agorska's library 51 articles Export

	Congenital hypopituitarism as a cause of undetectable estriol levels in the maternal triple-marker screen. [My Copy] The Journal of clinical endocrinology and metabolism, Vol. 88, No. 9. (September 2003), pp. 4144-4148. by I. Marshall, F. Ugrasbul, F. Manginello, et al.M. P. Wajnrajch, C. H. Shackleton, M. I. New, M. V. Vogiatzi posted to estriol cphd acth by agorska on 2009-12-11 20:33:29 as
	Prevalence of adrenocorticotropin deficiency in children with idiopathic growth hormone deficiency. [My Copy] The Journal of clinical endocrinology and metabolism, Vol. 89, No. 10. (October 2004), pp. 5030-5034. by Emily C. Walvoord, Marc B. Rosenman, Erica A. Eugster posted to cphd acth by agorska on 2009-12-11 20:25:11 as
	Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations. [My Copy] The Journal of clinical endocrinology and metabolism, Vol. 90, No. 3. (March 2005), pp. 1323-1331. by Sophie Vallette-Kasic, Thierry Brue, Anne-Marie M. Pulichino, et al.Magali Gueydan, Anne Barlier, Michel David, Marc Nicolino, Georges Malpuech, Pierre Déchelotte, Cheri Deal, Guy Van Vliet, Monique De Vroede, Felix G. Riepe, Carl-Joachim J. Partsch, Wolfgang G. Sippell, Merih Berberoglu, Begüm Atasay, Francis de Zegher, Dominique Beckers, Jennifer Kyllo, Patricia Donohoue, Martin Fassnacht, Stefanie Hahner, Bruno Allolio, C. Noordam, Leo Dunkel, Matti Hero, B. Pigeon, Jacques Weill, Sevket Yigit, Raja Brauner, Juan Jorge J. Heinrich, Elizabeth Cummings, Christie Riddell, Alain Enjalbert, Jacques Drouin posted to t-pit acth by agorska on 2009-12-11 20:13:14 as
	An update on the biochemical diagnosis of congenital ACTH insufficiency. [My Copy] Clinical endocrinology, Vol. 62, No. 3. (March 2005), pp. 307-314. by Ameeta Mehta, Peter C. Hindmarsh, Mehul T. Dattani posted to testy acth by agorska on 2009-12-11 20:09:45 as
	Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects. [My Copy] European journal of endocrinology / European Federation of Endocrine Societies, Vol. 153, No. 3. (September 2005), pp. 389-396. by Jan Lebl, Jan Vosáhlo, Roland W. Pfaeffle, et al.Heike Stobbe, Jana Cerná, Dana Novotná, Jirina Zapletalová, Bozena Kalvachová, Václav Hána, Vladimír Weiss, Werner F. Blum posted to propcphd by agorska on 2009-12-11 20:04:30 as
	Absent or delayed adrenarche in Pit-1/POU1F1 deficiency. [My Copy] Hormone research, Vol. 64, No. 4. (2005), pp. 175-179. by Doris Taha, Primus E. Mullis, Lourdes Ibáñez, Francis de Zegher posted to pouf1f1 cphd by agorska on 2009-12-11 20:02:34 as
	Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene. [My Copy] Pediatrics, Vol. 117, No. 2. (February 2006) by Naomi Weintrob, Jacques Drouin, Sophie Vallette-Kasic, et al.Ellen Taub, Daphna Marom, Yael Lebenthal, Gil Klinger, Efrat Bron-Harlev, Mordechai Shohat posted to t-pit acth by agorska on 2009-12-11 20:00:02 as
	Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe. [My Copy] Clinical endocrinology, Vol. 66, No. 1. (January 2007), pp. 95-102. by Maria Edna E. Melo, Suemi Marui, Luciani Renata R. Carvalho, et al.Ivo Jorge Prado J. Arnhold, Claudia Costa C. Leite, Berenice Bilharinho B. Mendonça, Mirta Knoepfelmacher posted to cphdacthlhx4hesx1 by agorska on 2009-12-11 19:52:43 as
	Prolonged hypocortisolemia in hydrocortisone replacement regimens in adrenocorticotrophic hormone deficiency. [My Copy] Pediatrics, Vol. 120, No. 1. (July 2007) by Ann M. Maguire, Geoffrey R. Ambler, Bin Moore, Mark McLean, Marina G. Falleti, Christopher T. Cowell posted to leczenie cphd acth by agorska on 2009-12-11 19:46:11 as
	Effect of growth hormone deficiency and recombinant hGH (rhGH) replacement on the hypothalamic-pituitary-adrenal axis in children with idiopathic isolated GH deficiency. [My Copy] Clinical endocrinology, Vol. 68, No. 2. (February 2008), pp. 247-251. by Claudia Giavoli, Silvia Bergamaschi, Emanuele Ferrante, et al.Cristina L. Ronchi, Andrea G. Lania, Roberto Rusconi, Anna Spada, Paolo Beck-Peccoz posted to acth by agorska on 2009-12-11 19:42:32 as
	Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies. [My Copy] The Journal of clinical endocrinology and metabolism, Vol. 93, No. 3. (March 2008), pp. 1062-1071. by Roland W. Pfaeffle, Chad S. Hunter, Jesse J. Savage, et al.Mario Duran-Prado, Rachel D. Mullen, Zachary P. Neeb, Urs Eiholzer, Volker Hesse, Nadine G. Haddad, Heike M. Stobbe, Werner F. Blum, Johannes F. Weigel, Simon J. Rhodes posted to lhx4 cphd by agorska on 2009-12-11 19:39:31 as
	Gonadotrophic status in adolescents with pituitary stalk interruption syndrome. [My Copy] Clinical endocrinology, Vol. 69, No. 1. (July 2008), pp. 105-111. by Diane Rottembourg, Agnès Linglart, Catherine Adamsbaum, et al.Najiba Lahlou, Cécile Teinturier, Pierre Bougnères, Jean-Claude C. Carel posted to gonadotropiny cphd by agorska on 2009-12-11 19:36:45 as
	The impact of fasting and treatment omission on susceptibility to hypoglycaemia in children and adolescents with GH and cortisol insufficiency. [My Copy] Clinical endocrinology, Vol. 69, No. 3. (September 2008), pp. 436-442. by Helen C. Johnstone, Richard J. McNally, Tim D. Cheetham posted to acth by agorska on 2009-12-11 19:33:17 as
	Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss. [My Copy] Human molecular genetics, Vol. 17, No. 14. (15 July 2008), pp. 2150-2159. by Anna Rajab, Daniel Kelberman, Sandra C. de Castro, et al.Heike Biebermann, Hala Shaikh, Kerra Pearce, Catherine M. Hall, Guftar Shaikh, Dianne Gerrelli, Annette Grueters, Heiko Krude, Mehul T. Dattani posted to lhx3 cphd by agorska on 2009-12-11 19:28:45 as
	A prismatic case: A 31-year old man who did not miss his pituitary. [My Copy] Hormones (Athens, Greece), Vol. 7, No. 3. (p 2008), pp. 263-270. by Stefanie Petzold, Alexandra Keller, Eberhardt Keller, et al.Christof Meigen, Wolfgang Hirsch, Jürgen Kratzsch K. Kratzsch, Wieland Kiess, Roland Pfäffle posted to cphd by agorska on 2009-12-11 19:24:09 as
	Isolated adrenocorticotropic hormone deficiency presenting as an acute neurologic emergency in a peripubertal girl. [My Copy] Journal of pediatric endocrinology & metabolism : JPEM, Vol. 21, No. 8. (August 2008), pp. 799-803. by Andrew A. Bremer, Sayali Ranadive, Susan C. Conrad, Sophie Vallette-Kasic, Stephen M. Rosenthal posted to acth by agorska on 2009-12-11 19:21:27 as
	A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency. [My Copy] The Journal of clinical endocrinology and metabolism, Vol. 93, No. 11. (November 2008), pp. 4351-4359. by Daniel Diaczok, Christopher Romero, Janice Zunich, Ian Marshall, Sally Radovick posted to otx2 cphd by agorska on 2009-12-11 19:18:47 as
	Congenital hypopituitarism: clinical, molecular and neuroradiological correlates. [My Copy] Clinical endocrinology, Vol. 71, No. 3. (September 2009), pp. 376-382. by Ameeta Mehta, Peter C. Hindmarsh, Hiten Mehta, et al.James P. Turton, Isabelle Russell-Eggitt, David Taylor, W. K. Chong, Mehul T. Dattani posted to prop1 cphd by agorska on 2009-12-11 19:08:54 as
	Premature differentiation and aberrant movement of pituitary cells lacking both Hes1 and Prop1. [My Copy] Developmental biology, Vol. 325, No. 1. (1 January 2009), pp. 151-161. by Ashley D. Himes, Lori T. Raetzman posted to rozwoj prop1 by agorska on 2009-11-11 17:58:11 as
	Genetic Screening of Combined Pituitary Hormone Deficiency: Experience in 195 Patients [My Copy] J Clin Endocrinol Metab, Vol. 91, No. 9. (1 September 2006), pp. 3329-3336. by Rachel Reynaud, Magali Gueydan, Alexandru Saveanu, et al.Sophie Vallette-Kasic, Alain Enjalbert, Thierry Brue, Anne Barlier posted to prop1 by agorska on 2009-11-02 19:11:00 as
	The fetal and neonatal hypothalamic-pituitary-adrenal axis [My Copy] Arch. Dis. Child. Fetal Neonatal Ed., Vol. 82, No. 3. (1 May 2000), pp. F250-254. by P. C. Ng posted to nadnercza by agorska on 2008-11-02 22:05:34 as
	The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency. [My Copy] J Clin Endocrinol Metab, Vol. 83, No. 9. (September 1998), pp. 3346-3349. by J. D. Cogan, W. Wu, J. A. Phillips, et al.I. J. Arnhold, A. Agapito, O. V. Fofanova, M. G. Osorio, I. Bircan, A. Moreno, B. B. Mendonca posted to prop1 by agorska on 2007-03-25 17:34:36 as
	Panhypopituitarism: genetic versus acquired etiological factors. [My Copy] J Pediatr Endocrinol Metab, Vol. 20, No. 1. (January 2007), pp. 27-36. by R. Coya, A. Vela, G. Pérez de Nanclares, et al.I. Rica, L. Castaño, M. A. Busturia, P. Martul, posted to prop1 by agorska on 2007-03-25 17:31:51 as
	Endocrine disorders in pediatric - onset Langerhans Cell Histiocytosis. [My Copy] Horm Metab Res, Vol. 38, No. 11. (November 2006), pp. 746-751. by M. C. Amato, L. L. Elias, J. Elias, et al.A. C. Santos, A. D. Bellucci, A. C. Moreira, M. De Castro posted to histiocytosis by agorska on 2007-03-23 22:17:55 as
	Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation. [My Copy] J Clin Endocrinol Metab, Vol. 86, No. 9. (September 2001), pp. 4353-4357. by F. G. Riepe, C. J. Partsch, O. Blankenstein, H. Mönig, R. W. Pfäffle, W. G. Sippell posted to guzy prop1 by agorska on 2007-03-23 22:02:42 as
	Oncocytic transformation in pituitary adenomas: immunohistochemical analyses of 65 cases. [My Copy] Arch Pathol Lab Med, Vol. 128, No. 7. (July 2004), pp. 776-780. by M. Niveiro, F. I. Aranda, A. Payá, E. Boix, G. Peiró, A. Picó posted to guzy prop1 by agorska on 2007-03-23 21:59:12 as along with 1 person Marcory
	PROP1 Gene Mutations and Pituitary Size: A Unique Case of Two Consecutive Cycles of Enlargement and Regression. [My Copy] Horm Res, Vol. 67 Suppl 1 (2007), pp. 109-113. by P. Xekouki, A. Sertedaki, S. Livadas, M. Argyropoulou, A. Voutetakis posted to guzy prop1 by agorska on 2007-03-23 20:23:34 as
	Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD) [My Copy] Clinical Endocrinology, Vol. 63, No. 1. (July 2005), pp. 10-18. by James P. Turton, Ameeta Mehta, Jamal Raza, et al.Kathryn S. Woods, Anatoly Tiulpakov, Joseph Cassar, Kling Chong, Paul Q. Thomas, Marumudi Eunice, Ariachery C. Ammini, Pierre M. Bouloux, Jerzy Starzyk, Peter C. Hindmarsh, Mehul T. Dattani posted to prop1 by agorska on 2007-03-23 20:20:57 as
	Prop-1 gene expression in human pituitary tumors. [My Copy] J Clin Endocrinol Metab, Vol. 84, No. 7. (July 1999), pp. 2581-2584. by S. Nakamura, A. Ohtsuru, N. Takamura, et al.G. Kitange, Y. Tokunaga, A. Yasunaga, S. Shibata, S. Yamashita posted to prop1 by agorska on 2007-03-23 20:16:08 as
	Cell proliferation and vascularization in mouse models of pituitary hormone deficiency. [My Copy] Mol Endocrinol, Vol. 20, No. 6. (June 2006), pp. 1378-1390. by R. D. Ward, B. M. Stone, L. T. Raetzman, S. A. Camper posted to prop1 by agorska on 2007-03-23 20:13:29 as
	Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia [My Copy] Clinical Endocrinology, Vol. 62, No. 2. (February 2005), 163. by L. A. Rainbow, S. A. Rees, M. G. Shaikh, et al.N. J. Shaw, T. Cole, T. G. Barrett, J. M. W. Kirk posted to prop1 by agorska on 2007-03-23 20:11:45 as
	Ovulation induction and successful pregnancy outcome in two patients with Prop1 gene mutations. [My Copy] Fertil Steril, Vol. 82, No. 2. (August 2004), pp. 454-457. by A. Voutetakis, A. Sertedaki, S. Livadas, et al.M. Maniati-Christidi, I. Mademtzis, I. Bossis, C. Dacou-Voutetakis, I. E. Messinis posted to prop1 by agorska on 2007-03-23 20:08:27 as
	Oncocytic and granular cell neoplasms of the central nervous system and pituitary gland. [My Copy] Semin Diagn Pathol, Vol. 16, No. 2. (May 1999), pp. 91-97. by F. Giangaspero, G. Cenacchi posted to guzy prop1 by agorska on 2007-03-23 20:03:13 as
	The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation. [My Copy] Mol Endocrinol, Vol. 10, No. 12. (December 1996), pp. 1570-1581. by P. J. Gage, M. L. Brinkmeier, L. M. Scarlett, L. T. Knapp, S. A. Camper, K. A. Mahon posted to guzy prop1 by agorska on 2007-03-23 19:58:10 as
	Familial hypopituitarism with large sella turcica. [My Copy] N Engl J Med, Vol. 298, No. 13. (30 March 1978), pp. 698-702. by J. S. Parks, A. Tenore, A. M. Bongiovanni, R. T. Kirkland posted to guzy prop1 by agorska on 2007-03-22 19:25:53 as
	Anterior pituitary cells defective in the cell-autonomous factor, df, undergo cell lineage specification but not expansion. [My Copy] Development, Vol. 122, No. 1. (January 1996), pp. 151-160. by P. J. Gage, M. L. Roller, T. L. Saunders, L. M. Scarlett, S. A. Camper posted to guzy prop1 by agorska on 2007-03-22 19:08:51 as
	PROP1 Mutations Cause Progressive Deterioration of Anterior Pituitary Function including Adrenal Insufficiency: A Longitudinal Analysis [My Copy] J Clin Endocrinol Metab, Vol. 89, No. 10. (1 October 2004), pp. 5256-5265. by Antje Bottner, Eberhard Keller, Jurgen Kratzsch, et al.Heike Stobbe, Johannes F. W. Weigel, Alexandra Keller, Wolfgang Hirsch, Wieland Kiess, Werner F. Blum, Roland W. Pfaffle posted to prop1 nadnercza by agorska on 2007-03-22 18:52:56 as
	Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C). [My Copy] J Clin Endocrinol Metab, Vol. 83, No. 10. (October 1998), pp. 3727-3734. by C. Flück, J. Deladoey, K. Rutishauser, et al.A. Eblé, U. Marti, W. Wu, P. E. Mullis posted to prop1 by agorska on 2007-02-18 19:11:13 as
	Clinical characteristics and molecular analysis of PIT1, PROP1,LHX3, and HESX1 in combined pituitary hormone deficiency patients with abnormal pituitary MR imaging. [My Copy] Horm Res, Vol. 60, No. 6. (2003), pp. 277-283. by S. S. Kim, Y. Kim, Y. L. Shin, G. H. Kim, T. U. Kim, H. W. Yoo posted to prop1 by agorska on 2007-02-18 19:00:40 as
	Transcription factors regulating pituitary development. [My Copy] Growth Horm IGF Res, Vol. 9 Suppl B (June 1999) by J. S. Parks, M. R. Brown posted to guzy prop1 by agorska on 2007-02-18 18:53:16 as
	Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion [My Copy] Clinical Endocrinology, Vol. 65, No. 3. (September 2006), pp. 294-300. by Abrao, M. G., Leite, et al. M. V., Carvalho, L. R., Billerbeck, A. E. C., Nishi, M. Y., Barbosa, A. S., Martin, R. M., Arnhold, I. J. P., Mendonca, B. B. posted to prop1 by agorska on 2007-02-11 09:33:25 as
	Cushing's syndrome. [My Copy] Lancet, Vol. 367, No. 9522. (13 May 2006), pp. 1605-1617. by J. Newell-Price, X. Bertagna, A. B. Grossman, L. K. Nieman posted to kurs cushing by agorska on 2007-01-25 15:54:04 as along with 1 person guhjy
	Medical progress: Acromegaly. [My Copy] N Engl J Med, Vol. 355, No. 24. (14 December 2006), pp. 2558-2573. by S. Melmed posted to kurs acromegaly by agorska on 2007-01-24 14:49:50 as along with 2 people guhjy Amazoness
	Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism? [My Copy] J Endocrinol Invest, Vol. 29, No. 5. (May 2006), pp. 462-466. by A. Voutetakis, A. Sertedaki, S. Livadas, et al.P. Xekouki, I. Bossis, C. Dacou-Voutetakis, M. I. Argyropoulou posted to guzy prop1 by agorska on 2007-01-07 19:07:45 as
	Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT). [My Copy] J Pediatr Endocrinol Metab, Vol. 19, No. 4. (April 2006), pp. 491-498. by O. Nose, K. Tatsumi, Y. Nakano, N. Amino posted to prop1 by agorska on 2006-12-17 19:33:53 as
	Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. [My Copy] J Clin Endocrinol Metab, Vol. 85, No. 1. (January 2000), pp. 390-397. by F. Pernasetti, S. P. Toledo, V. V. Vasilyev, et al.C. Y. Hayashida, J. D. Cogan, C. Ferrari, D. M. Lourenço, P. L. Mellon posted to guzy prop1 by agorska on 2006-12-17 19:26:02 as
	Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay. [My Copy] J Clin Endocrinol Metab, Vol. 88, No. 1. (January 2003), pp. 38-44. by T. C. Vieira, M. R. Dias da Silva, J. M. Cerutti, et al.E. Brunner, M. Borges, L. T. Arnaldi, P. Kopp, J. Abucham posted to prop1 cphd by agorska on 2006-12-17 19:10:54 as
	Role of PROP1 in pituitary gland growth. [My Copy] Mol Endocrinol, Vol. 19, No. 3. (March 2005), pp. 698-710. by R. D. Ward, L. T. Raetzman, H. Suh, B. M. Stone, I. O. Nasonkin, S. A. Camper posted to guzy prop1 by agorska on 2006-12-17 19:07:15 as along with 1 person mzygmunt
	Waxing and waning of a pituitary mass in a young woman with combined pituitary hormone deficiency (CPHD) due to a PROP-1 mutation [My Copy] Pituitary, Vol. 9, No. 1. (March 2006), pp. 47-52. by Nascif, Sergio, Vieira, et al. Teresa, Ramos-Dias, Joao, Lengyel, Ana-Maria, Abucham, Julio posted to guzy prop1 by agorska on 2006-12-17 19:06:58 as along with 1 person mzygmunt
	The spectrum of hypopituitarism caused by PROP1 mutations. [My Copy] Best Pract Res Clin Endocrinol Metab, Vol. 16, No. 3. (September 2002), pp. 421-431. by S. Mody, M. R. Brown, J. S. Parks posted to guzy prop1 by agorska on 2006-12-17 19:06:41 as along with 1 person mzygmunt

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agorska's library 51 articles Export

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