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

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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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Genetic forms of hypopituitarism and their manifestation in the neonatal period von Alatzoglou, Kyriaki S, Dattani, Mehul T

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Novel FGF8 Mutations Associated with Recessive Holoprosencephaly, Craniofacial Defects, and Hypothalamo-Pituitary Dysfunction von McCabe, Mark J, Gaston-Massuet, Carles, Tziaferi, Vaitsa, Gregory, Louise C, Alatzoglou, Kyriaki S, Signore, Massimo, Puelles, Eduardo, Gerrelli, Dianne, Farooqi, I. Sadaf, Raza, Jamal, Walker, Joanna, Kavanaugh, Scott I, Tsai, Pei-San, Pitteloud, Nelly, Martinez-Barbera, Juan-Pedro, Dattani, Mehul T

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Variations in PROKR2, But Not PROK2, Are Associated With Hypopituitarism and Septo-optic Dysplasia von McCabe, Mark J, Gaston-Massuet, Carles, Gregory, Louise C, Alatzoglou, Kyriaki S, Tziaferi, Vaitsa, Sbai, Oualid, Rondard, Philippe, Masumoto, Koh-hei, Nagano, Mamoru, Shigeyoshi, Yasufumi, Pfeifer, Marija, Hulse, Tony, Buchanan, Charles R, Pitteloud, Nelly, Martinez-Barbera, Juan-Pedro, Dattani, Mehul T

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The role of SOX proteins in normal pituitary development von Alatzoglou, Kyriaki S, Kelberman, Daniel, Dattani, Mehul T

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Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD) von McCabe, Mark J., Hu, Youli, Gregory, Louise C., Gaston-Massuet, Carles, Alatzoglou, Kyriaki S., Saldanha, José W., Gualtieri, Angelica, Thankamony, Ajay, Hughes, Ieuan, Townshend, Sharron, Martinez-Barbera, Juan-Pedro, Bouloux, Pierre-Marc, Dattani, Mehul T.

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Increased Transactivation Associated with SOX3 Polyalanine Tract Deletion in a Patient with Hypopituitarism von Alatzoglou, Kyriaki S, Kelberman, Daniel, Cowell, Christopher T, Palmer, Rodger, Arnhold, Ivo J. P, Melo, Maria E, Schnabel, Dirk, Grueters, Annette, Dattani, Mehul T

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SOX2 haploinsufficiency is associated with slow progressing hypothalamo-pituitary tumours von Alatzoglou, Kyriaki S., Andoniadou, Cynthia L., Kelberman, Daniel, Buchanan, Charles R., Crolla, John, Arriazu, Maria Cristina, Roubicek, Martin, Moncet, Daniel, Martinez-Barbera, Juan P., Dattani, Mehul T.

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Phenotype-Genotype Correlations in Congenital Isolated Growth Hormone Deficiency (IGHD) von Alatzoglou, Kyriaki S., Dattani, Mehul T.

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Acanthosis Nigricans and Insulin Sensitivity in Patients with Achondroplasia and Hypochodroplasia due to FGFR3 Mutations von Alatzoglou, Kyriaki S., Hindmarsh, Peter C., Brain, Caroline, Torpiano, John, Dattani, Mehul T.

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Two cases of myomectomy complicated by intravascular hemolysis and renal failure: disseminated intravascular coagulation or hemolytic uremic syndrome? von Tsimpanakos, Ioannis, M.D, Connolly, John, Ph.D, Alatzoglou, Kyriaki S., M.Sc, Rowan, Camilla, M.B., B.S., B.Sc, Magos, Adam, M.D., B.Sc., M.B., B.S

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Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency von França, Marcela M, Jorge, Alexander A. L, Alatzoglou, Kyriaki S, Carvalho, Luciani R. S, Mendonca, Berenice B, Audi, Laura, Carrascosa, Antonio, Dattani, Mehul T, Arnhold, Ivo J. P

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Increased Transactivation Associated with SOX3 Polyalanine Tract Deletion in a Patient with Hypopituitarism von Alatzoglou, Kyriaki S, Kelberman, Daniel, Cowell, Christopher T, Palmer, Rodger, Arnhold, Ivo J. P, Melo, Maria E, Schnabel, Dirk, Grueters, Annette, Dattani, Mehul T

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Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency von Gregory, Louise Cheryl, Alatzoglou, Kyriaki Sandy, McCabe, Mark James, Hindmarsh, Peter Christopher, Saldanha, Jose William, Romano, Nicola, Le Tissier, Paul, Dattani, Mehul Tulsidas

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Phenotype-Genotype Correlations in Congenital Isolated Growth Hormone Deficiency (IGHD) : GROWT HORMONE-I von ALATZOGLOU, Kyriaki S, DATTANI, Mehul T

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Increased Transactivation Associated with SOX 3 Polyalanine Tract Deletion in a Patient with Hypopituitarism von Alatzoglou, Kyriaki S., Kelberman, Daniel, Cowell, Christopher T., Palmer, Rodger, Arnhold, Ivo J. P., Melo, Maria E., Schnabel, Dirk, Grueters, Annette, Dattani, Mehul T.

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Renal pseudotumor simulating malignancy in a patient with Adamantiades-Behçet's disease : Case report and review of the literature von AESSOPOS, A, ALATZOGLOU, K, KOROVESIS, K, TASSIOPOULOS, S, LEFAKIS, G, ISMAILOU-PARASSI, A

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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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