Zobrazeno 1 - 10
of 168
pro vyhledávání: '"P, Feuillan"'
Publikováno v:
Cellular and Molecular Biology of the Renin-Angiotensin System ISBN: 9781351070492
Cellular and Molecular Biology of the Renin-Angiotensin System
Cellular and Molecular Biology of the Renin-Angiotensin System
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::881f12ee70b250d227434874ce887a36
https://doi.org/10.1201/9781351070492-16
https://doi.org/10.1201/9781351070492-16
Autor:
P. P. Feuillan
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 80:1357-1360
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59ed106ed19f8a71d84f40e85188470d
https://doi.org/10.1210/jc.80.4.1357
https://doi.org/10.1210/jc.80.4.1357
Autor:
P. P. Feuillan
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 77:647-651
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7436fc01d03beced76d00093fee29ce0
https://doi.org/10.1210/jc.77.3.647
https://doi.org/10.1210/jc.77.3.647
Effects of estrogen on nonverbal processing speed and motor function in girls with Turner's syndrome
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(9)
The Turner syndrome (TS) phenotype is characterized by a specific neurocognitive profile of normal verbal skills, impaired visual-spatial and/or visual-perceptual abilities, and difficulty with motor function. In the current study, we investigated mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4473c56bc69e411b7074f1fb8a1dac92
https://pubmed.ncbi.nlm.nih.gov/9745426
https://pubmed.ncbi.nlm.nih.gov/9745426
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 39(2)
Somatostatin receptor scintigraphy was performed on a patient with McCune-Albright syndrome and acromegaly. No evidence of pituitary disease was found, but uptake of (111)In-pentetreotide was noted in areas of fibrous dysplasia. This uptake was not c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c07067a06e91952d8ba4d2aeb6c0d8ea
https://pubmed.ncbi.nlm.nih.gov/9476926
https://pubmed.ncbi.nlm.nih.gov/9476926
Publikováno v:
The Journal of clinical endocrinology and metabolism. 82(6)
Turner syndrome (TS) is a genetic disorder characterized by short stature, gonadal dysgenesis, and a particular neurocognitive profile of normally developed language abilities (particularly verbal IQ) and impaired visual-spatial and/or visual-percept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::928ac6d9c51ee2e4b1afb567bb599526
https://pubmed.ncbi.nlm.nih.gov/9543174
https://pubmed.ncbi.nlm.nih.gov/9543174
Autor:
P P Feuillan, Greti Aguilera
Publikováno v:
Endocrinology. 137(9)
Little is known about mineralocorticoid regulation in the neonate. Here, adrenocortical function in 7-day-old Sprague-Dawley rats was studied by measuring the effects of angiotensin II (Ang II) and ACTH on serum aldosterone (ALDO), corticosterone, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c68710bad6e0224a422bae7ee74f3381
https://pubmed.ncbi.nlm.nih.gov/8756576
https://pubmed.ncbi.nlm.nih.gov/8756576
Autor:
G B Cutler, Harvey Kushner, David P. Roeltgen, L Long, E McCauley, P Feuillan, Judith L. Ross
Publikováno v:
The Journal of clinical endocrinology and metabolism. 81(3)
Data on self-concept and behavior were gathered from 31 girls with Turner syndrome (TS) followed longitudinally between the ages of 12 and 16 and from 89 normal control girls recruited from public schools and assessed cross-sectionally. The two group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b40ba1cc8efeab380d868052a5307f9
https://pubmed.ncbi.nlm.nih.gov/8772552
https://pubmed.ncbi.nlm.nih.gov/8772552
Autor:
P P, Feuillan
Publikováno v:
Current therapy in endocrinology and metabolism. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9606c43e06152e0ad396922ce1e6bc43
https://pubmed.ncbi.nlm.nih.gov/7704715
https://pubmed.ncbi.nlm.nih.gov/7704715
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 31(9)
This study of 22 patients with the McCune-Albright syndrome examined the scintigraphic distribution of fibrous dysplasia. The most frequently affected areas were the base of the skull (82% of patients), mandible (50%), facial bones (45%), femora (59%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3370ed840ca3fe2bf516fd9b8498ba81
https://pubmed.ncbi.nlm.nih.gov/2395015
https://pubmed.ncbi.nlm.nih.gov/2395015