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au.\*:("QUIGLEY, Charmian A")

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Growth hormone treatment of non-growth hormone-deficient growth disordersQUIGLEY, Charmian A.Endocrinology and metabolism clinics of North America. 2007, Vol 36, Num 1, issn 0889-8529, ix-x, 131-186 [58 p.]Article

Genomic imprinting in turner syndrome : Effects on response to growth hormone and on risk of sensorineural hearing lossHAMELIN, Catherine E; ANGLIN, Greg; QUIGLEY, Charmian A et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 8, pp 3002-3010, issn 0021-972X, 9 p.Article

Massive ischemic intestinal necrosis at the onset of diabetes mellitus with ketoacidosis in a three-year-old girlDIMEGLIO, Linda A; CHAET, Mark S; QUIGLEY, Charmian A et al.Journal of pediatric surgery. 2003, Vol 38, Num 10, pp 1537-1539, issn 0022-3468, 3 p.Article

Growth hormone and low dose estrogen in Turner syndrome: Results of a United States multi-center trial to near-final heightQUIGLEY, Charmian A; CROWE, Brenda J; ANGLIN, D. Greg et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 5, pp 2033-2041, issn 0021-972XArticle

Hypogonadism and CHARGE associationWHEELER, Patricia G; QUIGLEY, Charmian A; SADEGHI-NEJAD, Ab et al.American journal of medical genetics. 2000, Vol 94, Num 3, pp 228-231, issn 0148-7299Article

Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency : Two-year results of a randomized, controlled, multicenter trialBLUM, Werner F; CROWE, Brenda J; QUIGLEY, Charmian A et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 1, pp 219-228, issn 0021-972X, 10 p.Article

Differences in follicle-stimulating hormone secretion between 45,X monosomy turner syndrome and 45,X/46,XX mosaicism are evident at an early ageFECHNER, Patricia Y; DAVENPORT, Marsha L; QUALY, Rebecca L et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 12, pp 4896-4902, issn 0021-972X, 7 p.Article

Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH2- and carboxyl-terminal interactionQUIGLEY, Charmian A; TAN, Jiann-An; WILSON, Elizabeth M et al.Mechanisms of ageing and development. 2004, Vol 125, Num 10-11, pp 683-695, issn 0047-6374, 13 p.Article

The phenotype of short stature homeobox gene (SHOX) deficiency in childhood : Contrasting children with leri-weill dyschondrosteosis and turner syndromeROSS, Judith L; KOWAL, Karen; QUIGLEY, Charmian A et al.The Journal of pediatrics. 2005, Vol 147, Num 4, pp 499-507, issn 0022-3476, 9 p.Article

Ascertainment bias in Turner syndrome: New insights from girls who were diagnosed incidentally in prenatal lifeGUNTHER, Daniel F; EUGSTER, Erica; ZAGAR, Anthony J et al.Pediatrics (Evanston). 2004, Vol 114, Num 3, pp 640-644, issn 0031-4005, 5 p.Article

Growth Hormone plus Childhood Low-Dose Estrogen in Turner's SyndromeROSS, Judith L; QUIGLEY, Charmian A; DACHUANG CAO et al.The New England journal of medicine. 2011, Vol 364, Num 13, pp 1230-1242, issn 0028-4793, 13 p.Article

Effect of growth hormone treatment on adult height in peripubertal children with idiopathic short stature: A randomized, double-blind, placebo-controlled trialLESCHEK, Ellen Werber; ROSE, Susan R; CUTLER, Gordon B et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 7, pp 3140-3148, issn 0021-972X, 9 p.Article

Development of additional pituitary hormone deficiencies in pediatric patients originally diagnosed with idiopathic isolated GH deficiencyBLUM, Werner F; DEAL, Cheri; ZIMMERMANN, Alan G et al.European journal of endocrinology. 2014, Vol 170, Num 1, pp 13-21, issn 0804-4643, 9 p.Article

Effect of growth hormone (GH) treatment on bone in postpubertal GH-deficient patients: A 2-year randomized, controlled, dose-ranging studySHALET, Stephen M; SHAVRIKOVA, Elena; ATTANASIO, Andrea F et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 9, pp 4124-4129, issn 0021-972X, 6 p.Article

Brain responses to sexual images in 46,XY women with complete androgen insensitivity syndrome are female-typicalHAMANN, Stephan; STEVENS, Jennifer; VICK, Janice Hassett et al.Hormones and behavior (Print). 2014, Vol 66, Num 5, pp 724-730, issn 0018-506X, 7 p.Article

Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450sccCHAN JONG KIM; LIN LIN; NINGWU HUANG et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 3, pp 696-702, issn 0021-972X, 7 p.Article

Genotypes and phenotypes in children with short stature : clinical indicators of SHOX haploinsufficiencyRAPPOLD, Gudrun; BLUM, Werner F; SHAVRIKOVA, Elena P et al.Journal of medical genetics. 2007, Vol 44, Num 5, pp 306-313, issn 0022-2593, 8 p.Article

Growth hormone treatment of early growth failure in toddlers with turner syndrome : A randomized, controlled, multicenter trialDAVENPORT, Marsha L; CROWE, Brenda J; HUSEMAN, Carol et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 9, pp 3406-3416, issn 0021-972X, 11 p.Article

Safety of growth hormone treatment in pediatric patients with idiopathic short statureQUIGLEY, Charmian A; GILL, Anne M; REKERS-MOMBARG, Lyset T. M et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 9, pp 5188-5196, issn 0021-972X, 9 p.Article

Psychological adaptation in children with idiopathic short stature treated with growth hormone or placeboROSS, Judith L; SANDBERG, David E; CUTLER, Gordon B et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 10, pp 4873-4878, issn 0021-972X, 6 p.Article

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