Zobrazeno 1 - 10
of 32
pro vyhledávání: '"G L Warne"'
Autor:
Lucila Leico Kagohara Elias, Martin O. Savage, Peter E. Clayton, Louise A. Metherell, Maria Luisa Manca Bitti, Adrian J. L. Clark, Angela Huebner, Atilio Canas, G. L. Warne, Stefano Cianfarani
Publikováno v:
Clinical Endocrinology. 53:423-430
OBJECTIVE Familial glucocorticoid deficiency (FGD) has frequently been associated with tall stature in affected individuals. The clinical, biochemical and genetic features of five such patients were studied with the aim of clarifying the underlying m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::620bef91d5292a7c3fba714193c721ea
https://doi.org/10.1046/j.1365-2265.2000.01122.x
https://doi.org/10.1046/j.1365-2265.2000.01122.x
Autor:
Margaret Zacharin, G L Warne
Publikováno v:
Archives of Disease in Childhood. 76:495-499
Accepted 26 February AIMS—Long acting subcutaneous testosterone pellets are of proved efficacy for the treatment of hypogonadal men, but have not been reported as a treatment modality in adolescent boys. Pharmacodynamic studies of subcutaneous test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4dde36359ddc170514d305d22b193aa
https://doi.org/10.1136/adc.76.6.495
https://doi.org/10.1136/adc.76.6.495
Autor:
N. J. Howard, F. Wilson, M.T. Epstein, Christopher T. Cowell, Gordon Ennis, M. Silink, Michael J. Thomsett, A.L. Clarke, G. Antony, G.C. Byrne, D.A. Perry-Keane, H. Gold, Irene L. Hudson, G. L. Warne, C A Quigley, George A. Werther, P.T. Pullan
Publikováno v:
Journal of Paediatrics and Child Health. 26:4-8
A multi-centre open trial of Buserelin, a luteinizing hormone-releasing hormone (LHRH) analogue, was conducted in 13 children with central precocious puberty. Eleven children (eight girls and three boys), aged 3.4-10.2 years at commencement, complete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87e73112783e8b37ff1311ce98bf9bbf
https://doi.org/10.1111/j.1440-1754.1990.tb02369.x
https://doi.org/10.1111/j.1440-1754.1990.tb02369.x
Publikováno v:
Journal of paediatrics and child health. 39(3)
Increasing survival after treatment for childhood cancer in recent years has left many patients with long-term sequelae. Following cranial irradiation, changes in hypothalamic-pituitary function evolve over several years and multiple hormone deficien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a26c1b0894448712aa568ab4e91a34a
https://pubmed.ncbi.nlm.nih.gov/12654151
https://pubmed.ncbi.nlm.nih.gov/12654151
Autor:
L L, Elias, A, Huebner, L A, Metherell, A, Canas, G L, Warne, M L, Bitti, S, Cianfarani, P E, Clayton, M O, Savage, A J, Clark
Publikováno v:
Clinical endocrinology. 53(4)
Familial glucocorticoid deficiency (FGD) has frequently been associated with tall stature in affected individuals. The clinical, biochemical and genetic features of five such patients were studied with the aim of clarifying the underlying mechanisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60f4ee198bea02ee77d8be1cde5b3667
https://pubmed.ncbi.nlm.nih.gov/11012566
https://pubmed.ncbi.nlm.nih.gov/11012566
Publikováno v:
Neuropsychology. 14(3)
A battery of tests was administered to 17 patients with congenital adrenal hyperplasia (CAH) and 17 normal controls to investigate the effect of prenatal androgen exposure on cerebral lateralization and cognitive performance. Individuals were compare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b44eac3492f9f4f397a41d19da6936e
https://pubmed.ncbi.nlm.nih.gov/10928740
https://pubmed.ncbi.nlm.nih.gov/10928740
Autor:
P Dissaneevate, G L Warne
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 11
Six adolescents, five males with prolactin-secreting pituitary macroadenomas and one female with idiopathic hyperprolactinaemia, are described. Their ages at presentation ranged from 13 years 7 months to 16 years 6 months. Presenting symptoms include
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d71201d8357e11ad36995b194ea30e0
https://doi.org/10.1515/jpem.1998.11.4.531
https://doi.org/10.1515/jpem.1998.11.4.531
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 11
Objective To describe the clinical features, laboratory investigation and treatment of Kallmann syndrome. Design A retrospective study of patients treated in the Endocrine Clinic of the Royal Children's Hospital and St Vincent's Hospital, Melbourne,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58475b57ad26128837095b204435b37f
https://doi.org/10.1515/jpem.1998.11.5.631
https://doi.org/10.1515/jpem.1998.11.5.631
Publikováno v:
Journal of paediatrics and child health. 33(3)
17alpha-hydroxylase deficiency is a rare form of congenital adrenal hyperplasia (CAH) that affects both glucocorticoid and sex hormone biosynthesis. We report a case of an unambiguous female with testes and hypertension. She was found to have deficie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a575907393a51193198047f6b5ffbba4
https://pubmed.ncbi.nlm.nih.gov/9259306
https://pubmed.ncbi.nlm.nih.gov/9259306
Autor:
M, Lagerström-Fermér, M, Sundvall, E, Johnsen, G L, Warne, S M, Forrest, J D, Zajac, A, Rickards, D, Ravine, U, Landegren, U, Pettersson
Publikováno v:
American journal of human genetics. 60(4)
We present a linkage analysis and a clinical update on a previously reported family with X-linked recessive panhypopituitarism, now in its fourth generation. Affected members exhibit variable degrees of hypopituitarism and mental retardation. The mar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e4fe4b4783112a87b87d7b67b501cce
https://pubmed.ncbi.nlm.nih.gov/9106538
https://pubmed.ncbi.nlm.nih.gov/9106538