About: Jean-François Chateil

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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 = 0000-0002-6143-7607

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) wetenschapper (nl) дослідник (uk) researcher ORCID ID = 0000-0002-6143-7607 (en)
rdfs:label	Jean-François Chateil (en) Jean-François Chateil (es) Jean-François Chateil (fr) Jean-François Chateil (nl) Jean-François Chateil (ast)
skos:prefLabel	Jean-François Chateil (en) Jean-François Chateil (es) Jean-François Chateil (fr) Jean-François Chateil (nl) Jean-François Chateil (ast)
name	Jean-François Chateil (en) Jean-François Chateil (es) Jean-François Chateil (fr) Jean-François Chateil (nl) Jean-François Chateil (ast)
given name	wds:Q58831547-F0B8FB37-A9BC-477E-8CF4-DF0CCF3B0C87
given name	Jean-François
instance of	wds:Q58831547-1D8AEB14-95F7-401F-82AE-F0FA3126FED3
instance of	Homo sapiens
doctoral student	wds:Q58831547-7FE69335-C972-4B86-A540-168D77448136
doctoral student	Jean-Jacques Nathan
occupation	wds:Q58831547-FED7285D-A6C4-44AC-AED1-2A7F5962949D
employer	wds:Q58831547-5B50040D-904D-4FD0-8841-5835F2D632F3
sex or gender	wds:Q58831547-79304c11-7451-413e-b66e-31339e3bcc00
ISNI	wds:Q58831547-1E932231-187F-4068-BDB2-3E4B52A00685
VIAF ID	wds:Q58831547-36523F8B-ACB0-4A09-8900-C481F68B4E11
IdRef ID	wds:Q58831547-D34E33E0-AD64-4C32-A6CF-6AB5A03D0E6E
date of birth	wds:Q58831547-500AD34A-E5C6-48B1-9B1F-B0FAE1BFCB04
VIAF ID	http://viaf.org/viaf/69151958
IdRef ID	http://www.idref.fr/061732184/id
occupation	researcher
employer	University of Bordeaux
sex or gender	male
ISNI	0000000358895292
VIAF ID	69151958
IdRef ID	061732184
date of birth	1958-01-01 00:00:00Z (xsd:dateTime)
ORCID iD	wds:Q58831547-E8E0991F-F57B-475C-BFBC-8001EC700E3A
ORCID iD	https://orcid.org/0000-0002-6143-7607
ORCID iD	0000-0002-6143-7607
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58831547
is author of	Water excitation as an alternative to fat saturation in MR imaging: preliminary results in musculoskeletal imaging. Are the studies on cancer risk from CT scans biased by indication? Elements of answer from a large-scale cohort study in France Quiet Submillimeter MR Imaging of the Lung Is Feasible with a PETRA Sequence at 1.5 T. Bardet-biedl syndrome and brain abnormalities. Costello syndrome and neurological abnormalities Breast metastases in adolescent girls: US findings Imaging referral guidelines in Europe: now and in the future-EC Referral Guidelines Workshop Proceedings A prospective study of risk for Sturge-Weber syndrome in children with upper facial port-wine stain [Including exposure dose in radiological reports: how? why?] Radiation exposure from CT in early childhood: a French large-scale multicentre study. X-linked dominant chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia. Cranial aneurysmal bone cysts presenting with raised intracranial pressure: report of two cases [Para-articular and intraosseous synovial cysts and articular mucoid cysts] Radiography of scoliosis: Comparative dose levels and image quality between a dynamic flat-panel detector and a slot-scanning device (EOS system). Abdominal cystic lymphangiomas in children: presurgical evaluation with imaging MRI and clinical differences between optic pathway tumours in children with and without neurofibromatosis. Lung morphology assessment of cystic fibrosis using MRI with ultra-short echo time at submillimeter spatial resolution. [New tools in cystic fibrosis]. Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases [Radiation protection: current considerations] [Imaging of scoliosis] Capillary haemangioma of the greater omentum in a 5-month-old female infant: a case report [Superior sagittal sinus thrombosis in children during the first year of life: clinical aspects, imaging and development] Giant cystic Schmorl's nodes: imaging findings in six patients [French regulation for radiation dose control in paediatric radiography]. Diagnostic performance of an unenhanced MRI exam for tumor follow-up of the optic pathway gliomas in children [Imaging of Erdheim-Chester disease] 2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene. Ostéoarthropathie hypertrophique primitive familiale et dermatite atopique (maladie de Currarino) [Fetus in fetu and acardiac monster: can the similar patterns of these 2 malformations be explained by a common morphogenic mechanism?] [Acute torsion of an accessory spleen] Association of external auditory canal atresia, vertical talus, and hypertelorism: Confirmation of rasmussen syndrome Portal vein thrombosis after splenectomy for hereditary stomatocytosis in childhood Oculo-ectodermal syndrome: a new tumour predisposition syndrome [Radiologic change of cartilage of the pelvis and the upper end of the femur during growth. Application to the surveillance of scolioses] Duplication of PTHLH causes osteochondroplasia with a combined brachydactyly type E/A1 phenotype with disturbed bone maturation and rhizomelia Brachydactyly type A1 with short humerus and associated skeletal features Allergic Bronchopulmonary Aspergillosis in Cystic Fibrosis: MR Imaging of Airway Mucus Contrasts as a Tool for Diagnosis. Prognostic value of MR in term neonates with neonatal hypoxic-ischemic encephalopath: MRI score and spectroscopy. About 26 cases Childhood CT scans and cancer risk: impact of predisposing factors for cancer on the risk estimates. A patient with hydranencephaly and PEHO-like dysmorphic features. Cranial ultrasonography and transfontanellar Doppler in premature neonates (24-32 weeks of gestation): dynamic evolution and association with a severe adverse neurological outcome at hospital discharge in the Aquitaine cohort, 2003-2005. Phenotypic variability in van der Woude syndrome SMAD4 Germinal Mosaicism in a Family with Juvenile Polyposis and Hypertrophic Osteoarthropathy [Value of x-ray computed tomography in histiocytic involvements of the base of the skull in children] Antenatal diagnosis of lung malformations. Apropos of 9 case reports [Ectasia of the umbilical recess during the antenatal period. 3 case reports] Severe presentation of Peters'-Plus syndrome Abdominal lymphatic dysplasia and 22q11 microdeletion Pelizaeus-Merzbacher disease: the diagnostic contribution of MRI [Color Doppler sonography of superficial capillary hemangiomas] [Tuberous sclerosis (Bourneville disease)]

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