Mitochondrial disease and endocrine dysfunction von Chow, Jasmine, Rahman, Joyeeta, Achermann, John C., Dattani, Mehul T., Rahman, Shamima

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Isolated Growth Hormone Deficiency (GHD) in Childhood and Adolescence: Recent Advances von Alatzoglou, Kyriaki S, Webb, Emma Alice, Le Tissier, Paul, Dattani, Mehul T

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Progression from isolated growth hormone deficiency to combined pituitary hormone deficiency von Cerbone, Manuela, Dattani, Mehul T.

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Evaluation of growth hormone stimulation testing in children von Chesover, Alexander D., Dattani, Mehul T.

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Recent advances in central congenital hypothyroidism von Schoenmakers, Nadia, Alatzoglou, Kyriaki S, Chatterjee, V Krishna, Dattani, Mehul T

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Impact of short stature on quality of life: A systematic literature review von Backeljauw, Philippe, Cappa, Marco, Kiess, Wieland, Law, Lisa, Cookson, Charlotte, Sert, Caroline, Whalen, John, Dattani, Mehul T.

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Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation von Klammt, Jürgen, Neumann, David, Gevers, Evelien F., Andrew, Shayne F., Schwartz, I. David, Rockstroh, Denise, Colombo, Roberto, Sanchez, Marco A., Vokurkova, Doris, Kowalczyk, Julia, Metherell, Louise A., Rosenfeld, Ron G., Pfäffle, Roland, Dattani, Mehul T., Dauber, Andrew, Hwa, Vivian

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Genetic Regulation of Pituitary Gland Development in Human and Mouse von Kelberman, Daniel, Rizzoti, Karine, Lovell-Badge, Robin, Robinson, Iain C. A. F, Dattani, Mehul T

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Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome von Ara, Laura Bosch i, Katugampola, Harshini, Dattani, Mehul T.

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Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans von Gaston-Massuet, Carles, Andoniadou, Cynthia Lilian, Signore, Massimo, Jayakody, Sujatha A, Charolidi, Nicoletta, Kyeyune, Roger, Vernay, Bertrand, Jacques, Thomas S, Taketo, Makoto Mark, Le Tissier, Paul, Dattani, Mehul T, Martinez-Barbera, Juan Pedro

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Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma von Andoniadou, Cynthia L., Gaston-Massuet, Carles, Reddy, Rukmini, Schneider, Ralph P., Blasco, Maria A., Le Tissier, Paul, Jacques, Thomas S., Pevny, Larysa H., Dattani, Mehul T., Martinez-Barbera, Juan Pedro

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Septo-optic dysplasia and other midline defects: The role of transcription factors: HESX1 and beyond von McCabe, Mark James, PhD, Alatzoglou, Kyriaki S., MSc, MRCPCH, Dattani, Mehul T., FRCPCH, FRCP, MD

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Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism von Hietamäki, Johanna, Gregory, Louise C, Ayoub, Sandy, Iivonen, Anna-Pauliina, Vaaralahti, Kirsi, Liu, Xiaonan, Brandstack, Nina, Buckton, Andrew J, Laine, Tiina, Känsäkoski, Johanna, Hero, Matti, Miettinen, Päivi J, Varjosalo, Markku, Wakeling, Emma, Dattani, Mehul T, Raivio, Taneli

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Genetic Overlap in Kallmann Syndrome, Combined Pituitary Hormone Deficiency, and Septo-Optic Dysplasia von Raivio, Taneli, Avbelj, Magdalena, McCabe, Mark J, Romero, Christopher J, Dwyer, Andrew A, Tommiska, Johanna, Sykiotis, Gerasimos P, Gregory, Louise C, Diaczok, Daniel, Tziaferi, Vaitsa, Elting, Mariet W, Padidela, Raja, Plummer, Lacey, Martin, Cecilia, Feng, Bihua, Zhang, Chengkang, Zhou, Qun-Yong, Chen, Huaibin, Mohammadi, Moosa, Quinton, Richard, Sidis, Yisrael, Radovick, Sally, Dattani, Mehul T, Pitteloud, Nelly

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Challenges in the care of individuals with severe primary insulin-like growth factor-I deficiency (SPIGFD): an international, multi-stakeholder perspective von Backeljauw, Philippe F, Andrews, Mary, Bang, Peter, Dalle Molle, Leo, Deal, Cheri L, Harvey, Jamie, Langham, Shirley, Petriczko, Elżbieta, Polak, Michel, Storr, Helen L, Dattani, Mehul T

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Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans von Gualtieri, Angelica, Kyprianou, Nikolina, Gregory, Louise C., Vignola, Maria Lillina, Nicholson, James G., Tan, Rachael, Inoue, Shin-ichi, Scagliotti, Valeria, Casado, Pedro, Blackburn, James, Abollo-Jimenez, Fernando, Marinelli, Eugenia, Besser, Rachael E. J., Högler, Wolfgang, Karen Temple, I., Davies, Justin H., Gagunashvili, Andrey, Robinson, Iain C.A.F., Camper, Sally A., Davis, Shannon W., Cutillas, Pedro R., Gevers, Evelien F., Aoki, Yoko, Dattani, Mehul T., Gaston-Massuet, Carles

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SOX2 regulates the hypothalamic-pituitary axis at multiple levels von Jayakody, Sujatha A, Andoniadou, Cynthia L, Gaston-Massuet, Carles, Signore, Massimo, Cariboni, Anna, Bouloux, Pierre M, Le Tissier, Paul, Pevny, Larysa H, Dattani, Mehul T, Martinez-Barbera, Juan P

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Sotos Syndrome Presenting with Neonatal Hyperinsulinaemic Hypoglycaemia, Extensive Thrombosis, and Multisystem Involvement von Cerbone, Manuela, Clement, Emma, McClatchey, Martin, Dobbin, Joanna, Gilbert, Clare, Keane, Morgan, Boukhibar, Lamia, Williams, Hywel, Gagunashvili, Andrey, Dattani, Mehul T., Hurst, Jane, Shah, Pratik

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A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome von Roche, Edna F., McGowan, Anne, Koulouri, Olympia, Turgeon, Marc‐Olivier, Nicholas, Adeline K., Heffernan, Emmeline, El‐Khairi, Ranna, Abid, Noina, Lyons, Greta, Halsall, David, Bonomi, Marco, Persani, Luca, Dattani, Mehul T., Gurnell, Mark, Bernard, Daniel J., Schoenmakers, Nadia

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Transcription factor 7-like 1 is involved in hypothalamo–pituitary axis development in mice and humans von Gaston-Massuet, Carles, McCabe, Mark J., Scagliotti, Valeria, Young, Rodrigo M., Carreno, Gabriela, Gregory, Louise C., Jayakody, Sujatha A., Pozzi, Sara, Gualtieri, Angelica, Basu, Basudha, Koniordou, Markela, Wu, Chun-I, Bancalari, Rodrigo E., Rahikkala, Elisa, Veijola, Riitta, Lopponen, Tuija, Graziola, Federica, Turton, James, Signore, Massimo, Gharavy, Seyedeh Neda Mousavy, Charolidi, Nicoletta, Sokol, Sergei Y., Andoniadou, Cynthia Lilian, Wilson, Stephen W., Merrill, Bradley J., Dattani, Mehul T., Martinez-Barbera, Juan Pedro

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