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

Por Sani, Ilaria, Albanese, Assunta
Publicado no Neuro Oncol (2016)

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

Por Wei, Christina, Albanese, Assunta
Publicado no Children (Basel) (2014)

Suppression of menstruation in adolescents with severe learning disabilities

Por Albanese, Assunta, Hopper, Neil W
Publicado em 2007

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

Por Lashkari, Harsha Prasada, Nash, Ruth, Albanese, Assunta, Okoye, Bruce, Millar, Robert, Pritchard-Jones, Kathy
Publicado em 2013

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

Por Rose, Susan R, Carlsson, Martin, Grimberg, Adda, Aydin, Ferah, Albanese, Assunta, Hokken-Koelega, Anita C S, Camacho-Hubner, Cecilia
Publicado no 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

Por 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.
Publicado em 2007

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

Por 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
Publicado no Neuro Oncol (2018)

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

Por 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
Publicado no 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...

Por 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
Publicado no J Clin Oncol (2016)