About: Philippe Chanson

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher ORCID ID = 0000-0001-5096-5722

Attributes	Values
rdf:type	Item
description	forskare (sv) forsker (nb) 연구원 (ko) araştırmacı (tr) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) investigador francés (es) chercheur français (fr) investigador francés (ast) Frans onderzoeker (nl) ikertzaile frantziarra (eu) investigador francès (ca) investigador francés (gl) investigador francês (pt) ricercatore francese (it) researcher ORCID ID = 0000-0001-5096-5722 (en)
rdfs:label	P. Chanson (nl) P. Chanson (sl) P. Chanson (ast) Philippe Chanson (ca) Philippe Chanson (en) Philippe Chanson (es) Philippe Chanson (fr) Philippe Chanson (nb)
skos:prefLabel	P. Chanson (nl) P. Chanson (sl) P. Chanson (ast) Philippe Chanson (ca) Philippe Chanson (en) Philippe Chanson (es) Philippe Chanson (fr) Philippe Chanson (nb)
name	P. Chanson (nl) P. Chanson (sl) P. Chanson (ast) Philippe Chanson (ca) Philippe Chanson (en) Philippe Chanson (es) Philippe Chanson (fr) Philippe Chanson (nb)
given name	wds:Q58441504-213BCBE9-A07A-41EF-A99F-1332326AB055
given name	Philippe
instance of	wds:Q58441504-D7DA1588-7986-47AD-B547-985260E7219E
instance of	Homo sapiens
skos:altLabel	P. Chanson (en)
occupation	wds:Q58441504-75AD30AE-1AA1-46D3-B606-938E77483C34
KBR person ID	wds:Q58441504-D4DE14AE-501E-4B21-93D3-8B2C55CBA6B0
NUKAT ID	wds:Q58441504-1FC791EF-0EF7-44BA-8A05-B84BA46564A9
languages spoken, written or signed	wds:Q58441504-AB197A17-4468-47D8-B458-96118A4F9F31
sex or gender	wds:Q58441504-E32F9324-0DA0-4FD1-A28C-FDE30E12FC84
ISNI	wds:Q58441504-2820E92B-1B62-4235-99F8-8BBE8282AD19
VIAF ID	wds:Q58441504-98C22F6E-4AC8-40D5-9E31-C3B9E66034A6
GND ID	wds:Q58441504-28a1b680-0893-44cc-b628-580b28aa8580
IdRef ID	wds:Q58441504-299CE860-CAA3-470A-A5BD-8C02BFC680F2
country of citizenship	wds:Q58441504-7B6282A7-ED57-4835-818B-049D86905646
date of birth	wds:Q58441504-77AB9DD5-C8D7-4F96-9D9E-5A23DCAF0DA9
National Library of Israel J9U ID	wds:Q58441504-D2C001D2-ABFF-4F74-B1B0-508D005E99CF
VIAF ID	http://viaf.org/viaf/45356370
GND ID	https://d-nb.info/gnd/1103821237
IdRef ID	http://www.idref.fr/029294452/id
occupation	researcher
KBR person ID	14033993
NUKAT ID	n2014009227
languages spoken, written or signed	French
sex or gender	male
ISNI	0000000035894746
VIAF ID	45356370
GND ID	1103821237
IdRef ID	029294452
country of citizenship	France
date of birth	1955-01-01 00:00:00Z (xsd:dateTime)
National Library of Israel J9U ID	987007376169905171
ORCID iD	wds:Q58441504-80B81F8F-B0BB-4FC2-B18C-F1EF798E3872
ORCID iD	https://orcid.org/0000-0001-5096-5722
ORCID iD	0000-0001-5096-5722
ResearcherID	wds:Q58441504-8142B31B-E857-4FF1-90E5-15AA45F869EB
ResearcherID	F-8511-2013
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58441504
is author of	Impact of growth hormone (GH) treatment on cardiovascular risk factors in GH-deficient adults: a Metaanalysis of Blinded, Randomized, Placebo-Controlled Trials Impact of successful treatment of acromegaly on overnight heart rate variability and sleep apnea Expert consensus document: A consensus on the medical treatment of acromegaly Gross total resection or debulking of pituitary adenomas improves hormonal control of acromegaly by somatostatin analogs. Metabolic syndrome in Cushing's syndrome Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation Acromegaly Pituitary magnetic resonance imaging findings do not influence surgical outcome in adrenocorticotropin-secreting microadenomas Place of cabergoline in acromegaly: a meta-analysis. The European Registry on Cushing's syndrome: 2-year experience. Baseline demographic and clinical characteristics Cinacalcet reduces serum calcium concentrations in patients with intractable primary hyperparathyroidism Germline AIP mutations in apparently sporadic pituitary adenomas: prevalence in a prospective single-center cohort of 443 patients. Epithelial sodium channel is a key mediator of growth hormone-induced sodium retention in acromegaly. Effects of somatostatin analogs on glucose homeostasis: a metaanalysis of acromegaly studies. Outcome of gamma knife radiosurgery in 82 patients with acromegaly: correlation with initial hypersecretion GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships Kallmann's syndrome: a comparison of the reproductive phenotypes in men carrying KAL1 and FGFR1/KAL2 mutations Long-term effects of pegvisomant on comorbidities in patients with acromegaly: a retrospective single-center study.

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