Zobrazeno 1 - 10
of 370
pro vyhledávání: '"M. Decoulx"'
Publikováno v:
Annales d'Endocrinologie. 67:32-38
We describe the clinical presentation, biochemical features, diagnostic criteria, clinical course and differential diagnosis in three cases of feminizing adreno-cortical carcinoma (FACC) with a review of the literature. Patients From 1970 throughout
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d98e5612ea7ab496ec27bafa27bf8a5
https://doi.org/10.1016/s0003-4266(06)72537-9
https://doi.org/10.1016/s0003-4266(06)72537-9
Autor:
X. Marchandise, Didier Dewailly, C. Cortet, Bernard Cortet, Michèle d’Herbomez, J.-L. Wémeau, M. Decoulx, F. Blanckaert
Publikováno v:
Europe PubMed Central
Quantitative ultrasound (QUS) of bone is a valuable tool in the assessment of postmenopausal osteoporosis. QUS and new markers of bone turnover have been poorly assessed in Cushing's syndrome, however. Twenty-five patients with Cushing's syndrome (20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::140d3fe51b4c74badb9701939c9a4e16
https://doi.org/10.1007/s001980170143
https://doi.org/10.1007/s001980170143
Autor:
C. Cortet, Ch. Proye, Catherine Bauters, Degand Pm, C. Waterlot, M. Decoulx, Aubert Jp, J.-L. Wémeau, Didier Dewailly, Porchet N
Publikováno v:
Clinical Endocrinology. 51:109-113
OBJECTIVE Multiple endocrine neoplasia type 1 (MEN1) is an autosomal genetic disorder, the clinical phenotype of which includes tumours of the parathyroids and/or anterior pituitary and/or endocrine pancreas. The genetic defect has been mapped to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28c5cef977b0dbbc3187269b30178451
https://doi.org/10.1046/j.1365-2265.1999.00747.x
https://doi.org/10.1046/j.1365-2265.1999.00747.x
Autor:
Jean Lefebvre, M. Decoulx, François Pattou, Charles Proye, Bruno Carnaille, Michèle d’Herbomez
Publikováno v:
World Journal of Surgery. 22:1218-1224
Intraoperative hormonal measurements have been used successfully to guide the surgical treatment of various endocrine diseases. In this study, we report the results of intraoperative insulin measurement (IIM) in patients with organic hypoglycemia. II
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1dc10fcf1752455630a68973b476d34
https://doi.org/10.1007/s002689900548
https://doi.org/10.1007/s002689900548
Autor:
M Brouillard, A Louville, JM Gillot, I Tillie, B. Devulder, M Decoulx, Emmanuel Delaporte, André-Bernard Tonnel, E. Hachulla, P.Y. Hatron, E Houvenagel, Frédéric Piette
Publikováno v:
La Revue de Médecine Interne. 17:541-544
Resume La polychondrite atrophiante est une maladie inflammatoire revelee une t'ois sur deux par une chondrite caracteristique auriculaire ou nasale, plus rarement par des manifestations beaucoup moins evocatrices comme une polyarthrite, une Symptoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60680abf3978caac20792c15ea752901
https://doi.org/10.1016/0248-8663(96)83089-x
https://doi.org/10.1016/0248-8663(96)83089-x
Autor:
C. A. G. Proye, D. H. R. Dromer, B. M. Carnaille, A. J. P. Gontier, A. Goropoulos, P. Carpentier, J. Lefebvre, M. Decoulx, J. L. Wemeau, P. Fossati, C. Sulman
Publikováno v:
World Journal of Surgery. 16:640-645
From 1964 to 1989, bone metastases were found in 28 of 600 patients operated on for differentiated thyroid carcinoma. Bone metastasis was the presenting symptom in 15 (54%) patients, was detected from the initial symptom in 4 (14.5%) patients, and oc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfa6fb3946a9f1d4a23193cca8d01c64
https://doi.org/10.1007/bf02067343
https://doi.org/10.1007/bf02067343
Autor:
Jean-Louis Wémeau, Armelle Fayard, Michèle d’Herbomez, Catherine Bauters, M. Decoulx, Virginie Vlaeminck-Guillem, Pascal Pigny
Publikováno v:
The Journal of clinical endocrinology and metabolism. 86(7)
Pseudohypoparathyroidism Ia (PHP Ia) is characterized by resistance to PTH and many other stimuli because of deficiency of stimulatory G protein alpha-subunit. To determine the incidence, natural history, and mechanism of C cell dysfunction in PHP, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33aa24ea0790ba943b36ccff8fd5adc6
https://pubmed.ncbi.nlm.nih.gov/11443172
https://pubmed.ncbi.nlm.nih.gov/11443172
Publikováno v:
Presse medicale (Paris, France : 1983). 30(2)
THE APOPTOTIC FAS/FAS-L PATHWAY: Represents a major apoptotic pathway and involves the specific interaction between a membrane receptor, Fas, harbored by the target cell and a membrane ligand, Fas-L, harbored by the cytotoxic cell. FAS AND NORMAL THY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22daffdf8a62b01798cbdda2ee92d8b6
https://pubmed.ncbi.nlm.nih.gov/11244819
https://pubmed.ncbi.nlm.nih.gov/11244819
Autor:
D, Ferriby, J, de Seze, T, Stojkovic, E, Hachulla, B, Wallaert, S, Blond, A, Destée, P Y, Hatron, M, Decoulx, P, Vermersch
Publikováno v:
Revue neurologique. 156(11)
Neurological impairment is a frequent cause of morbidity and mortality in patients with sarcoidosis. The aim of this study was to evaluate the clinical manifestations of the disease, the response to corticosteroids and alternative treatments. During
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51b6db93885250dcc804ac7b8a3cc9c4
https://pubmed.ncbi.nlm.nih.gov/11119048
https://pubmed.ncbi.nlm.nih.gov/11119048
Publikováno v:
Annales d'endocrinologie. 61(3)
Syndromes of resistance to thyroid hormone (RTH) are almost always linked to a defective triiodothyronine-receptor B gene (TRB). Only six families with RTH exhibiting a normal TRB gene have been reported so far. We report another and discuss possible
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0801b597d60bd98feca32212c69f5298
https://pubmed.ncbi.nlm.nih.gov/10970943
https://pubmed.ncbi.nlm.nih.gov/10970943