NF1) AND PPTIC PATHWAY GLIOMA (OPG)

di Sani, Ilaria, Albanese, Assunta
Pubblicato in Neuro Oncol (2016)

Endocrine Disorders in Childhood Cancer Survivors Treated with Haemopoietic Stem Cell Transplantation

di Wei, Christina, Albanese, Assunta
Pubblicato in Children (Basel) (2014)

Suppression of menstruation in adolescents with severe learning disabilities

di Albanese, Assunta, Hopper, Neil W
Pubblicazione 2007

Treatment of High Risk Sertoli–Leydig Cell Tumors of the Ovary Using a Gonadotropin Releasing Hormone (GnRH) Analog

di Lashkari, Harsha Prasada, Nash, Ruth, Albanese, Assunta, Okoye, Bruce, Millar, Robert, Pritchard-Jones, Kathy
Pubblicazione 2013

Response to GH Treatment After Radiation Therapy Depends on Location of Irradiation

di Rose, Susan R, Carlsson, Martin, Grimberg, Adda, Aydin, Ferah, Albanese, Assunta, Hokken-Koelega, Anita C S, Camacho-Hubner, Cecilia
Pubblicato in J Clin Endocrinol Metab (2020)

Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function

di Lin, Lin, Philibert, Pascal, Ferraz-de-Souza, Bruno, Kelberman, Daniel, Homfray, Tessa, Albanese, Assunta, Molini, Veruska, Sebire, Neil J., Einaudi, Silvia, Conway, Gerard S., Hughes, Ieuan A., Jameson, J. Larry, Sultan, Charles, Dattani, Mehul T., Achermann, John C.
Pubblicazione 2007

CRAN-08. NATIONAL UK GUIDELINES FOR THE INVESTIGATION, TREATMENT AND LONG-TERM FOLLOW-UP OF PAEDIATRIC CRANIOPHARYNGIOMA

di Gan, Hoong-Wei, Aquilina, Kristian, Morillon, Paul, Albanese, Assunta, Barkas, Konstantinos, Chandler, Chris, Chang, Yen-Ching, Daousi, Christina, Drimtzias, Evangelos, Farndon, Sarah, Jacques, Tom, Korbonits, Marta, Kuczynski, Adam, Limond, Jennifer, Robinson, Louise, Simmons, Ian, Thomas, Nick, Thomas, Sophie, Thorpe, Nicola, Vargha-Khadem, Faraneh, Warren, Daniel, Zebian, Bassel, Mallucci, Conor, Gamble, Ashley, Wilne, Sophie, Harrison, Barney, Spoudeas, Helen
Pubblicato in Neuro Oncol (2018)

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

di Nicholas, Adeline K., Serra, Eva G., Cangul, Hakan, Alyaarubi, Saif, Ullah, Irfan, Schoenmakers, Erik, Deeb, Asma, Habeb, Abdelhadi M., Almaghamsi, Mohammad, Peters, Catherine, Nathwani, Nisha, Aycan, Zehra, Saglam, Halil, Bober, Ece, Dattani, Mehul, Shenoy, Savitha, Murray, Philip G., Babiker, Amir, Willemsen, Ruben, Thankamony, Ajay, Lyons, Greta, Irwin, Rachael, Padidela, Raja, Tharian, Kavitha, Davies, Justin H., Puthi, Vijith, Park, Soo-Mi, Massoud, Ahmed F., Gregory, John W., Albanese, Assunta, Pease-Gevers, Evelien, Martin, Howard, Brugger, Kim, Maher, Eamonn R., Chatterjee, V. Krishna K., Anderson, Carl A., Schoenmakers, Nadia
Pubblicato in J Clin Endocrinol Metab (2016)

Recommendations for Premature Ovarian Insufficiency Surveillance for Female Survivors of Childhood, Adolescent, and Young Adult Cancer: A Report From the International Late Effects...

di van Dorp, Wendy, Mulder, Renée L., Kremer, Leontien C.M., Hudson, Melissa M., van den Heuvel-Eibrink, Marry M., van den Berg, Marleen H., Levine, Jennifer M., van Dulmen-den Broeder, Eline, di Iorgi, Natascia, Albanese, Assunta, Armenian, Saro H., Bhatia, Smita, Constine, Louis S., Corrias, Andreas, Deans, Rebecca, Dirksen, Uta, Gracia, Clarisa R., Hjorth, Lars, Kroon, Leah, Lambalk, Cornelis B., Landier, Wendy, Levitt, Gill, Leiper, Alison, Meacham, Lillian, Mussa, Alesandro, Neggers, Sebastian J., Oeffinger, Kevin C., Revelli, Alberto, van Santen, Hanneke M., Skinner, Roderick, Toogood, Andrew, Wallace, William H., Haupt, Riccardo
Pubblicato in J Clin Oncol (2016)